Sunday, April 16, 2017

Dialysis and Engineering an Artificial Kidney Update, Dialysis Ethics

Kidney Research

From Engineering.com, by Michael Molitch-Hou

How to Engineer a Kidney

In 1982, a young student named Dahai Ding sat glumly in his classroom at Worcester Polytechnic Institute when his English professor, Kay Draper, asked him about what appeared to be a deep depression. He told her that his sister, Dadi Ding, was stuck in China, suffering from end-stage kidney disease, where, without access to dialysis or a kidney transplant, she would die.

It was then that Draper was introduced by the dean of the university to my mother, Dr. Susan Hou, then a nephrologist at Tufts University. Along with my family and her local community, Draper launched a campaign to get Dadi to the United States, where she would receive her first kidney transplant.

Kidney transplants and dialysis are the only methods for treating kidney failure. These solutions, however, have proven problematic for numerous reasons, causing researchers to explore new ways of treating kidney failure, including the construction of artificial, biomechanical kidneys or bioprinting new organs from the patient’s own cells.

Such exciting treatments aren’t yet available to kidney patients, but many people are eagerly waiting for science fiction like artificial and bioprinted kidneys to become a reality. To learn about these technologies and how they could play a role in the lives of people like my godmother, Dadi, and my own mother, I spoke to a variety of researchers in the field.


A Kidney Patient in China

Jump back to 1956, in Shanghai. Dadi and her family learned that she had kidney problems when she was just two years old, because there was blood in her urine. Her doctor’s treatment involved a mix of herbal remedies and Western medicine, but the treatment was not successful, and every time she caught a cold, the disease would be exacerbated. The situation did not change until she was about eight years old, when she met a doctor who tried to strengthen her immune system and, therefore, reduce the frequency with which she would have a cold and blood in her urine. The treatment seemed to work for sometime, but, when the Cultural Revolution occurred, her primary doctor was sent to perform custodial work, according to Dadi. Meanwhile, Dadi’s parents, U.S.-educated professors, were sent to labor camps. A 12-year-old living alone in Shanghai, Dadi said that she sought relief from the foul-tasting Chinese herbal medicine she had to take regularly and decided to skip out on the treatment altogether.

After several years, without the proper medication, Dadi’s body became very swollen and she began excreting protein in her urine. By the time the Cultural Revolution was over and her doctor was allowed to return to his practice, there was little he could do to reverse the damage already done to her kidneys. In China at the time, dialysis was not available, while kidney transplants had only been performeda handful of times at an experimental level.

“I was admitted to the hospital and there was a girl in the same ward with me, a little bit older than me—in her twenties,” Dadi said. “And she just died. I saw her die in the bed right next to me because of exactly the same disease I had. I realized that that could be me. I saw a lot of a doctors, even went to different cities to see famous doctors, and they all said the same thing.” Without a transplant or dialysis, the consensus opinion from all of the doctors that she saw—even those considered the most qualified experts in the country—was the same: her condition was fatal.

Thankfully, Dahai was already in the U.S. where such treatments were available. Draper was able to set up a nonprofit organization with which to legally raise funds for Dadi. Japan Airlines agreed to fund half of her airfare to travel to the United States and, over the course of a couple of months, Draper managed to raise the over $40,000 necessary to perform a kidney transplant.

How Does the Kidney Work?

Made up of about one million filtering units called nephrons, the kidney is essential to filtering the waste that passes through the bloodstream, as well as participating in homeostasis in the body. Within a nephron, the glomeruli are an elaborate tuft of blood vessels that keep proteins inside the blood vessels and filter out other material.

The resulting fluid is passed through a structure called the tubule, where specialized cells in its lining reabsorb water and necessary minerals back into the body, while the remaining waste-containing liquid is sent to the bladder to be excreted as urine.

Throughout the long, windy structure of each nephron, minerals and other molecules are reabsorbed into the body, while waste is sent to the bladder for excretion. (Image courtesy of Wikipedia.)


The nephrons don’t just arbitrarily reabsorb what the body needs and get rid of what it doesn’t, but do so at levels appropriate for the body to maintain homeostasis. For instance, if you drink too much water, the kidney will send more of the liquid to be excreted as urine. If you drink too little, the kidney will ensure that more water is reabsorbed into the bloodstream. The same is true for molecules like glucose and calcium. If a disease or toxin disrupts the function of the kidneys, waste may not be disposed of properly or homeostasis may be disrupted.


Kidneys in America

When you think about it, even the most rudimentary forms of organ transplant are fascinating. Taking a vital piece of one person’s body and placing it into another’s is mad science at its best, but getting those organs to work isn’t easy. Not only must the blood types of donors and recipients be compatible, but so must their human leukocyte antigen (HLA) type. HLA antigens are what enable the immune system to distinguish between one person and a foreign body, such as a transplanted organ. Once the immune system recognizes the kidney as being foreign, it treats it like bacterial in an infection and tries to destroy it.

Dahai was set to be Dadi’s donor, but the siblings learned that their crossmatch was positive. Upon introducing her blood to his, their antibodies immediately reacted to destroy the foreign element. This positive crossmatch suggested that Dahai’s kidney would be instantly rejected if it were implanted into Dadi. A transplant from her brother was not the only option, however. “In 1982, a surgeon that received a deceased donor was required to give one kidney to the national waiting list, but was able to give the other to his or her own patient,” my mother explained. “So, when a deceased donor came into Tufts, the surgeon was able to give one of the kidneys to Dadi.”

The donor kidney came from a young person who had died in a motorcycle accident, meaning that the kidney was relatively healthy. Nevertheless, it lasted only a week before Dadi’s body rejected it and the organ had to be removed. “At the time, the immunosuppressants weren’t as effective as what we use today,” Dadi told me. “A new medication called cyclosporine was in experimental trials, but not at Tufts, where I was having my transplant done.”

Dadi was then placed on the national waiting list, as she awaited another deceased donor. This process can take quite a long time; in her case, it was seven years. During that time, Dadi studied to become a nephrology nurse, got married and her life was sustained by peritoneal dialysis (PD).


Peritoneal Dialysis vs. Hemodialysis

Outside of actual kidney transplants, any technology used to treat kidney failure attempts to replicate the function of an actual kidney. This is done through the use of a system that features a semipermeable membrane for removing waste and excess water from the blood.
PD is a more affordable form of dialysis because it does not require a machine or specialized dialysis facility for treatment. (Image courtesy of Wikipedia.)

In the case of PD, that membrane is already in the body. PD gets its name because, to replace the function of the kidney, it relies on the peritoneum, a membrane coating the abdomen that is responsible for exchanging fluid and dissolved substances with the blood. A catheter is inserted into the abdominal cavity, which is filled with a specialty solution called dialysate. The membrane ultra filters the blood, causing waste products and excess fluid to flow into the dialysate, which is then drained and replaced with fresh solution.

While on PD and studying at nursing school, Dadi said that it was possible for her to fill her abdomen with fresh dialysate before heading to class until, after about four or five hours, she would go somewhere private, drain the waste fluid, and pour in some new dialysate once again. Although this process of continuous ambulatory peritoneal dialysis made it possible for Dadi to go about her daily life while undergoing treatment, she ultimately began to suffer from complications. The glucose in the solution caused her peritoneum to thicken to the point that it no longer functioned as an effective filter.

At this point, she switched to hemodialysis. Instead of an organic membrane within the body, hemodialysis relies on an external machine. Blood flows from a surgically altered blood vessel called a fistula in a patient’s arm into the dialysis machine, which includes a dialyzer made up of hollow synthetic fibers that ultrafilter out waste and excess fluid while dialysate cleans the blood. The cleaned blood is then returned to the body through a second needle. This process continues for three to four hours and must be performed at least three times a week to effectively clean the blood.
In hemodialysis, blood is pumped out of the patient into a filtering system, where the blood is cleaned and sent back into the patient’s body. The process only removes about 15 percent of the body’s necessary waste. (Image courtesy of Wikipedia.)

Switching to hemodialysis, Dadi was able to trade in the complications of PD for a whole new set. Although hemodialysis is more efficient at removing waste from the body and causes no risk to the abdomen, as with PD, it is necessary in this process for the patient to receive treatment at specific facilities overseen by trained staff.

By this time, Dadi actually became one of these trained staff members as a registered nurse who oversaw a dialysis unit. As it is for all such dialysis patients, she found it difficult to both work and dialyze three to four hours three days a week. Fortunately for her, she adopted home hemodialysis. This has allowed her to perform the treatment during flexible hours, usually at night while she tries to sleep.

Dadi explained that dialysis is only capable of removing about 15 percent of the waste that must be removed from her body. My mom pointed out that this can be improved by dialyzing longer, more frequently or through improvements in the machine technology. “The efficiency of a dialysis machine is determined by the size and how fast the blood moves through the dialyzer,” my mom explained, “as well as how big the holes are in the dialyzer. They have to be big enough to get rid of the waste, but without removing blood cells and proteins.”


The Artificial Kidney: The Future of Dialysis?

Dr. Shuvo Roy, of the University of California San Francisco, and Dr. William H. Fissell IV, of Vanderbilt University Medical Center, are in the process of developing a unique device that acts almost as a biomechanical, implantable dialysis machine. While it is mechanical in nature, the “artificial kidney” uses kidney cells and silicon membranes to replicate the function of a kidney, providing additional functions beyond current dialysis machines. I asked Dr. Roy to explain exactly how it works.
The artificial kidney will be roughly the size of a coffee cup and powered by the pumping of the body’s own blood. (Image courtesy of UCSF.)

“The artificial kidney device consists of two implanted modules that work together to get rid of wastes,” Dr. Roy said. “First, a hemofilter module processes incoming blood to create a watery ultrafiltrate that contains dissolved toxins as well as sugars and salts. Second, a bioreactor of kidney cells processes the ultrafiltrate and sends the sugars and salts back into the blood. In the process, water is also reabsorbed back into the body, concentrating the ultrafiltrate into ‘urine,’ which will be directed to the bladder for excretion.”

Key to the device is the use of actual kidney proximal tubule cells, which are grown on silicon nanomembranes, according to Dr. Roy. This makes it possible for water, salts, glucose, amino acids and other small molecules to pass through the device freely. “These nourish the kidney cells, and the porous nature of the membranes also allows the cells to dispose of small wastes, such as carbon dioxide,” Dr. Roy explained. “The silicon nanomembranes also provides immunoisolation for the kidney cells. The immune system relies on fairly large molecules (antibodies) to identify and attach foreign intruders, which are a thousand times larger than small nourishing components such as glucose. These molecules are too large to penetrate the sieve of the membrane supporting the kidney cells.”

Altogether, the device may be more effective than dialysis, not only because it provides continuous blood filtration, but also because it does so with silicon nanomembranes and actual kidney cells. These silicon nanomembranes make it possible to shrink the device down to an implantable size, but also perform better than the plastic components used in existing dialysis machines. Whereas hemofilters for dialysis machines have a surface area of about 2 square meters, the silicon filters that Roy’s lab uses are one-twentieth of the size.

“Traditional dialysis machines remove blood from the patient, filter it through an external machine, and then return the blood to the patient,” Dr. Roy said. “The implanted artificial kidney will allow the filtration to occur continuously, and within the patient’s body, removing the need to be tethered to an external machine. Human kidneys conduct these functions through hundreds of thousands of kidney cells. The artificial kidney performs blood filtration through the use of silicon nanomembranes instead of polymer membranes that are used in conventional dialysis. In addition, the artificial kidney contains kidney cells in the bioreactor to provide biological functions that dialysis simply cannot.”

For the team, the long-term challenges associated with the artificial kidney are keeping it operational and troublefree after implantation. All of the potential issues won’t be known until clinical trials begin in the next year or so. For the time being, Dr. Roy is examining ways for increasing the lifetime of the kidney cells and methods for

ensuring the absence of blood clots. This includes coating the nanomembranes with molecules that make them “blood-friendly.”

As a part of a three-phase program, the lab has already established concept feasibility for externally testing the hemofilter and bioreactor in ICU patients before shrinking the size of the device so that it can be small enough for permanent implantation.

“Currently, we are in Phase II,” Dr. Roy explained. “We are working on engineering refinements to the device components, continuing experiments on the bioreactor to study the conditions that allow the kidney cells to grow and remain healthy, and we have begun a rigorous series of preclinical animal studies for the hemofilter.”

Phase III will begin in late 2017 or in 2018, at which point clinical trials of the hemofilter will begin to demonstrate the device’s safety. This may expedite clinical trials of the combined hemofilter and bioreactor design and, ultimately, pave the way for more streamlined testing of the combined device.

“Once the bioreactor has completed its own set of rigorous preclinical animal studies, we will begin the combined device clinical trials. During clinical trials, we will work with manufacturers to discuss and manage the details of production. Once the clinical trials are complete, we anticipate that the device will be available for patients shortly thereafter,” Dr. Roy said.

Although Dr. Roy’s team uses 3D printing to create plastic housing for the lab’s prototypes and evaluate surgical considerations for the implanted design, no bioprinting is currently used for the kidney cells. That possibility has not yet been ruled out, however. “Bioprinting may be an interesting tool to use in the development of the bioreactor,” Dr. Roy explained. “As bioprinting technology matures for various kidney cells, we could explore it as an advanced tactic to creating a bioartificial kidney.” [Read more]


Dialysis

From Medscape, by Tejas P. Desai, MD



The Monetary Strains of Dialysis Therapy

Think of a nephrologist, and you will invariably think of dialysis. Perhaps no treatment is as synonymous with a kidney doctor as this remarkable procedure. Since its first use in the mid-twentieth century, dialysis has extended and saved innumerable lives while concomitantly helping to usher modern medicine into a new world.

In this world, many of the physiologic functions of the kidney are married with the automation of machines. Elapsing decades have seen refinements in the procedure. Years of research have culminated in an improved understanding of how best to use dialysis to achieve better clinical outcomes.

Today, dialysis machines are smaller, portable, more efficient, and safer for patients. Indeed these refinements have spread throughout the world, and more patients today have access to and receive dialysis therapy than at any time previously.

Despite these advances and the overwhelming, undeniable progress that scientists have made, dialysis therapy remains a challenging option for many patients. Perhaps that is because kidney transplantation (also starting near the mid-twentieth century) has arguably surpassed dialysis progress in two important areas: clinical outcomes and long-term financial costs. Indeed, the latter appears to be the "Achilles heel" for dialysis. The passage of time has not yielded a sufficiently cost-effective model for chronic dialysis administration. Providing modern dialysis therapy to patients is increasingly expensive no matter where in the world you are. The monetary strains are apparent to many global nephrology providers.

Couple the expense with clinical outcomes that have fallen behind those seen after kidney transplantation, and many wonder if it is time to limit the use of dialysis. A number of providers and governmental bodies have linked the outcomes of dialysis with its costs and the costs for alternative care. Many have concluded that "less bang for more bucks" does not justify dialysis administration as it currently exists.


Four Things to Consider in the Ethical Delivery of Dialysis

So can providers develop rational constraints, possibly grounded in the ethics of modern medicine, to simultaneously provide dialysis therapy to patients and ease the financial strain shouldered by those patients (or their national/local governments)? A recent publication in the Lancet tackles the issues surrounding this question.[1]

For those providers who aren't experts in medicine, a good rule of thumb to ensure that our decisions are ethically sound is to question whether we are acting in the best "interest" of our patient. I contend that the real question isn't what's in the best interest of a patient but rather what are the patient's interests.

This article touches on four areas of interest that can affect the ethical delivery of dialysis therapy. To start, the most obvious patient interest is the quality of dialysis care received. Patients and providers want to provide the highest-quality dialysis care, but in many healthcare systems, such care is costly, and those costs are borne by the providers themselves.

The authors note: "Physicians and dialysis centres might also compromise patient care to reduce costs, increase profits, or provide care to more patients." In some cases, the quality of preventive care is strikingly low because existing financial constructs disincentivize providers from investing in such strategies. No single provider can mitigate financial considerations that deter the delivery of the highest quality dialysis care. What we need are institutional or system-level changes to ensure that the patients' interest in quality of care is aligned with financing mechanisms that incentivize its delivery.

A second patient interest focuses on direct medical costs. For many patients around the world, the costs of each dialysis session are borne exclusively by them. Patients in many low-income countries (LICs) or low-middle income countries (LMICs) do not receive subsidized medical care and must pay a la carte for the dialysis therapy they receive. While the actual cost of a year's worth of dialysis is considerably less in LICs or LMICs (eg, US$3200 in India vs US$31,000 in the United States), the vast majority of patients would not be able to afford it. [Read more]
 

Sunday, April 9, 2017

PKD Treatment: Tolvaptan Update , PKD Research: Genes Linked to PKD, Challenging PKD Disability Decision

PKD Treatment

From Renal and Urology News, Jody A. Charnow, Editor
Tolvaptan Offers Sustained Slowing of Renal Function Decline in ADPKD


Tolvaptan treatment has a sustained disease-modifying effect on estimated glomerular filtration rate (eGFR) in autosomal dominant polycystic kidney disease (ADPKD), but the effects of five compared to two years of treatment on total kidney volume (TKV) were not significantly different, according to a new study.

The open-label extension trial, TEMPO (Tolvaptan Efficacy and safety in Management of Polycystic kidney disease and its Outcomes) 4:4, provided an additional 2 years of data on the long-term safety and efficacy of tolvaptan on TKV and eGFR among patients completing the pivotal TEMPO 3:4 trial. In TEMPO 3:4, tolvaptan, a vasopressin V2 receptor antagonist, slowed TKV growth by 49.2% and eGFR decline by 26% compared with placebo.

Of 1445 patients randomized to TEMPO 3:4, 871 (60.3%) enrolled in TEMPO 4:4. The group included 557 patients who received prior tolvaptan (early-treated group) and 314 who received prior placebo (delayed-treated group) in TEMPO 3:4.

From TEMPO 3:4 baseline to TEMPO 4:4 Month 24, TKV increased by 29.9% in early-treated patients and 31.6% in delayed-treated patients, a between-group difference that was not statistically significant, Vicente E. Torres, MD, of Mayo Clinic in Rochester, Minnesota, and colleagues reported in a paper published online ahead of print in Nephrology Dialysis Transplantation. TKV increases in both early- and delayed-treated patients were less than the increase estimated to have occurred without treatment (approximately 40%). The inability to demonstrate that the early treatment advantage on TKV achieved during TEMPO 3:4 was maintained at the end of TEMPO 4:4 may be accounted for by randomization imbalances that developed in the transition from TEMPO 3:4 to TEMPO 4:4 and by the fact that the tolvaptan effect on TKV is greatest during the first year of treatment, according to the investigators. Adjusting for baseline covariates improved the TKV treatment difference at month 24 in TEMPO 4:4 from 1.70% to 4.15% between the groups, a statistically significant difference.

Slopes of TKV growth during TEMPO 4:4 were higher in early- versus delayed-treatment groups (6.16% vs 4.96% per year).

Data showed that the effect of tolvaptan on slowing renal function decline in TEMPO 3:4 was maintained for an additional 2 years in TEMPO 4:4. The eGFR slopes in TEMPO 4:4 were similar in early and delayed-treated patients (−3.26 and −3.14 mL/min/1.73 m2 per year, respectively) compared with placebo.

The tolvaptan safety profile in TEMPO 4:4 was similar to that in TEMPO 3:4, Dr Torres' team reported.




PKD Research

From Yale News, Yale University, By Ziba Kashef

Study finds four genes linked to cystic diseases of the liver and kidney


Yale researchers are studying kidney and liver diseases to determine which genes are involved in the formation of cysts.

In order to diagnose and find treatments for a genetic disorder, scientists need to identify which gene mutations cause the disease. A common and often devastating genetic disease known as polycystic kidney disease (PKD) results in cysts in both the kidney and liver. Cysts are pockets of fluid in an organ that develop over time and crowd out the normal functioning parts. The more common form of PKD that affects adults and approximately half of their children, typically leads to kidney failure by the sixth decade of life. It is caused by mutations in the genes PKD1 or PKD2. The more rare juvenile form is caused by mutations inherited from both parents in a gene called PKHD1.

Researchers in the lab of Yale nephrologist Dr. Stefan Somlo have found that some patients have only liver cysts, not kidney cysts, and thus don’t get kidney failure. This disease, known as isolated polycystic liver disease (PCLD), is typically benign but can lead to symptoms in rare cases where the liver becomes very large. Nonetheless cysts form due to a dysregulation of the same disease process as those in the kidney, the details of which are an important area of investigation. To deepen understanding of why liver and kidney cysts form, a Yale-led research team examined the genes of patients with liver cysts.

Through sequencing of patient genomes and computer analyses, the researchers identified four additional genes associated with PLCD. This discovery demonstrated that many different genes are involved in the process of cyst formation. Interestingly, one of the identified genes was PKHD1, suggesting that a subset of carriers of PKHD1 mutations (parents of children with the juvenile form of PKD) can present with PCLD.

This finding supports a common mechanism of disease between both the adult and juvenile PKD and PCLD. Researchers, such as first author Whitney Besse, a clinical fellow in medicine, hope that through improving understanding of the genes involved in cyst formation, an effective treatment can be developed. It could be hypothesized now that blocking a single pathway could cure all of these diseases, said Besse. She and her colleagues plan to further study the underlying mechanisms of these diseases and how they might interact.

Read the fully study, published in the Journal of Clinical Investigation.




Living with PKD

From Central Maine.com, BY BETTY ADAMS

West Gardiner man with kidney disease challenges state decision to deny him disability payments

Terrence Marks, 55, of West Gardiner, talks about his kidney disease and retirement case during an interview on Thursday in his West Gardiner home.


Terrence Marks, 55, of West Gardiner, talks about his kidney disease and retirement case during an interview on Thursday in his West Gardiner home. Staff photo by Joe Phelan


AUGUSTA — Terrence “Terry” Marks has kidneys that are twice the normal size and are doing less than a quarter of the work they should be doing to filter toxins from his system.

Symptoms of his polycystic kidney disease — now at stage 4 — forced the West Gardiner man from his job in November 2015 as part of a state highway maintenance crew that plowed roads in winter and did other jobs in the summer.

Marks, 55, has seen his disability retirement application rejected by the Maine Public Employees Retirement System, has been declared ineligible to collect a military retirement because his wife earns $29,000 as a clerk for the Town of West Gardiner, and is ineligible for Social Security disability benefits.

He went to the State House Friday morning to speak in favor L.D. 176, a bill that he hopes will change the laws regarding state disability retirement benefits.

However, the Legislature’s Appropriations and Financial Affairs Committee only briefly considered the bill before agreeing to carry it over to the next session. Marks was out of the hearing room when the public was invited to comment, and he missed the opportunity. In fact, no one spoke about the bill, which is a concept only and lacks specific language.

But he and his wife, Tina Marks, still plan to support a law change so others don’t run into similar problems.

“There’s no help in the state system,” Terry Marks said on Thursday as he considered what he wanted to tell the committee. “My money is sitting in the state retirement system. My money’s there. I’m getting nothing. My future retirement money’s sitting there.”

Marks was terminated in November 2015 because he was no longer physically able to perform his job after 19 years and 11 months working for the state.

For a year, the family was OK financially because he had purchased income protection insurance, but that support ended in November 2016. Now things are much tighter.

While he has medical insurance through his wife’s job, he said, “There’s lots of bills coming in that aren’t covered by insurance. I have an old junked-out pickup truck. There’s the phone, lights, heating. Once there’s no paycheck, we’re scrimping, downsizing, everything you can imagine we’re trying to streamline.”

They feel powerless.

“This isn’t my master plan,” Marks said. “We were going to retire and venture out and do the day trips. We were going to enjoy our retirement. Our plan was not to be sick. We were going to buy a camper and go camping on weekends and travel around the state of Maine. My retirement has been altered. My plan wasn’t to get sick and end up suffering in end-stage kidney failure.”

He got news of his latest denial from the Maine Public Employees Retirement System on Wednesday.

According to Michael Colleran, general counsel for MainePERS, Marks’ case now will be considered by the system’s board of trustees. If the board upholds the hearing officer’s denial, then Marks’ only appeal would be to a superior court judge.

Data from MainePERS indicates that 82 of the 121 disability applications handled in 2016 were denied initially. It also shows that of the 73 appeals completed that year, 23 were granted.

State Sen. Shenna Bellows, D-Manchester, who is not on the committee but who attempted to aid the Marks, said afterward, “It strains credibility to me that 62 percent of the applicants for disability can be denied.”

She said she worries about how the families can survive.

“I would like to see something done that will try to make the system work for the people it’s designed to serve,” she said.

Just prior to the committee’s consideration of L.D. 176, introduced by state Rep. Robert A. Foley, R-Wells, the MainePERS system and the MainePERS Disability Retirement Task Force made presentations to the committee that appeared to address some of the concerns that Marks and others face.

Sandy Matheson, executive director of MainePERS, noted that 1,300 of 38,500 retirement member are on disability; the others are on service retirement. Another 51,000 are active members, paying into the plan.

She noted that members of MainePERS “experience varying levels of difficulty and frustration when applying for disability retirement.”

Specifically, Matheson said, the statute limits the MainePERS benefit to permanent disability.

“We know there’s a misperception of what our program is that really causes a lot of hardship and heartache for people,” Matheson told the committee.

She said that the task force looked into the costs for long-term disability insurance, which would fill in when the short-term income protection ends.

“We’re hoping to make it an opt-out, so people are aware there could be a gap in income and don’t think of our plans as disability insurance,” she said.

State Rep. Brian Hubbell, D-Bar Harbor, who serves on the committee, said, “I’m convinced we need to do that. We have to have some system to tell employees what our disability retirement program is and isn’t.”

Matheson said later that MainePERS is trying to refine its internal process to educate members and employers that the retirement system is not for long-term disability.

“You retire because you’re permanently disabled,” she said.

She told the committee that problems arise when members essentially apply too soon, when they find work difficult but are not yet permanently disabled.

Matheson also indicated that Foley’s bill is a placeholder should the agency need changes in the law.

State Sen. Roger Katz, R-Augusta, also presented a bill to give state disability retirement benefits to someone who becomes disabled after leaving state service, who is ineligible for social security disability and who prevails in or settles a claim under the state’s Whistleblowers’ Protection Act.

The first person to testify in favor of the bill was Sharon Leahy-Lind of Portland, who meets all those requirements.

In 2013, Leahy-Lind, who was director of the CDC’s Division of Local Public Health, disclosed that she was ordered by her superiors to shred documents related to competitive grant awards in the Healthy Maine Partnerships program. The documents shed light on irregularities and possible illegal activity in the way certain grants were awarded.

She later filed a whistle-blower complaint in federal court alleging retaliation for refusing to shred the documents. The lawsuit was settled.

Leahy-Lind said bonafide whistleblowers should not be denied benefits. She told the committee she had been diagnosed with pancreatic cancer after leaving state service and that the bill could potentially benefit her and protect future whistle-blowers.

“I’m not here today to seek your sympathy,” she told them. “What I’m afraid of is to live with no income, continue to liquidate my assets and leave my daughters with debt.”

Friends and former coworkers of Leahy-Lind spoke in support of the bill as well.



Betty Adams — 621-5631

Sunday, April 2, 2017

PKD Foundation Video Series, PKD: Obesity is an Issue, PKD: Its Runs in the Family, Dialysis on Cyprus

PKD Life

From PKD Foundation

Video series: Give hope

All month long, we have followed the inspiring PKD stories of the Phelps and the Wiesman families - but their journeys are far from over. Watch our video to hear more about how their connections with the PKD Foundation have helped them along the way and their hopes for the future.




From NorthGlen News, South Africa

Obesity a strong factor in developing kidney disease



OBESITY poses a huge threat in the development of kidney disease. Experts say that there is a strong link between the development of kidney disease and obesity.

“Our kidneys are one of those things we take for granted until we’re diagnosed with kidney problems only then do we start being more careful,” said Gopalan Gounden, a 62 year-old former police officer who says he had to retire due to health problems. Gounden suffers from Polycystic Kidney Disease, a hereditary illness. He urged people to take care of their body’s organs. “When you have be placed on dialysis, like me, the machine only removes certain toxins from your body, so you have to take various injections as well. Dialysis is not a replacement for all the work which your kidneys naturally do for you.”

Risk factors

Obesity increases the risk of developing factors associated with Chronic Kidney Disease (CKD), like diabetes and hypertension. These risk factors have a direct impact on the development of CKD and end stage renal disease. This is because in individuals affected by obesity, the kidneys have to work harder to filter more blood than normal to meet the metabolic demands of the increased body weight. The increase in function can damage the kidney and raise the risk of developing CKD in the long-term.
The kidneys are an essential organ to the human body. They remove toxins and excess water from the blood. Kidneys also help to control blood pressure, produce red blood cells and keep bones healthy.

Being proactive

“It’s important that people are careful and become more proactive with their health,” Gounden said. “In my case, I want people to know that taking their organs for granted has a serious impact on your lifestyle. I have to have dialysis three times a week and if I want to travel I need to make arrangements for a dialysis unit wherever I go. You also can’t travel to places where you can easily pick up an infection.”

The International Society of Nephrology and The International Federation of Kidney Foundations (the organisers of the annual awareness campaign) say that obesity, as well as CKD, is largely preventable. Education and awareness of the risks of obesity and a healthy lifestyle, including proper nutrition and exercise, can dramatically help in preventing obesity and kidney disease.




From Times-News, Burlington, By Bill Cresenzo

Mother of three, 9-year-old friend seek kidneys

Hope Foster needs a kidney.

But really she wants two: one for her young friend, Kenon, and another for herself.

Foster, 41, lives in Burlington with her husband, Danny, and her children, Kameron and twins Hayden and Sophia.

Three decades ago, her father, Duain Penland, who suffered from polycystic kidney disease, received a kidney from his wife, Nancy.

He’s done great for the past 30 years, despite other health problems.

“We call him the ‘Energizer Bunny,’” Foster said. “He ‘takes a lickin’ and keeps on tickin’.’”

Now, Foster, who inherited her father’s disease, is the one in need of a new kidney.

She recently began dialysis, three days a week for three hours and 45 minutes each time.

She spends that time volunteering for the Clover Garden Charter School parent/teacher group “to keep me busy and to not go crazy.”

FOSTER ALSO HAS forged a special bond with Kenon McCollum, a third-grader who attends Clover Garden with her son, Kameron.

The boys are good friends. They have sleepovers, and Foster is generous with pizza.

Kenon is a polite boy with a cute grin. He answers “good” to a lot of questions. He loves to play baseball and wants to be a pro baseball player when he grows up.

He helps his parents, Ashly and Brad, take care of his little brothers.

Kenon had a kidney transplant when he was just 22 months old.

But now, that kidney is failing.

So Kenon, like Foster, needs a kidney.

They have the same blood type, so they are looking for the same type of match.

“If there was an option, and if it came down to me and him, I would want him to have it first,” Foster said.

Both Foster and Kenon are on the national transplant list. The average wait time for a kidney is five to eight years.

People have been tested to see whether their kidneys were a match for Foster, but they weren’t. Even so, “they are angels,” Foster said.

The first one to test was her husband, Danny.

He wasn’t a match, but they discovered during the testing that he had kidney cancer.

He’s fine now.


APRIL IS NATIONAL Donate Life Month.

Foster and her father are encouraging people to become organ donors, whether living or deceased.

The living procedure is done laparoscopically, with doctors accessing the kidney through three little holes in the abdomen.

“It’s a gift,” Penland said.

The father and daughter say that many people are scared of the prospect of donating to someone.

“My view on organ donation is very familiar,” Foster said. “But it’s a touchy subject. If you really understand organ donation and how it works, and how many people can be affected, I think you would change your mind. No one will ever know the true meaning of organ donation until it hits your family. When it hits your family, it’s a whole different ballgame.”

For more information about becoming a living donor, got to the UNC kidney donor website athttps://tinyurl.com/mue2wlm, or contact Amy Woodard, UNC Hospitals’ living donor coordinator, at 984-974-7568.




From Cyprus Mail, by BEJAY BROWNE

Kidney charity to supply two more dialysis units

Kidney charity to supply two more dialysis units


Graham Brown receiving treatment



A PAPHOS charity is again stepping in to donate two further lifesaving dialysis machines for Paphos renal unit, which the government is unable to fund, according to the charity head.

Graham Brown, the chairman of the Paphos Kidney Association, who has hereditary polycystic kidney disease and receives regular dialysis treatment at the unit to keep him alive, told the Sunday Mail that Paphos general hospital had requested their help.

Since 2000, they have donated 12 machines.

Each hemodiafiltration (HDF) unit comes with a 25,000 euro price tag. If a patient doesn’t receive dialysis when needed, they will die within five days.

“A few weeks ago the hospital asked us to donate two more dialysis machines as the government are not helping,” Brown said. “I told them we have enough money for one, and we are collecting for the second one. We are almost there, we have about ten thousand euros to go, and we hope to get that in around six weeks.”

He added that the charity aims to supply the unit with two new machines every year to replace old ones which have a lifespan of around 14 years.

Brown said that huge efforts are being made by the community, British expat residents in particular, to support the registered charity, and that they are hoping to do more to encourage Cypriots to join in.

“We are asking the mayor of Paphos, Phedonas Phedonos, if he will be our patron, to try and get more Cypriots involved.”

Following the removal of one of his kidneys at a Paphos hospital, Brown started dialysis treatment in November 2013. He is now one of many patients who need regular dialysis treatment to keep him alive.

He said that the renal unit at Paphos general hospital now has 16 machines which are working, some better than others.

“Five are new in the last few years, their lifespan is around 14 years but many others are getting worn out,” he said, concerned that the ageing machines are unable to cope with the growing demand for lifesaving treatment. Chronic kidney failure is permanent and irreversible and the only chance of survival is to wait for a transplant.

Nurses at the unit are having to work night shifts to keep up with the demand and a much-needed proposed extension, which has been backed by the hospital director, looks set to go ahead. The extension will create at least five more beds, making treatment easier for both patients and nurses.

“We have been pushing for an extension as there are now around 75 patients needing treatment and negotiations are coming to an end and it’s looking good.”

He said the extension is vital as the current one is cramped, and there is no room between the beds.

“You can’t even get a wheel chair down the middle of them,” he said.

Currently, 12 patients receive dialysis machines in the morning, 12 in the afternoon and three times a week, eight at night time

Brown has just completed his 500th dialysis treatment, each one takes five hours and he needs them three times a week to keep him alive. It costs around €50,000 to treat each patient a year.

Brown said he can’t fault the treatment itself, or the level of care and professionalism by staff at the hospital.

“The nurses are wonderful and the support of my wife Heather has been instrumental in keeping me going, she is my rock. Without this treatment, Heather would have been a widow four years ago.”

Although Brown’s condition is getting steadily worse, he remains a driving force behind the charity and was awarded the Heart of Gold award Cyprus for his efforts in 2015.

The association has done much to improve the unit, by raising money and purchasing a huge amount of equipment since its inception 15 years ago.

“It will cost around 170,000 euros to fully equip the extension and I hope that we can achieve that also,” he said.

Brown has just been presented with a cheque for 5,500 euros from Minthis Hills golf course, and a regular monthly ‘kidney quiz’ which is held at the UKCA organised by a British expat Peter Milligan, helps too, he said.



Further information is available at the charity’s Facebook page.

To organise an event for the Paphos Kidney Association: (00 357) 99244679 www.cypruskidney.com

Sunday, March 26, 2017

PKD Life Finds a Way: Need Kidneys: Facebook in Stratford CT, Train Ads in Portland, OR

PKD Life

From Stratford Daily Voice, CT, by Donna Christopher and Karen Tensa

Retired Counselor From Bunnell High Needs Life-Saving Kidney Donation

Fairfield resident Peggy Karbovanec has stage 4 kidney disease and needs to find a donor soon.



FAIRFIELD, Conn. -- A former high school guidance counselor from Fairfield needs a kidney soon to replace her failing two.

Margaret Karbovanec has an inherited condition known as polycystic kidney disease.

She recently started a Facebook page and website to appeal to the public for help finding a live donor.

Meanwhile, Karbovanec continues to be on two deceased donor lists, one at Yale-New Haven Hospital and one at New York Presbyterian.

Between the two, she could potentially receive a kidney in as little as five years or up to 15 years.

"That might be too long," said Karbovanec who though not on dialysis yet, has only 13 percent of her own kidney function left.

"I have Stage 4 kidney disease. My doctors say it's better to receive a live donor kidney. I follow a very strict diet and try to stay healthy with walking and other ways."

Retired from Bunnell High School in Stratford Karbovanec was also an elementary school teacher in her career.

Today she enjoys bridge, travel, reading, cooking and has a full life, she said.

"I loved my career and love my life now. I want to get a kidney and continue with it," she said.

Turning to social media was a big step for this "very private person."

For a long time I didn't tell anyone I have kidney disease," she said. "I didn't use Facebook. I want people to know they can live with one kidney. If I get one they won't take the other two out, just add the third."

Karbovanec's mother had the same inherited kidney disease, but the relatives on "the other side" of her family had longevity.

"Since retiring I helped my elderly aunts, 102 and 104. I'm hoping to get rid of this problem and get on with my life."

Click here for Margaret Karbovanec's Facebook page and here for her website.





From KCBY, CBS Affiliate Coos Bay, Oregon, by Katherine Kisiel, KATU (Portland)

Man's family buys ad space on train: 'My brother needs a kidney'


PORTLAND, Ore. (KATU) — It's not a typical ad plastered on the side of the Max train. The headline: "My brother needs a kidney."

"It was the most effective thing we could imagine," said Barry Maynard. His adult son Jim suffers from polycystic kidney disease. Something that runs in the family.

Seventeen years ago Maynard donated his kidney to his wife. Now, his son is in need.

Maynard said they took a chance with the ad and it was promising at first.

"We had a flurry of responses," said Maynard.

He said nearly 25 people inquired. Ultimately, the donors fell through for one reason or another.

Then the family got another setback. Jim came down with pneumonia this winter.

"And that really took him down, and it failed rather rapidly after that," said Maynard.

Jim's scheduled for surgery next month to remove his kidney that's now the size of a football. If he doesn't get a healthy kidney by then, he'll continue with dialysis.

"Dialysis keeps you alive, but it's a hard life and there are a lot of limitations with it," said Laura Ellsworth, with Donate Life NW.

Ellsworth said there are many families who can identify with the Maynards. She said there are 800 people in Oregon and Southwest Washington on the waiting list for a new kidney. And the wait time is between three and five years.

She said many people are now turning to ads and social media to get their loved ones help.

"Their health is on hold. They're getting by day to day, and they're looking at that second chance at life and health any way they can find it," said Ellsworth.

Sunday, March 19, 2017

PKD Life: Enid, OK; PKD Research: Symposium at Harvard, PKD Gene Detection, Epidemiology Forecast

PKD Life

From Enid News, OK, By James Neal


New group improving education, support for kidney disease patients


Patients diagnosed with kidney disease are faced with new challenges in their lives, and many see the diagnosis as the end of life as they know it. A new support group met Wednesday in hopes of dispelling those fears, and giving patients the education and support they need.

The Polycystic Kidney Disease Support Group had its inaugural meeting in a basement classroom at St. Mary's Regional Medical Center, with almost 40 new members in attendance. They gathered to gain education on their disease and to support each other.

Dr. Rashmi Vijayvargiya, attending nephrologist and medical director of the dialysis unit at St. Mary's, said the purpose of the group is to provide kidney disease patients with support, education on disease prevention and treatment, and to "improve the quality of care for patients with chronic kidney disease."

Vijayvargiya said mutual support is essential for kidney disease patients.

"They feel their life is falling apart," Vijayvargiya said, "but when they see other patients who have been there, they see they can continue their life and it gives them faith and hope to continue their life.

"They feel this is the end of life, and their feeling is, 'Am I going to live?' I explain 'This is just a phase of life, we're going to get through this and we're going to have a good quality of life.'"

Vijayvargiya said the support group is not associated with any particular hospital, and is open to any kidney disease patient in the community.

In addition to mutual support, Vijayvargiya told the assembled patients she hoped the group would facilitate education on their disease and its treatment.

"I believe knowledge is power," Vijayvargiya said. "To educate patients is the highest form of care we can give. The more we educate patients the more they will be able to take care of themselves."

Vijayvargiya told the group members early detection and intervention is essential to improving outcomes in treating kidney disease.

She said patients can take steps like quitting smoking, exercising and managing their diets, and control kidney disease risk factors like obesity, high cholesterol and high blood pressure.

Melissa Thomas, who worked with Vijayvargiya to found the support group, said she hopes education and support will help fellow patients to take control of their care.

"I wanted there to be some education to it," Thomas said in an earlier News & Eagle interview. "Even through we cannot control the progression of the disease there are things we can do to help control it. We want the support group to be some education on how we can help ourselves, what we should and should not be doing."

Thomas was diagnosed six years ago with PKD and currently is on a transplant list for a new kidney.

She stressed to her fellow patients that kidney disease, even to the point of being placed on the transplant list, does not have to stop your daily activities. She still works full-time and volunteers with Habitat for Humanity.

Major Rowe rose to speak to the group, and said it's not uncommon to be scared when first diagnosed with kidney disease — especially without a support group.

"I had nothing to start with," Rowe said, "so you're scared every time you turn around."

Rowe underwent dialysis care for three years, and received a kidney transplant last year. He said the key to success in that process is to keep looking to the future, and have a positive attitude.

"You should enter this with looking forward," Rowe said. "Don't put yourself down or others down, and be congenial with those helping with your care."

Barbara Cink, who manages her dialysis with an in-home machine, said her diagnosis came as a shock.

"I was in a very dark place," Cink said. "If it had not been for my husband and family at home it would have been really terrible."

"I know it sounds scary," Cink said. But, she added, patients can overcome that fear "with the trust you have in your physician, with your ability to learn what's best for you, and by really taking your training seriously."

Dallas Winter sought to encourage his fellow patients, especially those early in the process. Winter takes an all-night dialysis treatment each night in his home. And, at age 90, he still enjoys fishing and looks forward to resuming bowling.

"It's no big deal," Winter told his fellow patients of dialysis. "You can still handle it. It's going to be fine."

For more information on the support group call Vijayvargiya at (580) 233-4444. The group will meet from 5:30-7 p.m. the third Friday of every month in basement classroom C at St. Mary's Regional Medical Center.



PKD Research

From EventBrite.com

10th Annual Symposium on Polycystic Kidney Disease

Free Symposium: 

This symposium is organized by the Harvard Center for Polycystic Kidney Disease Research (Director Dr. Jing Zhou). We will update you with the most recent advances in the cilia-PKD field and progresses made by members of the PKD Center at several Harvard Institutions in the past year and other distinguished investigators of the field.

All undergraduate, graduate students, medical students, residents, clinical and research fellows, physicians and basic science faculty members who are interested in kidney disease, cilia or epithelial biology would benefit from attending this conference. See more information at the Center website: http://pkdcenter.bwh.harvard.edu.


DATE AND TIME


Mon, May 8, 2017

8:00 AM – 5:00 PM EDT

Add to Calendar

LOCATION


The Joseph B. Martin Conference Center at Harvard Medical School

Boston, MA | The Joseph B. Martin Conference Center at Harvard Medical School (Bray Room)

77 Avenue Louis Pasteur

Boston, Massachusetts 02115

View Map




From MedGadget

Latest News on Polycystic kidney disease (PKD)-Epidemiology Forecast To 2023 Analysis

Summary
Orbis Research Present’s Polycystic kidney disease (PKD)-Epidemiology Forecast To 2023 And has been prepared based on an in-depth market analysis with inputs from industry experts.

Description

“Polycystic kidney disease (PKD) – Epidemiology Forecast To 2023” provides an overview of the epidemiology trends of Polycystic kidney disease (PKD) in seven major markets (US, France, Germany, Italy, Spain, UK and Japan). It includes 10 years epidemiology historical and forecasted data of Polycystic kidney disease (PKD) prevalent or incident cases segmented by age, sex and subpopulations. The Report also discusses the prevailing risk factors, disease burden with special emphasis on the unmet medical need associated with the Polycystic kidney disease (PKD). The report is built using data and information sourced from proprietary databases, primary and secondary research and in-house Forecast model analysis by team of industry experts.

Request a sample of this report @ http://www.orbisresearch.com/contacts/request-sample/220950

Scope of the Report
The Report includes the prevalent population and how will it change over the next eight years.
Prevalent or incident cases segmented by age and sex.
Coverage of key Polycystic kidney disease (PKD) subpopulations and its prevalent or incident cases
The key differences in epidemiology patterns across the seven market segments

Purchase a copy of this report @ http://www.orbisresearch.com/contact/purchase/220950 .




From NIH, National Institutes of Health

Pkd mutations and evaluation of same (U.S. Patent Number 20100047785 A1)

The present invention relates to methods of detecting novel mutations in a PKD1 and/or PKD2 gene that have been determined to be associated with autosomal dominant polycystic kidney disease (ADPKD) in order to detect or predict the occurrence of ADPKD in an individual. For more information please contact Johns Hopkins University's Technology Ventures office.

Sunday, March 12, 2017

PKD Screening Kidney Donors, PKD Research: Targeting MicroRNA-17, Gift of Life: Kerrville, TX

Kidney Donors

From MedScape.com, American Journal of Transplantation

Screening of Living Kidney Donors for Genetic Diseases Using a Comprehensive Genetic Testing Strategy


Abstract

Related living kidney donors (LKDs) are at higher risk of end-stage renal disease (ESRD) compared with unrelated LKDs. A genetic panel was developed to screen 115 genes associated with renal diseases. We used this panel to screen six negative controls, four transplant candidates with presumed genetic renal disease and six related LKDs. After removing common variants, pathogenicity was predicted using six algorithms to score genetic variants based on conservation and function. All variants were evaluated in the context of patient phenotype and clinical data. We identified causal variants in three of the four transplant candidates. Two patients with a family history of autosomal dominant polycystic kidney disease segregated variants in PKD1. These findings excluded genetic risk in three of four relatives accepted as potential LKDs. A third patient with an atypical history for Alport syndrome had a splice site mutation in COL4A5. This pathogenic variant was excluded in a sibling accepted as an LKD. In another patient with a strong family history of ESRD, a negative genetic screen combined with negative comparative genomic hybridization in the recipient facilitated counseling of the related donor. This genetic renal disease panel will allow rapid, efficient and cost-effective evaluation of related LKDs.

Introduction

Kidney transplantation is superior to long-term dialysis for the management of end-stage renal disease (ESRD) because it provides greater long-term survival and better quality of life. Nevertheless, there is an ever-increasing gap between the need for transplantation and the availability of donor kidneys, with >120 000 patients currently on the deceased donor waitlist in the United States alone. This has resulted in an increasing push to encourage living donation, and today there are almost as many living donors as deceased donors annually in the United States.[1] Living kidney donor (LKD) transplants, for those fortunate to receive one, bypass the long waiting time, reduce the likelihood of death while waiting and provide better long-term allograft and recipient survival compared with deceased donor kidneys.[2,3] In some parts of the world, LKDs are the principal or only source of transplanted organs, and where long-term dialysis is prohibitively expensive or unavailable, LKD transplants provide the only available therapy for ESRD.

Living donor nephrectomy is generally considered acceptable medical practice, even though there are real risks for the donor, including death, serious injury and failure of the remaining kidney. Recent retrospective studies examining long-term outcomes of living donation compared with matched nondonor cohorts reported an increased 15-year and lifetime risk of ESRD for LKDs.[4,5] Although the absolute risk is arguably small, the relative risk is 30 per 10 000 over 15 years and 90 per 10 000 over a lifetime compared with four per 10 000 and 14 per 10 000 in matched controls. Within subpopulations, black men have a 15-year risk of 90 per 10 000 compared with just nine per 10 000 for white women.[4]Although not statistically significant, there is a twofold increased risk of ESRD among biologically related LKDs compared with unrelated LKDs.[4] The increased risk may reflect shared inheritance of genetic variants that are deleterious or a common environmental exposure that increases susceptibility to kidney disease.

In the United States, 40% of all LKDs are biologically related to their recipients.[1] Many are siblings or adult children of patients with ESRD and are in their third and fourth decades of life, making it difficult to predict future risk of kidney disease. In addition, to guide focused genetic testing of related family members for a specific inherited disease, the transplant recipient's cause of ESRD must be known. Together, diabetes and hypertension are the two most important reported causes of ESRD and account for 60% of the waitlist.[1,6] Most patients with diabetes and/or hypertension and chronic kidney disease (CKD) do not receive a kidney biopsy to verify the diagnosis, and recent studies estimated that as many as 35% of patients with presumed diabetic or hypertensive nephropathy may actually have an alternative diagnosis.[7–9]

Traditionally, establishing and/or confirming the diagnosis of a presumed genetic disease has required Sanger sequencing of the suspected gene for pathogenic variants.[10] When candidate genes are large, like COL4A5, sequencing is costly and time consuming. When the disease is heterogeneous, like focal segmental glomerulosclerosis (FSGS), serial gene-by-gene screening approaches are inefficient and impractical. These constraints can be largely overcome by using high-throughput approaches to DNA sequencing (i.e. next-generation sequencing [NGS] or massively parallel sequencing [MPS]) to sequence a large number of genes simultaneously. Targeted NGS panels have been developed to evaluate patients with a single phenotype, such as steroid-resistant nephrotic syndrome, FSGS and some ciliopathies.[11–14]

We developed a targeted renal panel that includes 115 genes implicated in a variety of kidney diseases to facilitate a diagnosis in patients with suspected genetic renal disease. We validated this panel for the evaluation of selected LKDs in whom the related transplant recipient's phenotype raised suspicion of or clearly indicated an inherited renal disease. We reported our findings from a pilot study of six controls, four transplant candidates and their six related donors. [Read more]




PKD Research

From Nature.com

MicroRNA-17: a new drug target for ADPKD

New data suggest that the microRNA-17 (miR-17) family promotes the progression of autosomal dominant polycystic kidney disease (ADPKD) and is a promising target for therapy. “Anti-miRs work best in the liver and kidney and have a long duration of action,” explains researcher Vishal Patel. “These attributes make them ideal therapeutic…




Gift of Life

From Hill Country Community Journal, by Tammy Prout

When KPD officer needs kidney, locals, girlfriend respond

When KPD officer needs kidney, locals, girlfriend respond


Misty Cass (left) has no doubts about donating a kidney to save the life of her boyfriend, Kerrville Police Department Investigator Darin Trahan (right). Both of Trahan’s kidneys are failing due to Polycystic Kidney Disease.


The remarkable chain of events and community support have been overwhelming to a local police officer, who will be receiving a new kidney and a new chance at life and in the process save the lives of many others.

Kerrville Police Department Investigator Darin Trahan thought he had some sort of infection when he made a doctor’s appointment in 2005.

He expected to receive the usual prescription for antibiotics and then he would go on with his life. Instead, Trahan discovered his illness could someday take his life.

“I thought I had a kidney infection or something,” Trahan said. “But they came back and said I had Polycystic Kidney Disease.”

Trahan said he was told there was no cure for the disease and that he would eventually need a kidney transplant, as the disease is affecting both of his kidneys.

“They said to go on with my life and try to eat healthy and be active,” Trahan said. “They said, eventually my kidneys would begin to fail and then we would look at getting on a kidney transplant list.”

Trahan said doctors told him that his kidneys would have to be functioning at less than 20 percent capacity before being accepted on the national organ donor list.

So Trahan went about his daily routine, never missed a day of work, and quietly dealt with the reality of his illness.

“I didn’t really tell anyone,” Trahan said. “I didn’t even tell my children. I felt there was no reason to worry anyone at that time. I decided to wait and tell them when it was absolutely necessary.”

It became necessary nearly 11 years later, when Trahan’s kidney function began to drastically decrease.

“My kidney function is now at 17 percent,” Trahan said.

Trahan began the process of being accepted into the organ donation program. He made an appointment at the Methodist Specialty and Transplant Hospital to begin testing, so that a match could be identified. He was accompanied by his girlfriend of nearly two years, Misty Cass.

Cass chose to also be tested to see if she was a match, however, she was not.

The remarkable chain of events that were alluded to earlier begin here.

While Cass was not a blood match for Trahan, she was told she could become an “Altruistic Donor,” which means that she and Trahan would be paired in a donor pool. Cass’ kidney would go to someone who was paired with an altruistic donor that matched Trahan.

“The process is very complicated,” Trahan said. “In total, there will be 16 people involved, providing kidney transplants for eight people.”

Trahan said the surgeries will take two days to complete and will begin this week on Wednesday, March 8.

“Misty and I will go for our pre-op on Monday and Tuesday,” Trahan said.

When speaking of Cass’ willingness to donate a kidney on his behalf, Trahan gets a little emotional.

“She’s my hero,” Trahan said. “I’ve told her she didn’t have to do it. I’ve tried to talk her out of it.”

Cass said she did not hesitate when presented with the opportunity.

“He is a good man. He has served his community well and I love him,” Cass said. “This (surgery) will save his life. To be honest, I would do it for anyone I care about.”

Cass is not the only person who stepped up to help Trahan. In fact, the community support for Trahan, a public servant, has been phenomenal.

“After I told my family about my disease, my brother posted something on Facebook, asking for prayers,” Trahan said. “Just from that post, I have received offers from at least 40-50 people, who said they would be willing to get to tested to donate as well. I told them ‘thank you,’ and explained how much I appreciated their offer, but I have a donor.”

One donor, however, would not relent.

Trahan said Caitlin Eubank, the wife of a former KPD officer, was insistent that she help. Knowing that she was not a blood-match, but could assist in being an altruistic donor fueled Eubank’s cause. [Read more]

Sunday, March 5, 2017

PKD Kidney Patient Summit: Washington DC, PKD Families Needs Kidney:Council Bluffs, New Orleans

PKD Community

From Yahoo News

Advocates Across U.S. to Bring "My Kidneys, My Life" Mantra to Washington DC for 4th Annual Kidney Patient Summit

Getty Images/iStockphoto/ThinkStock



Nearly 150 advocates from six kidney organizations around the country will converge on Capitol Hill, March 6-7, 2017, to meet personally with lawmakers and put a human face on kidney disease during the 4thAnnual Kidney Patient Summit organized and led by the National Kidney Foundation (NKF). This largest event to date brings together, in a unified voice, NKF's Kidney Advocacy Committee members and advocates from Alport Syndrome Foundation, Polycystic Kidney Disease Foundation, NephCure Kidney International, Home Dialyzors United and American Association of Kidney Patients.

Among the attendees, 70 advocates selected by NKF to represent nearly all 50 states – learn who they are– will share their stories and urge Members of Congress to support a pilot program which seeks to improve early detection, care and outcomes for people with chronic kidney disease (CKD); support H.R. 1270, The Living Donor Protection Act 2017, which was just introduced by Representatives Jerrold Nadler (D-NY) and Jaime Herrera Beutler (R-WA) and would prohibit discrimination in life, disability or long-term care insurance for living organ donors and add living donation to the Family Medical Leave Act; and support funding for CKD programs run by the Centers for Disease Control and Prevention, National Institute of Diabetes and Digestive and Kidney Diseases, and Health Resources and Services Administration.

At the Summit, individuals who have kidney disease, dialysis patients, living donors, family members and caregivers will be united by the affirmation and hashtag "My Kidneys, My Life" (#MyKidneysMyLife) to underscore the direct relationship between having at least one healthy kidney and living at all.

"Coming together for the Kidney Patient Summit is personal for me and the many people traveling from throughout the country who seek to be heard and affect real change for those suffering from kidney disease," said National Kidney Foundation CEO Kevin Longino, who received a kidney transplant 12 years ago. "'My Kidneys, My Life' is not just a slogan. It's a mantra based on facts and a plea for more public awareness," he added.

More than 26 million Americans are affected by kidney disease but 90 percent don't even know they have it. Once kidneys fail, dialysis or a transplant is needed just to stay alive.

In addition to advocates' visits with lawmakers scheduled on Tuesday, March 7, this year, a special Summit press conference focused on living donation will be held the same day from 1 -2 p.m. EST, on Capitol Hill in 902 Hart Senate Office Building. Living organ donors and kidney recipients will share their stories, demonstrate the urgent need to increase living donation, and provide hope to more than 100,000 Americans waiting for a kidney transplant right now.

Press conference speakers will include: Kevin Longino, CEO, NKF; Representative Brett Guthrie, (R-KY); Kent Bressler, recipient, Kerrville, TX; Kelly Cline, mother of recipient Hannah Shelton, Glen Allen, VA; Alex Fox, donor, Star, ID; Ewo, Harrell, recipient, Providence, RI; Christopher Melz, donor, Huntington Station, NY; Luis and Noelia Rodriguez, recipient and donor, Sioux Falls, SD; Matthew Scroggy, recipient, Columbus, OH; and Joe Vohs, donor, Half Moon Bay, CA. See snapshots of their stories .

The Summit kicks off Monday, March 6, at the Holiday Inn Washington Capitol with a morning meeting of the Kidney Advocacy Committee, comprised of the advocates along with their family members and care partners, to use their collective experiences to champion NKF's priorities. This meeting will be followed by the annual Advocacy Awards Presentation luncheon, the Summit training to prepare advocates for their Tuesday visits on Capitol Hill, then dinner and organization presentations.

Whether traveling from far away or locally; or by air, rails, bus or car, the Summit has become a must-attend event – especially for patients despite constant health challenges, medical appointments, and reliance on dialysis. Event organizers work personally with patients well in advance to help accommodate any special needs they will have while staying in Washington, DC. This includes setting up on-site or local dialysis treatments, shipping dialysis supplies to the hotel, providing refrigerators in rooms for medications, allowing wheelchair or scooter access, and addressing dietary requests or restrictions.

Kidney Disease Facts

1 in 3 American adults is at risk for kidney disease. 26 million American adults have kidney disease—and most aren't aware of it. Risk factors for kidney disease include diabetes, high blood pressure, family history, and age 60+. People of African American; Hispanic; Native American; Asian; or Pacific Islander descent are at increased risk for developing the disease. African Americans are 3 ½ times more likely, and Hispanics 1 ½ times more likely, to experience kidney failure.

The National Kidney Foundation (NKF) is the largest, most comprehensive and longstanding organization dedicated to the awareness, prevention and treatment of kidney disease. For more information about the NKF visit www.kidney.org.


To view the original version on PR Newswire, visit:http://www.prnewswire.com/news-releases/advocates-across-us-to-bring-my-kidneys-my-life-mantra-to-washington-dc-for-4th-annual-kidney-patient-summit-300416773.html




PKD Life

From The Daily Non Pareil, Council Bluffs, Iowa, By Kristan Gray

Clarinda native seeks transplant to overcome hereditary kidney disease

Clarinda native seeks transplant to overcome hereditary kidney disease


A southwest Iowa man is one of 174 patients from Nebraska Medicine who are awaiting a new kidney.

Chris Hitt, a 1988 Clarinda High School graduate, now lives in Bennington, Nebraska, near Nebraska Medicine where he visits once a month for blood testing.

As he faces his 47th birthday on March 16, he’s praying to be matched with a donor.


“My kidneys are both the size of footballs,” Hitt said. “I just got out of the hospital this past week. I’m blessed that I haven’t had too many issues until now, but I have had some cysts burst the past few years.

“I’m at what they call stage 5, so I should be on dialysis. But, they’re functioning just enough to get by – at 10 percent between the two of them.”

Chris was diagnosed 21 years ago but only qualified to be on the transplant waiting list last year.

While polycystic kidney disease can affect cognitive ability, Hitt said his concentration has been only mildly affected. He continues to work full time as an engineer for Phillips Manufacturing in Omaha.

The disease runs in his family. Although Chris’s brother Jesse does not have the disease, his brother Ben received a kidney from their father, Steve Hitt, in 2008. His mother, Ann Hitt, has the disease as well.

His grandfather was a research doctor at the University of Kansas and studied the disease aggressively in the 1960s and ‘70s, even performed home dialysis for Chris’ grandmother in the 1970s and ‘80s.

For several years, Chris and his mother participated in the study his grandfather started at KU, he added.

Chris’ wife, Amy Hitt, said high blood pressure prevents her and her extended family members from becoming donors.

“But there’s definitely someone out there who will be a match,” she said. “Chris has been really lucky to be able to play normally with our son, Caleb, who’s 8. The wonderful thing is that he’s adopted, so we don’t have to worry about him having this genetic disease.”

The living donor program at Nebraska Medicine makes it possible for a donor who is not a match for Chris to possibly match with any of the 120,000 on the national waiting list.

Vicki Hunter, kidney and pancreas transplant manager at Nebraska Medicine, said those who wish to donate can first complete a brief online questionnaire. Then, the review process can take up to eight weeks.

“We do vigorous testing first, and the entire process is free of cost for donors in every way — the recipient’s insurance pays for everything,” Hunter said. “We want to ensure our patients that donors can live with just one kidney. Even those who do not have a gall bladder donate.”

Dr. Arika Hoffman, a transplant surgeon at Nebraska Medicine, said there are no dietary restrictions. Patients who donate can live normal lives with a normal lifespan. That includes pregnancy after donation, returning to work and being as active as they were before donating a kidney.


Because the screening process is stringent, Hoffman said only the healthiest people may donate.

“We do anywhere from 115 to 170 transplants every year. There’s always a small risk for patients who don’t take care of themselves afterward, but it’s just the same as anyone who doesn’t stay healthy,” Hoffman said.

Once approved, the surgery is most often scheduled within a month’s time. The donor has no restrictions after about six weeks. During that time, they cannot lift more than 10 pounds. Most donors go back to work after about two weeks. Those who are concerned about unpaid time off of work can put their minds at ease: The National Living Kidney Donor Fund can replace the donor’s loss of time from work.

The success rate of a living donor kidney regaining function in a new body is more than 99 percent, Hoffman said.

“I want to be a part of something that helps bring joy to patients — that gives them their life back so they can spend time with family and friends and do all they want to do,” she said. “The day we call patients and tell them they’re going to get a transplant is the best day of their lives. It’s a surreal job we work in every day.”

Hunter added that she and Hoffman are both passionate about transplantation and are vested in every patient.

“I encourage everyone out there to look at the numbers — there are over 120,000 people in America waiting for an organ transplant,” Hunter said. “There are 174 patients on the active waiting list in Nebraska who need a kidney. We only need one for each patient. If you’re medically and psychologically stable, please think about giving them back a chance at life.”

To register for donation, visit secure.nebraskamed.com/livingdonor. To specify an attempt to match with Christopher Hitt, his date of birth is March 16, 1970.





From The Times-Picayune, By Celeste Turner

Two New Orleans area residents battle kidney disease, lean on hope through transplants

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This is a tale of two local survivors, Collin Berg, a 13-year-old Holy Cross High School seventh grader who recently received a new kidney, and Agnieszka Nance, a 43-year-old Executive Director of the Center for Public Service at Tulane University, who is waiting for a kidney.

Both had similar dire health needs, but different personal experiences with kidney disease. Berg, who lives in Metairie, was born with a rare genetic disorder called Autosomal Recessive Polycystic Kidney disease (ARPKD), and his family knew that at some point, he would need a transplant.

"At 6 months old, we knew Collin was born with ARPKD," said Chris Berg, Collin's father. "We were trying to get the surgery done before Collin would need dialysis.

"Both my wife and I took the test to see if we could donate a kidney and, surprisingly, we were both compatible. But, we both felt my wife was a better donor. We both knew the day would come when Collin would need surgery."

On Jan. 31, 2017, Berg and his mother, Karen, underwent surgery. Doctors removed one of Karen's kidneys and transplanted it into her son.

Notably, Karen was the first living donor of a kidney at Tulane Lakeside Hospital, and Berg was the first recipient of a kidney from a living donor at this hospital in Metairie. After a total of five surgeries, 32 staples and more than three weeks in the hospital, Berg is home now but, still waiting for his new kidney to fully "wake up."

"We are waiting to hear from the kidney doctor," said Chris, who was at his son's bedside throughout the ordeal. "We were excited when they put the kidney in Collin because everything was going good."

It hasn't been smooth sailing, however. Right after the transplant surgery, Berg took a turn for the worse.

"Then, the ultrasound showed that the kidney was not receiving good blood flow, and hours later, Collin had a massive arterial bleed-out on the table. His blood pressure plummeted. I stood there in shock, while everyone tried to stop the bleeding," Chris said.

The words no father ever wants to hear were uttered next.

"We're losing him," Chris overheard the doctor say about his son.

"The doctors said that the kidney had no color, so they were talking about taking the kidney out to save (Berg's) life," Chris said.

By the next morning, Chris was awakened by good news.

"It's a miracle. ...The kidney is pink and it has blood in it," he was told.

The future is still uncertain.

"We are now waiting for the nuclear test to tell us how viable this kidney can be," Chris said. "This test results will indicate if the kidney is functioning properly, because there is still a chance he could lose this kidney."

Nance is also dealing with uncertainty.

Nance lives Uptown with her husband David and four dogs. To all around her, she's the picture of health and she's in the business of making others healthier.

Nance is an exercise instructor in her spare time, teaching eight classes a week at Franco's Athletic Club on Magazine Street. Two years ago, however, she noticed a strange allergic skin rash and some weird swelling that prompted a doctor's visit.

She was stunned to get a diagnosis of end stage kidney disease in April 2015.

"My team of doctors (allergy specialist and my nephrologists) ran all kinds of blood and urine tests and determined that I was in a dire need of dialysis. I was 41 at that time," stated Nance, who moved to New Orleans with David a week before Hurricane Katrina. "I feel like we talk about other problems like heart disease, or lung disease and do not address the kidneys. Kidney disease is a silent killer."

For patients like Nance, end-stage kidney or renal disease (ESRD) is the final stage of chronic kidney disease in which the kidneys no longer function well enough to meet the needs of daily life. The treatments for ESRD are dialysis or kidney transplant.

"There is no known solution to kidney failure," Nance explained. "Kidneys don't regenerate themselves so patients with that disease have to dialyze either daily or multiple times per week. I opted to do hemodialysis, which means that I go to a clinic three times a week for five-hours-long treatment. The treatment is not painful - however, it can be draining. During hemodialysis, a machine is pumping my blood out, cleaning it and sending it back to my veins."

The treatments are layered into an already high-octane life for Nance. But hemodialysis isn't the final solution. She yearns for a kidney transplant so her life can return to normal.

"Transplant is a wonderful way of ending dialysis and live a free life," she said.

In the meantime, Nance does everything she can to remain healthy and active while waiting for a kidney. But it's hard to do "normal" activities. Even going to lunch with friends is hard because her diet is severely limited while on hemodialysis. She can't eat bananas, potatoes, tomatoes, cheese or beans as well as foods with sodium. Even water is restricted.

"For me, the most difficult is the fluid restriction. We are allowed 30 oz. a day but I personally had to go lower to 15 oz. (about one bottle) per day," Nance said. "Since your kidneys filter all the liquids, you want to eliminate the pressure on the organs particularly the heart and limit your fluid intake."

Under the supervision of the staff at Tulane Hospital, Nance is presently waiting for a kidney transplant, and urges everyone to sign up as an organ donor when you apply for driver's license.

"Right now, I'm still waiting to receive a transplant. The average waiting time for a kidney transplant in the U.S. is 3.6 years," Nance said. "I am very fortunate to have family members and friends offering to get tested to be a donor. I am also listed on the UNOS list (https://www.unos.org/) for a transplant from a deceased donor. I'd really like to encourage anyone to put the little heart on your driver's license showing the willingness to donate your organs. One donor can save up to eight lives."

Since kidneys for transplantation can come from two sources, a living donor or a deceased donor, MatchingDonors.com, a nonprofit and the nation's largest living organ donor organization, can help facilitate the process by finding and registering living organ donors for people needing organ transplants in the United States.

Statistics show that on average approximately 22 people die every day while waiting on the government's deceased donor list. And those that live and get a transplant from that list wait seven to 12 years for their organ. In an effort to combat that waiting period, MatchingDonors has provided a forum for all people in need of lifesaving transplants to match with living, altruistic donors. Many patients may receive their kidney transplant within six months of registering on MatchingDonors.com.

Luckily for Berg, the wait for a kidney transplant is over and he has left the hospital with his new working kidney.

"Doctor said that Collin's reaction was rare in the hospital," Chris said. "Collin still has a drain and a pick line but they don't see a rejection. His blood work is good. But, every week, we will go for blood work and continue to tweak all his medication."

Nance is still waiting, thriving on hope despite some recent disappointments. Twice, she has had living donors volunteer only to get medically disqualified before transplant.

"I feel like my disability is special because it is not visible. I am thankful because I am physically able to do things that some healthy people cannot do. And yes, I'm there to support people on their journey to health and fitness, showing that it is possible to be healthy and strong, and overcome any obstacles," Nance said.

Celeste Turner is a fitness guru who writes news about East Jefferson and around the New Orleans metro area. Please send any health and fitness news, special events or East Jefferson news items to: cmturner10966@gmail.com.