Sunday, August 27, 2017

PKD Research: Reducing Cyst Growth with Cancer Drug, Using PDG to Eradicate PKD

PKD Research

From Science Daily

Cancer drug may benefit patients with inherited form of kidney disease


A cancer drug called bosutinib may inhibit the growth of cysts in patients with autosomal dominant polycystic kidney disease (ADPKD), according to a study appearing in an upcoming issue of the Journal of the American Society of Nephrology (JASN). The findings point to a potential new treatment strategy for affected patients, but the long-term benefits remain to be determined.

ADPKD is an inherited disorder that affects up to 1 in 1000 people and is characterized by cysts in the kidney and other organs. As patients' kidney volume increases due to cyst growth, they gradually lose their kidney function and often develop kidney failure. Current treatments are primarily supportive, such as focusing on hypertension and other secondary complications.

The inherited mutations that cause ADPKD affect a protein involved in various signaling pathways that often involve enzymes called tyrosine kinases. Therefore, a team led by Vladimir Tesar, MD, PhD (Charles University and General University Hospital, in the Czech Republic) tested the potential of an investigational drug called bosutinib that inhibits a particular tyrosine kinase called Src/Bcr-Abl.

The phase 2 study included patients with ADPKD who were randomized 1:1:1 to bosutinib 200 mg/day, bosutinib 400 mg/day, or placebo. Of 172 patients enrolled, 169 received at least one treatment. The higher dose of bosutinib was not well tolerated.

The annual rate of kidney enlargement was reduced by 66% for patients receiving bosutinib 200 mg/day vs. those receiving placebo (1.63% vs. 4.74%, respectively) and by 82% for all patients receiving bosutinib vs. those receiving placebo (0.84% vs. 4.74%, respectively). The study was not powered to demonstrate a treatment effect on kidney function, but there was no evidence of a benefit associated with bosutinib compared with placebo over the 2-year treatment period.

"The reduction in growth of cysts through treatment with bosutinib was confirmed, although gastrointestinal side effects (primarily diarrhea), which were partly dose-dependent, may represent a substantial drawback for the further development of the drug for patients with ADPKD," said Prof. Tesar.



From Rare Disease Report, by James Radke

Can Preimplantation Genetic Diagnosis (PGD) Eradicate Genetic Diseases?

Last week in Nature, an article by David Cyranoski was published regarding the rise of preimplantation genetic diagnosis (PGD) in Chinese fertility clinics with the intention of eradicating genetic diseases.

PGD was first performed in England almost 2 decades ago to preferentially select for female embryos to be implanted in parents at risk for X-linked genetic conditions. Since then, the technique has advanced significantly; while many countries are performing PGD, the article in Nature indicates that China is outperforming all other countries, and furthermore, PGD is not considered to be part of an ethical issue there as it is in other countries.

Using PGD, Chinese clinics have reported being able to avoid producing children with, or at risk for, retinoblastoma, short-rib-polydactyly syndrome, Brittle-bone disease, Huntington’s disease, polycystic kidney disease and deafness.

The eradication of a genetic, chronic condition could have a significant impact on healthcare costs. For example, the cost for a PGD to avoid having a child with cystic fibrosis would be $57,000. While seemingly expensive, a cystic fibrosis patient incurs about $2.3 million in medical costs over his or her lifetime.

Similarly to the way that Iceland’s eradication of Down syndrome has led to concerned tweets like the one below, similar concerns could be justified.




Specifically, PGD raises concerns that it will be used only by the well-off to create an elite genetic class. It is an expensive procedure, likely to be limited to families with better healthcare coverage.

In China, while many parents are concerned about genetic diseases, some parents are trying to weed out genetic anomalies to create a superior child. Sijia Lu, chief technology officer of Yikon Genomics has stated some couples are asking to weed out the mutation that renders many Asians unable to process alcohol. Right now, such selection is not allowed.

While such queries are theoretically a concern, some argue that it shouldn’t be. Joe Leigh Simpson, a medical geneticist at Florida International University in Miami said, “With every reproductive-biology advance, we get the same questions: ‘won’t there be a slippery slope that leads to abuse?’ But it never happens.”

As for using PGD for its intended use – to screen for genetic diseases – its use in the United States remains limited right now, partly because is very expensive and insurance generally does not cover it.

Sunday, August 20, 2017

PKD Foundation News: PKD Awareness Day, CRISPR Research, Toddler Walks 100 KM for PKD, Gift of Life, PKD Real Costs

PKD Foundation News

From PKD Foundation

#PKDAwarenessDay is fast approaching

We need your voice in the weeks leading up to Awareness Day on Monday, September 4. With an estimated 600,000 Americans suffering from the effects of PKD, the Average American is just 1.2 degrees of separation from someone with PKD. Visit our page to download and share #PKDAwarenessDay social resources and spread the word now. Your voice is the most important to finding treatment options for this chronic, genetic disease.


CRISPR Research Update

A recent article in the New York Times announced that scientists have successfully edited genes in a human embryo to repair a mutation. Peter Harris, Ph.D., Mayo Clinic geneticits, director of the ADPKD genetic mutation database and former PKD Foundation Scientific Advisory Committee (SAC) member, has written a piece about this discovery and what its implications are for PKD. You can read his take on the science on our website.



Register today and Walk for PKD

Bring your family and friends and join over 10,000 participants that will be walking for PKD. With 100% of donations funding research your donations have never been more powerful! You can help us accelerate treatments to patients faster: register for your local Walk and start fundraising today.


From Fort Saskatchewan Record, By Leanne Delong

Toddler walking 100 KM’s for kidney foundation

Two and a half year old Sam McKail is 81 kilometres into his 100 kilometre goal and will walk his final kilometre with those partaking in the Calgary Kidney Foundation March Sept. 8-10.


Fort Saskatchewan toddler Sam McKail is on a mission to walk 100 kilometres in 100 days in support of the Calgary Kidney Foundation’s annual kidney walk and as of Aug. 14 he has already reached 81 kilometres.

The kidney walk will take place Sept. 8 - 10 with participants marching 100 kilometres in three days from K-Country to Calgary and Sam will walk his last kilometre down the hill of Calgary’s Olympic Park with family and other marchers.

“I’m kind of amazed because when we first started, pretty much everybody asked if he could actually walk 100 kilometres a day for 100 days and at that point he was only two years and four months old and that is a pretty high expectation, so I was a little nervous,” said his mother Kirstin Lehmann.

What started as a light hearted joke in her family last year has turned into a solid commitment between mother and son.

Lehmann decided to fully commit to the challenge on May 5 and she let the kidney foundation know that Sam, now two and a half years old, would be partaking in the march in his own way.

“They have thrown themselves behind Sam and made him his own mini marcher t-shirt and a little name tag,” she said.

Every time Sam completes ten kilometres Lehmann makes a video, which is posted online.

“He just keeps on going and it’s been a great way to explore Fort Saskatchewan,” she noted.

She said they moved to the Fort in April from Calgary.

Why they support the kidney foundation

Lehmann and her family have been involved with the kidney foundation for many years.

“The story dates back to 2010, long before Sam was even born. My uncle, even though he had been a remarkably healthy active person, couldn’t beat genetics and developed polycystic kidney disease and he needed a kidney transplant or dialysis,” she explained.

Her mother had volunteered to donate a kidney and completed all the prep work but at the last minute another family member stepped in to donate.

Lehmann’s mother felt that donating a kidney was meant to be so she called the Kidney Foundation and asked if they wanted a kidney. Her kidney was donated to the Paired Exchange program and because of that, a new kidney was able to go to someone on the transplant list.

“80 per cent of the people on the organ transplant waiting list are waiting for a kidney, so this was huge for somebody else. The thing was my mom was in her early 60’s at this point and people assumed her lifestyle would be extremely compromised due to only having one kidney,” said Lehmann.

People would worry about her mother every time she got a cold.

“It’s amazing how many people don’t realize you can live with one kidney and still live a very functional life,” she noted.

Her mother decided to prove all these people wrong and walk the kidney march’s 100 kilometres in three days, just to show them that they are wrong.

Her mother will now be marching for her fifth year come September.

“Over the five years she has raised almost $20,000. She is just $700 shy of reaching that goal within the next couple of weeks leading up to this year’s march,” said Lehmann.

She said if that was not enough to get her son involved, Lehmann’s cousin is also marching this year with her parents as well.

For more information on the kidney foundation visit, www.kidney.ca.

To follow Sam’s journey visit Lehmann’s blog, www.greatnorthernfamily.com.




Gift of Life

From New York Post, By Christian Gollayan
World’s best student donates kidney to teacher

Wanna be a teacher’s pet for life? Don’t give an apple — give a kidney.

That’s what Ali Golian, 30, did for his former teacher Sonia Leonardo.

Golian and Leonardo go back to 2010, when he studied radiology under the now-42-year-old at London’s Kings College Hospital. “Sonia was an incredible teacher,” Golian tells South West News Service. He credits her with inspiring his career track (he’s now a radiology-equipment tutor).

After Golian graduated from school, he landed a job at Leonardo’s hospital. The two became fast friends, and worked together for two years. But they fell out of touch after she changed jobs.

Fast forward to five years later, when a Facebook post caught Golian’s eye. Leonardo’s sister was thanking friends for sending get-well flowers on her sister’s behalf. Concerned, Golian texted Leonardo.

His mentor and friend, he learned, was home on sick leave due to complications from polycystic kidney disease. The genetic disorder had caused cysts to grow in her kidneys, and she was in dire condition: Her kidney function had been reduced to 10 percent.

The transplant list, she told Golian, had a projected wait list of three years — and in the meantime, staying alive would mean enduring five half-hour dialysis sessions every single day. [Read more]




From MedicalXpress


A new analysis indicates that few strategies to increase living kidney donation have been evaluated effectively; however, educational strategies targeted to recipients and their family and friends have the best evidence of being successful. The analysis, which appears in an upcoming issue of the Clinical Journal of the American Society of Nephrology (CJASN), also provides possible suggestions that could help investigators, organizations, and policy makers determine which, out of the many strategies that may be used to increase living donation, should be considered.

There is a critical need to increase rates of living kidney donation to address the growing organ shortage; however, it's unclear which strategies are effective. To investigate, Scott Klarenbach, MD, MSc (University of Alberta) and his colleagues summarized the breadth and quality of the evidence on approaches to increase living kidney donation.

When the researchers conducted a search of the medical literature, they found very few high quality studies. The most evidence related to educational strategies: those directed at both the potential recipient and their close social network. Of the 7 studies that focused on educational strategies, 2 studies that targeted the potential recipient's close social network reported significant benefits. Other approaches were also identified, but their impact was assessed through less rigorous study designs.

"Living kidney donation is the optimal treatment for patients with kidney failure, who would otherwise be treated with dialysis. It improves survival and quality of life, and is less resource intensive and can be safely performed with appropriate donor selection," said Dr. Klarenbach. "There are large numbers of patients with kidney failure waiting for a kidney transplant, and increasing living kidney donation would reduce their wait time and improve outcomes."

In an accompanying editorial, Krista Lentine, MD, PhD (Saint Louse University School of Medicine) Didier Mandelbrot, MD (University of Wisconsin School of Medicine) noted that certain steps are needed for practitioners and policymakers to expand living donor kidney transplantation. "We and others believe that the strategies that have the potential to improve informed consent and access to living kidney donor transplantation include: (a) broader and repeated living donor kidney transplantation education beginning at earlier stages of kidney disease and involving the patient's social network, (b) removal of disincentives to donation, (c) optimized efficiency in the evaluation of donor candidates, and (d) improving the safety and defensibility of donor selection," they wrote.




PKD Research

From FigShare


Abstract Background There is limited real-world data on the economic burden of patients with autosomal dominant polycystic kidney disease (ADPKD). The objective of this study was to estimate the annual direct and indirect costs of patients with ADPKD by severity of the disease: chronic kidney disease (CKD) stages 1–3; CKD stages 4–5; transplant recipients; and maintenance dialysis patients. Methods A retrospective study of ADPKD patients was undertaken April–December 2014 in Denmark, Finland, Norway and Sweden. Data on medical resource utilisation were extracted from medical charts and patients were asked to complete a self-administered questionnaire. Results A total of 266 patients were contacted, 243 (91%) of whom provided consent to participate in the study. Results showed that the economic burden of ADPKD was substantial at all levels of the disease. Lost wages due to reduced productivity were large in absolute terms across all disease strata. Mean total annual costs were highest in dialysis patients, driven by maintenance dialysis care, while the use of immunosuppressants was the main cost component for transplant care. Costs were twice as high in patients with CKD stages 4–5 compared to CKD stages 1–3. Conclusions Costs associated with ADPKD are significant and the progression of the disease is associated with an increased frequency and intensity of medical resource utilisation. Interventions that can slow the progression of the disease have the potential to lead to substantial reductions in costs for the treatment of ADPKD.

World’s best student donates kidney to teacher

Sunday, August 13, 2017

Living with PKD: Columbus, IN, New Zealand, Walk for PKD: Milwaukee, Dialysis Membrane Technology

Living with PKD

From The Republic, Columbus, IN, by Brian Blair

Fighting together: Mom, daughter wage battle against disease

photo



Suffering through physical weakness, weariness and memory fog amid an incurable disease is one thing.

But painstakingly waiting is quite another — waiting for news that another person will grant the gift of renewed life with a donated organ.

Or the terrible-news-turned-redeeming-sacrifice that one who has died was altruistic enough to sign up for organ donation.

Columbus resident Debbie Patterson, 57, needs a kidney transplant as soon as possible. Thirty-year-old daughter Casey Durnil, also of Columbus, will need one soon enough.

Both have progressive polycystic kidney disease. It causes numerous fluid-filled cysts to grow in the kidneys, reducing kidney filtering function and eventually leading to organs failure, according to the National Kidney Foundation.

The mother has only 15 percent kidney function. The daughter only 12 percent, although she must make other medical-related adjustments before she can be considered for a transplant.

“There’s got to be at least one person out there who has an O (blood type) kidney for my wife,” said Gerry Jones, Patterson’s husband of seven years. “So I pray that someone else has the heart and soul to care enough to donate a matching one for Debbie. This is my prayer every minute of every day.”

Patterson recently sat in their 31st Street living room with a textbook-thick binder filled with medical background and notes, much of it highlighted in yellow marker, about her and daughter’s condition.

The mother suffered through back pain at work just that day from problems in her left kidney. There’s not much she can do for such obstacles other than taking acetaminophen.

Patterson was diagnosed in March 2010. Doctors diagnosed Durnil a year and a half later.

Durnil could begin daily dialysis within a few weeks as a step to help her. Both still work full-time at Phoenix Quality Management, a supply chain services company in Walesboro.

But Patterson notices regular reminders that her kidneys are struggling. Partly because she is low on absorption of iron and other vitamins, she couldn’t even muster the strength to drive a small yard-sale stake into the soft, rain-soaked ground of her lawn recently. But still, she managed to laugh at her plight.

“What else am I going to do?” Patterson asked. “Sit here and cry?”

She has been on the organ-donor waiting list for a year amid a process that sometimes stretches to five years.

She knows the number of people in the United States waiting for a kidney is more than four times greater than the number of transplants.

The United Network for Organ Sharing shows that in 2016, there were 19,060 kidney transplants nationally. And there are currently 96,966 people in the United States on the waiting list for a kidney.

The network also shows that kidneys rank as the most in-demand organ for transplants, far outpacing the need for other organs such as livers, hearts, and lungs, needed in that order.

Dr. Jennifer Bucki, Patterson’s nephrologist with Indiana Kidney Specialists in Indianapolis, said she has straightforwardly laid out the facts about the average wait for a new kidney, and other factors affecting Patterson’s situation “hopefully without being too blunt.” But the physician also mentioned that her patients also must remember that she has seen firsthand a number of transplant success stories among those she has treated.

Bucki complimented Patterson’s upbeat ways amid substantial challenges.

“She has a good attitude, even though she has experienced her share of ups and downs, including seeing changes in her body, and changes in her endurance as her disease has become symptomatic,” Bucki said.

The specialist supports publicity about cases such as Patterson’s.

“It helps the community become involved not only in thinking about their own health, but also with them thinking about becoming organ donors,” Bucki said.

Jones, a semi-truck driver in Indiana and Kentucky, soon will spread the word about needing a kidney donor by posting a message on his vehicle as he roams the interstates.

“There’s got to be at least one person out there (who’s a donor match),” said Jones, who is the wrong blood type to be a donor.

A number of people have tried to donate. But none who were a blood type O match made it through the initial phone-screening interview as a viable donor candidate.

So they wait. And hope. And pray, along with others. [Read more]




From Stuff, New Zealand

Kiwi basketball great Kenny McFadden diagnosed with serious kidney disease

Kenny McFadden (R) played a huge part in Steven Adams' development.

Kenny McFadden (R) played a huge part in Steven Adams' development.


Kenny McFadden, Kiwi basketball great and mentor to Steven Adams, has been struck down by a serious kidney disease.

The American-born former Wellington Saints player-coach was rushed to hospital several weeks ago with acute respiratory failure.

While he managed to pull through following a night of "extreme medical intervention", McFadden was subsequently diagnosed polycystic kidney disease, a genetic disorder that requires regular dialysis until a suitable kidney donor can be found, his friends say.

For more than 30 years McFadden has made a significant impact on basketball in this country as both a player and coach.

However, a Give A Little page set up by friends and colleagues of his partner, Angelia Beamsley, said the illness has left him unable to work.

"This is placing heavy financial strain on him and his partner which on top of regular visits to the hospital is making a tough time that much harder," a statement on the page said.

"By creating this page we are attempting to raise funds to help with his quality of life and to ease the burden on his partner and family."

After playing for Washington State University in the USA, McFadden moved to Wellington in 1982 where he enjoyed great success with the Saints.

He led the team to seven finals appearances, winning five NBL titles between 1982 to 1988.

Following his retirement in 1996, McFadden became heavily involved with junior player development, founding his own hoops academy in Wellington as well as coaching the Junior Tall Blacks to the under-19 World Championships in 2009.

It was through his coaching work that he met Adams, and he went on to play a key role in the Kiwi's miraculous rise to the top of the basketball world with the NBA's Oklahoma City Thunder.

McFadden first took Adams under his wing as a 14-year-old who had been shifted by an elder sibling to the capital from Rotorua in order to get his life back on track.

He has been the young man's mentor ever since, refining his skills early on at his academy and then later providing the guidance and advice as the young man headed stateside to chase his dreams.





PKD Walk

From Milwaukee Journal Sentinal

Milwaukee Walk for PKD:

Event is 2.5 mile benefit for polycystic kidney disease, 10 a.m. Sept. 10. Registration begins at 8:30 a.m. Bayshore Town Center, 5800 N. Bayshore Drive, Glendale. Registration is free; donation requested. walkforpkd.org/milwaukee




Dialysis Research

From WOW News, Malaysia

UTM researchers develop haemodialysis system using membrane technology



Statistically, it is estimated that one in twelve Malaysians has kidney failure and millions more are at risk. Commonly, these patients need dialysis treatment when they reach the final stage of kidney failure or typically known as the end-stage renal failure (ESRF), where they lose 85% to 90% of their kidney function.

In Malaysia, the number of dialysis patients keeps increasing with the estimation of 5,000 new cases of ESRF being reported each year. The statistics from the National Kidney Foundation Malaysia reveals worrying figures where the total number of haemodialysis patients had increased from 12,182 patients in 2005 to 38,157 patients at the end of 2016. In fact, with he right projection there will be 43,000 haemodialysis patients altogether by the end of 2017.

Every year, the government allocates RM50 million to cater to the cost of treatment of around 38,000 ESRF patients. However, only 35,580 patients from that number undergo haemodialysis treatment. Out of the 35,580 patients, government hospitals are able to cover the expenses for only 8,000 patients. The remaining patients have to solely rely on the subsidy from the Government and NGOs. According to local sources, the amount paid by each patient for every session is RM162 (around USD$38 with government subsidy), and part of the amount comes from the cost of the haemodialyser. It is known that the market price for an imported haemodialyser can be as high as RM125 (US$30) per dialyser depending on the brand and packing size. Therefore, immediate action is needed to compensate and reduce at least the cost of haemodialyser.

To that end, UTM made it a mission to establish its own brand for renal products, starting with the production of a haemodialyser. In order to do that, Prof Dr Ahmad Fauzi Ismail and his team from the Advanced Membrane Technology Research Centre (AMTEC), Universiti Teknologi Malaysia (UTM), began their research into creating a home-grown haemodialysis system for blood purification using membrane technology that would greatly reduce the cost of treatment for Malaysian ESRF patients, and the government and NGOs who are subsidising treatment. This is because at present, hospitals and haemodialysis centres in Malaysia solely depend on imported renal products from modern countries like Japan and Germany.

The project started with the development of a high performance haemodialysis membrane, where prior to membrane fabrication process, a polymer solution was prepared by mixing 18 wt.% polysulfone and 8 wt.% polyvinylpyrrolidone in N-methyl-2-pyrrolidone as the solvent. Both membrane and haemodialyser were produced using in-house equipment and instruments producing a well-optimised membrane specifically designed to remove critical uremic toxins while retaining essential proteins like albumin in blood, resulting in an optimised blood purification process. Further, along with the low production cost and high flux achievement, this home-grown haemodialyser is capable of removing sufficient amounts of uremic toxins from a patient’s blood including a large fraction of recalcitrant middle molecular weight molecules.

It is anticipated that the reduced price of this home-grown haemodialyser, in addition to the product’s trusted performance, will heighten the chances of market penetration in Malaysia, with the potential to greatly reduce costs borne by patients, the government, and NGOs, freeing up valuable resources to be used in other high impact projects that cater to the nation’s needs. With such an impact to Malaysian society as a whole, it is little wonder that UTM’s long-term goals include making Malaysia a regional base for renal products in Southeast Asia, and perhaps one day, the world.

Sunday, August 6, 2017

PKD Chain of Life, Donor Kidneys Rejected, DonateLife Week, PKD Creates Giant Liver

Gift of Life

From US News & World Report, By Dennis Thompson


A donated kidney is turned away for transplant an average of seven times before reaching the patient who finally receives it, a new study shows.

Transplant centers regularly reject kidneys based on a donor's age or perceived quality of the organ, even though these kidneys are eventually accepted and work well for people farther down the waiting list, explained lead researcher Dr. Anne Huml, a nephrologist and health disparities fellow with Case Western Reserve University in Cleveland.

The centers are likely being appropriately picky in selecting organs, to ensure the greatest chance of success by carefully matching each kidney to each recipient, Huml said.

"If someone's been waiting five years, why rush and take the first kidney offered when within a month they'll be offered a better kidney and their outcome will be better?" Huml said.

But such hesitation can mean that patients high on the waiting list remain on dialysis while organs that would have suited them fine pass down to others who've waited less time, said Dr. Sumit Mohan, an associate professor for medicine and epidemiology at Columbia University's Mailman School of Public Health.

"The general sense is that surgeons are less willing to take risks, so what ends up happening is there are a large number of kidneys that people say no to that end up getting transplanted way down the list," said Mohan, who co-authored an editorial accompanying the study. Both appear in the July 27 issue of the Clinical Journal of the American Society of Nephrology.

Worse, patients rarely are told that their transplant center has passed on a donor kidney offered to them, Mohan said.

"If your surgeon says no, I don't want that kidney, you're never informed. You're not even told that's the case," Mohan said. "Patients need to be more engaged in the process and have a better understanding of what's being agreed to on their behalf."

More than 100,000 people currently are waiting for a kidney transplant in the United States, Mohan said.

Despite this, nearly 1 in 5 deceased donor kidneys are discarded annually. Nearly 15 percent of organs are tossed away because no recipient can be located, Mohan said.

Dialysis keeps a delay in receiving a kidney from becoming immediately life-threatening, Huml said. However, there is a high mortality rate associated with dialysis, and people who are on dialysis longer don't do as well once they have received a kidney, Mohan said.

For the study, Huml and her colleagues reviewed more than 7 million organ offers that were made for 31,230 kidneys from deceased donors between 2007 and 2012. All the kidneys were eventually transplanted.

The researchers found that donor kidneys were offered a median of seven times to different patients before being accepted for transplantation.

Centers most often gave a pass to a donated kidney either based on donor-related factors such as age of the person or quality of the organ, or because the minimal acceptable criteria for a transplant center had not been met. Each of those two general reasons accounted for 3.2 million rejected offers, or around 45 percent.

Transplant centers largely pass on kidneys from donors with high blood pressure, a history of diabetes, reduced kidney function or death related to heart problems, the researchers found.

In those cases, centers that want to keep their success rates high are rejecting organs that appear dicey, even though they end up being successfully transplanted into another patient, Mohan said.

The study also found that transplant centers are more picky in choosing kidneys for patients who are male, Hispanic, overweight or obese, or suffering from high blood pressure resulting from kidney failure, Huml said.

Patients with medical problems such as excess weight or high blood pressure likely face more difficult surgeries, and so doctors are more choosy about the kidney that's right for them, Mohan explained. [Read more]




From Hartford Courant, CT

Yale-New Haven Hospital Puts Connections On Display In 18-Patient, 9-Kidney Exchange

Yale Kidney Chain

As Janet Labati, a small, thin woman from Newtown, sat next to her kidney donor Laura Miller, of Old Lyme, the two women whispered and laughed like old friends. However, it was the first time they had ever met.

"She's my angel," Labati said as she rested her hand on Miller's arm. "I'm so grateful just to be able to walk around and feel good again."

Emotions ran high on Thursday at the Yale-New Haven Hospital when nine kidney transplant patients met their donors for the first time. All had been strangers, but they are forever linked in an 18-patient, nine-kidney exchange; the largest exchange ever performed in Connecticut.

When a previous transplant failed, Labati said she thought she was out of options.

"Kidney disease had taken a toll on my body," she said. "I contacted the hospice to discuss end of life care, I never dreamed I would have a third chance."

But her husband, Jim Labati, wouldn't give up on her. He said he donated one of his kidneys through Yale's kidney exchange program in the hopes that his wife would receive a kidney and no longer require the use of a dialysis machine to filter toxins from her bloodstream.

"Being on dialysis is surviving but it's not living," he said. "I donated a kidney so Janet could receive a kidney."

Miller said she had originally wanted to donate to her friend Randy Smith of Old Lyme.

"I feel rewarded and pleased that I saved a life," Miller said. "How many people can say that at the end of the day?"

The mastermind behind the exchange was Dr. Peter Yoo, director of Yale's program in paired organ exchange. He said it started with one altruistic donor, Robin Gilmartin, of West Hartford. Gilmartin and her wife, Diane Mack, both said they decided to donate their kidneys after reading an article in the Hartford Courant about a four-way kidney exchange performed at the hospital. Her only motive was to help others, she said.

"Donating a kidney is an extremely low-risk surgery. It doesn't change your functioning in the least," Gilmartin said. "For relatively little inconvenience, it's a tremendous reward."

Little did Gilmartin know that her decision to donate would set off a chain reaction in which Yoo was able to match 18-patients together. [Read more]




From Bendigo Advertiser, Australia, by Mark Kearney

Bendigo kidney recipients use DonateLife Week to describe how organ donation changed their lives


On meeting Maree Derby, it is impossible to tell that just five weeks ago she was the recipient of a kidney transplant.

Her mood is upbeat, her eyes are bright and 18 months of dialysis at Bendigo Health already feels like a distant memory.

“Sometimes I’ve got to remind myself to slow down, that I’ve had a major operation,” Ms Derby, who suffered from polycystic kidney disease, said.

Speaking during DonateLife Week, an annual initiative encouraging organ and tissue donation, the 52-year-old explained how gifted organs transformed her family’s life.

Not only was Ms Derby an organ recipient, her mother, Gwen, also underwent a kidney transplant for polycystic kidney disease.

Her 25-year-old daughter has also been diagnosed with the hereditary condition.

“It does follow you around a little bit, but you have to get on with it,” she said when asked how it felt knowing this was a process she would eventually endure.

“I also think it gives you time to accept it.”

Peter Van Schajik, another Bendigo kidney recipient, did not have so long to prepare; he was struck down last year with an aggressive case of IgA nephropathy, a build-up of antibodies in the kidneys.

Eight weeks ago, a transplant operation freed him from four days of dialysis every week. It also put to an end a horror three-year period during which time a workplace accident left Mr Van Schajik with burns to 35 per cent of his body.




Living with PKD

The Sydney Morning Herald, Australia, by Rachel Clun

Woman donates 12 kilogram liver to university learning museum

Fiona Murray with her donated liver.



Fiona Murray's liver was large. So large people would often ask her when her baby was due.

A healthy human liver weighs about 1.5 kilograms, but Ms Murray's weighed a massive 12.08 kilograms when it was removed.

"When I actually had the operation I said, 'can somebody take a photo of it for me' but they took one step forward and said,'well actually, the fellow in pathology said could we actually have it for the museum'," she said.

And after receiving a donor liver and kidney herself, Ms Murray said she jumped at the chance to donate her own to science.

"I just said, 'yeah that would be great, I don't mind, I don't need it'."

The Brisbane woman's liver was donated to the University of Queensland's Integrated Pathology Learning centre, where she said students can now use it as a learning tool.

"If someone's donating to me, for me to live and do all the things that I love to do so if someone would like to learn from my donation, then that was pretty much just giving the gift of knowledge," she said during DonateLife Week.

Ms Murray, now 47, was diagnosed with polycystic kidney disease when she was 25 years old. When she was in her 30s the disease spread to her liver, which continued to grow.

"(It was) rather uncomfortable, it's pretty much like being pregnant for years and years," she said.

Strangers would often ask her when she was due, but rather than get annoyed Ms Murray said she would use it as a way of bringing up the topic of organ donation.

"I didn't get sick of that totally; sometimes it was just more of an avenue to tell people, 'oh no that's not a baby bump, it's actually polycystic liver due to polycystic kidneys and I need a donation of a liver and kidney."

While Ms Murray said she didn't feel particularly unwell, she realized her condition was serious when dialysis failed to improve her health.

"It was making it worse: I lost a lot of weight, I was cramping up on the chair, my liver was so big it was encroaching and sitting and suffocating all the other organs when I was sitting on the dialysis chair," she said.

She was on the transplant list for just a couple of weeks before receiving a donor kidney and liver in early 2014.

As well as being able to now bend down and do up her own shoelaces, Ms Murray said she had been enjoying the freedom the transplant had given her.

"Life now is my own journey, I don't have to think about having to go on dialysis, I can do whatever I want now, I can choose," said Ms Murray, who has just completed a course in medical administration and plans on studying to be a radiographer. [Read more]