Sunday, January 31, 2016

PKD Treatment: Eating Less; 3D Printing Aids Kidney Transplant

PKD Research

From Eureka Alert

A diet dividend

Members of the Thomas Weimbs Lab at UCSB demonstrate that reducing food intake in mice diminishes the growth of their polycystic kidneys

UNIVERSITY OF CALIFORNIA - SANTA BARBARA

What if polycystic kidney disease (PKD) could be combatted with a strategy as simple as dieting? Such a finding would surely be welcome news to the 12 million people worldwide with the genetic disease.

New research from UC Santa Barbara suggests that reducing food intake may slow the growth of the cysts that are symptomatic of PKD, an inherited disorder in which clusters of cysts develop in the kidneys.

A study by biologist Thomas Weimbs and colleagues has demonstrated that in mouse models, a modest decrease in food intake resulted in substantially diminished cyst growth. The findings appear in the American Journal of Physiology - Renal Physiology.

"Amazingly, the growth of polycystic kidneys was quite strongly inhibited with the reduced food intake, suggesting that these organs are much more sensitive to nutrients than the rest of the body," said Weimbs, a professor in UCSB's Department of Molecular, Cellular, and Developmental Biology. "That's very interesting because if we translate this to a human population, the regimen should be something that would be potentially feasible for PKD patients to follow."

The researchers were particularly interested in the mTOR pathway, the mechanistic target of a drug called rapamycin, which has been studied as a potential treatment for PKD. When nutrients are abundant, the mTOR pathway -- important in regulating cell growth and proliferation -- is highly active. So the investigators hypothesized that limiting nutrient supply might affect the pathway's activity and tested their theory in mice with polycystic kidneys.

Animals in the control group had free access to food and showed a kidney weight increase of 151 percent during the study period. Those in the experimental group, in which food intake was reduced 23 percent, experienced only a 41 percent gain in kidney weight. "That's pretty substantial," said Weimbs. "The reduction is similar to what we would see with rapamycin treatment but without the side effects."

The researchers also looked at other parameters, such as proliferation of the cysts and the inhibition of other molecular pathways. "Not only did the size of cysts decrease significantly but pathways were inhibited as we expected them to be," Weimbs said. "All of this made sense with our initial hypothesis."

Moving from animal to human studies, however, would require additional research as well as clinical trials. Still to be determined is whether the sizable effects seen in this study are due to simply decreasing caloric intake or to a reduction in a particular nutrient group, such as carbohydrates, lipids or proteins.

"That's something we really don't know, but it's something that can be easily tested and should be, because potentially we only have to reduce one nutrient group and not all of the others," Weimbs explained. "Or maybe it's just the caloric intake. We need to know which before it makes sense to move forward with a clinical trial."

The results of the Weimbs Lab's research are similar to another recent study conducted at the Mayo Clinic in Rochester, Minnesota. While that group used slightly different mouse models and a more severe level of food restriction -- 40 percent -- the results also demonstrated a reduction in cyst growth.

"Two groups using different protocols and different models that come to the same conclusion strengthens the overall findings and makes a clinical trial much more justifiable," Weimbs concluded.




Kidney Dialysis News

From Belfast Telegraph, Northern Ireland, By Joanne Sweeney

Little Lucy Boucher in world first as she receives father's kidney with help of 3D printing

Daniel, Ciara, Chris and Lucy Boucher

Little Lucy Boucher has made medical history by receiving the world's first successful transplantation of an adult kidney into a child aided by 3D printing.

The three-year-old Antrim girl received her father Chris' kidney when she underwent the pioneering operation last November.

3D printing was used by the surgical team at Guy's and St Thomas' and Great Ormond Street Hospital in London to intricately plan the complex operation.

By producing life-sized plastic anatomically correct models of both the father's kidney and his daughter's much smaller abdomen, the team were able to see beforehand the challenges they faced in transplanting the larger organ.

The 3D printer produces a model of liquid plastic, based on measurements taken through CT and MRI scans.

Last night, her father described Lucy - who suffered heart failure at just four weeks old - as the "bubbliest, bounciest, happiest, active little girl" around.

And he revealed that the medical challenge of keeping Lucy alive resulted in a ground-breaking dialysis machine being adapted to suit her needs, which will benefit other infants in the future.

He said: "There was some worry that Lucy had also experienced neurological damage but she's met every developmental milestone: she's talking, she's counting, she's getting up to everything.

"We are so thankful to all the medical teams who have helped her along the way and our families and friends who supported us."

Mr Pankaj Chandak, a transplant registrar at Guy's and St Thomas', whose idea it was to use 3D printouts, said: "Lucy has been through a tremendous amount. She's great-spirited and her family were fantastic. It was a great pleasure to have helped her and to do this kind of work."

Sunday, January 24, 2016

Gift of Life Continues: Toddlers, Father-Son, Rival Baseball Fans; PKD Proteins Team up on Cilia

Gift of Life

From People Magazine, BY ROSE MINUTAGLIO

Adorable Toddlers Become Best Friends After Receiving Kidney Transplants: 'Their Friendship Is so Amazing'

Toddlers Find Love in a Hospital

Aubrey and Ayden have become best friends
KATHERINE C. COHEN/BOSTON CHILDREN’S HOSPITAL

When the going gets tough, it's nice to have a best friend to lean on.

Ayden Mosher, 3, and his bestie Aubrey Ferrell, 2, met in September in the lobby of Boston Children's Hospital while receiving outpatient care for their respective successful kidney transplants.

The two have been inseparable ever since.

"It was like love at first sight!" Boston Children's renal transplant coordinator and nurse practitioner Courtney Loper tells PEOPLE. "They connected with each other over a coloring book and just had this instant bond."

Ayden, of Herkimer, New York, and Aubrey, a Milan, Tennessee, native, only see each other while in Boston for follow-up appointments, so hospital staff always makes sure to schedule the two on the same day.

"We have a lot of kids come in here and play together, but these two were something else," Dr. Nancy Rodig, medical director of renal transplant at Boston Children's, tells PEOPLE. "Aubrey would come out and search the hallways for him, calling his name. She would be on a mission to find him!"

The doctor adds with a laugh, "Oh, and Ayden absolutely loves the attention she pours on him. It's so, so adorable."

Ayden was born with polycystic kidney disease, a disorder which causes clusters of cysts to form within the kidneys.

The toddler received a transplant from his aunt in September and has been coming to Boston Children's Hospital for outpatient care ever since.

"He used to be upset that he had to get his blood work done, and we'd say, 'Well, Aubrey has to do it too!' " Ayden's mother, Cindy Davis tells PEOPLE. "It makes him feel better to know she is going through the same thing, they benefit each other. They help each other to be strong." [Read more]




From Today FM, Dublin, Ireland

DAD SAVES SON'S LIFE WITH KIDNEY TRANSPLANT

Today FM image

Darren and Mike Burns (pic with thanks to Tralee Today)

19-year old Darren Burns from Kevin Barry's Villas owes his new lease of life to his dad Mike, who donated one of his kidneys to his son during a five-hour procedure at Beaumont Hospital earlier this month.

Big-hearted Tralee man Mike saved the life of his son Darren (19) by donating him one of his kidneys and says everyone should carry a donor card, as someone’s life is literally in your hands. He told Anton Savage on the Anton Savage Show today that he did not give donating his kidney to Darren a second thought. For one week of soreness, his son has a life, he revealed.

The pair were cool as a cucumber about the procedure, which took place at Dublin’s Beaumont Hospital, which carries out all adult kidney transplants in Ireland.

Darren diagnosed with Polycystic Kidney Disease at 9 years of age but as he tells Anton it didn’t get in the way of an active life. “I just belted away with it” he said. He had thought pain was appendicitis as it felt like a stitch, but thanks to his mothers determination to get to the bottom of it and her sense that something wasn’t right, he was diagnosed in time.

He could have had a massive heart attack at just 9 years of age if he had not been diagnosed in time.

He’s been on a strict medication regime ever since to keep the condition under control but carried on with his life. “It’s pointless thinking about it, you just belt away,” the positive-thinking lad told Anton.

Back in 2013 his condition began to deteriorate and 4 months ago he was referred to Beaumont Hospital having been told that he needed a life-saving kidney transplant. Luckily, both of Darren's parents Mike and Denise were deemed suitable donors. Not all parents are suitable donors, explained Mike

As the pair recuperate at home in Tralee, they will be in and out of hospital for tests, but Darren says he will be up and running soon and wants to carry on playing football with Tralee’s Na Gaeil. In fact, he played football right up until day before transplant!




From Total Pro Sports

Cubs Fan Donates Kidney to Five-Year-Old White Sox Fan

cubs fan donates kidney to 5-year-old white sox fan drew duszynski


Five-year-old White Sox fan Drew Duszynski was recently given the most amazing gift he’ll ever get in his life. And it came from a complete stranger who just so happens to be a Cubs fan.

Drew was born with a condition called autosomal recessive polycystic kidney disease, which basically means his kidneys just didn’t work properly from day one. For the first three years of his life Drew was able to manage his condition by taking up to six medications daily to control high potassium, high phosphorous, and high blood pressure. However, by year four his kidney function started to decline rapidly. And by June 2015 both of Drew’s kidneys were removed, meaning he had to undergo dialysis every single day.

At that point, all Drew’s parents could do was sit around and pray that an adult donor would come forward in time to save their son. Meanwhile, friends and family started holding fundraisers and spreading the word via social media, hoping for a miracle.

Then, one day, a 35-year-old man named Chris White came into their lives. He had heard about Drew from his wife, who had heard about him through a friend, who had heard about him through mom’s group on Facebook. White immediately knew that, if he was a match, he wanted to donate a kidney to Drew. His own son, Jack, was also five years old. And he had witnessed first-hand the difference he could make in Drew’s life because his wife donated a kidney to her father years before.

Fortunately, it turned out that Drew and Chris were a match. So the procedure took place last month at Children’s Hospital of Milwaukee.

The fact that Drew is a White Sox fan and Chris is a Cubs fan was not lost on no one.

“I hope that my donation might, at some point, set him straight and influence Drew’s choice in baseball teams,” Chris told Redeye Chicago.

Of course, if you know anything about the Cubs-White Sox rivalry, you know that not even a life-saving act of kindness will be enough to change Drew’s loyalties.




From GazettExtra, Walworth County, Wisconsin, by Catherine W. Idzerda

Janesville couple gives life, gets life



Imagine this: a flock of airborne kidneys, migrating across country in quest of a new home.

It's a migration that requires perfect matches, perfect timing and perfect love.

In exchange, participants get a chance at life.

In December, Gail Chesmore gave her husband, Dan Chesmore, her kidney. Or rather, she exchanged her kidney for someone's healthy one, a swap likely to save at least two lives—perhaps more.

The Chesmores' story started several years ago, when Dan discovered he had polycystic kidney disease, an inherited condition.

Like many other people with the disease, Dan ended up needing a kidney transplant. In 2010, he was lucky enough to get one from his uncle.

But Dan's body started to reject the kidney, and by August 2014, he found himself in the hospital again. Doctors gave him steroids to help reverse the rejection. But the steroids caused a stomach ulcer that led to additional surgery.

By the time his stomach healed, his kidney had failed.

In April 2015, doctors removed the kidney.

“It just wasn't doing him any good,” said Gail.

Throughout this time, Dan was going to dialysis four hours a day, every other day.

In March, Gail decided she would be a living donor for her husband, and doctors said she was a match.

Surgery was scheduled July 1.

“Two weeks before the surgery, they told me I was no longer a match,” Gail said. “It really sucked.”

Dan's antibodies, the substances the body uses to fight infection and foreign pathogens, had changed too much.

“I was disappointed,” Dan said. “We were all ready to go. We were all hoping for this.”

On July 23—Dan's birthday—Gail told him she was willing to take part in the paired kidney exchange program at the University Hospital.

“There are other couples like us out there,” Gail said. “They have a willing donor, but there's not a match.”

In the paired kidney exchange, donors and recipients are entered into a database, and the hunt for donor-recipient pairs begins.

It can be two couples, or it could be many more. Think of it as a large circle of donors and recipients with the lines of connection crisscrossing the center.

“In Madison, they said they had a chain that effected 70 people,” Gail said.

More than 50 transplant centers involved in the “paired kidney exchange” greatly increases the number of compatible matches, according to the University Hospital's program.

In addition, living donors improve patients survival rates and better long-term function for the transplanted organ, according to the transplant program.

Gail and Dan think there were three couples involved in their exchange.

For the paired exchanges to work, donor and recipient surgeries are scheduled the same day. Gail had her surgery in the morning. Meanwhile, Dan's donor was having surgery in another part of the country. There might have been other donors in their exchange, as well.[Read more]



PKD Research

From Journal of Neuroscience (PDF of article available)

Pkd Proteins Team Up to Tell Cilia Which Way to Go
 



Living with PKD

From The Houma Courier, Houma, LA, By Kevinisha Walker

Houma woman waiting on kidney transplant

Some days, Joan Ledet Stoks is in good spirits. Other days, she's extremely tired and exhausted. She often can't stand for very long because her back aches so badly.

"Even sweeping the floor is painful," the Houma native said.

While Stoks' pains seem run of the mill, the disease that causes them isn't.

Stoks is suffering with Polycystic Kidney Disease, which is a genetic disease that causes uncontrolled growth of cysts in the kidney.

Stoks' father, who died from complications stemming from the disease, passed it down to her and her siblings.

In addition to large cyst growth, symptoms include back aches, high blood pressure, blood in the urine, kidney infections, kidney stones, kidney failure, aneurysm of the brain and enlarged bellies.

Her sister Jeanine Louviere died from the disease's complications in 2012, and while her brother Mark died a year later from lung cancer, he suffered with the illness, too.

Now, Stoks and her brother Leonard Ledet, Jr. are the only two living siblings.

"I just can't put into words what it means to have these two kids with me now because I lost my other two," EraMae Halbert said of her remaining children.

Eight years ago, Ledet, Jr. received a kidney transplant as he was suffering with complications of PKD.

Currently, Stoks is hoping for a miracle as a chance encounter over the summer with a California woman may lead to a kidney transplant.

The 57-year-old attended her stepdaughter's graduation party in San Diego last June. And after sharing her PKD struggles with Rebecca Quinones Sergi at the party, Sergi offered to get tested for the kidney transplant.

Sunday, January 17, 2016

Two Day Break in Dialysis Could be Fatal; Gift of Life; Inhibiting Aerobic Glycolysis

Living with PKD

From MedicalXpress

Two day break in treatment for dialysis patients could be fatal, study finds

Patients who have kidney dialysis three times a week are more likely to be admitted to hospital or die after a two day break, according to a study by a leading kidney researcher at the University of Sheffield.

Dr James Fortheringham from the Sheffield Kidney Institute has found there is a 69 per cent increase in hospital admissions and a 22 per cent increase in deaths after a two day break in three times a week haemodialysis.

To help reduce hospital admissions and boost the survival prospects of kidney dialysis patients, Dr Fotheringham has now been awarded a five year fellowship by the National Institute of Health Research (NIHR) Clinician Scientist Award panel – one of only six researchers to be awarded the fellowship this year.

Building on this study, James will now continue his work to understand and reduce the harm being caused by the two day break.

"I'm trying to identify who it is that is getting admitted to hospital and dying after this two day break and why. Harnessing existing data including the valuable UK Renal Registry I will examine if wider use of some of the care techniques we already use here in the UK can combat the two day break problem," Dr Fotherigham said. [Read more]


PKD Research

From National Institutes of Health (NIH)

Inhibition of Aerobic Glycolysis Attenuates Disease Progression in Polycystic Kidney Disease

Abstract

Dysregulated signaling cascades alter energy metabolism and promote cell proliferation and cyst expansion in polycystic kidney disease (PKD). Here we tested whether metabolic reprogramming towards aerobic glycolysis ("Warburg effect") plays a pathogenic role in male heterozygous Han:SPRD rats (Cy/+), a chronic progressive model of PKD. Using microarray analysis and qPCR, we found an upregulation of genes involved in glycolysis (Hk1, Hk2, Ldha) and a downregulation of genes involved in gluconeogenesis (G6pc, Lbp1) in cystic kidneys of Cy/+ rats compared with wild-type (+/+) rats. We then tested the effect of inhibiting glycolysis with 2-deoxyglucose (2DG) on renal functional loss and cyst progression in 5-week-old male Cy/+ rats. Treatment with 2DG (500 mg/kg/day) for 5 weeks resulted in significantly lower kidney weights (-27%) and 2-kidney/total-body-weight ratios (-20%) and decreased renal cyst index (-48%) compared with vehicle treatment. Cy/+ rats treated with 2DG also showed higher clearances of creatinine (1.98±0.67 vs 1.41±0.37 ml/min), BUN (0.69±0.26 vs 0.40±0.10 ml/min) and uric acid (0.38±0.20 vs 0.21±0.10 ml/min), and reduced albuminuria. Immunoblotting analysis of kidney tissues harvested from 2DG-treated Cy/+ rats showed increased phosphorylation of AMPK-α, a negative regulator of mTOR, and restoration of ERK signaling. Assessment of Ki-67 staining indicated that 2DG limits cyst progression through inhibition of epithelial cell proliferation. Taken together, our results show that targeting the glycolytic pathway may represent a promising therapeutic strategy to control cyst growth in PKD.



Gift of Life

From Birmingham Mail, United Kingdom

Brave Birmingham police worker to donate a kidney to save his brother's life



As a Birmingham police officer he is used to protecting the public - and now David Footman is preparing to help save his brother’s life.

The big-hearted Police Community Support Officer is donate a kidney to his older sibling Paul who desperately needs a transplant.

Paul, aged 39, was diagnosed with adult polycystic kidney disease 15 years ago but his condition has begun to deteriorate in recent years.

When the Birmingham chef was told that without a transplant he faced kidney failure, his brother David was quick to offer to donate one of his own kidneys in a bid to save him.

David, a dad-of-two from Kings Norton, said: “We didn’t really have a conversation, I knew he was getting worse and he needed to have this done.

“I am just grateful I am able to help. I like to make a difference as a PCSO and with it being family this was always something I was going to do.

“Hopefully, we can raise awareness of kidney disease and the importance of diagnosis.

“The force has been really supportive and I am looking forward to joining back up with the rest of the team afterwards.”

The 37-year-old will go under the knife in the next few months and said he will return to pounding the streets of Stechford and Yardley after he has had time to recuperate from the operation.  [Read more]




From CBS Affiliate, Channel 2, Los Angles, CA

Diamond Bar Man Celebrates Gift Of New Kidney From Wife Of An Old Coast Guard Buddy

A Diamond Bar father has gotten a new lease on life following a life-saving kidney transplant.

CBS2’s Michele Gile says his Coast Guard family stepped up in a big day.

Frank Maggelet and Patricia Lovenstein had only met twice but she had no doubt that he — a retired Coast Guard Port security chief — would get her kidney.

“Well, first of all there was no if,” she said, “I knew that it was going to happen.”

She considers him, a husband and father, like her own family.

A decade ago, her husband was his senior officer — buddies in the Coast Guard, stationed together in Boston.

A few months ago, Lovenstein — a former nurse — read on Facebook that Maggelet needed help and was in dire need of a new kidney after he developed polycystic kidney disease.

“He still has never asked me for my kidney,” she said, with a laugh, “it’s already in him. It’s a little late for that. But he’s never asked. No one ever asked me to do this.”

The transplant took place at UCI Medical Center in Orange on Tuesday.

Her left kidney now sits in his right abdomen.

Today was the first day the two got to share a private moment without family around. He was able to whisper a “thank you” to Lovenstein, grateful that the transplant came at just the right time. He was left with a kidney that barely functioned.

He learned on Thanksgiving night that he will have many more years to spend with his wife and young daughters.

“Patricia called, and the hospital called. ‘You’re a match.’ And the four of us, Thanksgiving evening, we cried,” said Maggelet, “because it was like a miracle.”




From WKRN, ABC affiliate Channel 2, Nashville, TN

Michigan woman donates kidney to husband

Courtesy: WOOD-TV



GRAND RAPIDS, Mich. (WOOD) — A Michigan man celebrated his 55th birthday Thursday with a gift from his wife he’ll likely never be able to match.

Jim Sisson suffered from polycystic kidney disease, a rare genetic disorder.

His father died from complications of the disease in the 1980s.

Sisson got on a waiting list for a new kidney, joining more than 100,000 people nationwide. He was prepared for a wait that could last years.

But it turned out a match was living under the same roof – his wife Laurie.

“We’ve been very blessed. There’s so many people out there that are not this fortunate,” Laurie Sisson said.

On Monday, the transplant team at Mercy Health Saint Mary’s hospital in Grand Rapids, Michigan took one of Laurie’s kidneys and put it inside Jim.

“He kept saying he didn’t want me to of it. He wouldn’t think any less of me if I didn’t. I said, ‘God didn’t make me a match for me to be selfish and keep the kidney to myself,’” Laurie Sisson said.

“There was never once I looked back thinking I don’t want to do this.”

Laurie’s kidney worked for her husband — in more ways than one.

“I’ve been praying for a long time that we could reignite a spark. You know, when you’re married 35 years sometimes it takes a little oomph to get things where they should be,” Laurie Sisson said.

“You’ve got to be careful what you pray for.”

If there’s one message the couple wants to get out, it’s the importance of organ donation.

In Michigan alone, the waiting list for a new kidney is longer than 2,800 people. More than 350 people are waiting for a call from Mercy Health Saint Mary’s transplant program.

Jim Sisson said he was looking at a wait of up to eight years for a new kidney.

“If I would have went to Ohio, I could have got one within a year or two maybe because they have a lot more people that signed the registered donor list,” he explained.

Thursday, just three days after receiving his new kidney, Sisson celebrated his 55th birthday. His next challenge, he said, will be coming up with a gift for his wife.

“Always wanted to go on a trip,” Laurie Sisson hinted.

“Wherever she want to go now. Who’s she kidding?” her husband said.

Sunday, January 10, 2016

Kidney Allocation Debate; Finding a Kidney; Decline in Living Kidney Donors; Location, Location

Getting a Kidney

From Nephrology News, by LANA SCHMIDT, MBA

Is the new kidney transplant allocation system fair?

We have an epidemic in the United States—a shortage of kidneys. But older patients and those who have been on dialysis a long time waiting for a kidney are least likely to receive a deceased donor kidney transplant with the new kidney allocation system.

At 57 years old and over 13 years on dialysis when the new Kidney Allocation System was implemented last year, I immediately dropped significantly from the top percent of the list. Years on dialysis is no longer a factor in moving candidates up the list, in fact, it is the exact opposite. Years on dialysis now only is considered if there is a tie for a kidney. With KAS’s new goals of matching kidneys with similar age recipients and the effort to maximize the life of a kidney, it has reduced the chances of a deceased donor transplant for those over 50 and who have been on dialysis a long time waiting for a kidney.

Preliminary study suggests new rules also increased transplantation rates for adults under 50 but significantly lowers them in those over 50. More

The Kidney Allocation System new calculation, “Estimated Post Transplant Survival (EPTS)” score is assigned to all adult transplant candidates on the waiting list. If a candidate has a score of 20% or above then the transplant candidate will be eligible for available kidneys rated in the top 20% by KDPI (Kidney Donor Risk Index) calculation.

KAS’s new calculation method EPTS of prioritizing candidates for a kidney transplant is faulty in many ways.

In summary, the EPTS assumes a kidney will last longer with a candidate that is 35 years and younger compared to those 50 years and older, and it assumes that those who have been on dialysis a long time waiting for a kidney are least likely to keep a kidney for a long time. Also the EPTS calculation does not include proper criteria for determining a persons’ state of health.

Although this new system cannot be defined as “age-matching,” age is one major factor being used to determine transplant candidates’ placement on the waitlist. As a kidney dialysis patient waiting on the transplant list, it is hard to believe there is “age discrimination” in receiving a kidney transplant in the U.S.

Each day that I get older and each day that I am on dialysis, I get further away from receiving a deceased donor kidney.

Patients can go to OPTN website to see if they fall in the top 20% of donor recipients. If they do they will be eligible for available kidneys rated in the top rated 20%.




Finding a Kidney

From Fox TV 5 Atlanta, Athens, Georgia, by Katie Muse


Athens Chick-fil-A Rallies around Manager in Need of Kidney


Employees at an Athens Chick-fil-A are rallying together to help their coworker find a new kidney.

Shelley Kurasaka, 39, has been diagnosed with Polycystic Kidney Disease, which is a genetic disease in which cysts grow on the kidneys and eventually cause them to fail. She will soon be in need of dialysis as her kidney function continues to drop.

The Snellville native moved to Athens two years ago when she was offered a position as a manager at the Chick-fil-A on Epps Bridge Parkway. That’s how FOX 5 first learned about Kurasaka’s story. Some of her coworkers took to social media and shared a post pleading for prayers and a kidney donor on the restaurant's Facebook page.

Kurasaka’s kidneys are failing and she’s been accepted as a transplant candidate at the Emory University Transplant Center. Kurasaka said since May, there has been a significant decline in her kidney function.

“I have placed my future in God’s hands and trust that He will lead someone to come forward and graciously provide this gift of life,” she said.

Kurasaka wants to continue leading an active and involved life with her family and friends and said a new kidney would allow her to do so.

“I want to continue my great career at Chick-fil-A in Athens,” she said. “I also believe that God has called me to be a good steward and to serve others. I am involved with the local food bank because it is dear to my heart and I want to continue serving as God leads.”

On Tuesday, Kurasaka and her fellow coworkers gathered at Chick-fil-A and took photos with Georgia-based photographer Brandy Angel, who started Be the Change -- Brandy Angel Foundation. Angel helps those in need by sharing their images and stories with the world through social media.




Kidney Donor Decline

From The Journal, Ireland

Concern over ‘significant decline’ in kidney transplants from living donors

Dialysis patient waiting for treatment at hospital (File photo).


THE IRISH KIDNEY Association has expressed its disappointment in the decrease of transplants carried out in 2015.

In 2014, there were 112 deceased kidney transplants from 63 donors. In 2015, there were 81 donors and 120 deceased kidney transplants.

The IKA said this represents “a significant decline in utilisation of available kidneys”.

“It is evident that this will require further investigation to understand exactly why this has come about. For the first time in the modern living donor kidney transplant programme fewer kidney transplants were performed than the previous year,” a statement noted.

There were a total of 153 kidney transplants performed in 2015, down from the 2011 peak of 192 kidney transplants.

A statement released by Health Minister Leo Varadkar this evening said there were 266 transplants carried out in 2015, an increase of 15 on the previous year.

“This includes overall increases in kidney (deceased and living donor combined), lung and liver transplants and the first ever combined heart and lung transplant. I want to welcome this progress and acknowledge the work of our health service staff who made this improvement possible,” Varadkar said.




Dialysis News: Location, Location, Location       

From Pasadena Star-News, by Courtney Tompkins

New San Gabriel dialysis center opponents score victory as council denies project


San Gabriel City Council rejected a proposed development project at the corner of Las Tunas and Country Club drives, near the San Gabriel Country Club. The now vacant site, pictured Jan. 4, 2016, formerly housed a used-car dealership. Photo by Leo Jarzomb/Pasadena Star-News

City officials on Tuesday overturned an approved development project contested by neighbors who felt it would bring unwanted noise and traffic to an affluent neighborhood near the San Gabriel Country Club.

The item brought hundreds of people to City Hall on Tuesday, and members of the city police and fire departments were turning people away at the door because the chambers were filled to capacity.

Mayor Jason Pu said the project, as proposed, was not consistent with the city’s general plan goals nor was it a good fit for that lot or the surrounding neighborhood. The council voted 4-1 against the project.

“We went through each of the elements that needed to be found in order to uphold the two conditional use permits, and on a pretty fair number of those, the council as a whole could not reach the findings required,” Pu said.


THE SCOPE OF THE PROJECT

The project, first approved by the Planning Commission in November, would have been a 12,285-square-foot kidney dialysis center on the corner of Las Tunas and Country Club drives.

The applicant, Dr. Priya Sakhrani, requested two variances, one for the building’s size because it was larger than 10,000 square feet and the other for a 20 percent reduction in the required number of parking spaces.

Sakhrani, who owns and operates Quality Dialysis, a similar facility on San Gabriel Boulevard, said he was disappointed with the decision and surprised by the council’s vote.

“They chose to ignore the commission, ignore their own staff, ignore the surveillance videos and parking study, and instead listen to anectdotal evidence,” he said. “These residents of Country Club Drive, they feel that they are priveleged and the selfish concern about someone parking outside their homes is frivolous.”


THE ISSUES RAISED BY RESIDENTS

The concerns raised by residents revolved primarily around the business’ proposed operating hours, which would have been between 4 a.m. and 10 p.m.

Neighbors said they were concerned about the noise from over a dozen people coming and going early in the morning and late at night in addition to concerns over parking on the street as a result of the requested parking reduction.

Attorney Charles D. Cummings, who appealed the commission’s decision on behalf of about 100 residents and business owners, called the decision a “big victory” for the neighborhood.

“I think the City Council listened to the arguments and to the residents,” he said. “I also think they were really taken with the fact that there had been a parking study done, but there was also evidence that the study had been manipulated.”


QUESTIONS ABOUT THE PARKING STUDY


Residents presented photographs to the council that had been taken one week after the parking study was done, showing the parking lot at Sakhrani’s other facility filled nearly to capacity and it has 41 parking spots, in contrast to the proposed facility, which was designed with 28 spaces.

Cummings alleged the employees parked on the street during the week of the parking study to make it appear emptier.

Sakhrani dismissed any allegations the study was manipulated and said the evidence was unsubstantiated. He also questioned why Planning Commissioner Camelia Vera spoke in opposition to the project during public comments, but did not identify herself as a member of the board.

Vera, who voted against the project in November, spoke Tuesday as a member of the community, she said.

City staff will bring back a resolution detailing the council’s findings at its next regularly scheduled meeting on Jan. 19.

Sunday, January 3, 2016

Lab Grown Kidneys; Make Kidney Donation Easier; Animation Shows Process; Kidney Rejection Fears

Living with PKD

From The Washington Post, In Theory, By Benjamin Humphreys

Will lab-grown kidneys fix our transplant waiting lists?

 

Scientists removed the cells from a rat kidney, leaving only its collagen scaffolding, then re-seeded the scaffolding with neonatal kidney cells and endothelial cells, producing a functional man-made kidney that, when transplanted into rats, filters waste and produces urine. It raises hopes for a bioengineered human kidney. (Ott Laboratory/Massachusetts General Hospital Center for Regenerative Medicine via Reuters)


Each week, In Theory takes on a big idea in the news and explores it from a range of perspectives. This week we’re talking about government compensation for organ donors. Need a primer? Catch up here.

Benjamin D. Humphreys is a nephrologist and chief of the division of nephrology at Washington University in St. Louis. He cares for patients with kidney disease and runs a research laboratory aimed at developing new therapies to treat kidney disease, including stem-cell-based therapies.

Kidney failure is a growing problem in the United States, with more than 100,000 new cases per year. There are not enough kidneys available to transplant all of these patients, so the majority are treated with dialysis. The therapy is certainly life-saving but is also costly, inconvenient for patients and itself causes accelerated heart disease. The risk of death for an average dialysis patient is 20 percent per year.

Dialysis patients make up about one percent of the Medicare population, but paying for dialysis costs seven percent of the entire Medicare budget. Clearly there is a strong need for innovative new therapies and approaches to the problem. We already have some new ideas being developed — at-home and portable dialysis, for example. Yet simply improving the existing technology is an evolutionary change, one that falls well short of what is actually needed: a new kidney that frees patients from devices entirely.

[Other perspectives: The moral case for paying kidney donors]

It is here that the stem-cell revolution of the past 10 years offers a measure of hope. To understand the challenges in growing a kidney from stem cells, it is useful to compare the stem-cell approaches to kidney failure with those for diabetes. Patients with Type 1 diabetes suffer from the failure of a single cell type in the pancreas, called the beta cell. Over the past 10 years, scientists have been successful in generating beta cells in the lab — billions of them — and now the only remaining challenge to cure Type 1 diabetes is find a way to deliver those cells to a patient and keep them alive.

Kidney failure, on the other hand, represents failure of an entire organ comprised of over 30 distinct cell types, all organized in an intricate and complicated pattern. The challenge is not only to grow 30 different cell types, but also how to arrange them in proper orientation. Until two years ago, the prospects for surmounting these challenges appeared slim, despite decades of effort by large teams of scientists around the world.

But recent breakthroughs using human pluripotent stem cells have demonstrated that growing a kidney in a dish may be feasible. Pluripotent stem cells are special in that they possess the ability to differentiate into any cell type in the human body.

By coaxing stem cells to differentiate into two different types, kidney-specific stem cells, then combining them, scientists have discovered that these cells will continue to differentiate on their own, generating a wide variety of cells that are found in a mature kidney. Moreover, the cells pattern themselves into nephrons — the functional unit of the kidney — and these nephrons are structurally quite similar to real nephrons in our own kidney.

This remarkable and surprising advance has, in a short time, changed the way many of us think about the problem of growing an artificial kidney. While still an enormous undertaking, the problem may have a potential solution. Rather than the challenge of generating 30 different cell types, we may only need to develop the two critical kidney stem cells and make sure the conditions in the dish encourage these two cell types to do what they want to do.

A powerful aspect of this human stem-cell approach is that it can be tailored specifically for each patient. Transplant patients generally must take immunosuppressive drugs for the remainder of their lives, to prevent rejection of their kidney by the immune system. This same problem would exist if an artificial kidney were grown in the laboratory using cells from someone other than the patient receiving the kidney.

[Generosity won’t fix our shortage of organs for transplants]

However, we now have the ability to turn any patient’s cells — from skin or blood on the inside of the mouth, for example — into pluripotent stem cells. One can imagine generating patient-specific stem cells from a patient with kidney failure, using these cells to generate a kidney in a laboratory, and then transplanting that kidney into the same patient. In this scenario, there would be no a need for immunosuppression, and limited ethical concerns.

Of course, a number of very substantial challenges remain. The nephrons that can be grown in the dish currently number only in the hundreds, and a human kidney contains about 400,000 nephrons. Furthermore, the nephrons are not attached to blood vessels, and there is no clear way to insert the kidney into a patient’s blood supply. There is also no way to drain the urine that such a kidney would produce. This will require learning how to grow the drainage system — ureters — that could then be attached to the patient’s bladder.

I was formerly skeptical about the prospects for growing a kidney, but the developments over the past two years have convinced me that this could be a viable option. Realistically, we are still probably 15 to 25 years away from success, so it remains important to pursue other avenues to increase the pool of transplantable kidneys. But certainly our patients have reason for cautious optimism. [Read more]


 

From The Washington Post, Letters to the Editor

Let’s make kidney donation easier and more common


Slow healing wounds from dialysis on the arms of kidney recipient Cynthia Decker before her transplant on Dec. 1. (Linda Davidson/The Washington Post)

The Dec. 24 front-page article “The offering” told a poignant story of one person’s gift of life to a stranger. Toni Badinger saved Cynthia Decker from a life on dialysis. Yet there is a subtle tragedy in the tale that other dialysis patients will instantly recognize: “The other patients [on dialysis machines] — almost all gaunt and gray-haired, offered congratulations, speaking to [Ms. Decker] as if she were a fellow prisoner who had just been pardoned.” That is exactly what happened.

I have been on dialysis for four years while awaiting a transplant. Many have been on dialysis for 20 or more years, their bodies ravaged by the side effects. The article was accurate: A high percentage of the 100,000 people waiting for a transplant will die before one is available. The hidden tragedy is that many of these deaths are unnecessary.

An August opinion piece in the New York Times pleaded for a system run by the government in which organ donors were compensated. It would not be perfect, but it would be intended to meet a desperate need while preventing scammers and brokers from profiting. Many doctors also advocate such a system. Why has this not happened? The National Kidney Foundation and other players with big money at stake are opposed.

We all should look forward to the day when Ms. Decker’s joyful outcome is the norm.


Neil Williamson, Greenbelt

Children from the Eagle dialysis ward team up with an animator from the Foundling museum to show the process of dialysis through to kidney transplant.



From Tap Into Summit, Summit, NJ, By GREG ELLIOTT


Dana and Karen - Update



Dana Henderson, boyfriend of Summit Police Department records clerk Lauren Karsen, gave the gift of life to his girlfriend's mother Karen, donating a kidney in a transplant procedure performed on December 1.

The procedure was a completed success, and Henderson relays, "Karen and I are both doing well. We got to spend Christmas and New Year's together."

Karen has Polycystic Kidney Disease (PKD), a hereditary disease that is passed down through families and in which manyclusters of cysts form in the kidneys, causing them to become enlarged.

What exactly triggers the cysts to form is unknown. The disease is associated with the aortic aneurysms, brain aneurysms, cysts in the liver, pancreas, and testes, and diverticulaof the colon.

Currently, no preventative treatment can prevent the cysts from forming or enlarging, and the disease gets worse slowly. Eventually it leads to end-stage kidney failure, the treatments for which may include dialysis or a kidney transplant.

Henderson, a Muhlenberg College nursing student with two semesters remaining, works full-time as a patient care technician at Overlook Medical Center in Summit. He also volunteers one day each week at the Summit Volunteer First Aid Squad.

Henderson further reports that Dr. Stuart Geffner and the renal transplant team at St. Barnabas Medical Center were "nothing short of remarkable." Henderson explained, "We were both discharged three days post-surgery, and I have been completely pain free for the past three weeks or so. The recovery was much better than my two previous surgeries. In fact, on one or two occasions, I've had people ask me how I was feeling and for a split second I have to remind myself, 'I donated a kidney just a few weeks ago'."

Henderson's blood work post surgery has all been good, he has been cleared to go back to work again starting January 4, and he begins nursing school again January 25.

Lauren's mother Karen's recovery has, understandingly, been much more challenging than Henderson's, but she had been making significant progress. Most importantly, all of her blood work post surgery has also been good.

According to Henderson, there have been no unexpected "hiccups, knock on wood," and Karen has just recently been cleared to drive again. She does have restrictions on the types of places she can be in public because she is immunocompromised, but has a very positive outlook and has "taken everything in stride."

As it currently stands, Karen is expecting to return back to work in March.

"All in all, we couldn't be happier with the outcome of all of this. We all have had a lot to be thankful for this holiday season," said Henderson.




From Yorkshire Evening Post, by Jonathan Brown

Fresh start hoped for defiant Leeds teenager Akash after kidney transplant rejection fears

Akash Suryavansi, from Harehills, with his mum Tina. Picture by Tony Johnson.

Akash Suryavansi, from Harehills, with his mum Tina. Picture by Tony Johnson.

A 17-year-old Leeds boy is hoping the New Year will signal a new start for him after a second lifesaving kidney transplant proved a success.

Akash Suryavansi, from Harehills, was born with polycystic kidney disease and after years of dialysis and a transplant from his mother Tina in his youth, his donated organ began to fail in July.

His desperate wait for a second transplant saw his health deteriorate, with 12-hour days of dialysis taking their toll and leading him to suffer a stroke in October.

Doctors eventually gave the teen’s dad Aky the go-ahead to donate one of his kidneys in November but following the complex procedure, Akash’s body began to reject the new organ before Christmas.

Tina revealed that following an anxious few weeks her son appears to have weathered the storm after he was plied with steroids and anti-rejection drugs to rescue his kidney.

“It’s the best Christmas present we could have hoped for,” she said. “He’s drinking normally, he’s got his energy back and he’s looking better and putting weight on. We are just grateful top have come through the last 12 months.”

She explained that Akash is now progressing well at home and is in temporary isolation until March to steer him clear of infection, which is an increased risk due to the nature of his transplant.

When Akash first needed a transplant 11 years ago both parents offered to be donors but Aky was rejected because his blood group did not match. But these ABO-incompatible transplants are now possible with the use of drugs to suppress the immune system.

The average wait for a kidney transplant in Yorkshire is 1,114 days but due to a shortage of donors from ethnic minorities, Akash could have been made to wait a year longer without Aky’s donation.

Tina said: “Next year is going to be a new start – it’s his third chance at life. We’ve had a lovely, big family Christmas this year and Akash is just enjoying being well.”

The family have been major supporters of the YEP-backed Be A Hero campaign, led by LTH, which saw around 27,000 people sign the NHS Organ Donor Register in its first three months this year.

Aiming to tackle a Tough Mudder challenge in August in aid of LTH’s Leeds Children’s Transplant Team, the Suryavansis, who were praised in the YEP Best of Health Awards 2015 for their bravery, are keen to continue to offer their support.

“We want to continue with organ donation awareness and that’s still at the top of our agenda and always will be,” Tina added.




PKD Fundraising

From The Valley Voice, Champlain Valley Vermont

VUHS Teens Set Goal To Raise $6,000 For Polycystic Kidney Disease

As the year winds down the goals for 2016 are being set around the county and the VUHS National Honor Society members have a busy year ahead. The group is determined to help support research for local people battling Polycystic Kidney Disease (PKD) and have set up numerous fundraisers to reach their goal.
First and foremost the teens want to increase awareness of the struggles for people facing this disease and the lack of funding and community understanding. Polycystic Kidney Disease is an inherited disorder that has been diagnosed in 600,000 Americans which causes many cysts to grow in the kidneys and while the cysts are noncancerous they damage the kidneys and can lead to kidney failure. The cysts are different sizes and grow as they accumulate fluid and in addition to the kidneys which in some people require a transplant, the cysts are also found in the liver and other parts of the body. Complications of this disease include high blood pressure. While the disease can vary greatly in each person at present it is not curable. New research is working on possible cures but it is costly and not many Americans even know about the disease or how it impacts families.

“We are raising money for PKD research to honor a NHS member and her family,” shared NHS president Nathan Rowell. “We are performing numerous fundraisers as well as accepting sponsors and donations to go toward PKD research. We are really hoping to raise both funding and awareness.” The group plans on a media campaign in and outside of Addison County and hopes to draw sponsors for their participation in the Polar Bear Challenge Obstacle Race taking place on Saturday, February 6th in Benson, Vermont.
Rowell and his fellows NHS members are hoping that community members might consider making a donation or if there is a small job that the group could do for donation toward the cause, please contact Rowell at nrowell@anwsu.org or the faculty adviser at lkayhart@anwsu.org . “When my mother had breast cancer many members of our community helped my family stay strong by bringing us warm meals and smiles. That kind of community needs to be sustained and focused to help those dealing with PKD.” Research is often slow but the recent discovery of a new gene editing technique is just one of many different areas where research is slowly beginning to unravel the mysteries of the genes that bring PDK into the lives of so many Vermonters and Americans.

So check your list of projects and see if you have a project that could be handled by willing hands or maybe consider making a donation to help the teens reach their goal. But most importantly please get on the web and read up on this disease that impacts so man.