Gene Mutation Linked to Inherited ALS

Discovery might one day lead to additional treatments, experts say

Posted: February 26, 2009

THURSDAY, Feb. 26 (HealthDay News) -- A new gene has been identified as playing a role in the inherited form of amyotrophic lateral sclerosis, or ALS, say researchers at the University of Massachusetts Medical School and King's College, London.

The discovery, a mutation in the FUS/TLS gene, is the fourth gene linked to the neurological disorder, also known as Lou Gehrig's disease. The finding was reported in the Feb. 27 issue of the journal Science.

"We found a series of mutations in a gene that interacts with biological pathways already implicated in ALS and other neurological diseases, resulting in familial ALS of differing inheritance patterns and varying severity," Dr. Thomas Kwiatkowski, of the Institute for Neurodegenerative Disease at Massachusetts General Hospital and lead author of the report, said in a news release from the hospital.

The discovery "puts us closer to identifying the link between inherited and sporadic ALS as well as to new targets for drug design," he said.

In people with ALS, motor neurons in the central nervous system begin to die, compromising the brain's ability to send signals to the muscles. As the disease progresses, people lose voluntary muscle movement, develop paralysis and eventually die from respiratory failure. About 10 percent of ALS cases are inherited, but the cause of most cases of ALS is unknown.

The researchers discovered the FUS/TLS gene mutation on both copies of chromosome 16 in four family members with ALS who live on a small Cape Verde island. Three other family members also had two mutated copies of FUS/TLS but had not yet reached the age of onset of ALS. Several unaffected family members had a single copy of the mutation. No FUS/TLS mutations were found in a control group of 1,446 North Americans.

Eventually, the researchers found FUS/TLS mutations in other families involved in earlier research efforts, leading to the discovery of 13 different FUS/TLS mutations in 17 families with inherited ALS.

Dr. Robert Brown, the study's senior author, said in the news release that the discovery "will almost certainly lead to new animal- and cell-based models for this disease, which should accelerate efforts to find a therapy for ALS."

More information

The U.S. National Institute of Neurological Disorders and Stroke has more about ALS.

Als

Hello,

My mother died of ALS related symptoms 1 1/2 years after being diagnosed and right from the start it was a nightmare for her and my family. It started when she was diagnosed first with lymphoma, for which she received radiation treatments. We thought she lost her ability to swallow and speak shortly after that due to the radiation and later found out she had ALS. She lived an agonizing year after that and slowly lost her ability to eat, walk and communicate. She went from 130 pds. down to 80 pds. She had a feeding tube and trach and the worst part was that she knew what was ahead for her. At that time the news was filled with euthanasia featuring an ALS patient. Please donate to the ALS Foundation and ask the Goverment to fund more scientific research on this merciless disease. Not enough is being done to stamp this out! My mother suffered in silence but the sadness we all feel after almost ten years remains stronger than if it happened yesterday.

Sincerely,

Long Island Daughter

Long Island Daughter of NY @ Mar 21, 2009 20:37:52 PM

Hi

Booby,

When you have some time I would like to chat with you on your project and also other thoughts. Hugs, Frank 415-6906399

Frank Corsini of MA @ Feb 28, 2009 09:08:58 AM

Cure for ALS

I have been trying to keep up with all of the research going on in the ALS community. My wonderful husband of 21 years was diagnosed with the disease in 2008. He has a trach and feeding tube, but can still walk. He keeps an amazing, positive outlook. This disease needs to be stomped out! I have held three fundraisers to benefit ALS TDI(Therapy Development Institute) and believe that 2009 is going to be a banner year. So far, there have been some positive events happening. I just want to tell everyone out there who is afflicted with this horrific disease that there is HOPE! My husband is a very strong-willed person and believes that one day the world will be rid of this "Satan's disease". I don't want to see any other families endure this pain. As a caregiver, I feel helpless, but believe that God will answer prayer and help in this war against Amyotropic Lateral Sclerosis. We also have Jerry Lewis and his Telethon donating to ALS research. There are so many players in the game. On July 4, 2009 Major League Baseball will be having an auction to benefit ALS research. I am reaching out to as many people as possible to help in any way possible.

This disease affects 30,000 people in the United States and at least 6000 are newly diagnosed every year. July 4th will mark Lou Gehrig's 70th anniversary of his retirement from baseball. What a wonderful thing for the players to do to help rid the world of ALS. I would like to see the rest of the sports teams follow in their footsteps. I know there are other diseases out there that need a cure as well, but ALS is one of the worst because it takes away all of the things that make life worth living.

To all of those families living with ALS patients- please keep the faith and trust in the power of prayer. There are support groups out there and there is much information. My family and I are praying every day for a cure or at least an effective treatment. Don't let the doctors tell you that there is no hope. We had three neurologists tell us that- one more negative than the next. Find a doctor who believes in LIFE and not just the fatality of the disease. It is true that the disease has no cure, at least for now.

We are a family at war against this disease and will not stop helping to find a cure or something to slow down the progression of the disease.

Right now my husband is doing well. The disease appears to be in remission. He is not going to let it beat him! Please keep on staying positive and learning as much as you can about the disease. One book, in particular, is called "Eric is Winning". Eric Edney is the author and has had the disease for 14 years. He is beating the disease. This book has been very inspirational to me. Thank you for letting me tell my story. I know there are many more families out there that want their voices heard.

United for a Cure,

Debbie Barry, Longmont, CO

Debbie Barry of CO @ Feb 27, 2009 11:50:16 AM

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