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Ysobelle
08-02-2007, 10:44 AM
I thought this might be of interest to a few of us.


http://www.usatoday.com/news/health/2007-07-29-multiple-sclerosis_N.htm


Multiple sclerosis findings could help pinpoint cause
By Kathleen Fackelmann, USA TODAY
Gene hunters from the USA and Europe have located two genes that appear to increase the risk of developing multiple sclerosis, studies released Sunday show.
The findings are widely expected to help scientists figure out what causes MS, a baffling disease of the central nervous system that afflicts about 350,000 people in the USA. The hope is that new knowledge will lead to the development of more targeted treatments, says Jonathan Haines, director of the Center for Human Genetics Research at Vanderbilt University in Nashville.

"We've been trying to identify the genetic basis of MS for a long time," Haines says. Researchers discovered one gene in the 1970s called HLA (human leukocyte antigen) that raises the risk of developing MS, and they knew that other genes probably play a role, he says.

But the intense search to find them has been disappointing — until now.

In the July 29 online edition of Nature Genetics, Haines and his colleagues pored over previous studies to identify genes that appeared to have a role in the disease. They then collected blood from more than 10,000 people, MS patients and healthy subjects alike.

The DNA was extracted from the samples, and researchers homed in on suspect genes. They found that a variation in the interleukin 7 receptor gene increased the risk of developing MS by 20% to 30%.

A second study in Nature Genetics confirmed that finding.

A person who inherits this gene variation, however, isn't guaranteed to get MS, Haines says. To actually get the disease, people probably need to inherit other genes that put them at higher risk, says study co-author Margaret Pericak-Vance of the University of Miami School of Medicine. In addition, the disease might require a trigger — such as exposure to a virus, says John Richert of the National Multiple Sclerosis Society in New York.

David Hafler of the Harvard Medical School and an international consortium of researchers also identified the interleukin 7 receptor gene as a risk factor for MS. But Hafler's team identified a second gene that might play a role: the interleukin 2 receptor gene. Hafler's team gathered DNA from about 12,000 people, both MS patients and healthy subjects.

The team reports in the July 29 online edition of The New England Journal of Medicine that two variations of the interleukin 2 receptor gene raise the risk of developing MS by about 20%.

The interleukin genes are thought to help regulate specialized immune cells called T-cells, Hafler says. Researchers have long speculated that MS is an autoimmune disease that occurs when immune cells mistakenly attack the coating, or myelin, that protects nerve fibers. If that's true, drug developers might be able to craft a compound that could block or stop the attack, Richert says.

People who have MS often experience attacks of weakness and tremors. Over time — especially if the current lineup of drugs stop working — they can develop permanent disability. "Some people end up in a wheelchair," Haines says.

Although researchers are now racing to find better drug compounds, that effort might take years, Richert says.

"I don't expect a cure here," says Martha Crowninshield, a former venture capitalist who donated $1 million to finance the research that led to the The New England Journal of Medicine results. Still, Crowninshield, who has the disease, says she believes additional research into the interleukin genes "will accelerate the process of finding therapies."

Gellis Indigo
08-02-2007, 10:50 AM
A former student of mine was diagnosed with MS his senior year of high school, at the age of 18. What a way to start out your adult life.
He's such a strong young man and is handling it with grace and dignity.

daBaroness
08-03-2007, 03:57 AM
While it's a long way from a cure - it's VERY good news. MS is an incidious disease and can manifest symptoms in so many different ways. Some people go a long time - years even - without a proper diagnosis. There are several varieties - one that's pretty much ongoing and constantly deteriorating its host - the other comes and goes - with sometimes years in between flare ups. But each flare-up damages the brain and the nervous system in ways the body cannot repair. Some people react well to treatments - others have tried everything from drugs to bee sting therapy with little or no benefit. It's a terrible disease that causes its sufferers to waste away and lose the ability to function as they'd like - often times making them completely dependent in terms of even their basic needs. It simply sucks!

I hope for all those who have MS or have a loved one with the disease that this research continues and a cure is ultimately found. Shame on those who would disapprove of gene therapy and research!

Ysobelle
08-03-2007, 05:23 AM
Relapsing-remitting and secondary progressive. Sometimes, the former can become the latter, which will eventually put you in a wheelchair and make your life hell. It's a horrible, nasty, evil, taunting disease and I fucking hate it. I've known too many wonderful people who fight it every day. If it were a person I'd kill it with my bare hands-- maybe using a rusty hedge clipper.

Not that I'm bitter or anything.

KissMeKate
08-03-2007, 01:56 PM
A former student of mine was diagnosed with MS his senior year of high school, at the age of 18. What a way to start out your adult life.
He's such a strong young man and is handling it with grace and dignity.

That's very unusual, but I'm glad his doctors got his diagnosis right so early. My sister was diagnosed when she was 23, which is also young, but not so unusual as MS seems to affect more women than men.

Luckily she was admitted into the clinical trial for Betaseron and has been on it ever since. She calls it better living through chemistry (she has drugs to counteract side effects and drugs to counteract the side effects of the side effect meds), but she is able to walk and function, and is even working again. She's very lucky!

I agree with Nikki, if I could eradicate it with my bare hands, I would.

Lady Laurel
08-03-2007, 02:21 PM
I going to copy this on my LJ if that is okay. I talk to a couple of people that suffer from MS.

daBaroness
08-04-2007, 10:24 PM
Nikki - I'm with you! I've had a number of friends, family of friends and former coworkers with the disease. Most had relapsing-remitting. I learned TONS about the disease when I worked for Fleishman-Hillard PR. We were the agency that helped Teva Marion Partners (now just Teva) launch the MS drug, Copaxone. Doing a drug launch is an interesting process in, and of itself. But I got the opportunity to learn so much about it. One of the cool things Teva did was establish networks of people with MS as online support groups - the leaders of the networks were MS patients and it really allowed patients and families to connect with one another, offer support and gain information on new therapies and old. I personally had the opportunity to work with our local MS Society group on several events - and the people I met were simply awesome.

Ironically, about a year after the initial release of the drug, one of my bosses who had been one of the key people in the launch efforts was disagnosed with relapsing-remitting MS. She hadn't had an event in about 15 years at the time she relapsed - but this time - armed with the information about MS - she immediately went to her doctor and was pretty sure what it was. She started on a regimen of Copaxone and when last I talked to her, she was doing great!

You just never know when you are involved in something important - how very important it might become to you in the future!