Parkinson's Disease Tulip


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Old 08-26-2010, 06:08 AM #1
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Default Genetic Link Discovered Between Immune System, Parkinson's Disease

From http://www.sciencedaily.com/releases...0815162130.htm



In the study, researchers detected a new association with the HLA (human leukocyte antigen) region, which contains a large number of genes related to immune system function in humans. With the new findings, and link to HLA, researchers will now be encouraged to take a fresh look at the possible role of infections, inflammation and autoimmunity in Parkinson's disease.

HLA genes are essential for recognizing foreign invaders from the body's own tissues. Similarly, HLA molecules are supposed to recognize a body's own tissue as itself and prevent immune reactions against them. But the system doesn't always work perfectly. HLA genes are highly variable from individual to individual. Certain variants of the genes are associated with increased risk or protection against infectious disease, while other variants can induce autoimmune disorders in which the immune system attacks the body's own tissues. Multiple sclerosis, a neurological disease caused by autoimmunity, is also associated with HLA-DR. The genetic variant that is associated with Parkinson's disease is in the same region as the one associated with multiple sclerosis.
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Born in 1953, 1st symptoms and misdiagnosed as essential tremor in 1992. Dx with PD in 2000.
Currently (2011) taking 200/50 Sinemet CR 8 times a day + 10/100 Sinemet 3 times a day. Functional 90% of waking day but fragile. Failure at exercise but still trying. Constantly experimenting. Beta blocker and ACE inhibitor at present. Currently (01/2013) taking ldopa/carbadopa 200/50 CR six times a day + 10/100 form 3 times daily. Functional 90% of day. Update 04/2013: L/C 200/50 8x; Beta Blocker; ACE Inhib; Ginger; Turmeric; Creatine; Magnesium; Potassium. Doing well.
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Old 08-26-2010, 12:42 PM #2
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Default One just needs to come on over here!

If only researchers would read what Rick and some others have been posting about for years, I can't help but think it would push things forward by light years! Good find, Rick, thanks for sharing.
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Old 08-26-2010, 02:00 PM #3
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Thumbs Up Good timing!!!

Rick,

I am going for my 3 month visit with Neurologist Friday morning. I printed out the article to see if he has any comments. Will report back.

Mike
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Old 08-26-2010, 08:48 PM #4
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Default Wish we could take turns on PDOnline Research

Quote:
Originally Posted by lurkingforacure View Post
If only researchers would read what Rick and some others have been posting about for years, I can't help but think it would push things forward by light years! Good find, Rick, thanks for sharing.
Too bad that patients are not more welcome to post on the PDOnline Research wiki. I understand why they discourage it, but the wiki would be a great way for information exchange between researchers and those who live with the disease. Some of our experiences and anecdotes may even serve as a catalyst for new ways of looking at old, outworn ideas.

There are some creative ways to establish quality control. For instance, their could be patient liaisons or reps and Rick, Ron Hutton, and Girija would be perfect for that (others too).

Thanks, Rick!

Laura
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Old 08-27-2010, 08:39 AM #5
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Default

Heck, if they even cared enough to assign a grad student to liason with us it would be something. The unspoken message is we don't count. Or, to paraphrase George Carlin, "It's a great big club and YOU'RE not a member!"


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Originally Posted by Conductor71 View Post
Too bad that patients are not more welcome to post on the PDOnline Research wiki. I understand why they discourage it, but the wiki would be a great way for information exchange between researchers and those who live with the disease. Some of our experiences and anecdotes may even serve as a catalyst for new ways of looking at old, outworn ideas.

There are some creative ways to establish quality control. For instance, their could be patient liaisons or reps and Rick, Ron Hutton, and Girija would be perfect for that (others too).

Thanks, Rick!

Laura
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Born in 1953, 1st symptoms and misdiagnosed as essential tremor in 1992. Dx with PD in 2000.
Currently (2011) taking 200/50 Sinemet CR 8 times a day + 10/100 Sinemet 3 times a day. Functional 90% of waking day but fragile. Failure at exercise but still trying. Constantly experimenting. Beta blocker and ACE inhibitor at present. Currently (01/2013) taking ldopa/carbadopa 200/50 CR six times a day + 10/100 form 3 times daily. Functional 90% of day. Update 04/2013: L/C 200/50 8x; Beta Blocker; ACE Inhib; Ginger; Turmeric; Creatine; Magnesium; Potassium. Doing well.
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Old 08-27-2010, 12:51 PM #6
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Default havenot given up yet.........

Just wanted to add my two cents worth here. I have tried very hard to initiate discussions with PD researchers on the autoimmune component of PD, sent grant applications to test my hypothesis for atleast 2 years now. All I can say is I havent been successful yet.......... I am still trying....

Girija
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Old 08-27-2010, 02:34 PM #7
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Quote:
Originally Posted by girija View Post
Just wanted to add my two cents worth here. I have tried very hard to initiate discussions with PD researchers on the autoimmune component of PD, sent grant applications to test my hypothesis for atleast 2 years now. All I can say is I havent been successful yet.......... I am still trying....

Girija
Would Reflex Sympathetic Dystrophy and or Lou Gehrig's Disease (ALS) fall into this "Genetic Link Discovered Between Immune System" ?
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