Posted on 10/10/2006 5:51:08 PM PDT by blam
Psoriasis linked to tripled risk of heart attack
21:00 10 October 2006
NewScientist.com news service
Roxanne Khamsi
Patients with the common inflammatory skin condition psoriasis have a tripled risk of heart attack, a new study has revealed.
The studys researchers speculate that the systemic inflammation seen in psoriasis might weaken the cardiovascular system, thereby increasing the chance of such heart problems.
Psoriasis is an inflammatory system disorder that affects around 2% of people in the US and is characterised by sore, scaly patches of red skin. Recent studies suggest that genetic mutations and lifestyle factors such as stress and smoking may increase the risk of psoriasis.
Previous studies have linked other inflammatory illnesses, such as rheumatoid arthritis, to cardiovascular problems.
Joel Gelfand at the University of Pennsylvania School of Medicine in Philadelphia, US, and colleagues analysed five years of medical data from nearly 700,000 people. The sample included 4000 people with severe psoriasis and 130,000 with a milder form of the disease.
Relative risk
After controlling for other risk factors, such as high blood pressure, people with psoriasis were up to three times as likely to have a heart attack during that five-year period. The highest elevation of relative heart risk was seen in patients under 50.
(Excerpt) Read more at newscientist.com ...
Kind of brings new meaning to "The Heartbreak Of Psoriasis."
Are you sure about that diagnosis? The inside elbow surface is much much more typical of eczema (atopic dermatitis).
Inflammatory processes are associated with many diseases, including cancer. Preventing or minimizing inflammation wherever it's found in the body should be emphasized.
My son's second grade teacher died of ovarian cancer about a month ago. She had terrible psoriasis up until about 6 months before she died.
You know, you are right. It is raised hive like things that are really itchy...but it may be eczema. Thanks for pointing that out. We had planned to treat the arm thing once the Graves was under control...but viola! it disappeared, so it was never officially dealt with.
I just read this very quickly and thought "See, I'm NOT crazy." Thereby actually giving the doctors' opinions way more credence. LOL.
Oh well. This is why I'm not a scientist. : D.
My mom had Graves Disease, they ended up killing the thyroid with radioactive iodine and then she had to take medicine so she could regulate her metabolism.
I know its a very scary disease, my mom went from 120 to about 70lbs when she had it and literally looked like she was a walking skeleton, I wonder if thats where they get its name from?
IIRC, it's the name of the Doctor who discovered it, but I'm not sure. It was pretty scary, I'll have to tell you. My daughter was a skeleton as well. But she could eat two adult Mexican Restaurant meals and be hungry in a half an hour.
Unbelievable what it does to a person.
Wow, I have it right now. Have had it for about 5 weeks and this is the 4th outbreak right on top of the same places, over and over.
I thought it was an allergy, because it presented itself exactly the same way my contact dermatitis did, from poison ivy, more than a decade ago. And *that* was just like my metal allergy, to nickel and other non-gold base metals, when against my skin for a prolonged period of time (like the rivet on the back of the waist button on jeans).
It starts like tiny insect bites and I'm fooled every time, thinking that's all it is. I kinda scratch just a little bit. Next thing you know, there are tiny blisters popping out all around the original 1-2 bumps.
This time is much different from those others, which were years ago. It's mostly on the tops (backs) of my hands, more on the left than right. It's all across the upper part, towards the bottoms of the fingers. It "spread" (it doesn't really *spread* per se) to the webs between my fingers when it broke out the 2nd or 3rd time. Ouch, ouch, ouch.
The first outbreak, I traced it to what I thought was some damage I had done while preparing some Thanksgiving sugar pumpkins. I had scraped out 3 of them, holding the spoon handle very close to the bowl, and then repeatedly scraping the flesh out of the raw ones - each time, hitting the tops (backs) of my hands on the inside of the small pumpkins.
I would change hands once in a while, but did most of it with my left hand and a little bit with my right hand. I didn't notice any cuts or roughed-up skin, but it surely might have been there - little micro-abrasions.
Anyway, about 3-4 days later, I handled some jalapeno peppers when making jelly and my outbreak occurred probably 2-3 days after that. It was just terrible on my left hand, hundreds of small clear blisters erupting.
I knew not to scratch after that first accidental time - I've found a way to just run it under cold water till the itching stops. My doctor back on the poison ivy dx had told me never to use hydrocortisone cream, as it would leave scars. I can't afford a doctor now, so I just used the Domeboro Burow's solution he recommended for soaking the blisters, taking Benadryl and Advil or Tylenol, and using an oatmeal-based lotion or cream - or calamine.
My left hand really looked bad - all those blisters had to burst and crust over, in order to know it was healing. It was a real mess - looked like flesh-eating bacteria had attacked me. Hurt like heck, too. The worst was when it erupted on the palms of my hands - aaarrrggh!
I put gauze over both hands just to go to the store (the right hand just had red blisters on a finger knuckle, but was developing the tiny bumps elsewhere on the top of my hand by the 2nd week).
When it was almost gone, it came back again with a vengeance, which was not anything my allergies had ever done. A FReeper suggested maybe it was shingles, which several others had experienced. I yelled "no!" at her because I have so many medical problems I can't pay for - I just didn't need another chronic something.
I went into the med symptoms online and the only picture my outbreak matched was shingles. That also meant I could go get some hydrocortisone cream, so I did and it has been a godsend for the itching. Clears it all right up, right away. It's hard to keep it on my hands for long periods of time, because you have to wash and do things, but it does stop the messy part of the advance of the blisters.
That's all I know. The same hands that looked like Freaksville a week ago, even 3 days ago, look perfectly normal right now. There are a few spots left and I can feel that they're there, but they don't bother me. I do know that each outbreak, now that I know it's there, has been directly because of something I was stressing out about.
It's related to the chicken pox virus, so there really isn't anything that can be done medically - altho some people do go get a shot of something from their doctors.
I've never had shingles before, so don't know what it's *supposed* to feel like, but everyone I've talked to who has had them has said the same thing - that they're very painful. And most have had them on their torsos, not hands - so you're probably right.
This rash only hurt when the blisters had crusted over and then cracked open - but the spots do hurt now and then, as if they're on fire under the skin. That's right before the itching and eruptions start.
Someone suggested lupus, but I didn't have any of the other symptoms. My friend who had a terrible shingles outbreak on her stomach for 3 months, which later came and went for 3 years in various intensities, thought my hand looked like it was psoriasis - as in this article. I just don't think so - she saw it when it was well and the cortisone cream was dried and peeling off - lol, it wasn't dried skin.
I had another "theory" on mine, but it was another allergen or possibly fungus. This year was a bad year for pumpkin mold, worst in ages - I thought perhaps I got some kind of fungal thing, like athlete's foot - but I couldn't find anything to address that specifically.
Also, I had been working a jigsaw puzzle and had the pieces out on a white surface - I saw some paper mites (almost microscopic) moving around and my first instinct had been that those mites had bitten me and my system overreacted. My immunity is very low right now due to some extreme stress.
The little bumps *seemed* like they could've been bites from mites. However, when it came back right on top of itself, I ruled that out. Hadn't been near the puzzle.
I don't know what scabies is/are, but maybe I'll check it out. I know my GP won't have any better idea than I do what this is because he just calls it all contact dermatitis, even poison ivy, when I know exactly what it is.
All I know is I love hydrocortisone cream now! The marks *do* stay there, however. Please do let us know what you find out.
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