Guest guest Posted May 20, 2002 Report Share Posted May 20, 2002 , I find these references confusing. In particular, the abstract to the second reference doesn't support what's Dr. Nase's saying. The statistics described in the study are confusing, but at a minumum the authors found that 12 of the study's 24 rosaceans had tissue biopsy evidence of altered immune function, and 6 of the 24 had laboratory evidence of auto-immunity (remember, evidence of autoantibodies isn't enough to call a condition auto-immune). The abstract doesn't say how many of the controls had similiar findings, but Dr. Nase's " ...The average rosacea sufferer has a perfectly health immune system. " contradicts the authors' closing statement, " It is suggested that altered immune function plays a significant role in the pathogenesis of the disease. That study is published in a respected journal but it's 20 years old - - frankly, that's just too old to reference in this area, whatever the study found or didn't find. And the first reference comes from a 15 year old Proceedings. A proceeding is a short, non-peer-reviewed entry or presentation for a specific conference (each conference puts out its own Proceeding). Proceedings are used to keep everyone abreast of completed research during the year or two it takes for the study to be officially published in peer-review journal. Proceedings that are 1-3 years old are credible references, but referencing a 15 year old Proceeding doesn't carry the same credibility. Here's the second abstract. It does support what we've been talking about -- rosacea has features of a primary immune-mediated condition, and there is an association between rosacea and other auto-immune disorders: Br J Dermatol 1982 Aug;107(2):203-8 Involvement of immune mechanisms in the pathogenesis of rosacea. Manna V, Marks R, Holt P. Twenty-five patients with rosacea were compared with twenty-five control subjects for previous medical history and tests of immune function. cea patients were found to have a higher incidence of disorders of the auto-immune type and were significantly more difficult to sensitize to DNCB than the controls. In addition, twelve of the rosacea patients and eleven other rosacea patients had biopsies which were examined by the direct immunofluorescence technique. In only five was the test negative. In the remainder deposits of IgM and/or IgG and/or complement were found at the dermo- epidermal junction and/or in the dermal collagen. Serum from the rosacea patients was also examined by the indirect technique and in six cases a circulating antinuclear antibody of IgM type was found. It is suggested that altered immune function plays a significant role in the pathogenesis of the disease. Marjorie Marjorie Lazoff, MD > Hi, > > While we're on the topic of rosacea / auto-immune disease, there is a > snippet in Dr. Nase's book (http://www.drnase.com) on page 93 which > gives the flip-side of the coin. I'll quote the main point here. > > " It is important for rosacea sufferers and general physicians to > understand that rosacea is _NOT_ an auto-immune disease (242, 243). > The immune system does _NOT_ produce antibodies or > specifically " attack " the facial skin and blood vessels. The average > rosacea sufferer has a perfectly health immune system. (242, 243) > > [emphasis in book is bold and underlined lower-case where I have used > _THIS_ format] > > The references are as follows: > > 242: Marks, R. " cea: hopeless hypotheses, marvellous myths and > dermal disorganisation " . In: Proceedings of an international > symposium, Cardiff, edited by R. Marks and G. Plewid. Cardiff: > Dunitz Ltd, 1988, p.293-299 > > 243: Manna, V., R. Marks, and P. Hold. Involvement of immune > mechanisms in the pathogenesis of rosacea. Br J Dermatol 107:203- > 208, 1982 > > . Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 21, 2002 Report Share Posted May 21, 2002 Hi, I've not read the full papers myself (and you're right, they are old) so can't really make a comment as educated as I'd like. I can say that on the same page as I took the direct quotes from, Nase explains how the immune system reacts to the chronic flushing environment and the side-effects that causes. I will dig out any further references tonight. The hypothesis which you wrote in your message last week is most closely mirrored by Lupus which presents rosacea-like symptoms on the facial skin (permanent facial redness) but which also affects other organs in the body. I haven't studied Lupus in any depth at all, however I don't believe it has flushing as a symptom -- unlike rosacea, where flushing to triggers (usually transient) is the first symptom and primary cause and mediator of the disease process. It seems that if rosacea was an auto-immune disease like Lupus, but only affecting the skin, the symptoms would mirror Lupus, i.e. NOT be flushing to triggers causing vascular damage, but the onset of permanent redness without a flushing pattern. Those are just my thoughts, . > > , I find these references confusing. In particular, the > abstract to the second reference doesn't support what's Dr. Nase's > saying. > > The statistics described in the study are confusing, but at a minumum > the authors found that 12 of the study's 24 rosaceans had tissue > biopsy evidence of altered immune function, and 6 of the 24 had > laboratory evidence of auto-immunity (remember, evidence of > autoantibodies isn't enough to call a condition auto-immune). The > abstract doesn't say how many of the controls had similiar findings, > but Dr. Nase's " ...The average rosacea sufferer has a perfectly > health immune system. " contradicts the authors' closing > statement, " It is suggested that altered immune function plays a > significant role in the pathogenesis of the disease. > > That study is published in a respected journal but it's 20 years old - > - frankly, that's just too old to reference in this area, whatever > the study found or didn't find. And the first reference comes from Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 21, 2002 Report Share Posted May 21, 2002 Hi, I've not read the full papers myself (and you're right, they are old) so can't really make a comment as educated as I'd like. I can say that on the same page as I took the direct quotes from, Nase explains how the immune system reacts to the chronic flushing environment and the side-effects that causes. I will dig out any further references tonight. The hypothesis which you wrote in your message last week is most closely mirrored by Lupus which presents rosacea-like symptoms on the facial skin (permanent facial redness) but which also affects other organs in the body. I haven't studied Lupus in any depth at all, however I don't believe it has flushing as a symptom -- unlike rosacea, where flushing to triggers (usually transient) is the first symptom and primary cause and mediator of the disease process. It seems that if rosacea was an auto-immune disease like Lupus, but only affecting the skin, the symptoms would mirror Lupus, i.e. NOT be flushing to triggers causing vascular damage, but the onset of permanent redness without a flushing pattern. Those are just my thoughts, . > > , I find these references confusing. In particular, the > abstract to the second reference doesn't support what's Dr. Nase's > saying. > > The statistics described in the study are confusing, but at a minumum > the authors found that 12 of the study's 24 rosaceans had tissue > biopsy evidence of altered immune function, and 6 of the 24 had > laboratory evidence of auto-immunity (remember, evidence of > autoantibodies isn't enough to call a condition auto-immune). The > abstract doesn't say how many of the controls had similiar findings, > but Dr. Nase's " ...The average rosacea sufferer has a perfectly > health immune system. " contradicts the authors' closing > statement, " It is suggested that altered immune function plays a > significant role in the pathogenesis of the disease. > > That study is published in a respected journal but it's 20 years old - > - frankly, that's just too old to reference in this area, whatever > the study found or didn't find. And the first reference comes from Quote Link to comment Share on other sites More sharing options...
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