Ultraviolet radiation intensity predicts the relative distribution of dermatomyositis and anti-Mi-2 autoantibodies in women.
Ultraviolet radiation intensity predicts the relative distribution of dermatomyositis and anti-Mi-2 autoantibodies in women.
复制标题
DOI:
10.1002/art.24702
复制
发表时间:
2009-08
影响因子:
--
通讯作者:
Miller, Frederick W.
中科院分区:
文献类型:
--
作者:
Love, Lori A.;Weinberg, Clarice R.;McConnaughey, D. Robert;Oddis, Chester V.;Medsger, Thomas A., Jr.;Reveille, John D.;Arnett, Frank C.;Targoff, Ira N.;Miller, Frederick W.
Because studies suggest that ultraviolet radiation (UVR) modulates myositis phenotype and Mi-2 autoantigen expression, we conducted a retrospective investigation to determine if UVR may influence the relative prevalence of dermatomyositis and anti-Mi-2 autoantibodies in the United States. We assessed the relationship between surface UVR intensity in the state of residence at the time of onset with the relative prevalence of dermatomyositis and myositis autoantibodies in 380 myositis patients from referral centers in the U.S. Myositis autoantibodies were detected by validated immunoprecipitation assays. Surface UVR intensity was estimated from UV index data collected by the U.S. National Weather Service. UVR intensity was associated with the relative proportion of patients with dermatomyositis (odds ratio [OR] 2.3, 95% confidence interval [CI] 0.9–5.8) and with the proportion of patients expressing anti-Mi-2 autoantibodies (OR 6.0, CI 1.1–34.1). Modeling of these data showed that these associations were confined to women (OR 3.8, CI 1.3–11.0 and OR 17.3, CI 1.8–162.4, respectively) and suggests that gender influences UVR effects on autoimmune disorders. Significant associations were not seen in men, nor were UVR levels related to the presence of anti-synthetase or anti-signal recognition particle autoantibodies. This first study of the distribution of myositis phenotypes and UVR exposure in the United States showed that UVR may modulate the clinical and immunologic expression of autoimmune disease in women. Further investigation of the mechanisms by which these effects are produced may give insights into pathogenesis and suggest therapeutic or preventative strategies.
登录
查看更多内容
影响因子:
4.8
作者:
Yamaguchi, Yuji;Takahashi, Kaoruko;Hearing, Vincent J.
通讯作者:
Hearing, Vincent J.
影响因子:
4.8
作者:
Burd, Craig J.;Kinyamu, H. Karimi;Archer, Trevor K.
通讯作者:
Archer, Trevor K.
DOI:
10.1016/j.pbiomolbio.2006.02.011
发表时间:
2006-09-01
影响因子:
3.8
作者:
Gallagher, Richard P.;Lee, Tim K.
通讯作者:
Lee, Tim K.
影响因子:
6.5
作者:
Damian, Diona L.;Patterson, Clare R. S.;Halliday, Gary M.
通讯作者:
Halliday, Gary M.
影响因子:
27.4
作者:
Chinoy, Hector;Fertig, Noreen;Cooper, Robert G.
通讯作者:
Cooper, Robert G.