Female Gender and Reproductive Factors Affecting Risk, Relapses and Progression in Multiple Sclerosis

被引:34
作者
D'hooghe, M. B. [1 ,2 ]
D'Hooghe, T. [3 ]
De Keyser, J. [2 ,4 ]
机构
[1] Natl Ctr Multiple Sclerosis, Melsbroek, Belgium
[2] VUB, Ctr Neurosci, Dept Neurol UZ Brussels, Brussels, Belgium
[3] Univ Hosp Gasthuisberg, Leuven Fertil Ctr, Dept Obstet & Gynecol, Louvain, Belgium
[4] Univ Groningen, Univ Med Ctr Groningen, Dept Neurol, NL-9713 AV Groningen, Netherlands
关键词
Multiple sclerosis; Female gender; Pregnancy; Menarche; Oral contraceptives; IN-VITRO FERTILIZATION; ORAL-CONTRACEPTIVES; NATURAL-HISTORY; ENVIRONMENTAL GENETICS; CLINICAL PREDICTORS; POSTPARTUM RELAPSES; CONTROLLED TRIAL; MENSTRUAL-CYCLE; SEX-HORMONES; MAJOR CAUSE;
D O I
10.1159/000346319
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Multiple sclerosis (MS), a chronic inflammatory demyelinating and degenerative disease of the central nervous system, is a frequent cause of neurological disability in young adults. Female predominance has increased over the last decades. Although female gender carries a higher risk of developing relapsing remitting MS, being female and at child-bearing age also appears to provide some protection against cognitive decline and against progressive onset MS, an adverse predictive factor when considering long-term disability in MS. The risk of MS in women has been associated with an earlier age at menarche. In most studies, parity did not impact MS risk. However, the recently published association of higher parity and offspring number with a reduced risk of a first demyelinating event suggests a potential suppressive effect. Pregnancy in MS patients has been associated with a reduced relapse rate and a reduction of neurological symptoms, especially in the third trimester. Despite the increased relapse risk in the postpartum period, there is no indication of an adverse effect of childbirth on the long-term course of MS. Fertility treatment in MS has been associated with an increased relapse risk in the following 3-month period, especially when the procedure did not result in pregnancy and gonadotrophin-releasing hormone agonists were used. Altogether, there is substantial evidence to support a regulatory role of sex steroid hormones in MS. In the absence of correlations with single hormone blood levels, we can only speculate about the underlying mechanisms. In conclusion, the increased MS risk in women and the changes in relapse and progression risk in association with reproductive events suggest significant and complex interactions between immune, neuroendocrine and reproductive systems in MS. Copyright (C) 2013 S. Karger AG, Basel
引用
收藏
页码:73 / 84
页数:12
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