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首页> 外文期刊>Lancet Neurology >Autoimmune disease in families with multiple sclerosis: a population-based study.
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Autoimmune disease in families with multiple sclerosis: a population-based study.

机译:多发性硬化症家庭的自身免疫性疾病:一项基于人群的研究。

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BACKGROUND: Evidence of an association between multiple sclerosis (MS) and other autoimmune diseases would substantiate the hypothesis that MS is an autoimmune disease, and implicate a common mechanism. We aimed to investigate and compare the rate of autoimmune disease in MS patients, in their first-degree relatives, and in their unrelated spouses. METHODS: We used data from a national, multicentre, population-based sample to investigate the rate of autoimmune disease in 5031 MS patients, 30 259 of their first-degree relatives, and 2707 spousal controls. We asked patients and controls whether they had any of ten autoimmune diseases: Crohn's disease, ulcerative colitis, rheumatoid arthritis, type 1 diabetes, psoriasis, pernicious anaemia, systemic lupus erythematosus, autoimmune thyroid disease, vitiligo, and myasthenia gravis. MS probands were also asked whether their first-degree relatives had Crohn's disease, ulcerative colitis, rheumatoid arthritis, or type 1 diabetes. FINDINGS: After correction forage and sex, we did not identify any increased risk of autoimmune diseases in MS patients compared with their spousal controls (odds ratio [OR]=1.07, 95% CI 0.86-1.23, chi(2)=0.47, p=0.49), or in the first-degree relatives of MS probands compared with controls (OR=0.89, 0.63-1.17, chi(2)=1.11, p=0.29). However, the reported frequency of autoimmune diseases did differ according to the sex of the interviewee (female vs male patients chi(2)=92.2, p<0.0001; female vs male spousal controls chi(2)=87.1, p<0.0001). MS patients had slightly higher rates of thyroid disease and pernicious anaemia than did controls, which is consistent with MHC associations for these diseases, but this effect disappeared when results were adjusted for sex. For eight other diseases the rates were similar in MS patients and controls. Families with multiple cases of MS were no more likely to report autoimmune diseases than families with single MS cases. INTERPRETATION: When data were adjusted for sex, no excess of common autoimmune diseases could be identified in MS patients or their families, including multicase pedigrees. Our results suggest that women are more aware of family medical histories than men, which emphasises the potential for ascertainment bias in unstratified data for a sex-limited disease. Family histories should thus be taken from male patients in the presence of a spouse.
机译:背景:多发性硬化症(MS)与其他自身免疫性疾病之间存在关联的证据将证实MS是一种自身免疫性疾病的假说,并暗示一个共同的机制。我们的目的是调查和比较MS患者,其一级亲属和其无亲属的配偶的自身免疫性疾病的发生率。方法:我们使用来自全国性,多中心,基于人群的样本数据调查了5031名MS患者,30 259名一级亲属和2707名配偶对照的自身免疫性疾病发病率。我们询问患者和对照对象是否患有十种自身免疫性疾病:克罗恩病,溃疡性结肠炎,类风湿性关节炎,1型糖尿病,牛皮癣,恶性贫血,系统性红斑狼疮,自身免疫性甲状腺疾病,白癜风和重症肌无力。还向MS先证者询问其一级亲属是否患有克罗恩病,溃疡性结肠炎,类风湿性关节炎或1型糖尿病。结果:校正草料和性别后,我们没有发现与配偶对照相比MS患者自身免疫性疾病的风险增加(优势比[OR] = 1.07,95%CI 0.86-1.23,chi(2)= 0.47,p = 0.49),或与对照相比MS先证者的一级亲属(OR = 0.89,0.63-1.17,chi(2)= 1.11,p = 0.29)。但是,根据受访者的性别,报告的自身免疫性疾病的发病率确实有所不同(女性与男性患者chi(2)= 92.2,p <0.0001;女性与男性配偶对照chi(2)= 87.1,p <0.0001)。 MS患者的甲状腺疾病和恶性贫血的发生率比对照组稍高,这与这些疾病的MHC关联是一致的,但是对性别进行调整后,这种影响消失了。对于其他八种疾病,MS患者和对照组的发病率相似。多发性MS病例的家庭比单发性MS病例的家庭更不可能报告自身免疫性疾病。解释:调整性别数据后,MS患者或其家属(包括多病例谱系)未发现过多的常见自身免疫性疾病。我们的研究结果表明,女性比男性更了解家庭医疗史,这强调了在未分层的性别受限疾病数据中确定偏倚的可能性。因此,应在有配偶的情况下从男性患者那里获取家族史。

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