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格雷夫斯病的流行病学:遗传和环境因素的证据。

The epidemiology of Graves' disease: evidence of a genetic and an environmental contribution.

机构信息

Division of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 580, D-69120 Heidelberg, Germany.

出版信息

J Autoimmun. 2010 May;34(3):J307-13. doi: 10.1016/j.jaut.2009.11.019. Epub 2009 Dec 28.

Abstract

Previous family and twin studies have indicated that Graves' disease has a heritable component. Family studies have also shown that some autoimmune disease cluster in families and genetic studies have been able to show shared susceptibility genes. In the present nation-wide study we describe familial risk for Graves' disease among parents and offspring, singleton siblings, twins and spouses with regard to age of onset, gender and number and type of affected family members. Additionally familial association of Graves' disease with any of 33 other autoimmune and related conditions was analyzed. The Swedish Multigeneration Register on 0-75-year-old subjects was linked to the Hospital Discharge Register from years 1987-2007. Standardized incidence ratios (SIRs) were calculated for individuals whose relatives were hospitalized for Graves' disease compared to those whose relatives were unaffected. The total number of hospitalized Graves' patients was 15,743. Offspring with an affected family member constituted 3.6% of all patients among offspring. The familial SIR was 5.04 for individuals whose sibling was affected but it increased to 310 when two or more siblings were affected; the SIR in twins was 16.45. Familial risks were higher for males than for females. The SIR was increased to 6.22 or 30.20 when parental age was limited to 50 or 20 years, respectively. Graves' disease associated with 19 other autoimmune and related conditions, including Addison's disease, type 1 diabetes mellitus, Hashimoto/hypothyroidism, pernicious anemia, polymyositis/dermatomyositis, myasthenia gravis, discoid lupus erythematosus and localized scleroderma. Remarkably, there was a high disease concordance of 2.75 between spouses. The clustering between spouses suggests environmental effects on Graves' disease which may contribute to the observed gender effects. The demonstrated high risks should be considered in clinical counseling and in prevention plans.

摘要

先前的家族和双胞胎研究表明,格雷夫斯病具有遗传成分。家族研究还表明,某些自身免疫性疾病在家族中聚集,遗传研究已经能够显示出共同的易感基因。在本项全国性研究中,我们描述了父母和子女、单胎兄弟姐妹、双胞胎和配偶中格雷夫斯病的家族发病风险,涉及发病年龄、性别以及受影响家庭成员的数量和类型。此外,还分析了格雷夫斯病与 33 种其他自身免疫性和相关疾病的家族关联性。利用瑞典 0-75 岁人群的多代注册信息,与 1987 年至 2007 年的住院登记信息相链接。通过比较亲属患有格雷夫斯病和未患病的个体,计算个体的标准化发病比(SIR)。患有住院治疗的格雷夫斯病的患者总数为 15743 例。患病亲属的子女占所有患者的 3.6%。如果一个个体的兄弟姐妹患病,其家族 SIR 为 5.04;如果两个或更多的兄弟姐妹患病,SIR 增加至 310;如果是双胞胎,SIR 为 16.45。男性的家族风险高于女性。当父母年龄限制在 50 岁或 20 岁时,SIR 分别增加到 6.22 或 30.20。格雷夫斯病与 19 种其他自身免疫性和相关疾病有关,包括艾迪生病、1 型糖尿病、桥本甲状腺炎/甲状腺功能减退、恶性贫血、多发性肌炎/皮肌炎、重症肌无力、盘状红斑狼疮和局限性硬皮病。值得注意的是,配偶之间的疾病一致性高达 2.75。配偶之间的聚集表明,环境因素可能对格雷夫斯病有影响,从而导致观察到的性别效应。所证明的高风险应在临床咨询和预防计划中加以考虑。

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