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原发性胆汁性肝硬化的地理聚集性。

Geographic clusters of primary biliary cirrhosis.

作者信息

Abu-Mouch Saif, Selmi Carlo, Benson Gordon D, Kenny Thomas P, Invernizzi Pietro, Zuin Massimo, Podda Mauro, Rossaro Lorenzo, Gershwin M Eric

机构信息

Hepatology Clinic, Hillel Yaffe Medical Center, Hadera, Israel.

出版信息

Clin Dev Immunol. 2003 Jun-Dec;10(2-4):127-31. doi: 10.1080/10446670310001626526.

Abstract

Genetic and environmental factors have been widely suggested to contribute to the pathogenesis of primary biliary cirrhosis (PBC), an autoimmune disease of unknown etiology leading to destruction of small bile ducts. Interestingly, epidemiologic data indicate a variable prevalence of the disease in different geographical areas. The study of clusters of PBC may provide clues as to possible triggers in the induction of immunopathology. We report herein four such unique PBC clusters that suggest the presence of both genetic and environmental factors in the induction of PBC. The first cluster is represented by a family of ten siblings of Palestinian origin that have an extraordinary frequency of PBC (with 5/8 sisters having the disease). Second, we describe the cases of a husband and wife, both having PBC. A family in which PBC was diagnosed in two genetically unrelated individuals, who lived in the same household, represents the third cluster. Fourth, we report a high prevalence of PBC cases in a very small area in Alaska. Although these data are anedoctal, the study of a large number of such clusters may provide a tool to estimate the roles of genetics and environment in the induction of autoimmunity.

摘要

遗传和环境因素被广泛认为与原发性胆汁性肝硬化(PBC)的发病机制有关,PBC是一种病因不明的自身免疫性疾病,可导致小胆管破坏。有趣的是,流行病学数据表明该疾病在不同地理区域的患病率各不相同。对PBC聚集病例的研究可能会为免疫病理学诱导中的潜在触发因素提供线索。我们在此报告了四个这样独特的PBC聚集病例,提示在PBC的诱导过程中存在遗传和环境因素。第一个聚集病例是以一个来自巴勒斯坦的十兄弟姐妹家庭为代表,他们中PBC的发病率异常高(8个姐妹中有5个患病)。其次,我们描述了一对夫妻均患有PBC的病例。在同一个家庭中,两名无血缘关系的个体被诊断出患有PBC的一个家庭代表了第三个聚集病例。第四,我们报告了阿拉斯加一个非常小的区域内PBC病例的高患病率。尽管这些数据只是轶事,但对大量此类聚集病例的研究可能会提供一种工具,以评估遗传和环境在自身免疫诱导中的作用。

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