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Familial Aggregation and Segregation Analysis in Families Presenting Autoimmunity Polyautoimmunity and Multiple Autoimmune Syndrome

机译:表现自身免疫多自身免疫和多种自身免疫综合症的家庭的家族聚集和分离分析

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摘要

Studies documenting increased risk of developing autoimmune diseases (ADs) have shown that these conditions share several immunogenetic mechanisms (i.e., the autoimmune tautology). This report explored familial aggregation and segregation of AD, polyautoimmunity, and multiple autoimmune syndrome (MAS) in 210 families. Familial aggregation was examined for first-degree relatives. Segregation analysis was implemented as in S.A.G.E. release 6.3. Data showed differences between late- and early-onset families regarding their age, age of onset, and sex. Familial aggregation of AD in late- and early-onset families was observed. For polyautoimmunity as a trait, only aggregation was observed between sibling pairs in late-onset families. No aggregation was observed for MAS. Segregation analyses for AD suggested major gene(s) with no clear discernible classical known Mendelian transmission in late-onset families, while for polyautoimmunity and MAS no model was implied. Data suggest that polyautoimmunity and MAS are not independent traits and that gender, age, and age of onset are interrelated factors influencing autoimmunity.
机译:研究表明发生自身免疫疾病(AD)的风险增加的研究表明,这些疾病具有多种免疫遗传机制(即自身免疫重言式)。本报告探讨了210个家庭的AD家族聚集和分离,多自身免疫和多发性自身免疫综合症(MAS)。检查家族聚集的一级亲属。分离分析的实施与S.A.G.E. 6.3版。数据显示,早发型和早发型家庭在年龄,发病年龄和性别方面存在差异。在晚期和早期发病的家庭中观察到AD的家族聚集。以多自身免疫为特征,在晚期发病家庭的兄弟姐妹对之间仅观察到聚集。没有观察到MAS的聚集。对AD的分离分析表明在晚期发病家庭中没有明显可辨别的经典已知孟德尔传播的主要基因,而对于多自身免疫和MAS则没有隐含模型。数据表明,多自身免疫和MAS不是独立的特征,性别,年龄和发病年龄是影响自身免疫的相关因素。

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