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自身免疫性疾病、多发性自身免疫性疾病和多重自身免疫综合征患者家庭中的家族聚集性和分离分析

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

作者信息

Castiblanco John, Sarmiento-Monroy Juan Camilo, Mantilla Ruben Dario, Rojas-Villarraga Adriana, Anaya Juan-Manuel

机构信息

Center for Autoimmune Diseases Research (CREA), School of Medicine and Health Sciences, Universidad del Rosario, Carrera 24 No. 63-C-69, Bogotá, Colombia ; Doctoral Program in Biomedical Sciences, Universidad del Rosario, Bogotá, Colombia.

Center for Autoimmune Diseases Research (CREA), School of Medicine and Health Sciences, Universidad del Rosario, Carrera 24 No. 63-C-69, Bogotá, Colombia.

出版信息

J Immunol Res. 2015;2015:572353. doi: 10.1155/2015/572353. Epub 2015 Nov 30.

Abstract

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.

摘要

记录自身免疫性疾病(AD)发病风险增加的研究表明,这些病症具有多种免疫遗传机制(即自身免疫性套套逻辑)。本报告探讨了210个家庭中AD、多自身免疫性疾病和多重自身免疫综合征(MAS)的家族聚集性和分离情况。对一级亲属进行了家族聚集性检查。采用S.A.G.E. 6.3版进行分离分析。数据显示,晚发型和早发型家庭在年龄、发病年龄和性别方面存在差异。观察到晚发型和早发型家庭中AD的家族聚集性。对于多自身免疫性疾病这一特征,仅在晚发型家庭的同胞对之间观察到聚集性。未观察到MAS的聚集性。AD的分离分析表明,晚发型家庭中存在主要基因,但没有明显可辨别的经典孟德尔遗传模式,而对于多自身免疫性疾病和MAS则未暗示任何模型。数据表明,多自身免疫性疾病和MAS不是独立的特征,性别、年龄和发病年龄是影响自身免疫性的相互关联因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/629d/4677210/d85dfa1f27a1/JIR2015-572353.001.jpg

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