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类风湿关节炎与其他自身免疫性疾病的家族聚集性。

Familial clustering of rheumatoid arthritis with other autoimmune diseases.

作者信息

Lin J P, Cash J M, Doyle S Z, Peden S, Kanik K, Amos C I, Bale S J, Wilder R L

机构信息

Genetic Studies Section, Laboratory of Skin Biology, Bethesda, MD 20892-2757, USA.

出版信息

Hum Genet. 1998 Oct;103(4):475-82. doi: 10.1007/s004390050853.

Abstract

Previous studies have shown that rheumatoid arthritis aggregates within families. However, no formal genetic analysis of rheumatoid arthritis in pedigrees together with other autoimmune diseases has been reported. We hypothesized that there are genetic factors in common in rheumatoid arthritis and other autoimmune diseases. Results of odds-ratio regression and complex segregation analysis in a sample of 43 Caucasian pedigrees ascertained through a rheumatoid arthritis proband or matched control proband, revealed a very strong genetic influence on the occurrence of both rheumatoid arthritis and other autoimmune diseases. In an analysis of rheumatoid arthritis alone, only one inter-class measure, parent-sibling, resulted in positive evidence of aggregation. However, three inter-class measures (parent-sibling, sibling-offspring, and parent-offspring pairs) showed significant evidence of familial aggregation with odds-ratio regression analysis of rheumatoid arthritis together with all other autoimmune diseases. Segregation analysis of rheumatoid arthritis alone revealed that the mixed model, including both polygenic and major gene components, was the most parsimonious. Similarly, segregation analysis of rheumatoid arthritis together with other autoimmune diseases revealed that a mixed model fitted the data significantly better than either major gene or polygenic models. These results were consistent with a previous study which concluded that several genes, including one with a major effect, is responsible for rheumatoid arthritis in families. Our data showed that this conclusion also held when the phenotype was defined as rheumatoid arthritis and/or other autoimmune diseases, suggesting that several major autoimmune diseases result from pleiotropic effects of a single major gene on a polygenic background.

摘要

先前的研究表明类风湿关节炎在家族中具有聚集性。然而,尚未有关于类风湿关节炎与其他自身免疫性疾病在系谱中的正式遗传学分析报告。我们推测类风湿关节炎与其他自身免疫性疾病存在共同的遗传因素。在通过类风湿关节炎先证者或匹配的对照先证者确定的43个白种人系谱样本中进行的优势比回归和复杂分离分析结果显示,类风湿关节炎和其他自身免疫性疾病的发生均受到非常强烈的遗传影响。单独对类风湿关节炎进行分析时,只有一种类内测量方法,即父母与兄弟姐妹之间的关系,得出了聚集的阳性证据。然而,三种类内测量方法(父母与兄弟姐妹、兄弟姐妹与后代以及父母与后代对)在对类风湿关节炎与所有其他自身免疫性疾病进行优势比回归分析时显示出家族聚集的显著证据。单独对类风湿关节炎进行分离分析表明,包括多基因和主基因成分的混合模型是最简约的。同样,对类风湿关节炎与其他自身免疫性疾病进行分离分析表明,混合模型对数据的拟合明显优于主基因模型或多基因模型。这些结果与先前的一项研究一致,该研究得出结论,包括一个具有主要作用的基因在内的几个基因导致了家族性类风湿关节炎。我们的数据表明,当将表型定义为类风湿关节炎和/或其他自身免疫性疾病时,这一结论同样成立,这表明几种主要的自身免疫性疾病是由单个主要基因在多基因背景上的多效性作用导致的。

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