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HLA相关的类风湿关节炎。

HLA-linked rheumatoid arthritis.

作者信息

Hasstedt S J, Clegg D O, Ingles L, Ward R H

机构信息

Department of Human Genetics, University of Utah, Salt Lake City 84112.

出版信息

Am J Hum Genet. 1994 Oct;55(4):738-46.

Abstract

Twenty-eight pedigrees were ascertained through pairs of first-degree relatives diagnosed with rheumatoid arthritis (RA). RA was confirmed in 77 pedigree members including probands; the absence of disease was verified in an additional 261 pedigree members. Pedigree members were serologically typed for HLA. We used likelihood analysis to statistically characterize the HLA-linked RA susceptibility locus. The genetic model assumed tight linkage to HLA. The analysis supported the existence of an HLA-linked RA susceptibility locus, estimated the susceptibility allele frequency as 2.16%, and estimated the lifetime penetrance as 41% in male homozygotes and as 48% in female homozygotes. Inheritance was recessive in males and was nearly recessive in females. In addition, the analysis attributed 78% of the variance within genotypes to genetic or environmental effects shared by siblings. The genetic model inferred in this analysis is consistent with previous association, linkage, and familial aggregation studies of RA. The inferred HLA-linked RA susceptibility locus accounts for approximately one-half of familial RA, although it accounts for only approximately one-fifth of the RA in the population. Although other genes may account for the remaining familial RA, a large portion of RA cases may occur sporadically.

摘要

通过对诊断为类风湿关节炎(RA)的一级亲属对确定了28个家系。在包括先证者在内的77名家系成员中确诊为RA;在另外261名家系成员中证实无疾病。对家系成员进行了HLA血清学分型。我们使用似然分析对与HLA连锁的RA易感基因座进行统计学特征描述。遗传模型假定与HLA紧密连锁。分析支持存在一个与HLA连锁的RA易感基因座,估计易感等位基因频率为2.16%,估计男性纯合子的终生外显率为41%,女性纯合子为48%。遗传方式在男性中为隐性,在女性中近乎隐性。此外,分析将基因型内78%的方差归因于兄弟姐妹共有的遗传或环境效应。本分析推断的遗传模型与先前关于RA的关联、连锁和家族聚集性研究一致。推断的与HLA连锁的RA易感基因座约占家族性RA的一半,尽管它仅占人群中RA的约五分之一。虽然其他基因可能解释其余的家族性RA,但很大一部分RA病例可能是散发性的。

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