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自身免疫性甲状腺疾病相关连锁位点的精细定位确定了新的易感基因。

Fine mapping of loci linked to autoimmune thyroid disease identifies novel susceptibility genes.

机构信息

Department of Medicine, Division of Endocrinology, Mount Sinai School of Medicine, New York, New York 10029, USA.

出版信息

J Clin Endocrinol Metab. 2013 Jan;98(1):E144-52. doi: 10.1210/jc.2012-2408. Epub 2012 Nov 1.

Abstract

CONTEXT

Genetic factors play a major role in the etiology of autoimmune thyroid disease (AITD) including Graves' disease (GD) and Hashimoto's thyroiditis (HT). We have previously identified three loci on chromosomes 10q, 12q, and 14q that showed strong linkage with AITD, HT, and GD, respectively.

OBJECTIVES

The objective of the study was to identify the AITD susceptibility genes at the 10q, 12q, and 14q loci.

DESIGN AND PARTICIPANTS

Three hundred forty North American Caucasian AITD patients and 183 healthy controls were studied. The 10q, 12q, and 14q loci were fine mapped by genotyping densely spaced single-nucleotide polymorphisms (SNPs) using the Illumina GoldenGate genotyping platform. Case control association analyses were performed using the UNPHASED computer package. Associated SNPs were reanalyzed in a replication set consisting of 238 AITD patients and 276 controls.

RESULTS

Fine mapping of the AITD locus, 10q, showed replicated association of the AITD phenotype (both GD and HT) with SNP rs6479778. This SNP was located within the ARID5B gene recently reported to be associated with rheumatoid arthritis and GD in Japanese. Fine mapping of the GD locus, 14q, revealed replicated association of the GD phenotype with two markers, rs12147587 and rs2284720, located within the NRXN3 and TSHR genes, respectively.

CONCLUSIONS

Fine mapping of three linked loci identified novel susceptibility genes for AITD. The discoveries of new AITD susceptibility genes will engender a new understanding of AITD etiology.

摘要

背景

遗传因素在自身免疫性甲状腺疾病(AITD)的病因学中起着重要作用,包括格雷夫斯病(GD)和桥本甲状腺炎(HT)。我们之前已经确定了三个位于染色体 10q、12q 和 14q 上的位点,它们分别与 AITD、HT 和 GD 有强烈的连锁关系。

目的

本研究的目的是确定 10q、12q 和 14q 位点的 AITD 易感基因。

设计和参与者

研究了 340 名北美白种人 AITD 患者和 183 名健康对照者。使用 Illumina GoldenGate 基因分型平台,通过对紧密间隔的单核苷酸多态性(SNP)进行基因分型,对 10q、12q 和 14q 位点进行精细作图。使用 UNPHASED 计算机包进行病例对照关联分析。在由 238 名 AITD 患者和 276 名对照者组成的复制组中重新分析了相关 SNP。

结果

AITD 位点 10q 的精细作图显示,AITD 表型(GD 和 HT 均包括在内)与 SNP rs6479778 存在复制关联。该 SNP 位于最近报道与日本的类风湿关节炎和 GD 相关的 ARID5B 基因内。GD 位点 14q 的精细作图显示,GD 表型与位于 NRXN3 和 TSHR 基因内的两个标记物 rs12147587 和 rs2284720 存在复制关联。

结论

三个连锁位点的精细作图确定了 AITD 的新易感基因。新 AITD 易感基因的发现将使人们对 AITD 的病因学有新的认识。

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