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亚洲人群中 HLA - DRB1 等位基因与格雷夫斯病的关联:一项荟萃分析。

Association Between HLA-DRB1 Alleles and Graves' Disease in Asian Populations: A Meta-Analysis.

作者信息

Li Wenyi, Ke Tingyu, Wang Jia, Zhu Fangling, Chi Yan

机构信息

Endocrinology Department, Kunming Medical University Second Affiliated Hospital, Kunming, China.

出版信息

Horm Metab Res. 2024 Dec;56(12):859-868. doi: 10.1055/a-2298-4366. Epub 2024 May 2.

Abstract

Graves' disease (GD) is an autoimmune disease that primarily affects the thyroid gland. It is the most common cause of hyperthyroidism. Genetic studies have shown that human leukocyte antigen (HLA) plays an important role in the development of GD. In this article, we performed a meta-analysis determined to evaluate the relationship between HLA-DRB1 alleles and GD. This meta-analysis included 9 studies (3582 cases in the case group and 23070 cases in the control group) and 27 alleles was performed. The combined results showed that, compared with the control group, GD patients have a significant increase in the frequency of DRB11403 (OR=2.50, 95% CI=1.78-3.51, pc<0.0001) and have a significant decrease in frequencies of DRB1 0101 (OR=0.45, 95% CI=0.34-0.59, pc<0.0001) and DRB10701 (OR=0.44, 95% CI=0.35-0.55, pc<0.0001). The meta-analysis indicated that, in Asian populations, DRB11403 is a risk allele for GD, and DRB10101 and DRB10701 are protective against the occurrence of GD. We surprisingly discovered that the susceptibility alleles for GD in Asian populations are completely different from Caucasians and the protective alleles for GD in Asians are quite similar to those of Caucasians. The results of our study may provide new opportunities for gene-targeted therapy for GD in Asian populations.

摘要

格雷夫斯病(GD)是一种主要影响甲状腺的自身免疫性疾病。它是甲状腺功能亢进最常见的病因。基因研究表明,人类白细胞抗原(HLA)在GD的发病过程中起重要作用。在本文中,我们进行了一项荟萃分析,旨在评估HLA - DRB1等位基因与GD之间的关系。该荟萃分析纳入了9项研究(病例组3582例,对照组23070例),并对27个等位基因进行了分析。合并结果显示,与对照组相比,GD患者中DRB11403的频率显著增加(OR = 2.50,95%CI = 1.78 - 3.51,pc < 0.0001),而DRB10101(OR = 0.45,95%CI = 0.34 - 0.59,pc < 0.0001)和DRB10701(OR = 0.44,95%CI = 0.35 - 0.55,pc < 0.0001)的频率显著降低。荟萃分析表明,在亚洲人群中,DRB11403是GD的风险等位基因,而DRB10101和DRB10701可预防GD的发生。我们惊讶地发现,亚洲人群中GD的易感等位基因与白种人完全不同,而亚洲人群中GD的保护等位基因与白种人非常相似。我们的研究结果可能为亚洲人群GD的基因靶向治疗提供新的机会。

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