Suppr超能文献

HLA 在格雷夫斯眼病发展中的意义。

Significance of HLA in the development of Graves' orbitopathy.

机构信息

Polish Mother's Memorial Hospital - Research Institute, Department of Endocrinology and Metabolic Diseases, Lodz, Poland.

Medical University of Lodz, Department of Immunology, Rheumatology and Allergy, Lodz, Poland.

出版信息

Genes Immun. 2023 Feb;24(1):32-38. doi: 10.1038/s41435-023-00193-z. Epub 2023 Jan 13.

Abstract

Graves' disease (GD), similarly to most autoimmune disease, is triggered by environmental factors in genetically predisposed individuals. Particular HLA alleles increase or decrease GD risk. No such correlation was demonstrated for Graves' orbitopathy (GO) in Caucasian population. HLA-A, -B, -C, -DQB1 and -DRB1 genotyping was performed using a high-resolution method in a total number of 2378 persons including 70 patients with GO, 91 patients with non-GO GD and 2217 healthy controls to compare allele frequencies between GO, non-GO and controls. Significant associations between GO and HLA profile were demonstrated, with HLA-A01:01, -A32:01, -B37:01, -B39:01, -B42:01, -C08:02, C03:02, DRB103:01, DRB114:01 and DQB102:01 being genetic markers of increased risk of GO, and HLA-C04:01, -C03:04, -C07:02 and -DRB115:02 being protective alleles. Moreover, correlations between HLA alleles and increased or decreased risk of non-GO GD, but with no impact on risk of GO development, were revealed. Identification of these groups of GO-related and GO-protective alleles, as well as the alleles strongly related to non-GO GD, constitutes an important step in a development of personalized medicine, with individual risk assessment and patient-tailored treatment.

摘要

格雷夫斯病(GD)与大多数自身免疫性疾病类似,是由遗传易感个体的环境因素引发的。特定的 HLA 等位基因增加或降低 GD 的风险。然而,在白种人群中,尚未发现格雷夫斯眼病(GO)与 HLA 之间存在这种相关性。我们使用高分辨率方法对总共 2378 人(包括 70 例 GO 患者、91 例非 GO GD 患者和 2217 名健康对照者)进行了 HLA-A、-B、-C、-DQB1 和 -DRB1 基因分型,以比较 GO、非 GO 和对照组之间的等位基因频率。结果表明,GO 与 HLA 谱之间存在显著关联,HLA-A01:01、-A32:01、-B37:01、-B39:01、-B42:01、-C08:02、C03:02、DRB103:01、DRB114:01 和 DQB102:01 是 GO 风险增加的遗传标志物,而 HLA-C04:01、-C03:04、-C07:02 和 -DRB115:02 是保护性等位基因。此外,还揭示了 HLA 等位基因与非 GO GD 风险增加或降低之间的相关性,但对 GO 发病风险没有影响。鉴定这些与 GO 相关和保护 GO 的等位基因组,以及与非 GO GD 密切相关的等位基因,是个体化医学发展的重要步骤,可进行个体风险评估和患者量身定制的治疗。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验