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人类白细胞抗原II类分子区分甲状腺自身免疫和多腺体自身免疫。

HLA Class II Differentiates Between Thyroid and Polyglandular Autoimmunity.

作者信息

Barkia Beradhi S, Flesch B K, Hansen M P, Matheis N, Kahaly G J

机构信息

Molecular Thyroid Research Laboratory, Johannes Gutenberg University (JGU) Medical Center, Mainz, Germany.

Laboratory of Immunogenetics/HLA (BKF), German Red Cross Blood Service West, Bad Kreuznach, Germany.

出版信息

Horm Metab Res. 2016 Apr;48(4):232-7. doi: 10.1055/s-0035-1559622. Epub 2015 Aug 28.

Abstract

The HLA class II genes are susceptibility genes for autoimmune endocrine diseases; however, scarce data are available pertaining to the determinants of genetic susceptibility to polyglandular autoimmunity (PGA). A total of 300 consecutive and unselected patients with either PGA or monoglandular autoimmune thyroid disease (AITD) and 100 healthy control subjects were genotyped for the HLA class II DRB1, -DQA1, and -DQB1 alleles. Compared to patients with AITD and controls, the HLA-DRB103 (pc =0.001), 04 (pc<0.001), -DQA103 (pc<0.001), and -DQB102 (pc =0.001) alleles were increased in patients with PGA. When dividing patients with Hashimoto's thyroiditis (HT) into those with PGA (PGA-HT) vs. those with HT as monoglandular disease, significant differences for the DRB103 (pc=0.001) and DQA103 (pc=0.001) alleles were observed. In contrast, the DQB102 allele was more prevalent in PGA patients with Graves' disease (PGA-GD) vs. those with monoglandular GD (pc=0.002). The HLA-DRB115 (pc =0.001), -DQA101 (pc =0.001), -DQB105 (pc =0.002) and -DQB1*06 (pc =0.002) alleles were significantly less present in PGA compared to monoglandular AITD and controls, thus indicating protective alleles. The HLA class II alleles differentiate between mono- and polyglandular autoimmunity in patients with autoimmune thyroid disease.

摘要

人类白细胞抗原(HLA)II类基因是自身免疫性内分泌疾病的易感基因;然而,关于多腺体自身免疫(PGA)遗传易感性决定因素的数据却很匮乏。对连续的300例未经选择的PGA患者或单腺体自身免疫性甲状腺疾病(AITD)患者以及100名健康对照者进行了HLA II类DRB1、-DQA1和-DQB1等位基因的基因分型。与AITD患者和对照相比,PGA患者中HLA-DRB103(pc =0.001)、04(pc<0.001)、-DQA103(pc<0.001)和-DQB102(pc =0.001)等位基因增加。将桥本甲状腺炎(HT)患者分为伴有PGA的患者(PGA-HT)和单腺体疾病的HT患者时,观察到DRB103(pc=0.001)和DQA103(pc=0.001)等位基因存在显著差异。相比之下,DQB102等位基因在伴有格雷夫斯病的PGA患者(PGA-GD)中比单腺体GD患者更为常见(pc=0.002)。与单腺体AITD患者和对照相比,PGA患者中HLA-DRB115(pc =0.001)、-DQA101(pc =0.001)、-DQB105(pc =0.002)和-DQB1*06(pc =0.002)等位基因明显较少,因此表明这些是保护性等位基因。HLA II类等位基因可区分自身免疫性甲状腺疾病患者的单腺体和多腺体自身免疫情况。

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