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Genome-wide association analysis suggests novel loci underlying thyroid antibodies in Hashimoto’s thyroiditis

机译:全基因组关联分析表明桥本甲状腺炎中潜在的新型甲状腺甲状腺抗体基因位点

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摘要

Thyroid antibodies against thyroglobulin (TgAb) and thyroid peroxidase (TPOAb) are key markers of Hashimoto’s thyroiditis (HT), the most common autoimmune thyroid disorder. Genetic determinants of thyroid antibodies are still poorly known, especially as they were not studied in patients with thyroid diseases. We performed the first genome-wide association analysis of thyroid antibodies in 430 HT patients that may be considered as population extremes for thyroid antibodies distribution. We detected two suggestively associated genetic variants with TgAb, rs6972286 close to ANKRD7 and LSM8 (P = 2.34 × 10−7) and rs756763 inside CA10 (P = 6.05 × 10−7), and one with TPOAb, rs12507813 positioned between TRIM61 and TRIM60 (P = 4.95 × 10−7). Bivariate analysis resulted with three suggestively associated genetic variants that predispose to both antibodies: rs13190616 inside RP11-138J23.1 (P = 2.01 × 10−6), rs561030786 close to DUBR (P = 7.33 × 10−6) and rs12713034 inside FSHR (P = 7.66 × 10−6). All identified genomic regions have a substantial literature record of involvement with female-related traits, immune-mediated diseases and personality traits that are all characterized by increased thyroid antibody levels. Our findings demonstrate the existence of genetic overlap between thyroid autoimmunity in HT and different non-thyroid diseases characterized by the presence of thyroid antibodies. We also suggest that genetic variants that regulate antibody levels may differ between HT patients and individuals with normal thyroid function.
机译:抗甲状腺球蛋白(TgAb)和甲状腺过氧化物酶(TPOAb)的甲状腺抗体是桥本甲状腺炎(HT)(最常见的自身免疫性甲状腺疾病)的关键标志。甲状腺抗体的遗传决定因素仍然知之甚少,特别是因为尚未在甲状腺疾病患者中进行研究。我们对430名HT患者进行了首次全基因组甲状腺抗体全基因组关联分析,这可能被认为是甲状腺抗体分布的极端人群。我们检测到两个暗示相关的TgAb遗传变异,靠近ANKRD7和LSM8的rs6972286(P = 2.34×10 -7 )和位于CA10内的rs756763(P = 6.05×10 −7 ),以及一个带有TPOAb的rs12507813,位于TRIM61和TRIM60之间(P = 4.95×10 -7 )。双变量分析产生了三个提示性相关的遗传变异,它们易感于两种抗体:RP11-138J23.1内部的rs13190616(P = 2.01×10 -6 ),rs561030786接近DUBR(P = 7.33×10 < FSHR中的sup> -6 )和rs12713034(P = 7.66×10 -6 )。所有确定的基因组区域都有大量涉及女性相关性状,免疫介导的疾病和人格性状的文献记录,这些特征均以甲状腺抗体水平升高为特征。我们的发现表明,HT甲状腺自身免疫与以甲状腺抗体为特征的不同非甲状腺疾病之间存在基因重叠。我们还建议调节抗体水平的遗传变异在HT患者和甲状腺功能正常的个体之间可能有所不同。

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