Ruijin Hospital, State Key Laboratory of Medical Genomics, Molecular Medicine Center, Shanghai Institute of Endocrinology, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
PLoS One. 2010 Mar 23;5(3):e9821. doi: 10.1371/journal.pone.0009821.
To determine whether genetic heterogeneity exists in patients with Graves' disease (GD), the cytotoxic T-lymphocyte associated 4 (CTLA-4) gene, which is implicated a susceptibility gene for GD by considerable genetic and immunological evidence, was used for association analysis in a Chinese Han cohort recruited from various geographic regions. Our association study for the SNPs in the CTLA4 gene in 2640 GD patients and 2204 control subjects confirmed that CTLA4 is the susceptibility gene for GD in the Chinese Han population. Moreover, the logistic regression analysis in the combined Chinese Han cohort revealed that SNP rs231779 (allele frequencies p = 2.81x10(-9), OR = 1.35, and genotype distributions p = 2.75x10(-9), OR = 1.42) is likely the susceptibility variant for GD. Interestingly, the logistic regression analysis revealed that SNP rs35219727 may be the susceptibility variant to GD in the Shandong population; however, SNP, rs231779 in the CTLA4 gene probably independently confers GD susceptibility in the Xuzhou and southern China populations. These data suggest that the susceptibility variants of the CTLA4 gene varied between the different geographic populations with GD.
为了确定 Graves 病(GD)患者中是否存在遗传异质性,我们使用细胞毒性 T 淋巴细胞相关蛋白 4(CTLA-4)基因进行关联分析,该基因有大量的遗传和免疫学证据表明其与 GD 易感性相关,我们从不同地理区域招募了中国汉族人群进行分析。我们对 2640 名 GD 患者和 2204 名对照者的 CTLA4 基因中的 SNP 进行了关联研究,证实 CTLA4 是中国汉族人群 GD 的易感基因。此外,在合并的中国汉族人群中进行的逻辑回归分析表明,SNP rs231779(等位基因频率 p = 2.81x10(-9),OR = 1.35,基因型分布 p = 2.75x10(-9),OR = 1.42)可能是 GD 的易感变异。有趣的是,逻辑回归分析表明,SNP rs35219727 可能是山东人群中 GD 的易感变异,但 CTLA4 基因中的 SNP rs231779 可能在徐州和中国南方人群中独立赋予 GD 易感性。这些数据表明,CTLA4 基因的易感变异在不同的 GD 地理人群中存在差异。