Li Yuan, Zhou Aihong, Lv Guanting, Li Ping, Chen Si, Li Jing, Wen Xiaoting, Wu Ziyan, Zhang Shulan, Wang Jibo, Zhang Fengchun, Li Yongzhe
Department of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Key Laboratory of Rheumatology and Clinical Immunology, Ministry of Education, 1 Shuaifuyuan, Dongcheng District, Beijing, 100730, China.
Department of Rheumatology, The Affiliated Hospital of Qingdao University, Qingdao, China.
Immunol Res. 2016 Feb;64(1):324-8. doi: 10.1007/s12026-015-8755-9.
Several novel susceptibility genes for systemic lupus erythematosus (SLE) and other nephropathy have been identified in recent genome-wide association studies. Membranous nephropathy is the most common diagnosis in adults with the nephrotic syndrome, and both idiopathic membranous nephropathy (IMN) and lupus nephritis (LN) are autoimmune diseases of the kidney; they may share common disease mechanisms that overlap with genetic susceptibility. Therefore, we sought to identify genetic variants associated with IMN in SLE/LN. The PLA2R1 single-nucleotide polymorphisms rs4664308, rs3828323, rs3792189, and rs3792192 were genotyped in a cohort of 1247 SLE patients and 1174 healthy controls, using the Sequenom MassArray system method. PLA2R1 displayed a nominally significantly genetic association with SLE [for rs4664308, P = 0.02, odds ratio (OR) 1.16, 95 % confidence interval (CI) 1.02-1.31; for rs3792192, P = 7.9 × 10(-3), OR 1.18, 95 % CI 1.05-1.34] and LN (for rs4664308, P = 0.04). The frequencies of genotypes of rs3792189 and rs3828323 were significantly different between the SLE patients and controls (all P < 0.05), and the haplotype (AA) formed by rs3792189 and rs3792192 was associated with SLE (P = 0.019). This was the first study to reveal that PLA2R1 polymorphisms were associated with SLE/LN patients, indicating that PLA2R1 might be a susceptibility gene for SLE/LN in a Chinese Han population.
在最近的全基因组关联研究中,已鉴定出几种系统性红斑狼疮(SLE)和其他肾病的新型易感基因。膜性肾病是成人肾病综合征最常见的诊断类型,特发性膜性肾病(IMN)和狼疮性肾炎(LN)均为肾脏自身免疫性疾病;它们可能具有与遗传易感性重叠的共同发病机制。因此,我们试图鉴定与SLE/LN中IMN相关的基因变异。使用Sequenom MassArray系统方法,对1247例SLE患者和1174例健康对照组成的队列进行了磷脂酶A2受体1(PLA2R1)单核苷酸多态性rs4664308、rs3828323、rs3792189和rs3792192的基因分型。PLA2R1与SLE显示出名义上显著的遗传关联[对于rs4664308,P = 0.02,优势比(OR)1.16,95%置信区间(CI)1.02 - 1.31;对于rs379219