Tripathi G, Rangaswamy D, Borkar M, Prasad N, Sharma R K, Sankhwar S N, Agrawal S
Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India ; Department of Pathology and Laboratory Medicine, Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada.
Department of Nephrology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
Indian J Nephrol. 2015 Jan-Feb;25(1):34-42. doi: 10.4103/0971-4065.135350.
We evaluated whether polymorphisms in interleukin (IL-1) gene cluster (IL-1 alpha [IL-1A], IL-1 beta [IL-1B], and IL-1 receptor antagonist [IL-1RN]) are associated with end stage renal disease (ESRD). A total of 258 ESRD patients and 569 ethnicity matched controls were examined for IL-1 gene cluster. These were genotyped for five single-nucleotide gene polymorphisms in the IL-1A, IL-1B and IL-1RN genes and a variable number of tandem repeats (VNTR) in the IL-1RN. The IL-1B - 3953 and IL-1RN + 8006 polymorphism frequencies were significantly different between the two groups. At IL-1B, the T allele of - 3953C/T was increased among ESRD (P = 0.0001). A logistic regression model demonstrated that two repeat (240 base pair [bp]) of the IL-1Ra VNTR polymorphism was associated with ESRD (P = 0.0001). The C/C/C/C/C/1 haplotype was more prevalent in ESRD = 0.007). No linkage disequilibrium (LD) was observed between six loci of IL-1 gene. We further conducted a meta-analysis of existing studies and found that there is a strong association of IL-1 RN VNTR 86 bp repeat polymorphism with susceptibility to ESRD (odds ratio = 2.04, 95% confidence interval = 1.48-2.82; P = 0.000). IL-1B - 5887, +8006 and the IL-1RN VNTR polymorphisms have been implicated as potential risk factors for ESRD. The meta-analysis showed a strong association of IL-1RN 86 bp VNTR polymorphism with susceptibility to ESRD.
我们评估了白细胞介素(IL-1)基因簇(IL-1α [IL-1A]、IL-1β [IL-1B] 和 IL-1 受体拮抗剂 [IL-1RN])中的多态性是否与终末期肾病(ESRD)相关。共对 258 例 ESRD 患者和 569 例种族匹配的对照进行了 IL-1 基因簇检测。对这些样本进行了 IL-1A、IL-1B 和 IL-1RN 基因中的五个单核苷酸基因多态性以及 IL-1RN 中的可变数目串联重复序列(VNTR)的基因分型。两组之间 IL-1B - 3953 和 IL-1RN + 8006 多态性频率存在显著差异。在 IL-1B 处,ESRD 患者中 - 3953C/T 的 T 等位基因增加(P = 0.0001)。逻辑回归模型显示,IL-1Ra VNTR 多态性的两个重复序列(240 碱基对 [bp])与 ESRD 相关(P = 0.0001)。C/C/C/C/C/1 单倍型在 ESRD 中更为常见(P = 0.007)。在 IL-1 基因的六个位点之间未观察到连锁不平衡(LD)。我们进一步对现有研究进行了荟萃分析,发现 IL-1 RN VNTR 86 bp 重复多态性与 ESRD 易感性之间存在强关联(优势比 = 2.04,95% 置信区间 = 1.48 - 2.82;P = 0.000)。IL-1B - 5887、+8006 和 IL-1RN VNTR 多态性被认为是 ESRD 的潜在危险因素。荟萃分析显示 IL-1RN 86 bp VNTR 多态性与 ESRD 易感性之间存在强关联。