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首页> 外文期刊>Journal of human genetics >Screening of 336 single-nucleotide polymorphisms in 85 obesity-related genes revealed McKusick-Kaufman syndrome gene variants are associated with metabolic syndrome.
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Screening of 336 single-nucleotide polymorphisms in 85 obesity-related genes revealed McKusick-Kaufman syndrome gene variants are associated with metabolic syndrome.

机译:在85个肥胖相关基因中筛选了336个单核苷酸多态性,发现McKusick-Kaufman综合征基因变异与代谢综合征相关。

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Genetic factors are important in the development of metabolic syndrome. However, the genetic background of metabolic syndrome remains unclear. We screened polymorphisms in 85 obesity-related genes to determine which may be associated with metabolic syndrome. A total of 336 single-nucleotide polymorphisms (SNPs) in 85 genes selected from the JSNP database were genotyped. We conducted case-control association analyses using patients with metabolic syndrome (n=1080) and control individuals (n=528) who had no risk of the metabolic syndrome. Three SNPs in the McKusick-Kaufman syndrome (MKKS) gene were significantly related to metabolic syndrome by case-control association study; rs1545 (odds ratio (OR) adjusted for age and gender, 1.45; 95% confidence interval (CI), 1.21-1.74; P=0.000043 (additive model)); rs1547 (OR, 1.45; 95% CI, 1.21-1.74; P=0.000041); and rs2294901 (OR, 1.46; 95% CI, 1.22-1.75; P=0.000033). We selected five tag SNPs (rs2294901, rs221667, rs6133922, rs6077785 and rs6108572) in the MKKS gene. They were in one linkage disequilibrium (LD) block and rs6133922 (P=0.00042), rs6077785 (P=0.000013) and rs6108572 (P=0.000019) as well as rs2294901 were significantly associated with metabolic syndrome. TGAAA haplotype was protective against the metabolic syndrome (P=0.0074), and CCGTT haplotype was susceptible (P=0.00070) to the metabolic syndrome. Our data suggest that genetic variations at MKKS gene influence the risk of metabolic syndrome.Journal of Human Genetics (2009) 54, 230-235; doi:10.1038/jhg.2009.16; published online 27 February 2009.
机译:遗传因素在代谢综合征的发展中很重要。然而,代谢综合征的遗传背景仍不清楚。我们筛选了85个肥胖相关基因的多态性,以确定哪些可能与代谢综合征相关。从JSNP数据库中选择的85个基因中共有336个单核苷酸多态性(SNP)。我们使用代谢综合征患者(n = 1080)和没有代谢综合征风险的对照组(n = 528)进行了病例对照关联分析。通过病例对照研究,McKusick-Kaufman综合征(MKKS)基因中的三个SNP与代谢综合征显着相关。 rs1545(针对年龄和性别调整的赔率(OR)为1.45; 95%置信区间(CI)为1.21-1.74; P = 0.000043(加性模型)); rs1547(OR,1.45; 95%CI,1.21-1.74; P = 0.000041);和。和rs2294901(OR为1.46; 95%CI为1.22-1.75; P = 0.000033)。我们在MKKS基因中选择了五个标记SNP(rs2294901,rs221667,rs6133922,rs6077785和rs6108572)。它们处于一个连锁不平衡(LD)区域,rs6133922(P = 0.00042),rs6077785(P = 0.000013)和rs6108572(P = 0.000019)以及rs2294901与代谢综合征显着相关。 TGAAA单倍型对代谢综合症具有保护作用(P = 0.0074),而CCGTT单倍型对代谢综合症易感(P = 0.00070)。我们的数据表明,MKKS基因的遗传变异影响代谢综合征的风险。《人类遗传学杂志》(2009)54,230-235; doi:10.1038 / jhg.2009.16; 2009年2月27日在线发布。

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