首页> 外文期刊>Annals of Human Genetics >Association study of the single-nucleotide polymorphisms-3971G/A and+276G/T in the adiponectin gene with type 2 diabetes in a North Indian Punjabi population
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Association study of the single-nucleotide polymorphisms-3971G/A and+276G/T in the adiponectin gene with type 2 diabetes in a North Indian Punjabi population

机译:北印度旁遮普人群中脂联素基因的单核苷酸多态性-3971g / a和+ 276g / t的结合研究

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Objective To investigate the role of ADIPOQ gene variants (-3971G/A rs822396 and +276G/T rs1501299) with type 2 diabetes risk in a North Indian Punjabi population. Methods Adiponectin is one of the most abundant circulating adipocytokines in the human body that plays an important role in the metabolic processes and positively regulates energy homeostasis and insulin secretion. Several studies have provided the evidence of adiponectin gene polymorphisms association with type 2 diabetes mellitus (T2DM) in different ethnic populations. A total of 616 subjects including 316 T2DM patients and 300 normal healthy controls from Punjab were genotyped for ADIPOQ polymorphisms (rs822396 and rs1501299) by using a polymerase chain reaction-based restriction fragment length polymorphism (PCR-RFLP) technique. Anthropometric, physiometric, and biochemical measurements were taken from each participant. Results Genotypic frequencies were significantly different in T2DM subjects and healthy controls for both polymorphisms (rs822396 and rs1501299). The risk genotype GG of -3971A/G and TT of +276G/T conferred an approximately twofold risk towards the development of T2DM and were found to be significantly higher in T2DM cases than control subjects (p = 0.006 and p = 0.019, respectively, after the Bonferroni correction). The recessive model of the ADIPOQ polymorphism rs822396 was significantly shown to confer a 3.63-fold risk towards type 2 diabetes after adjusting for confounding factors and Bonferroni correction [odds ratio (OR): 3.63 (1.20-10.96), p = 0.022]. rs1501299 gave a 3.82-fold risk towards development of T2DM but was not statistically significant after Bonferroni correction [OR: 3.82 (1.16-12.55), p = 0.027]. Meta-analysis also illustrated the overall effect of the minor allele of rs822396 (-3971A/G) polymorphism, providing a greater risk for the T2DM development. Conclusion Thus, we concluded on the basis of observed results that the ADIPOQ gene polymorphisms rs822396 and rs1501299 plays an important role in the development of type 2 diabetes in North Indian Punjabi population.
机译:目的探讨AdipoQ Gene Variants(-3971G / ARS822396和+ 276G / T RS1501299)的作用,北印度旁遮普人口2型糖尿病风险。方法脂联素是人体中最丰富的循环adipocytokines之一,在代谢过程中起重要作用,积极调节能量稳态和胰岛素分泌。几项研究已经提供了不同种族群体中与2型糖尿病(T2DM)的脂联素基因多态性联合的证据。通过使用基于聚合酶链反应的限制性片段长度多态性(PCR-RFLP)技术,共有616名受试者包括316个T2DM患者和来自旁遮普多态性(RS822396和RS1501299)的基因分型。从每个参与者采取人体测量,生理学和生物化学测量。结果基因型频率在T2DM受试者和对多态性的健康对照中显着不同(RS822396和RS1501299)。 -3971A / g的风险基因型GG和TT为+ 276g / T的促进T2DM发育的大约两倍的风险,并且在T2DM病例中发现显着高于对照受试者(P = 0.006和P = 0.019,在Bonferroni纠正之后)。 adipoq多态性RS822396的隐性模型显着显示在调整混淆因子和Bonferroni校正后对2型糖尿病进行3.63倍的风险[obferroni校正[赔率比(或):3.63(1.20-10.96),p = 0.022]。 RS1501299对T2DM的发展有3.82倍的风险,但在Bonferroni校正后没有统计学意义[或:3.82(1.16-12.55),P = 0.027]。 Meta分析还示出了RS822396(-3971A / g)多态性的次要等位基因的总体影响,为T2DM发育提供了更大的风险。结论因此,我们在观察结果的基础上得出结论,即AdipoQ基因多态性RS822396和RS1501299在北印度旁遮普人口2型糖尿病发育中发挥着重要作用。

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