过氧化物酶体增殖物激活受体γ辅助激活因子1 α基因变异与妊娠期糖尿病无关。

Heinz Leipold, Martin Knoefler, Christian Gruber, Ambros Huber, Peter Haslinger, Christof Worda
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引用次数: 15

摘要

目的:流行病学、病理生理学和遗传学数据表明妊娠期糖尿病(GDM)与2型糖尿病之间存在密切联系。关于过氧化物酶体增殖物激活受体γ共激活因子-1 α (PGC-1)基因变异对2型糖尿病发生的影响,以往的研究结果存在争议。因此,我们检测了GDM女性中该基因的两种常见单核苷酸多态性(SNP)。方法:采用口服葡萄糖耐量试验(OGTT)对875名女性进行评估。该人群中随机选择200名女性,100名OGTT异常患者和100名正常对照。采用聚合酶链反应(PCR)扩增和限制性内切分析的方法,对对照组和研究组血液中分离的DNA样本进行PGC-1基因Gly482Ser和Thr394Thr SNP的分析。此外,研究人员还调查了Gly482Ser和Thr394Thr变体之间对GDM风险的潜在相互作用。结果:GDM女性明显老年化(32.2 +/-5.5岁vs 29.7 +/- 6.1岁;P = .005),体重指数(BMI;28.0 +/- 7.1 kg/m2 vs 25.0 +/- 5.7 kg/m2;P = .002),血红蛋白A1c (HbA1c)值较高(5.6 +/- 0.9 vs 4.9 +/- 0.5;结论:根据我们的数据,PGC-1基因Gly482Ser和Thr394Thr多态性与GDM的发生无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Peroxisome proliferator-activated receptor gamma coactivator-1alpha gene variations are not associated with gestational diabetes mellitus.

Objective: Epidemiologic, pathophysiologic, and genetic data suggest a close link between gestational diabetes mellitus (GDM) and type 2 diabetes. Previous studies yielded controversial results on the impact of peroxisome proliferator-activated receptor gamma coactivator-1alpha (PGC-1) gene variations on the development of type 2 diabetes mellitus. Therefore, we examined two common single nucleotide polymorphisms (SNP) of this gene in women with GDM.

Methods: We assessed a total of 875 women by oral glucose tolerance testing (OGTT). Two hundred women of this population, 100 patients with an abnormal OGTT and 100 normal controls, were randomly selected. DNA samples isolated from the blood of the control and study groups were analyzed with respect to the SNP Gly482Ser and Thr394Thr of the PGC-1 gene using polymerase chain reaction (PCR) amplification and restriction analysis. Furthermore, a potential interaction between the Gly482Ser and the Thr394Thr variant on the risk of GDM was investigated.

Results: Women with GDM were significantly older (32.2 +/-5.5 years vs 29.7 +/- 6.1 years; P = .005), had higher body mass indices (BMI; 28.0 +/- 7.1 kg/m2 vs 25.0 +/- 5.7 kg/m2; P = .002) and displayed higher hemoglobin A1c (HbA1c) values (5.6 +/- 0.9 vs 4.9 +/- 0.5; P <.001). There was no significant difference between the allele distribution of the two polymorphisms in women with and without GDM. No significant associations between the two polymorphisms and BMI or OGTT values were observed. When the different haplotype combinations of the two loci were analyzed for the risk of GDM, no significant association could be found.

Conclusion: Based on our data, the Gly482Ser and the Thr394Thr polymorphisms of the PGC-1 gene are not associated with the development of GDM.

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