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转录因子7样2基因变异影响多囊卵巢综合征的代谢表型。

Transcription Factor-7-Like 2 Gene Variants Affect the Metabolic Phenotypes of Polycystic Ovary Syndrome.

作者信息

Gammoh Emily, Mahmood Naeema A, Madan Samira, Ebrahim Bashayer H, Mustafa Fekria E, Almawi Wassim Y

机构信息

Department of Medical Biochemistry, Arabian Gulf University, Manama, Bahrain.

出版信息

Ann Nutr Metab. 2015;67(4):228-35. doi: 10.1159/000439546. Epub 2015 Oct 20.

Abstract

BACKGROUND

Polycystic ovary syndrome (PCOS) is a common endocrinopathy, which shares genetic features with type 2 diabetes mellitus (T2DM). Insofar as transcription factor 7-like 2 (TCF7L2) is consistently replicated T2DM susceptibility locus, this study evaluates whether common TCF7L2 variants are associated with PCOS and related metabolic features.

METHODS

The association between TCF7L2 rs4506565, rs7903146, rs12243326, and rs12255372 SNPs and PCOS was tested in 242 women with PCOS and in 236 control women.

RESULTS

The allelic distribution of rs4506565, rs7903146, rs12243326, and rs12255372 TCF7L2 variants was not significantly different between women with PCOS and control women. The genotype distribution of the 4 TCF7L2 loci was comparable between PCOS cases and controls, irrespective of the genetic analysis model used (additive, dominant, recessive). Carriage of rs4506565 minor allele correlated with free insulin and homeostasis model assessment of insulin resistance, while the presence of rs12243326 and rs12255372 minor allele correlated with waist changes. Four-locus (rs4506565-rs7903146, rs12243326, and rs12255372) haplotype analysis identified PCOS-susceptible (ACTG) and -protective (TTTG) haplotypes, which remained significant after controlling for multiple comparisons and for key covariates.

CONCLUSIONS

Although individual TCF7L2 variants were not associated with the presence of PCOS in Bahraini women, specific TCF7L2 haplotypes were identified, which were both positively and negatively associated with PCOS.

摘要

背景

多囊卵巢综合征(PCOS)是一种常见的内分泌病,与2型糖尿病(T2DM)具有共同的遗传特征。鉴于转录因子7样2(TCF7L2)是一致重复出现的T2DM易感位点,本研究评估常见的TCF7L2变异体是否与PCOS及相关代谢特征相关。

方法

在242例PCOS女性和236例对照女性中检测TCF7L2 rs4506565、rs7903146、rs12243326和rs12255372单核苷酸多态性(SNP)与PCOS之间的关联。

结果

PCOS女性和对照女性之间,rs4506565、rs7903146、rs12243326和rs12255372 TCF7L2变异体的等位基因分布无显著差异。无论采用何种遗传分析模型(加性、显性、隐性),4个TCF7L2位点的基因型分布在PCOS病例组和对照组之间具有可比性。rs4506565次要等位基因的携带与游离胰岛素及胰岛素抵抗的稳态模型评估相关,而rs12243326和rs12255372次要等位基因的存在与腰围变化相关。四位点(rs4506565 - rs7903146、rs12243326和rs12255372)单倍型分析确定了PCOS易感单倍型(ACTG)和保护性单倍型(TTTG),在控制多重比较和关键协变量后,这些单倍型仍具有显著性。

结论

虽然单个TCF7L2变异体与巴林女性PCOS的存在无关,但确定了特定的TCF7L2单倍型,其与PCOS呈正相关和负相关。

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