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肿瘤坏死因子-α基因的-308 G/A 多态性改变了白种南非女性饱和脂肪摄入与血清总胆固醇水平之间的关联。

The -308 G/A polymorphism of the tumour necrosis factor-α gene modifies the association between saturated fat intake and serum total cholesterol levels in white South African women.

机构信息

UCT/MRC Research Unit for Exercise Science and Sports Medicine, Department of Human Biology, University of Cape Town, Newlands, Cape Town, South Africa.

出版信息

Genes Nutr. 2011 Nov;6(4):353-9. doi: 10.1007/s12263-011-0213-2. Epub 2011 Mar 8.

Abstract

This study explored interactions between dietary fat intake and the tumour necrosis factor-α gene (TNFA) -308 G/A polymorphism on serum lipids in white South African (SA) women. Normal-weight (N = 88) and obese (N = 60) white SA women underwent measurements of body composition, fat distribution, fasting serum lipids, glucose, insulin concentrations and dietary intake. Subjects were genotyped for the functional -308 G/A polymorphism within the TNFA gene. There were no significant differences in the genotype or allele frequencies between groups, and no significant genotype associations were found for body fatness or distribution, or serum lipid concentrations. However, there was a significant interaction effect between dietary saturated fat (SFA) intake (%E) and TNFA -308 genotypes on serum total cholesterol concentrations (P = 0.047). With increasing SFA intake (%E), serum total cholesterol levels decreased for the GG genotype and increased for the GA plus AA genotypes. The TNFA -308 G/A polymorphism appears to modify the relationship between dietary fat intake and serum total cholesterol concentrations in white SA women.

摘要

本研究探讨了南非白人女性饮食脂肪摄入与肿瘤坏死因子-α基因(TNFA)-308 G/A 多态性之间的相互作用对血清脂质的影响。正常体重(N=88)和肥胖(N=60)的南非白人女性接受了身体成分、脂肪分布、空腹血清脂质、葡萄糖、胰岛素浓度和饮食摄入的测量。对 TNFA 基因内的功能性-308 G/A 多态性进行了基因分型。两组间基因型或等位基因频率无显著差异,也未发现与体脂或分布或血清脂质浓度相关的显著基因型关联。然而,饮食饱和脂肪(SFA)摄入(%E)与 TNFA-308 基因型之间存在血清总胆固醇浓度的显著交互效应(P=0.047)。随着 SFA 摄入(%E)的增加,GG 基因型的血清总胆固醇水平降低,GA+AA 基因型的血清总胆固醇水平升高。TNFA-308 G/A 多态性似乎改变了南非白人女性饮食脂肪摄入与血清总胆固醇浓度之间的关系。

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