Seeking genetic determinants of selected metabolic disorders in women aged 45-60.

IF 1.2
Małgorzata Szkup, Jacek Brodowski, Anna Jurczak, Marzanna Stanisławska, Elżbieta Grochans
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引用次数: 3

Abstract

Introduction and objective: The biochemical and anthropometric consequences of metabolic disorders exert an enormous effect on the functioning of people worldwide. The aim of this study is to assess relationships between biochemical and anthropometric parameters associated with metabolic syndrome, and the presence of the PPAR-γ rs1801282, the FTO rs9939609, and the MC4R rs17782313 polymorphisms in women aged 45-60.

Material and methods: The study included 425 women, aged 45-59 years, from the general population of the West Pomeranian Province in north-west Poland. The research procedure involved a structured interview, anthropometric and blood pressure measurements, biochemical analysis of serum, and genetic analysis.

Results: The carriers of the A/A genotype of the FTO polymorphism had higher LDL levels than their counterparts with the T/T genotype (p = 0.01). The carriers of the T/T genotype of the MC4R polymorphism had lower non-HDL levels than those with the C/C and C/T genotypes (p = 0.019). Weight was related to the C/C and the C/G + G/G genotypes of the PPAR-γ gene polymorphism (p = 0.046). The model of inheritance for the MC4R polymorphism had a significant effect on TG (p = 0.039) and non-HDL (p = 0.05) levels.

Conclusions: The genotypes analyzed in the study had only a slight direct effect on the biochemical and anthropometric abnormalities typical of metabolic disorders. Nonetheless, the risk alleles (A allele of the FTO rs9939609 and the C allele of the MC4R rs17782313) were found to be related to lipid metabolism disorders in 45-60-year-old women.

寻找45-60岁女性选定代谢紊乱的遗传决定因素。
简介和目的:代谢紊乱的生化和人体测量后果对全世界人们的功能产生巨大影响。本研究的目的是评估与代谢综合征相关的生化和人体测量参数,以及45-60岁女性中PPAR-γ rs1801282、FTO rs9939609和MC4R rs17782313多态性的存在之间的关系。材料和方法:该研究包括425名年龄在45-59岁之间的女性,来自波兰西北部西波美拉尼亚省的普通人群。研究过程包括结构化访谈、人体测量和血压测量、血清生化分析和基因分析。结果:FTO多态性A/A基因型携带者LDL水平高于T/T基因型携带者(p = 0.01)。MC4R多态性T/T基因型携带者的非hdl水平低于C/C和C/T基因型携带者(p = 0.019)。体重与PPAR-γ基因多态性的C/C和C/G + G/G基因型相关(p = 0.046)。MC4R多态性的遗传模式对TG (p = 0.039)和non-HDL (p = 0.05)水平有显著影响。结论:研究中分析的基因型对代谢性疾病典型的生化和人体测量异常只有轻微的直接影响。尽管如此,风险等位基因(FTO rs9939609的A等位基因和MC4R rs17782313的C等位基因)被发现与45-60岁女性的脂质代谢紊乱有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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