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老年斯洛伐克人血管紧张素转换酶插入/缺失多态性及其与代谢综合征各组分的关系。

ACE insertion/deletion polymorphism and its relationships to the components of metabolic syndrome in elderly Slovaks.

作者信息

Siváková Daniela, Lajdová Alica, Basistová Zuzana, Cvícelová Marta, Blazícek Pavel

机构信息

Department of Anthropology, Faculty of Sciences, Comenius University, Bratislava, Slovak Republic

出版信息

Anthropol Anz. 2009 Mar;67(1):1-11.

Abstract

The purpose of this study was to assess clustering of Metabolic Syndrome components in aged Slovaks, and to investigate whether insertion/deletion (I/D) polymorphism of the human angiotensin-converting enzyme (ACE) gene is associated with this syndrome. Data were available from 374 Slovak participants (200 females and 174 males) ranging in age between 60 and 90 years. ACE I/D polymorphism was determined by PCR amplification of the ACE gene sequence. Metabolic Syndrome was diagnosed according to criteria in the NCEP ATP-III. Elderly males and females differ significantly in the prevalence of Metabolic Syndrome (females 45.1%, males 24.8%). The males and females including subjects with and without metabolic syndrome, respectively, did not differ significantly in the three genotype distributions (p = 0.603 and p = 0.247). The allele frequencies (D = 0.5483, I = 0.4517) in the entire sample fell within the Hardy-Weinberg equilibrium. There was no confirmed association between ACE genotype and phenotypic variation in the recognized risk components for Metabolic Syndrome in elderly Slovaks. Among other factors which may induce a difference in Metabolic Syndrome, significant effect was detected for sex, BMI, HDL, TG, glucose and the ApoB/ApoA1 ratio.

摘要

本研究的目的是评估老年斯洛伐克人代谢综合征各组分的聚集情况,并调查人类血管紧张素转换酶(ACE)基因的插入/缺失(I/D)多态性是否与该综合征相关。研究数据来自374名年龄在60至90岁之间的斯洛伐克参与者(200名女性和174名男性)。通过PCR扩增ACE基因序列来确定ACE I/D多态性。根据美国国家胆固醇教育计划成人治疗组第三次报告(NCEP ATP-III)的标准诊断代谢综合征。老年男性和女性在代谢综合征患病率上存在显著差异(女性为45.1%,男性为24.8%)。分别纳入有和无代谢综合征受试者的男性和女性在三种基因型分布上无显著差异(p = 0.603和p = 0.247)。整个样本中的等位基因频率(D = 0.5483,I = 0.4517)处于哈迪-温伯格平衡范围内。在老年斯洛伐克人中,未证实ACE基因型与代谢综合征公认风险组分的表型变异之间存在关联。在可能导致代谢综合征差异的其他因素中,检测到性别、体重指数(BMI)、高密度脂蛋白(HDL)、甘油三酯(TG)、血糖和载脂蛋白B/载脂蛋白A1比值有显著影响。

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