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巴西南部人群中 PPARA、RXRA、NR1I2 和 NR1I3 基因多态性与血脂和脂蛋白水平的关系。

PPARA, RXRA, NR1I2 and NR1I3 gene polymorphisms and lipid and lipoprotein levels in a Southern Brazilian population.

机构信息

Laboratório de Biologia Molecular, Programa de Pós-Graduação em Ciências da Saúde, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, Brazil.

出版信息

Mol Biol Rep. 2013 Feb;40(2):1241-7. doi: 10.1007/s11033-012-2166-y. Epub 2012 Oct 19.

Abstract

Cardiovascular disease is the main cause of death worldwide, and dyslipidemia is an important multifactorial risk factor. Considering the involvement of nuclear receptors in metabolic pathways, and that some of the receptors act in lipid metabolism and homeostasis, the aim of the present study was to investigate the influence of genetic variations in RXRA, PPARA, NR1I2, and NR1I3 on lipid and lipoprotein levels. Five polymorphisms in the aforementioned genes were genotyped in 622 Brazilians of European descent by PCR-RFLP or TaqMan genotyping assays. In general, carriers of the A insertion of RXRA rs11381416 polymorphism showed higher levels of triglyceride (TG; 1.80 ± 1.20 vs. 1.52 ± 1.20 mmol/L; P = 0.020). Moreover, sexual dimorphic association was found (gender*NR1I3 rs2501873 genotype interaction P < 0.001), males with NR1I3 rs2501873 G/G genotype had lower TG levels (ANCOVA, P = 0.009). Our results suggest that polymorphisms in the RXRA and NR1I3 genes influence lipid profile in a Southern Brazilian population. However, these general and gender association require confirmation in subsequent studies.

摘要

心血管疾病是全球主要死亡原因,血脂异常是一个重要的多因素危险因素。鉴于核受体参与代谢途径,并且一些受体作用于脂质代谢和稳态,本研究旨在研究 RXRA、PPARA、NR1I2 和 NR1I3 基因中的遗传变异对血脂和脂蛋白水平的影响。通过 PCR-RFLP 或 TaqMan 基因分型检测,在 622 名欧洲裔巴西人中共检测到上述 5 个基因中的 5 个多态性。一般来说,RXRA rs11381416 多态性 A 插入的携带者甘油三酯 (TG) 水平较高 (1.80 ± 1.20 与 1.52 ± 1.20 mmol/L;P = 0.020)。此外,还发现了性别二态性关联 (性别*NR1I3 rs2501873 基因型相互作用 P < 0.001),NR1I3 rs2501873 G/G 基因型的男性 TG 水平较低 (ANCOVA,P = 0.009)。我们的结果表明,RXRA 和 NR1I3 基因中的多态性影响南里奥格兰德州巴西人群的血脂谱。然而,这些总体和性别关联需要在后续研究中得到证实。

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