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2
Effect of the ADIPOQ Gene -11391G/A Polymorphism Is Modulated by Lifestyle Factors in Mexican Subjects.ADIPOQ基因-11391G/A多态性的影响受墨西哥人群生活方式因素的调节。
J Nutrigenet Nutrigenomics. 2014;7(4-6):212-24. doi: 10.1159/000371801. Epub 2015 Mar 12.
3
What We Know About Diet, Genes, and Dyslipidemia: Is There Potential for Translation?我们对饮食、基因和血脂异常的了解:是否有转化应用的潜力?
Curr Nutr Rep. 2013 Dec;2(4):236-242. doi: 10.1007/s13668-013-0065-z.
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Impact of body mass index and waist circumference on the cardiovascular risk and all-cause death in a general population: data from the PAMELA study.体重指数和腰围对一般人群心血管风险和全因死亡的影响:来自 PAMELA 研究的数据。
Nutr Metab Cardiovasc Dis. 2013 Jul;23(7):650-6. doi: 10.1016/j.numecd.2012.01.004. Epub 2012 May 26.
5
Multiple functions of microsomal triglyceride transfer protein.微粒体甘油三酯转移蛋白的多种功能。
Nutr Metab (Lond). 2012 Feb 21;9:14. doi: 10.1186/1743-7075-9-14.
6
Allele-specific regulation of MTTP expression influences the risk of ischemic heart disease.等位基因特异性调控 MTTP 表达影响缺血性心脏病的风险。
J Lipid Res. 2010 Jan;51(1):103-11. doi: 10.1194/jlr.M900195-JLR200.
7
Arlequin (version 3.0): an integrated software package for population genetics data analysis.Arlequin(版本 3.0):一个用于群体遗传学数据分析的集成软件包。
Evol Bioinform Online. 2007 Feb 23;1:47-50.
8
Association of the T54 allele of the FABP2 gene with cardiovascular risk factors in obese Mexican subjects.FABP2基因T54等位基因与肥胖墨西哥人群心血管危险因素的关联。
Diab Vasc Dis Res. 2007 Sep;4(3):235-6. doi: 10.3132/dvdr.2007.046.
9
Genetic factors in human obesity.人类肥胖中的遗传因素。
Obes Rev. 2007 Mar;8 Suppl 1:37-40. doi: 10.1111/j.1467-789X.2007.00315.x.
10
Intestinal fatty acid binding protein and microsomal triglyceride transfer protein polymorphisms in French-Canadian youth.法裔加拿大青少年肠道脂肪酸结合蛋白和微粒体甘油三酯转移蛋白的多态性
J Lipid Res. 2005 Feb;46(2):320-7. doi: 10.1194/jlr.M400346-JLR200. Epub 2004 Nov 16.

墨西哥人群中脂质基因变异体苏氨酸54(FABP2)和-493T(MTTP)与总胆固醇及低密度脂蛋白胆固醇水平的关联。

Associations of the lipid genetic variants Thr54 ( FABP2) and -493T ( MTTP) with total cholesterol and low-density lipoprotein cholesterol levels in Mexican subjects.

作者信息

Gonzalez-Becerra Karina, Ramos-Lopez Omar, Garcia-Cazarin Mary Lolis, Barron-Cabrera Elisa, Panduro Arturo, Martinez-Lopez Erika

机构信息

1 Medical Molecular Biology Service, "Fray Antonio Alcalde" Civil Hospital of Guadalajara, Department of Molecular Biology and Genomics, 42571 University Center of Health Sciences, University of Guadalajara , Guadalajara, Jalisco, Mexico.

2 Office of 171302 Disease Prevention, National Institutes of Health , Bethesda, MD, USA.

出版信息

J Int Med Res. 2018 Apr;46(4):1467-1476. doi: 10.1177/0300060517748518. Epub 2018 Jan 17.

DOI:10.1177/0300060517748518
PMID:29338565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6091818/
Abstract

Objective Mexico has one of the world's highest rates of obesity, which is influenced by lipid-genetic and lifestyle factors. This study aimed to determine whether FABP2 (Ala54Thr) and MTTP (-493 G/T) genetic polymorphisms are associated with metabolic disorders in Mexican subjects. Methods A total of 523 subjects participated in a cross-sectional study. Genotyping for FABP2 and MTTP was performed using real-time RT-PCR. Biochemical and anthropometric data were evaluated. Results The genetically at-risk group (Thr54/-493T) was associated with significantly higher total and low-density lipoprotein cholesterol levels (difference between genetically at-risk group and wild-type group: 10.6 mg/dL and 8.94 mg/dL, respectively). Carriers within the genetically at-risk group had a significantly higher prevalence rate of hypercholesterolaemia (42.5% vs. 32.0%) and higher LDL-C levels (37.6% vs. 26.4%) than did non-carriers. Conclusions Subjects who are genetically at risk (Thr54/-493T) have higher total cholesterol levels, low-density lipoprotein cholesterol levels, and prevalence rate of hypercholesterolaemia. These findings highlight the importance of basing nutritional intervention strategies for preventing and treating chronic diseases on individual genetic characteristics.

摘要

目的 墨西哥是世界上肥胖率最高的国家之一,肥胖受到脂质遗传和生活方式因素的影响。本研究旨在确定FABP2(Ala54Thr)和MTTP(-493 G/T)基因多态性是否与墨西哥人群的代谢紊乱有关。方法 共有523名受试者参与了一项横断面研究。使用实时RT-PCR对FABP2和MTTP进行基因分型。评估生化和人体测量数据。结果 遗传风险组(Thr54/-493T)与总胆固醇和低密度脂蛋白胆固醇水平显著升高相关(遗传风险组与野生型组之间的差异分别为10.6mg/dL和8.94mg/dL)。遗传风险组内的携带者高胆固醇血症患病率(42.5%对32.0%)和低密度脂蛋白胆固醇水平(37.6%对26.4%)显著高于非携带者。结论 遗传风险受试者(Thr54/-493T)的总胆固醇水平、低密度脂蛋白胆固醇水平和高胆固醇血症患病率更高。这些发现凸显了基于个体遗传特征制定预防和治疗慢性病营养干预策略的重要性。