共 3 条
Associations of the lipid genetic variants Thr54 (FABP2) and-493T (MTTP) with total cholesterol and low-density lipoprotein cholesterol levels in Mexican subjects
被引:3
|作者:
Gonzalez-Becerra, Karina
[1
]
Ramos-Lopez, Omar
[1
]
Lolis Garcia-Cazarin, Mary
[2
]
Barron-Cabrera, Elisa
[1
]
Panduro, Arturo
[1
]
Martinez-Lopez, Erika
[1
]
机构:
[1] Univ Guadalajara, Univ Ctr Hlth Sci, Fray Antonio Alcalde Civil Hosp Guadalajara, Med Mol Biol Serv,Dept Mol Biol & Genom, Guadalajara, Jalisco, Mexico
[2] NIH, Off Dis Prevent, Bldg 10, Bethesda, MD 20892 USA
关键词:
Lipid genetic variants;
hypercholesterolaemia;
polymorphism;
FABP2;
MTTP;
Mexico;
FATTY-ACID-BINDING;
TRIGLYCERIDE TRANSFER PROTEIN;
INSULIN-RESISTANCE;
POLYMORPHISM;
OBESITY;
CELLS;
D O I:
10.1177/0300060517748518
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
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.
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页码:1467 / 1476
页数:10
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