Associations between CD36 gene polymorphisms, fat tolerance and oral fat preference in a young-adult population

被引:5
作者
Jayewardene, A. F. [1 ]
Mavros, Y. [1 ]
Hancock, D. P. [2 ]
Gwinn, T. [1 ]
Rooney, K. B. [1 ]
机构
[1] Univ Sydney, Fac Hlth Sci, Discipline Exercise & Sport Sci, Lidcombe, NSW, Australia
[2] Univ Sydney, Sch Mol Biosci, Fac Sci, Camperdown, NSW, Australia
关键词
SKELETAL-MUSCLE FAT/CD36; DISEASE RISK-FACTORS; INSULIN-RESISTANCE; DIETARY LIPIDS; ACID OXIDATION; NULL MUTATION; OBESITY; IDENTIFICATION; QUESTIONNAIRE; TRIGLYCERIDES;
D O I
10.1038/ejcn.2016.132
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
BACKGROUND/OBJECTIVES: CD36 is known to be an orosensory receptor for dietary long-chain fatty acids, as well as being involved in the chemosensory mechanisms within the human gut. Recent data have demonstrated an association between CD36 single-nucleotide polymorphisms (SNPs) and lipid consumption behaviours in humans. This study aimed to test for associations between CD36 SNPs and response to a high-fat meal in a young healthy Australian cohort. Secondary associations were tested between CD36 gene variants and fasting lipid parameters, body composition, cardiovascular disease (CVD) risk factors and measures of oral fat preference. SUBJECTS/METHODS: Two SNPs (rs1527479 and rs1984112) were assessed for associations with response to a 75 g saturated fat oral fat tolerance test (OFTT), whole-body substrate oxidation, fasting plasma lipids, CVD risk factors and self-reported habitual diet questionnaires. Genotyping was performed using real-time polymerase chain reaction. RESULTS: Cross-sectional data were collected on 56 individuals (28 m, 28 f; 24.9 +/- 3.3 years), with 42 completing participation in a high-fat OFTT. No genotypic associations were evident in anthropometric data or self-reported fat preference measures. AA SNP carriers at rs1984112 exhibited significantly elevated fasting triglyceride when compared with non-carriers (P = 0.024). This group also tended to have an elevated response to a high-fat meal (P = 0.078). CONCLUSIONS: Although these data show the potential pleiotropic influence of CD36 SNP rs1984112 on lipoprotein accumulation in a young healthy cohort, further assessment in a larger cohort is warranted.
引用
收藏
页码:1325 / 1331
页数:7
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