APOA2, Dietary Fat, and Body Mass Index Replication of a Gene-Diet Interaction in 3 Independent Populations

被引:121
作者
Corella, Dolores [1 ,4 ,5 ]
Peloso, Gina [3 ]
Arnett, Donna K. [6 ,7 ]
Demissie, Serkalem [3 ]
Cupples, L. Adrienne [3 ]
Tucker, Katherine [2 ]
Lai, Chao-Qiang [1 ]
Parnell, Laurence D. [1 ]
Coltell, Oscar [8 ]
Lee, Yu-Chi [1 ]
Ordovas, Jose M. [1 ,9 ]
机构
[1] Tufts Univ, Nutr & Genom Lab, Jean Mayer US Dept Agr, Human Nutr Res Ctr Aging, Boston, MA 02111 USA
[2] Tufts Univ, Dietary Assessment & Epidemiol Res Program, Jean Mayer US Dept Agr, Human Nutr Res Ctr Aging, Boston, MA 02111 USA
[3] Boston Univ, Dept Biostat, Boston, MA 02215 USA
[4] Univ Valencia, Genet & Mol Epidemiol Unit, Valencia, Spain
[5] Univ Valencia, Ctr Invest Biomed Red Fisiopatol Obesidad & Nutr, Inst Salud Carlos III, Sch Med, Valencia, Spain
[6] Univ Alabama, Sch Publ Hlth, Dept Epidemiol, Birmingham, AL 35294 USA
[7] Univ Alabama, Clin Nutr Res Ctr, Birmingham, AL 35294 USA
[8] Jaume I Univ, Dept Comp Sci, Castellon de La Plana, Spain
[9] Natl Ctr Cardiovasc Invest CNIC, Dept Cardiovasc Epidemiol & Populat Genet, Madrid, Spain
关键词
APOLIPOPROTEIN-A-II; FOOD FREQUENCY QUESTIONNAIRE; INSULIN-RESISTANCE; GENETIC ASSOCIATIONS; PHYSICAL-ACTIVITY; LIPID-METABOLISM; TRANSGENIC MICE; PUERTO-RICAN; RISK-FACTORS; HEALTH;
D O I
10.1001/archinternmed.2009.343
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Nutrigenetics studies the role of genetic variation on interactions between diet and health, aiming to provide more personalized dietary advice. However, replication has been low. Our aim was to study interaction among a functional APOA2 polymorphism, food intake, and body mass index (BMI) in independent populations to replicate findings and to increase their evidence level. Methods: Cross-sectional, follow-up (20 years), and case-control analyses were undertaken in 3 independent populations. We analyzed gene-diet interactions between the APOA2 -265T>C polymorphism and saturated fat intake on BMI and obesity in 3462 individuals from 3 populations in the United States: the Framingham Offspring Study, (1454 whites), the Genetics of Lipid Lowering Drugs and Diet Network Study (1078 whites), and Boston-Puerto Rican Centers on Population Health and Health Disparities Study (930 Hispanics of Caribbean origin). Results: Prevalence of the CC genotype in study participants ranged from 10.5% to 16.2%. We identified statistically significant interactions between the APOA2 -265T>C and saturated fat regarding BMI in all 3 populations. Thus, the magnitude of the difference in BMI between the individuals with the CC and TT+TC genotypes differed by saturated fat. A mean increase in BMI of 6.2% (range, 4.3%-7.9%; P=.01) was observed between genotypes with high- (>= 22 g/d) but not with low-saturated fat intake in all studies. Likewise, the CC genotype was significantly associated with higher obesity prevalence in all populations only in the high-saturated fat stratum. Meta-analysis estimations of obesity for individuals with the CC genotype compared with the TT+TC genotype were an odds ratio of 1.84 (95% confidence interval, 1.38-2.47; P < .001) in the high-saturated fat stratum, but no association was detected in the low-saturated fat stratum (odds ratio, 0.81; 95% confidence interval, 0.59-1.11; P=18). Conclusion: For the first time to our knowledge, a gene-diet interaction influencing BMI and obesity has been strongly and consistently replicated in 3 independent populations.
引用
收藏
页码:1897 / 1906
页数:10
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