Nutrition and Genomics Laboratory, JM-USDA Human Nutrition Research Center on Aging at Tufts University, Boston, MA 02111-1524, USA.
Int J Obes (Lond). 2011 May;35(5):666-75. doi: 10.1038/ijo.2010.187. Epub 2010 Oct 26.
The APOA2 gene has been associated with obesity and insulin resistance (IR) in animal and human studies with controversial results. We have reported an APOA2-saturated fat interaction determining body mass index (BMI) and obesity in American populations. This work aims to extend our findings to European and Asian populations.
Cross-sectional study in 4602 subjects from two independent populations: a high-cardiovascular risk Mediterranean population (n = 907 men and women; aged 67 ± 6 years) and a multiethnic Asian population (n = 2506 Chinese, n = 605 Malays and n = 494 Asian Indians; aged 39 ± 12 years) participating in a Singapore National Health Survey. Anthropometric, clinical, biochemical, lifestyle and dietary variables were determined. Homeostasis model assessment of insulin resistance was used in Asians. We analyzed gene-diet interactions between the APOA2 -265T>C polymorphism and saturated fat intake (<or ≥ 22 g per day) on anthropometric measures and IR.
Frequency of CC (homozygous for the minor allele) subjects differed among populations (1-15%). We confirmed a recessive effect of the APOA2 polymorphism and replicated the APOA2-saturated fat interaction on body weight. In Mediterranean individuals, the CC genotype was associated with a 6.8% greater BMI in those consuming a high (P = 0.018), but not a low (P = 0.316) saturated fat diet. Likewise, the CC genotype was significantly associated with higher obesity prevalence in Chinese and Asian Indians only, with a high-saturated fat intake (P = 0.036). We also found a significant APOA2-saturated fat interaction in determining IR in Chinese and Asian Indians (P = 0.026).
The influence of the APOA2 -265T>C polymorphism on body-weight-related measures was modulated by saturated fat in Mediterranean and Asian populations.
载脂蛋白 A2(APOA2)基因在动物和人体研究中与肥胖和胰岛素抵抗(IR)有关,但结果存在争议。我们曾报告称,APOA2-饱和脂肪相互作用可决定美国人群的体重指数(BMI)和肥胖。本研究旨在将这些发现扩展至欧洲和亚洲人群。
在两个独立人群中进行了一项横断面研究:一个是高心血管风险的地中海人群(n=907 名男性和女性;年龄 67±6 岁),另一个是多民族亚洲人群(n=2506 名中国人、n=605 名马来人和 n=494 名印度人;年龄 39±12 岁),他们参加了新加坡国家健康调查。测定了人体测量、临床、生化、生活方式和饮食变量。亚洲人采用稳态模型评估胰岛素抵抗。我们分析了 APOA2-265T>C 多态性与饱和脂肪摄入量(每天≥22 克)之间的基因-饮食相互作用对人体测量和 IR 的影响。
人群间 APOA2-265T>C 多态性的 CC(纯合子携带较少的等位基因)频率不同(1-15%)。我们证实了 APOA2 多态性的隐性作用,并复制了 APOA2-饱和脂肪在体重方面的相互作用。在地中海人群中,高饱和脂肪饮食(P=0.018)但不是低饱和脂肪饮食(P=0.316)时,CC 基因型与 BMI 增加 6.8%有关。同样,仅在中国人和印度人中,高饱和脂肪饮食与 CC 基因型显著相关,肥胖发生率更高(P=0.036)。我们还发现 APOA2-饱和脂肪在中国人和印度人中对 IR 的影响存在显著的相互作用(P=0.026)。
APOA2-265T>C 多态性对体重相关指标的影响在地中海和亚洲人群中受到饱和脂肪的调节。