Hugh Sinclair Unit of Human Nutrition, Department of Food and Nutritional Sciences, University of Reading, Reading RG6 6DZ, UK.
Indonesia International Institute for Life Sciences, JI. Pulomas Barat Kav. 88, Jakarta Timur 13210, Indonesia.
Nutrients. 2022 Jun 29;14(13):2713. doi: 10.3390/nu14132713.
Abnormalities in lipid metabolism have been linked to the development of obesity. We used a nutrigenetic approach to establish a link between lipids and obesity in Asian Indians, who are known to have a high prevalence of central obesity and dyslipidaemia. A sample of 497 Asian Indian individuals (260 with type 2 diabetes and 237 with normal glucose tolerance) (mean age: 44 ± 10 years) were randomly chosen from the Chennai Urban Rural Epidemiological Study (CURES). Dietary intake was assessed using a previously validated questionnaire. A genetic risk score (GRS) was constructed based on cholesteryl ester transfer protein (CETP) and lipoprotein lipase (LPL) genetic variants. There was a significant interaction between GRS and saturated fatty acid (SFA) intake on waist circumference (WC) (Pinteraction = 0.006). Individuals with a low SFA intake (≤23.2 g/day), despite carrying ≥2 risk alleles, had a smaller WC compared to individuals carrying <2 risk alleles (Beta = −0.01 cm; p = 0.03). For those individuals carrying ≥2 risk alleles, a high SFA intake (>23.2 g/day) was significantly associated with a larger WC than a low SFA intake (≤23.2 g/day) (Beta = 0.02 cm, p = 0.02). There were no significant interactions between GRS and other dietary factors on any of the measured outcomes. We conclude that a diet low in SFA might help reduce the genetic risk of central obesity confirmed by CETP and LPL genetic variants. Conversely, a high SFA diet increases the genetic risk of central obesity in Asian Indians.
脂质代谢异常与肥胖的发生有关。我们采用营养遗传学方法,在亚洲人群中建立脂质与肥胖之间的联系,亚洲人普遍存在中心性肥胖和血脂异常。从 Chennai Urban Rural Epidemiological Study (CURES) 中随机选择了 497 名亚洲个体(260 名 2 型糖尿病患者和 237 名血糖正常者)(平均年龄:44 ± 10 岁)。使用先前验证过的问卷评估饮食摄入。基于胆固醇酯转移蛋白 (CETP) 和脂蛋白脂肪酶 (LPL) 遗传变异构建遗传风险评分 (GRS)。GRS 与饱和脂肪酸 (SFA) 摄入量在腰围 (WC) 上存在显著交互作用 (Pinteraction = 0.006)。尽管携带≥2 个风险等位基因,但 SFA 摄入量低(≤23.2 g/天)的个体与携带<2 个风险等位基因的个体相比,WC 更小(Beta = -0.01 cm;p = 0.03)。对于携带≥2 个风险等位基因的个体,SFA 摄入量高(>23.2 g/天)与 SFA 摄入量低(≤23.2 g/天)相比,WC 显著更大(Beta = 0.02 cm,p = 0.02)。在任何测量结果上,GRS 与其他饮食因素之间均无显著交互作用。我们得出结论,低 SFA 饮食可能有助于降低 CETP 和 LPL 遗传变异证实的中心性肥胖的遗传风险。相反,高 SFA 饮食会增加亚洲人群中心性肥胖的遗传风险。