de Luis Román Daniel A, Izaola Jáuregui Olatz, Primo David, Aller Rocio
Departamento de Endocrinología y Nutrición. Hospital Clínico Universitario.
Nutr Hosp. 2019 Dec 26;36(6):1288-1295. doi: 10.20960/nh.02390.
Background and objectives: genetic variants of the APOA1 gene have been related to lipid profile in obese subjects. Our aim was to analyze the effects of the rs670 APOA1 gene polymorphism on metabolic changes secondary to an enriched-polyunsaturated fat vs. an enriched-monounsaturated fat hypocaloric diet. Methods: 360 Caucasian obese subjects were randomly allocated to two groups. One group received an enriched-polyunsaturated fat (diet P) and the other an enriched-monounsaturated fat hypocaloric diet (diet M) during 12 weeks. The effects on serum biomarkers related to lipid and carbohydrate metabolism were evaluated before and after the dietary intervention. Results: after both diets, body mass index, weight, fat mass, waist circumference, systolic blood pressure, plasma leptin concentration, and waist circumference decreased in all patients. After 12 weeks of intervention with diet P, plasma insulin levels and HOMA-IR decreased in A-allele carriers: delta: -7.3 ± 2.2 IU/L (p = 0.01), and delta: -2.8 ± 0.5 units (p = 0.02), respectively. The same changes in delta were observed after diet M in A-allele carriers: insulin delta: -5.9 ± 1.2 IU/L (p = 0.01), and HOMA-IR delta: -2.1 ± 0.8 units (p = 0.02). In A-allele carriers, LDL-cholesterol decreased and HDL-cholesterol increased after the dietary intervention with diet P: delta: -12.1 ± 4.3 mg/dL (p = 0.01), and delta: 2.6 ± 0.7 mg/dL (p = 0.01), respectively. No differences in lipid profile were observed after diet M. These improvements were not observed in non-A-allele carriers after both interventions. Conclusions: our study showed the association of the rs670 ApoA1 polymorphism with insulin resistance changes as induced by both diets. An enriched-polyunsaturated fat diet produced an additional improvement of HDL-cholesterol and LDL-cholesterol in A-allele carriers.
APOA1基因的遗传变异与肥胖受试者的血脂水平有关。我们的目的是分析APOA1基因rs670多态性对富含多不饱和脂肪与富含单不饱和脂肪的低热量饮食继发的代谢变化的影响。方法:360名白种人肥胖受试者被随机分为两组。一组接受富含多不饱和脂肪的饮食(饮食P),另一组接受富含单不饱和脂肪的低热量饮食(饮食M),为期12周。在饮食干预前后评估对与脂质和碳水化合物代谢相关的血清生物标志物的影响。结果:两种饮食后,所有患者的体重指数、体重、脂肪量、腰围、收缩压、血浆瘦素浓度和腰围均下降。饮食P干预12周后,A等位基因携带者的血浆胰岛素水平和HOMA-IR下降:变化量分别为-7.3±2.2 IU/L(p=0.01)和-2.8±0.5单位(p=0.02)。饮食M后,A等位基因携带者也观察到相同的变化量:胰岛素变化量为-5.9±1.2 IU/L(p=0.01),HOMA-IR变化量为-2.1±0.8单位(p=0.02)。饮食P干预后,A等位基因携带者的低密度脂蛋白胆固醇下降,高密度脂蛋白胆固醇上升:变化量分别为-12.1±4.3 mg/dL(p=0.01)和2.6±0.7 mg/dL(p=0.01)。饮食M后未观察到血脂水平的差异。两种干预后,非A等位基因携带者未观察到这些改善。结论:我们的研究表明rs670 ApoA1多态性与两种饮食诱导的胰岛素抵抗变化有关。富含多不饱和脂肪的饮食在A等位基因携带者中使高密度脂蛋白胆固醇和低密度脂蛋白胆固醇有额外改善。