Xu Min, Ng San San, Bray George A, Ryan Donna H, Sacks Frank M, Ning Guang, Qi Lu
Department of Nutrition, Harvard School of Public Health, Boston, MA; Shanghai Clinical Center for Endocrine and Metabolic Diseases, Shanghai Institute of Endocrine and Metabolic Diseases, Shanghai, China;
Department of Molecular Genetics, GenoVive, New Orleans, LA;
J Nutr. 2015 Jun;145(6):1289-94. doi: 10.3945/jn.115.212514. Epub 2015 Apr 29.
Hepatic lipase (HL) plays a pivotal role in the metabolism of HDL and LDL. Recent genome-wide association studies have identified common variants in the HL gene (LIPC) associated with HDL cholesterol.
We tested the effect of a common variant in LIPC on changes in blood lipids in response to weight-loss diets in the Preventing Overweight Using Novel Dietary Strategies Trial.
We genotyped LIPC rs2070895 in 743 overweight or obese adults aged 30-70 y (61% women) who were assigned to high-fat (40% energy) or low-fat (20% energy) diets for 2 y. We measured serum concentrations of total cholesterol (TC), triglycerides, LDL cholesterol, and HDL cholesterol at baseline and 2 y of intervention.
At 2 y of intervention, dietary fat modified effects of the variant on changes in serum TC, LDL cholesterol, and HDL cholesterol (P-interaction: 0.0008, 0.004, and 0.03, respectively). In the low-fat group, as compared to the G allele, the A allele tended to be related to the decrease in TC and LDL cholesterol concentrations [TC (β ± SE): -5.5 ± 3.0, P = 0.07; LDL cholesterol: -4.8 ± 2.5, P = 0.06] and a lower increase in HDL cholesterol concentrations (β ± SE: -1.37 ± 0.69, P = 0.048), whereas an opposite effect in the high-fat diet group was evident [TC (β ± SE): 7.3 ± 2.7, P = 0.008; LDL cholesterol: 4.1 ± 2.3, P = 0.07], and there was no genetic effect on changes in HDL cholesterol concentrations (P = 0.54).
Dietary fat intake modifies the effect of a common variant in LIPC on changes in serum lipids during a long-term weight-loss intervention in overweight or obese adults. This trial was registered at clinicaltrials.gov as NCT00072995.
肝脂肪酶(HL)在高密度脂蛋白(HDL)和低密度脂蛋白(LDL)的代谢中起关键作用。最近的全基因组关联研究已经确定了HL基因(LIPC)中与HDL胆固醇相关的常见变异。
在“使用新型饮食策略预防超重”试验中,我们测试了LIPC中一种常见变异对减肥饮食后血脂变化的影响。
我们对743名年龄在30 - 70岁的超重或肥胖成年人(61%为女性)的LIPC rs2070895进行基因分型,这些人被分配到高脂肪(40%能量)或低脂肪(20%能量)饮食组,为期2年。我们在基线和干预2年后测量血清总胆固醇(TC)、甘油三酯、LDL胆固醇和HDL胆固醇的浓度。
在干预2年后,饮食脂肪改变了该变异对血清TC、LDL胆固醇和HDL胆固醇变化的影响(交互作用P值分别为0.0008、0.004和0.03)。在低脂组中,与G等位基因相比,A等位基因倾向于与TC和LDL胆固醇浓度的降低相关[TC(β±标准误):-5.5±3.0,P = 0.07;LDL胆固醇:-4.8±2.5,P = 0.06]以及HDL胆固醇浓度较低的升高(β±标准误:-1.37±0.69,P = 0.048),而在高脂饮食组中则有相反的效果[TC(β±标准误):7.3±2.7,P = 0.008;LDL胆固醇:4.1±2.3,P = 0.07],并且对HDL胆固醇浓度的变化没有遗传效应(P = 0.54)。
在超重或肥胖成年人的长期减肥干预期间,饮食脂肪摄入量改变了LIPC中一种常见变异对血清脂质变化的影响。该试验已在clinicaltrials.gov注册,注册号为NCT00072995。