Chan Edmund, Tan Chuen Seng, Deurenberg-Yap Mabel, Chia Kee Seng, Chew Suok Kai, Tai E Shyong
Department of Endocrinology, Singapore General Hospital, Block 6 level 6, Room B35, Outram Road, Singapore 169608, Republic of Singapore.
Atherosclerosis. 2006 Aug;187(2):309-15. doi: 10.1016/j.atherosclerosis.2005.10.002. Epub 2005 Nov 9.
Peroxisome proliferators activated receptor alpha (PPARalpha) regulates the transcription of several proteins involved in human lipoprotein metabolism. We screened the PPARA locus for polymorphisms in 20 unrelated subjects from each of three ethnic groups (Chinese, Malays and Asian Indians). Only the V227A polymorphism was observed. We genotyped 4248 subjects (2899 Chinese, 761 Malay and 588 Asian Indians) and found allele frequencies for the A227 allele of 0.04 in Chinese, 0.006 in Malays and 0.003 in Asian Indians. We examined the associations between this polymorphism and serum lipid concentrations in Chinese. In women, but not in men, the presence of the A227 allele was associated with lower serum concentrations of total cholesterol [5.38mmol/l (95%CI: 5.22-5.54) versus 5.21mmol/l (95%CI: 4.99-5.43), p=0.047] and triglycerides [1.19mmol/l (95%CI: 1.10-1.28) versus 1.09mmol/l (95%CI: 0.98-1.21), p=0.048]. We also found that the V227A polymorphism modulates the association between dietary polyunsaturated fatty acid intake and serum high density lipoprotein concentration (p-value for interaction=0.049). Our findings implicate PPARalpha in the lipid lowering associated with diets high in PUFA and suggests that genetic variation at the PPARA locus may determine the lipid response to changes in PUFA intake.
过氧化物酶体增殖物激活受体α(PPARα)调节参与人类脂蛋白代谢的几种蛋白质的转录。我们在来自三个种族群体(中国人、马来人和亚洲印度人)的每组20名无关个体中筛查了PPARA基因座的多态性。仅观察到V227A多态性。我们对4248名受试者(2899名中国人、761名马来人和588名亚洲印度人)进行了基因分型,发现中国人中A227等位基因的频率为0.04,马来人为0.006,亚洲印度人为0.003。我们研究了这种多态性与中国人群血清脂质浓度之间的关联。在女性中,而非男性中,A227等位基因的存在与较低的血清总胆固醇浓度[5.38mmol/l(95%CI:5.22 - 5.54)对5.21mmol/l(95%CI:4.99 - 5.43),p = 0.047]和甘油三酯浓度[1.19mmol/l(95%CI:1.10 - 1.28)对1.09mmol/l(95%CI:0.98 - 1.21),p = 0.048]相关。我们还发现V227A多态性调节饮食中多不饱和脂肪酸摄入量与血清高密度脂蛋白浓度之间的关联(交互作用的p值 = 0.049)。我们的研究结果表明PPARα参与了与高PUFA饮食相关的降脂作用,并提示PPARA基因座的遗传变异可能决定对PUFA摄入量变化的脂质反应。