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首页> 外文期刊>International Journal of Preventive Medicine >EFFECTS OF EICOSAPENTAENOIC ACID SUPPLEMENTATION ON LIPID AND LIPOPROTEIN PROFILE IN HYPERTRIGLYCERIDEMIC SUBJECTS WITH DIFFERENT PROLIFERATOR-ACTIVATED RECEPTOR ALPHA GENOTYPES
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EFFECTS OF EICOSAPENTAENOIC ACID SUPPLEMENTATION ON LIPID AND LIPOPROTEIN PROFILE IN HYPERTRIGLYCERIDEMIC SUBJECTS WITH DIFFERENT PROLIFERATOR-ACTIVATED RECEPTOR ALPHA GENOTYPES

机译:二十碳五烯酸补充对不同增殖型激活受体α基因型高甘油三酯血症患者脂质和脂蛋白谱的影响

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Background: We determined the blood lipid-lowering effects of eicosapentaenoic acid (EPA) on hypertriglyceridemic subjects with Leu 162/Val in exon 5 and G/C in intron7 polymorphism of peroxisome proliferator-activated receptor alpha (PPAR a ) genotypes that, to our knowledge, have not been previously studied.Methods: A total of 170 hypertriglyceridemic subjects were enrolled and genotyped for Ala54Thr, Leu162Val, and intron7 polymorphism by the use of a polymerase chain reaction–restriction fragment length polymorphism method. After determination of their genotypes, the first 23 eligible subjects who were found as Ala54 carriers and the first 23 eligible Thr54 carriers were enrolled in the study and stratified for PPAR a genotypes. Participants took 2 g of pure EPA daily for 8 weeks. Fasting blood lipid and lipoprotein profiles were determined and changes from baseline were measured.Results: We observed significant difference between EPA supplementation and Leu162 and Val162, Interon 7 (GG and GC) carriers (P Conclusions: EPA consumption has a lipid-lowering effect in hypertriglyceridemic subjects in both Leu162 and Val162 carriers. But there was no significant interaction between EPA supplementation and PPAR a genotypes. Thus, genetic variation within the PPAR a Leu162/Val cannot modulate the association of EPA intakes with lipid and lipoprotein profile. However, we must note that the sample size in this study was small.
机译:背景:我们确定了二十碳五烯酸(EPA)对高甘油三酸酯血症受试者的血脂降低作用,该受试者在外显子5中存在Leu 162 / Val,在过氧化物酶体增殖物激活受体α(PPAR a)基因型的intron7多态性中具有G / C。方法:采用聚合酶链反应-限制性片段长度多态性方法,共招募了170名高甘油三酯血症受试者,并对其Ala54Thr,Leu162Val和intron7多态性进行了基因分型。确定基因型后,将前23名符合条件的受试者作为Ala54携带者和前23名符合条件的Thr54携带者纳入研究,并对PPAR a基因型进行分层。参与者每天服用2克纯EPA,持续8周。结果:我们观察到EPA补充剂与Leu162和Val162,Interon 7(GG和GC)载体之间存在显着差异(P结论:EPA的摄入具有降低血脂的作用)。 Leu162和Val162携带者都患有高甘油三酸酯血症,但是EPA补充剂和PPAR a基因型之间没有显着的相互作用,因此,PPAR a Leu162 / Val内的遗传变异不能调节EPA摄入与脂质和脂蛋白谱的关系。必须注意,这项研究的样本量很小。

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