首页> 外文期刊>Alcoholism: Clinical and experimental research >Interactions Between the Apolipoprotein A1/C3/A5 Haplotypes and Alcohol Consumption on Serum Lipid Levels
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Interactions Between the Apolipoprotein A1/C3/A5 Haplotypes and Alcohol Consumption on Serum Lipid Levels

机译:载脂蛋白A1 / C3 / A5单倍型与饮酒对血脂水平的相互作用

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Background: The interactions between apolipoprotein (Apo) A1/C3/A5 haplotypes and alcohol consumption on serum lipid profiles have not been previously explored. The present study was undertaken to detect the polymorphisms of ApoA1 -75 bp G>A (rs1799837), ApoC3 3238C>G (rs5128), ApoA5 -1131T>C (rs662799), ApoA5 c.553G>T (rs2075291), and ApoA5 c.457G>A (rs3135507) and the interactions between their haplotypes and alcohol consumption on serum lipid levels. Methods: Genotyping was performed in 1,030 unrelated subjects (516 nondrinkers and 514 drinkers) aged 15 to 89. The interactions between ApoA1/C3/A5 haplotypes and alcohol consumption on serum lipid levels were detected by factorial regression analysis after controlling for potential confounders. Results: The frequencies of ApoC3 3238 CG/GG genotypes and ApoA1 -75 bp A allele in nondrinkers were higher in females than in males (p < 0.05). The frequencies of ApoC3 3238 CG/GG genotypes and G allele in drinkers were higher in females than in males (p < 0.05). The frequencies of ApoA1 -75 bp GA/AA genotypes and A allele in males were higher, and those of ApoC3 3238 CG/GG genotypes were lower in drinkers than in nondrinkers (p < 0.05 to 0.01). The frequency of ApoC3 3238 GG genotype in male drinkers was also higher in ≥25 g/d than in <25 g/d subgroups (p < 0.05). There were 11 haplotypes with a frequency >1% in our study population. The haplotypes of G-G-T-C-G (in the order of c.553G>T, c.457G>A, -1131T>C, 3238C>G, and -75 bp G>A), G-G-T-C-A, and G-G-C-G-G were shown consistent interactions with alcohol consumption to increase serum total cholesterol, high-density lipoprotein cholesterol (HDL-C), and ApoA1 levels (p < 0.05 to 0.001). The interactions between G-G-T-G-G (HDL-C and ApoA1), G-G-C-C-A (ApoA1), G-A-T-C-G (triglyceride), G-G-T-C-G (ApoA1/ApoB ratio), and G-G-C-G-G (ApoB) haplotypes and alcohol consumption on serum lipid levels were also detected (p < 0.05 to 0.001); the levels of these serum lipid parameters were significantly higher in drinkers than in nondrinkers. Conclusions: The differences in serum lipid parameters between drinkers and nondrinkers might partly result from different interactions between the ApoA1/C3/A5 haplotypes and alcohol consumption.
机译:背景:载脂蛋白(Apo)A1 / C3 / A5单倍型与饮酒对血脂水平之间的相互作用以前未曾探讨过。进行本研究以检测ApoA1-75 bp G> A(rs1799837),ApoC3 3238C> G(rs5128),ApoA5 -1131T> C(rs662799),ApoA5 c.553G> T(rs2075291)和ApoA5的多态性c.457G> A(rs3135507)及其单倍型与饮酒之间的相互作用对血脂水平的影响。方法:对1,030名年龄在15至89岁的无关受试者(516名非饮酒者和514名饮酒者)进行基因分型。在控制潜在的混杂因素后,通过因子回归分析检测了ApoA1 / C3 / A5单倍型与饮酒与血脂水平之间的相互作用。结果:非饮酒者中ApoC3 3238 CG / GG基因型和ApoA1 -75 bp A等位基因的频率在女性中高于男性(p <0.05)。女性饮酒者中ApoC3 3238 CG / GG基因型和G等位基因的频率高于男性(p <0.05)。男性中ApoA1 -75 bp GA / AA基因型和A等位基因的频率较高,饮酒者中ApoC3 3238 CG / GG基因型的频率比非饮酒者低(p <0.05至0.01)。 ≥25 g / d的男性饮酒者中ApoC3 3238 GG基因型的频率也高于<25 g / d的亚组(p <0.05)。在我们的研究人群中,有11种单倍型的频率> 1%。 GGTCG和GGCGG的单倍型(按c.553G> T,c.457G> A,-1131T> C,3238C> G和-75 bp G> A的顺序显示)与酒精消耗具有一致的相互作用增加血清总胆固醇,高密度脂蛋白胆固醇(HDL-C)和ApoA1水平(p <0.05至0.001)。还检测到GGTGG(HDL-C和ApoA1),GGCCA(ApoA1),GATCG(甘油三酸酯),GGTCG(ApoA1 / ApoB比)和GGCGG(ApoB)单倍型之间的相互作用以及酒精消耗对血脂水平的影响(p <0.05至0.001);饮酒者的这些血清脂质​​参数水平显着高于非饮酒者。结论:饮酒者和非饮酒者之间的血脂参数差异可能部分是由于ApoA1 / C3 / A5单倍型与饮酒之间的相互作用不同所致。

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