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载脂蛋白转化酶枯草溶菌素/克胰蛋白酶 9 基因 E670G 多态性与饮酒相互作用,调节血清脂质水平。

Proprotein convertase subtilisin/kexin type 9 gene E670G polymorphism interacts with alcohol consumption to modulate serum lipid levels.

机构信息

Department of Cardiology, Institute of Cardiovascular Diseases, the First Affiliated Hospital, Guangxi Medical University, 22 Shuangyong Road, Nanning 530021, Guangxi, China.

出版信息

Int J Med Sci. 2013;10(2):124-32. doi: 10.7150/ijms.5296. Epub 2012 Dec 30.

Abstract

BACKGROUND

Both alcohol consumption and the proprotein convertase subtilisin/kexin type 9 (PCSK9) gene polymorphism modulate serum lipid levels, but their interactions on serum lipid profiles are still unknown. The present study was undertaken to detect the interactions of PCSK9 E670G polymorphism and alcohol consumption on serum lipid levels.

METHODS

Genotypes of the PCSK9 E670G in 1352 unrelated subjects (785 non-drinkers and 567 drinkers) were determined by polymerase chain reaction and restriction fragment length polymorphism combined with gel electrophoresis, and then confirmed by direct sequencing. The interactions between PCSK9 E670G genotypes and alcohol consumption on serum lipid parameters were detected by using a factorial design covariance analysis after controlling for potential confounders.

RESULTS

The levels of serum triglyceride, high-density lipoprotein cholesterol, apolipoprotein (Apo) A1, and the ratio of ApoA1 to ApoB were higher in drinkers than in non-drinkers (P < 0.01 for all), whereas the levels of total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C) and ApoB were lower in drinkers than in non-drinkers (P < 0.001 for all). The genotypic and allelic frequencies of PCSK9 E670G were not different between non-drinkers and drinkers (P > 0.05 for each). The subjects with AA genotype in non-drinkers had higher serum LDL-C levels than the subjects with AG genotype, whereas the subjects with AG genotype in drinkers had higher serum TC levels than the subjects with AA genotypes (P < 0.05 for each). The effects of alcohol consumption on TC and LDL-C levels depended upon genotypes, the subjects with AA genotype had lower serum TC and LDL-C levels in drinkers than in non-drinkers.

CONCLUSIONS

Alcohol consumption can modify the effects of the PCSK9 E670G polymorphism on serum TC and LDL-C levels. The subjects with AA genotype of the PCSK9 E670G benefit more from alcohol consumption than the subjects with AG genotype in decreasing serum TC and LDL-C levels.

摘要

背景

饮酒和前蛋白转化酶枯草溶菌素/ 9(PCSK9)基因多态性均能调节血清脂质水平,但两者在血清脂质谱上的相互作用尚不清楚。本研究旨在检测 PCSK9 E670G 多态性与饮酒之间的相互作用对血清脂质水平的影响。

方法

采用聚合酶链反应和内切酶片段长度多态性结合凝胶电泳,对 1352 例无关个体(785 名非饮酒者和 567 名饮酒者)的 PCSK9 E670G 基因型进行检测,然后通过直接测序进行确认。采用协方差分析的析因设计,在控制潜在混杂因素后,检测 PCSK9 E670G 基因型与饮酒之间对血清脂质参数的相互作用。

结果

与非饮酒者相比,饮酒者的血清甘油三酯、高密度脂蛋白胆固醇、载脂蛋白(Apo)A1 水平以及 ApoA1/ApoB 比值较高(均 P<0.01),而总胆固醇(TC)、低密度脂蛋白胆固醇(LDL-C)和 ApoB 水平较低(均 P<0.001)。非饮酒者和饮酒者之间 PCSK9 E670G 的基因型和等位基因频率无差异(均 P>0.05)。非饮酒者中 AA 基因型的个体血清 LDL-C 水平高于 AG 基因型,而饮酒者中 AG 基因型的个体 TC 水平高于 AA 基因型(均 P<0.05)。饮酒对 TC 和 LDL-C 水平的影响取决于基因型,与非饮酒者相比,饮酒者中 AA 基因型的个体 TC 和 LDL-C 水平较低。

结论

饮酒可改变 PCSK9 E670G 多态性对血清 TC 和 LDL-C 水平的影响。与 AG 基因型相比,PCSK9 E670G 的 AA 基因型的个体从饮酒降低 TC 和 LDL-C 水平中获益更多。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c3a/3547209/1d96a9a01f03/ijmsv10p0124g01.jpg

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