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Associations of the ABCA1 and LPL Gene Polymorphisms With Lipid Levels in a Hyperlipidemic Population

机译:高血脂症人群中ABCA1和LPL基因多态性与脂质水平的关联。

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摘要

We conducted a cross-sectional study to investigate the effects of the adenosine triphosphate-binding cassette transporter 1 (ABCA1) I883M and lipoprotein lipase (LPL) HindIII polymorphisms on lipid levels in patients with hyperlipidemia. A total of 533 patients were enrolled. Serum lipid parameters were determined by an automatic biochemistry analyzer. Genotyping of the ABCA1 I883M and LPL HindIII was carried out using the polymerase chain reaction-restriction fragment length polymorphism technique. Multiple linear regression analysis was used to estimate the associations between serum lipid levels and the genetic polymorphisms. The frequency distribution of the ABCA1 I883M and LPL HindIII polymorphisms did not deviate from Hardy-Weinberg equilibrium. The major finding of our regression analysis showed that neither the ABCA1 I883M nor the LPL HindIII polymorphism was associated with baseline serum lipid levels in the total population. However, among patients with elevated alanine aminotransferase (ALT) levels (ALT ≥ 40 U/L), carriers of the M allele of the ABCA1 gene had lower levels of high-density lipoprotein cholesterol (HDL-C) and higher levels of low-density lipoprotein cholesterol (LDL-C) after adjusting for age, sex, smoking status, alcohol consumption, education level, occupation, and work intensity (P < .05 for both). A test on interaction terms between the ABCA1 I833M polymorphism and ALT on HDL-C and LDL-C levels also remained significant (P = .001 and P = .014, respectively). Our data suggest that there are significant interactive effects between ABCA1 I883M and ALT levels on HDL-C and LDL-C levels. However, the LPL HindIII polymorphism did not influence lipid levels.
机译:我们进行了一项横断面研究,以研究高脂血症患者三磷酸腺苷结合盒转运蛋白1(ABCA1)I883M和脂蛋白脂肪酶(LPL)HindIII多态性对血脂水平的影响。共有533名患者入组。血清脂质参数由自动生化分析仪确定。使用聚合酶链反应-限制性片段长度多态性技术进行ABCA1 I883M和LPL HindIII的基因分型。多元线性回归分析用于估计血清脂质水平和遗传多态性之间的关联。 ABCA1 I883M和LPL HindIII多态性的频率分布没有偏离Hardy-Weinberg平衡。我们回归分析的主要发现表明,ABCA1 I883M和LPL HindIII多态性均与总人群的基线血脂水平无关。然而,在丙氨酸氨基转移酶(ALT)水平升高(ALT≥40 U / L)的患者中,ABCA1基因的M等位基因携带者的高密度脂蛋白胆固醇(HDL-C)水平较低,而低密度脂蛋白水平较高。调整年龄,性别,吸烟状况,饮酒量,受教育程度,职业和工作强度后的密度脂蛋白胆固醇(LDL-C)(两者均P <0.05)。关于ABCA1 I833M多态性与ALT在HDL-C和LDL-C水平上相互作用的一项测试也仍然很有意义(分别为P = .001和P = .014)。我们的数据表明,ABCA1 I883M与ALT水平之间对HDL-C和LDL-C水平具有显着的交互作用。但是,LPL HindIII多态性不影响脂质水平。

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