Association of lipoprotein lipase gene polymorphisms with coronary artery disease among Filipinos.

International journal of molecular epidemiology and genetics Pub Date : 2019-12-15 eCollection Date: 2019-01-01
Ferdinand R Gerodias, Fabio Enrique B Posas, Michael O Baclig, Elmer Casley T Repotente, Jonnah Fatima B Pelat, Gregorio G Rogelio, Maria Cristina Z San Jose, Cynthia A Mapua, Ma Luisa G Daroy
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Abstract

Studies have shown association of lipoprotein lipase (LPL) polymorphisms with coronary artery disease (CAD); however, limited studies on the genetics of CAD have been done in the Philippines. Because of their effects on high-density lipoprotein and triglyceride metabolism, the G-allele of the Ser447X variant of LPL gene has been shown to be atheroprotective, while HindIII polymorphism has been shown to be pro-atherogenic. We assessed 1301 patients undergoing coronary angiography to determine the prevalence of HindIII and Ser447X polymorphisms and their association with angiographically significant CAD. Genotyping for HindIII and Ser447X variants were analyzed by real-time PCR. Multivariate analyses were performed to determine the interaction between LPL polymorphisms and risk factors of CAD. CAD+ group (72%) was predominantly male (76%) with a mean age of 60.17 ± 11.01 with hypertension (89%), dyslipidemia (84%) and smoking (54%) as the most common risk factors. HindIII carriage frequency among the CAD+ group was 20.3% with a genotypic distribution of 78.71% (T/T), 19.83% (T/G) and 1.46% (G/G). Ser447X carriage frequency among the CAD+ group was 8.0% with a genotypic distribution of 91.39% (C/C), 8.38% (C/G) and 0.23% (G/G). HindIII and Ser447X polymorphisms were both not significantly associated with CAD. LPL polymorphic allele HindIII was common, while Ser447X was rare. Present study did not show association of LPL polymorphisms with the development of CAD. However, among patients with dyslipidemia, presence of Ser447X allele is associated with an increased risk (OR 2.6; 95% CI 2.1-3.7; p value < 0.001) of developing CAD than those without LPL polymorphisms.

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脂蛋白脂肪酶基因多态性与菲律宾人冠状动脉疾病的关系
研究表明,脂蛋白脂肪酶(LPL)多态性与冠状动脉疾病(CAD)有关;然而,在菲律宾对CAD的遗传学研究有限。由于其对高密度脂蛋白和甘油三酯代谢的影响,LPL基因Ser447X变异的g等位基因已被证明具有动脉粥样硬化保护作用,而HindIII多态性已被证明具有促动脉粥样硬化作用。我们评估了1301名接受冠状动脉造影的患者,以确定HindIII和Ser447X多态性的患病率及其与血管造影上显著的CAD的关系。实时荧光定量PCR分析HindIII和Ser447X变异的基因分型。进行多变量分析以确定LPL多态性与CAD危险因素之间的相互作用。CAD+组(72%)以男性为主(76%),平均年龄60.17±11.01岁,高血压(89%)、血脂异常(84%)和吸烟(54%)是最常见的危险因素。CAD+组HindIII携带频率为20.3%,基因型分布分别为78.71% (T/T)、19.83% (T/G)和1.46% (G/G)。CAD+组Ser447X携带频率为8.0%,基因型分布分别为91.39% (C/C)、8.38% (C/G)和0.23% (G/G)。HindIII和Ser447X多态性均与CAD无显著相关性。LPL多态性等位基因HindIII较为常见,Ser447X较为少见。目前的研究没有显示LPL多态性与CAD的发展有关。然而,在血脂异常患者中,Ser447X等位基因的存在与风险增加相关(OR 2.6;95% ci 2.1-3.7;p值< 0.001)。
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