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希腊人群中CTH 1364 G>T基因多态性与冠状动脉疾病的关联研究。

Association study of the CTH 1364 G>T polymorphism with coronary artery disease in the Greek population.

作者信息

Giannakopoulou Efstathia, Konstantinou Fotios, Ragia Georgia, Gerontitis Zisis, Tavridou Anna, Papapetropoulos Andreas, Mikroulis Dimitrios, Manolopoulos Vangelis G

机构信息

Laboratory of Pharmacology, Medical School, Democritus University of Thrace, Alexandroupolis, Greece.

Department of Cardiothoracic Surgery, Academic General Hospital of Evros, Alexandroupolis, Greece.

出版信息

Drug Metab Pers Ther. 2019 Mar 12;34(1):dmpt-2018-0033. doi: 10.1515/dmpt-2018-0033.

DOI:10.1515/dmpt-2018-0033
PMID:30860977
Abstract

Background Cystathionine γ-lyase enzyme, which is encoded by the CTH gene, is responsible for hydrogen sulfide (H2S) production in the endothelium. The CTH 1364 G>T polymorphism may alter the CTH expression and H2S bioavailability, thus leading to atherosclerosis and coronary artery disease (CAD). We examined the potential association of the CTH 1364 G>T polymorphism with CAD. Methods The CTH 1364 G>T polymorphism was determined in 178 coronary artery bypass grafting (CABG) patients and 156 non-atherosclerotic controls of Greek Caucasian origin using the PCR-RFLP method. Results No significant difference in the frequency of the CTH 1364 G>T genotypes (p = 0.281) and alleles (p = 0.265) was found between the CABG patients and controls. After conducting stratification according to sex, analysis showed a numerical difference in the CTH 1364 TT genotype frequency in female participants that did not reach statistical significance (16.3% and 8.5% in the CABG and controls, respectively, p = 0.26). The frequency of the CTH 1364 TT genotype between the male CABG patients and controls did not differ (p = 0.507). Conclusions The CTH 1364 G>T polymorphism was not associated with CAD in the studied population. However, interestingly, a higher - if not significantly so - CTH 1364 TT genotype frequency was present in female CABG patients compared with female controls. Larger studies are necessary to conclude on the potential overall or gender-driven association between CTH 1364 G>T gene polymorphism and CAD.

摘要

背景

由CTH基因编码的胱硫醚γ-裂解酶负责在内皮中产生硫化氢(H2S)。CTH 1364 G>T多态性可能会改变CTH表达和H2S生物利用度,从而导致动脉粥样硬化和冠状动脉疾病(CAD)。我们研究了CTH 1364 G>T多态性与CAD之间的潜在关联。方法:采用PCR-RFLP方法,在178例希腊白种人来源的冠状动脉旁路移植术(CABG)患者和156例非动脉粥样硬化对照中测定CTH 1364 G>T多态性。结果:CABG患者和对照之间CTH 1364 G>T基因型频率(p = 0.281)和等位基因频率(p = 0.265)无显著差异。按性别分层后分析显示,女性参与者中CTH 1364 TT基因型频率存在数值差异,但未达到统计学意义(CABG组和对照组分别为16.3%和8.5%,p = 0.26)。男性CABG患者和对照之间CTH 1364 TT基因型频率无差异(p = 0.507)。结论:在研究人群中,CTH 1364 G>T多态性与CAD无关。然而,有趣的是,与女性对照相比,女性CABG患者中CTH 1364 TT基因型频率更高(即使未达到显著水平)。需要更大规模的研究来确定CTH 1364 G>T基因多态性与CAD之间潜在的总体或性别驱动的关联。

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