Butyrylcholinesterase K variants increase the risk of coronary artery disease in the population of western Iran.

A Vaisi-Raygani, Z Rahimi, H Entezami, H Kharrazi, F Bahrhemand, H Tavilani, M Rezaei, A Kiani, B Nomanpour, T Pourmotabbed
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引用次数: 18

Abstract

The conflicting results of several studies suggest that there is an association between the butyrylcholinesterase-K variant (BCHE-K, G1615A/Ala539Thr) and the risk of developing coronary artery disease (CAD) in diabetes and non-diabetic subjects. The objective of this study was to determine whether the presence of the BCHE-K variant exacerbates the risk of CAD in patients from western Iran with and without type 2 diabetes mellitus (T2DM). This case-control study comprised 464 subjects undergoing their first coronary angiography. They were matched and randomly assigned into four groups: CAD+T2DM+ (CAD/T2DM), CAD+DM(-) (CAD/ND), CAD(-)DM+ (T2DM/NCAD) and CAD(-)DM(-)(control). The BCHE-K variant was detected by PCR-RFLP. The BCHE-K allele frequency in CAD patients with and without T2DM [total CAD (TCAD)] and separately for each group (CAD/T2DM and CAD/ND) was significantly higher than in the control group (21.1 % versus 13.3 % (p = 0.001), 22.4 % versus 13.3 % (p = 0.001) and 19.7 % versus 13.3 % (p = 0.015), respectively). The odds ratios (ORs) for the BCHE-K heterozygous and homozygous variants in TCAD subjects were 1.65 (95 % CI 1.17-2.3; p = 0.004) and 4.3 (1.05-19.4; p = 0.048); for CAD/T2DM individuals 1.76 (1.2-2.6; p = 0.004) and 4.73 (0.96-23.3; p = 0.052); and for CAD/ND patients 1.53 (1.05-2.3; p = 0.029) and 3.88 (0.8-19.7; p = 0.7), respectively. The OR of the BCHE-K allele was found to be 1.74 (1.1-2.4; p = 0.001) in TCAD subjects, 1.87 (1.12-1.48; p = 0.001) in the CAD/T2DM group and 1.59 (1.04-1.4; p = 0.016) in CAD/ND subjects. These data suggest that the BCHE-K allele increases the risk of CAD in the population (with and without DM) in western parts of Iran, and its presence intensifies the risk of CAD in T2DM. The fact that the BCHE-K allele, even in the heterozygous form, exacerbates the risk of CAD in this population, suggests that a specific therapeutic intervention should be considered for this particular group of patients.

丁基胆碱酯酶K变异增加了伊朗西部人群冠状动脉疾病的风险
一些相互矛盾的研究结果表明,在糖尿病和非糖尿病受试者中,丁基胆碱酯酶k变异(BCHE-K, G1615A/Ala539Thr)与发生冠状动脉疾病(CAD)的风险之间存在关联。本研究的目的是确定BCHE-K变异是否会加剧伊朗西部伴有和不伴有2型糖尿病(T2DM)的患者发生CAD的风险。这项病例对照研究包括464名接受首次冠状动脉造影的受试者。他们被匹配并随机分为四组:CAD+T2DM+ (CAD/T2DM), CAD+DM(-) (CAD/ND), CAD(-)DM+ (T2DM/NCAD)和CAD(-)DM(-)(对照)。PCR-RFLP检测BCHE-K变异。合并和不合并T2DM的CAD患者[总CAD (TCAD)]以及每组(CAD/T2DM和CAD/ND)的BCHE-K等位基因频率均显著高于对照组(分别为21.1%对13.3% (p = 0.001)、22.4%对13.3% (p = 0.001)和19.7%对13.3% (p = 0.015))。TCAD受试者中BCHE-K杂合型和纯合型变异的比值比(or)为1.65 (95% CI 1.17-2.3;P = 0.004)和4.3 (1.05-19.4;P = 0.048);冠心病/T2DM患者1.76 (1.2-2.6);P = 0.004)和4.73 (0.96-23.3;P = 0.052);CAD/ND患者1.53 (1.05-2.3);P = 0.029)和3.88 (0.8-19.7;P = 0.7)。BCHE-K等位基因的OR为1.74 (1.1 ~ 2.4;p = 0.001), 1.87 (1.12-1.48;p = 0.001)和1.59 (1.04-1.4;p = 0.016)。这些数据表明,BCHE-K等位基因增加了伊朗西部人群(有和没有糖尿病)冠心病的风险,并且它的存在加剧了2型糖尿病患者冠心病的风险。事实上,BCHE-K等位基因,即使是杂合子形式,也会加剧这一人群中冠心病的风险,这表明应该考虑对这一特殊患者群体进行特定的治疗干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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