[GENES ALLELE STATUS OF ANGIOTENSINCONVERTING ENZYME (I/D) AND ENDOTHELIAL NITRIC OXIDE SYNTHASE (894 G > T) IN PATIENTS WITH ACUTE CORONARY SYNDROME].

Likars'ka sprava Pub Date : 2015-07-01
L P Sydorchuk, Y V Ursuliak
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Abstract

The association of genes polymorphism of angiotensin-converting enzyme ACE (I/D) and endothelial nitric oxide synthase eNOS (894 G > T) with acute myocardial infarction (MI) among residents of North Bukovina region was evaluated. II/GG and ID/GG haplotypesre associated with more frequent presence of Q-MI, with localization on anterior wall and primary appearance. ID/TT, or II/TG haplotypes are associated with the presence of a severe re-Q-MI, with localization on the posterior wall. ID/TG variant is associated in 93.7% of cases with Q-MI, regardless of its location and times of occurrence. ID/TG increased relative risk of Q-MI by 2,93 times (OR = 4,79; P = 0,002), which confirmed the severity of the disease and increases the risk of MI inanterior and higher in posterior walls of the left ventricle (OR = 4.31; P = 0.007 and OR = 4.6; P = 0.005, respectively) increases the likelihood of the first Ml by 2.88 times (OR = 4.62; P = 0.003) and its re-occurrence or recurrence--by 2.67 times (OR = 4; P = 0.022). Mutations absence: in haplotypes (II/GG) is a protective factor of Q-MI appearance (OR = 0.19; P = 0.004) and makes the chances for the first MI the lowest in observed population (OR = 0.36; P = 0.045).

[急性冠脉综合征患者血管紧张素转换酶(i / d)和内皮型一氧化氮合酶(894 g > t)基因等位基因状况]。
研究了北布科维纳地区居民血管紧张素转换酶ACE (I/D)和内皮型一氧化氮合酶eNOS (894 G > T)基因多态性与急性心肌梗死(MI)的相关性。II/GG和ID/GG单倍型与Q-MI更常见的存在相关,定位于前壁和原发外观。ID/TT或II/TG单倍型与严重的re-Q-MI存在相关,并定位于后壁。ID/TG变异与93.7%的Q-MI病例相关,无论其发生地点和时间如何。ID/TG使Q-MI的相对风险增加2,93倍(OR = 4,79;P = 0.002),这证实了疾病的严重性,并增加了左心室前壁和后壁心肌梗死的风险(OR = 4.31;P = 0.007, OR = 4.6;P = 0.005)使第一次Ml的可能性增加2.88倍(OR = 4.62;P = 0.003),再发生或复发- 2.67倍(or = 4;P = 0.022)。突变缺失:在单倍型中(II/GG)是Q-MI出现的保护因素(OR = 0.19;P = 0.004),并且使得第一次心肌梗死的几率在观察人群中最低(OR = 0.36;P = 0.045)。
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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