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本文引用的文献

1
PRISMA-combined Myeloperoxidase -463G/A gene polymorphism and coronary artery disease: A meta-analysis of 4744 subjects.PRISMA合并髓过氧化物酶-463G/A基因多态性与冠状动脉疾病:对4744名受试者的荟萃分析
Medicine (Baltimore). 2017 Mar;96(12):e6461. doi: 10.1097/MD.0000000000006461.
2
Myeloperoxidase G-463A polymorphism and susceptibility to coronary artery disease: a meta-analysis.髓过氧化物酶 G-463A 多态性与冠心病易感性的关系:一项荟萃分析。
Gene. 2013 Jul 10;523(2):152-7. doi: 10.1016/j.gene.2013.03.131. Epub 2013 Apr 10.
3
Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010.1990年和2010年20个年龄组中235种死因的全球和区域死亡率:全球疾病负担研究2010的系统分析
Lancet. 2012 Dec 15;380(9859):2095-128. doi: 10.1016/S0140-6736(12)61728-0.
4
Mortality from ischaemic heart disease by country, region, and age: statistics from World Health Organisation and United Nations.按国家/地区和年龄划分的缺血性心脏病死亡率:世界卫生组织和联合国的统计数据。
Int J Cardiol. 2013 Sep 30;168(2):934-45. doi: 10.1016/j.ijcard.2012.10.046. Epub 2012 Dec 4.
5
An epidemic of coronary heart disease.冠心病的一种流行情况。
QJM. 2012 Jun;105(6):509-18. doi: 10.1093/qjmed/hcr265. Epub 2012 Jan 19.
6
Myeloperoxidase G-463A polymorphism and risk of lung and prostate cancer in a Turkish population.髓过氧化物酶 G-463A 多态性与土耳其人群肺癌和前列腺癌风险的关系。
Mol Med Rep. 2011 Jan-Feb;4(1):87-92. doi: 10.3892/mmr.2010.378. Epub 2010 Oct 5.
7
Effects of myeloperoxidase -463 G/A gene polymorphism and plasma levels on coronary artery disease.髓过氧化物酶-463 G/A 基因多态性及其血浆水平对冠状动脉疾病的影响。
Mol Biol Rep. 2011 Feb;38(2):887-91. doi: 10.1007/s11033-010-0181-4. Epub 2010 Jun 22.
8
The optimal blood pressure target for patients with coronary artery disease.冠状动脉疾病患者的最佳血压目标。
Curr Cardiol Rep. 2010 Jul;12(4):302-6. doi: 10.1007/s11886-010-0112-y.
9
Serial analyses of C-reactive protein and myeloperoxidase in acute coronary syndrome.急性冠状动脉综合征中 C 反应蛋白和髓过氧化物酶的连续分析。
Clin Cardiol. 2009 Nov;32(11):E58-62. doi: 10.1002/clc.20462.
10
The myeloperoxidase gene and its influence on myocardial infarction in a Swedish population: protective role of the -129A allele in women.髓过氧化物酶基因及其对瑞典人群心肌梗死的影响:-129A等位基因在女性中的保护作用。
Coron Artery Dis. 2009 Aug;20(5):322-6. doi: 10.1097/MCA.0b013e32832da06d.

土耳其人群中α和β多态性对冠心病风险及患者生存的影响。

Effects of and - polymorphisms on coronary artery disease risk and patient survival in a Turkish population.

作者信息

Arslan Serdal, Berkan Öcal, Bayyurt Burcu, Beton Osman, Şahin Ni L Özbi Lüm, Aydemir Eylem Itır

机构信息

Department of Medical Biology, Faculty of Medicine, Cumhuriyet University, 58140 Sivas, Turkey.

Department of Cardiovascular Surgery, Heart Center, Cumhuriyet University, 58140 Sivas, Turkey.

出版信息

Biomed Rep. 2017 Dec;7(6):547-552. doi: 10.3892/br.2017.995. Epub 2017 Oct 3.

DOI:10.3892/br.2017.995
PMID:29188060
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5702965/
Abstract

Myeloperoxidase (MPO) is an oxidative hemoprotein compound expressed in polymorphonuclear leukocytes that contributes to inflammatory responses. Coronary artery disease (CAD), as the most prevalent form of heart disease, is considered to originate from an interaction between genetic and environmental factors. In the present study, the potential associations between and - polymorphisms with CAD were investigated in a Turkish population using a polymerase chain reaction-based restriction fragment length polymorphism (RFLP) assay technique. To the best of our knowledge, the study was the first to examine the association of and - with patient survival rate in a Turkish population. The study population consisted of 201 patients with CAD and 201 healthy controls. The results indicated that there was a significant association of the genotype of with the case population (P=0.048). Meanwhile, in the patients with CAD, the frequency distributions of the allele (P=0.006) and genotype (P=0.001) were significantly increased compared with the allele and genotype, respectively, in CAD patients. Additionally, compared with the genotype, the frequency distribution of was significantly increased in the patient group regarding smoking status (P=0.001) and the presence of hypercholesterolemia (P=0.028). However, survival analysis did not detect an effect of either polymorphism on the survival rate of the CAD patients (P>0.05). Therefore, the genotype may be a significant risk factor for the development of CAD.

摘要

髓过氧化物酶(MPO)是一种在多形核白细胞中表达的氧化血红素蛋白化合物,它参与炎症反应。冠状动脉疾病(CAD)作为最常见的心脏病形式,被认为源于遗传和环境因素之间的相互作用。在本研究中,使用基于聚合酶链反应的限制性片段长度多态性(RFLP)分析技术,在土耳其人群中研究了[具体基因]和[具体基因]多态性与CAD之间的潜在关联。据我们所知,该研究是首次在土耳其人群中研究[具体基因]和[具体基因]与患者生存率的关联。研究人群包括201例CAD患者和201名健康对照。结果表明,[具体基因]的[具体基因型]与病例组存在显著关联(P = 0.048)。同时,在CAD患者中,[具体基因]的[具体等位基因]频率分布(P = 0.006)和[具体基因型]频率分布(P = 0.001)分别与CAD患者中的[另一个等位基因]和[另一个基因型]相比显著增加。此外,与[另一个基因型]相比,在患者组中,关于吸烟状况(P = 0.001)和高胆固醇血症的存在(P = 0.028),[具体基因型]的频率分布显著增加。然而,生存分析未检测到任何一种多态性对CAD患者生存率的影响(P>0.05)。因此,[具体基因型]可能是CAD发生的一个重要危险因素。