染色体9p21遗传变异与中国汉族人群冠心病关系的病例对照研究及Meta-分析
ssociation between Genetic variations in 9p21 Region with Coronary Heart Disease in Chinese Han Population: case-control study and meta-analysis
目的:探讨染色体9p21区域rs2383206和rs2383207位点遗传变异与中国汉族人群冠心病的关系。方法:采用病例-对照方法,选择冠心病患者580例作为病例组,选择性别年龄与其匹配的正常人539例作为对照组,收集研究对象的一般人口学资料、病史资料和实验室检查资料,采用Sequenom MassARRAY飞行时间质谱法对rs2383206和rs2383207位点进行基因分型,采用SPSS17.0进行统计分析。全面检索中国生物医学文献数据库、中国知网和PubMed数据库,搜集中国汉族人群rs2383206和rs2383207位点基因多态性与冠心病关系的病例-对照研究,采用RevMan 5.0 软件对符合纳入标准的文献进行meta-分析。结果:吸烟、腰臀比、高血压病史、糖尿病史、收缩压、舒张压和总胆固醇在两组中差异显著,均具有统计学意义(P<0.05);rs2383206位点的基因型在病例组和对照组人群中分布差异无统计学意义(P>0.05),rs2383207位点基因型在病例组和对照组人群中分布差异显著,具有统计学意义(P<0.05),其中AA基因型在病例组分布频率(8.3%)显著低于对照组(13.6%)。Meta-分析共纳入6项研究,共累计病例4836 例,对照4789 例,meta-分析结果表明rs2383206位点AA基因型合并后OR值为0.77,其95%可信区间为(0.66,0.89);rs2383207位点AA基因型合并后OR值为0.75,其95%可信区间为(0.61,0.92)。结论:吸烟、腰臀比、高血压病史、糖尿病史、收缩压、舒张压和总胆固醇可能是冠心病的危险因素;9p21区域rs2383206和rs2383207位点AA基因型可能是冠心病的保护基因型。
Objective: To explore the association of rs2383206 and rs2383207 genetic variations in 9p21 region with coronary heart disease (CHD) in Chinese Han Population. Methods: We conducted a case-control study. Cases were CHD patients (n=580), controls were randomly selected age and sex matched normal people (n=539). General demographic data, medical history data and laboratory data were collected. Rs2383206 and rs2383207 loci were genotyped with Sequenom MassARRAY time of flight mass spectrometer (TOF); SPSS17.0 was used for result analysis. A thorough literature search about studies on the relationship between the polymorphism of rs2383206 and rs2383207 loci and CHD was performed among Chinese Biomedical Literature Database (CBM), Chinese Knowledge Internet (CNKI) and PubMed. Rev Man 5.0 software was used to perform the meta-analysis on those valid studies. Results: Smoking, waist-to-hip ratio (WHR), hypertension, diabetes mellitus, systolic blood pressure, diastolic blood pressure and total cholesterol were statistically different in two groups (P<0.05); No significant associations between rs2383206 and CHD was observed in the study (P>0.05), while rs2383207 was statistically different (P<0.05), the distribution of AA genotype in the patient group (8.3%) was significantly lower than the control group (13.6%). Six studies met the inclusion criteria, including 4836 patient s and 4789 controls. Meta-analysis demonstrated disease association for rs2383206 AA genotype (OR=0.77, 95% CI 0.66-0.89), rs2383207 AA genotype (OR=0.75, 95% CI 0.61-0.92). Conclusions: Smoking, waist-to-hip ratio, hypertension, diabetes mellitus, systolic blood pressure, diastolic blood pressure and total cholesterol may be risk factors for coronary heart disease; 9p21 rs2383206 and rs2383207 loci AA genotype may be the protection genotype of CHD.
王树越、郑东春、朱健、陈新、叶琳、周丽婷
基础医学内科学医学研究方法
染色体9p21冠心病遗传变异病例-对照研究meta-分析
hromosome 9p21Coronary heart diseaseGenetic variantsCase-control studyMeta-analysis
王树越,郑东春,朱健,陈新,叶琳,周丽婷.染色体9p21遗传变异与中国汉族人群冠心病关系的病例对照研究及Meta-分析[EB/OL].(2013-04-24)[2025-08-11].http://www.paper.edu.cn/releasepaper/content/201304-466.点此复制
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