{"title":"The Role of Integrin Beta 3 Polymorphisms in Coronary Artery Disease: A Systematic Review and Meta-analysis","authors":"Sana Ashiq, K. Ashiq, M. Sabar","doi":"10.47144/phj.v56i1.2362","DOIUrl":null,"url":null,"abstract":"Objectives: The literature on the role of integrin beta 3 (ITGB3) exonic variants in coronary artery disease (CAD) and lipid outcomes is scarce. However, the findings remained uncertain and still not clear. Therefore, the current study aims to determine the association of rs5918 polymorphism with coronary artery disease.\nMethodology: All the eligible literature published in the English language from February 3, 2005, up to December 19, 2021, were searched by using different electronic databases and extracted all the required information from the available literature. The statistical analysis was performed through the MetaGenyo program, and pooled odds ratios (ORs) were calculated to determine the association between rs5918 and CAD.\nResults: The final analysis includes four studies, and the overall rs5918 risk allele in all the tested genetic models as follow: allelic model: OR 0.80 CI 0.41-1.58; homozygote model: OR 1.66, 95% CI 0.20-2.16; recessive model: OR 0.71 CI 0.44-1.14; dominant model: OR 0.81 CI 0.22-3.03. In addition, the lipid outcomes, including lipoproteins, cholesterol, and triglycerides were associated with increased disease risk. The shapes of the funnel plots suggest no publication bias in our study.\nConclusion: In conclusion, our final pooled analysis revealed a non-significant role of this exonic polymorphism in coronary artery disease that may exert its effect by modulating various lipid parameters. However, more studies are required with a larger cohort size that may give us conclusive results in the future.","PeriodicalId":42273,"journal":{"name":"Pakistan Heart Journal","volume":" ","pages":""},"PeriodicalIF":0.2000,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pakistan Heart Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.47144/phj.v56i1.2362","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives: The literature on the role of integrin beta 3 (ITGB3) exonic variants in coronary artery disease (CAD) and lipid outcomes is scarce. However, the findings remained uncertain and still not clear. Therefore, the current study aims to determine the association of rs5918 polymorphism with coronary artery disease.
Methodology: All the eligible literature published in the English language from February 3, 2005, up to December 19, 2021, were searched by using different electronic databases and extracted all the required information from the available literature. The statistical analysis was performed through the MetaGenyo program, and pooled odds ratios (ORs) were calculated to determine the association between rs5918 and CAD.
Results: The final analysis includes four studies, and the overall rs5918 risk allele in all the tested genetic models as follow: allelic model: OR 0.80 CI 0.41-1.58; homozygote model: OR 1.66, 95% CI 0.20-2.16; recessive model: OR 0.71 CI 0.44-1.14; dominant model: OR 0.81 CI 0.22-3.03. In addition, the lipid outcomes, including lipoproteins, cholesterol, and triglycerides were associated with increased disease risk. The shapes of the funnel plots suggest no publication bias in our study.
Conclusion: In conclusion, our final pooled analysis revealed a non-significant role of this exonic polymorphism in coronary artery disease that may exert its effect by modulating various lipid parameters. However, more studies are required with a larger cohort size that may give us conclusive results in the future.
目的:关于整合素β3(ITGB3)外显子变体在冠状动脉疾病(CAD)和脂质结果中的作用的文献很少。然而,调查结果仍然不确定,仍然不清楚。因此,本研究旨在确定rs5918多态性与冠状动脉疾病的相关性。方法:使用不同的电子数据库搜索2005年2月3日至2021年12月19日以英语发表的所有符合条件的文献,并从现有文献中提取所有所需信息。通过MetaGenyo程序进行统计分析,并计算合并优势比(OR),以确定rs5918与CAD之间的相关性。结果:最终分析包括四项研究,并将rs5918总风险等位基因在所有测试的遗传模型中如下:等位基因模型:OR 0.80 CI 0.41-1.58;纯合模型:OR 1.66,95%CI 0.20-2.16;隐性模型:OR 0.71 CI 0.44-1.14;优势模型:OR 0.81 CI 0.22-3.03。此外,包括脂蛋白、胆固醇和甘油三酯在内的脂质结果与疾病风险增加有关。漏斗图的形状表明在我们的研究中没有发表偏倚。结论:总之,我们的最终汇总分析揭示了这种外显子多态性在冠状动脉疾病中的不显著作用,可能通过调节各种脂质参数发挥其作用。然而,还需要更多的研究,队列规模更大,这可能会在未来给我们带来结论性的结果。