Tara Reshadmanesh, Amir Hossein Behnoush, Maedeh Farajollahi, Amirmohammad Khalaji, Elina Ghondaghsaz, Hassan Ahangar
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Random-effect meta-analysis was performed for the calculation of standardized mean difference (SMD) and 95% confidence interval (CI). Blood calprotectin levels were compared between CAD patients and controls, as well as CAD subtypes.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>A total of 20 studies were included in the systematic review and meta-analysis, comprising 3300 CAD patients and 1230 controls. Patients with CAD had significantly higher calprotectin levels (SMD 0.81, 95% CI 0.32−1.30, <i>p</i> < 0.01). Similarly, patients with ACS were reported to have higher levels compared to those with stable CAD. However, there was no significant difference in terms of blood calprotectin levels between stable CAD cases and healthy controls. Finally, studies have shown that calprotectin could be used as a diagnostic biomarker of CAD while also predicting major adverse events and mortality in these patients.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Based on our findings, calprotectin, as an inflammatory marker, could be used as a possible biomarker for patients with CAD and ACS. These suggest the possibility of pathophysiological pathways for this involvement and warrant further research on these associations as well as their clinical utility.</p>\n </section>\n </div>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/clc.24315","citationCount":"0","resultStr":"{\"title\":\"Circulating Levels of Calprotectin as a Biomarker in Patients With Coronary Artery Disease: A Systematic Review and Meta-Analysis\",\"authors\":\"Tara Reshadmanesh, Amir Hossein Behnoush, Maedeh Farajollahi, Amirmohammad Khalaji, Elina Ghondaghsaz, Hassan Ahangar\",\"doi\":\"10.1002/clc.24315\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>Calprotectin, also known as MRP8/14, is generated by immune cells and is altered in several inflammatory diseases. 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引用次数: 0
摘要
背景:钙粘蛋白又称 MRP8/14,由免疫细胞生成,在多种炎症性疾病中会发生改变。有研究评估了冠状动脉疾病(CAD)及其亚型(稳定型 CAD 和急性冠状动脉综合征 [ACS])患者的钙粘蛋白水平。在此,我们旨在通过系统综述和荟萃分析系统地研究这些关联:方法:我们在四个在线数据库(包括 PubMed、Scopus、Embase 和 Web of Science)中进行了系统检索。对相关研究进行了检索、筛选和提取。进行随机效应荟萃分析,计算标准化平均差(SMD)和95%置信区间(CI)。比较了CAD患者和对照组以及CAD亚型的血液钙蛋白水平:系统回顾和荟萃分析共纳入了 20 项研究,包括 3300 名 CAD 患者和 1230 名对照组患者。CAD患者的钙粘蛋白水平明显较高(SMD 0.81,95% CI 0.32-1.30,P 结论:钙粘蛋白在CAD患者和CAD亚型中的作用是非常重要的:根据我们的研究结果,钙粘蛋白作为一种炎症标志物,可用作 CAD 和 ACS 患者的生物标志物。这表明这种参与可能存在病理生理途径,因此有必要对这些关联及其临床实用性进行进一步研究。
Circulating Levels of Calprotectin as a Biomarker in Patients With Coronary Artery Disease: A Systematic Review and Meta-Analysis
Background
Calprotectin, also known as MRP8/14, is generated by immune cells and is altered in several inflammatory diseases. Studies have assessed their levels in patients with coronary artery disease (CAD) and its subtypes (stable CAD and acute coronary syndrome [ACS]). Herein, we aimed to systematically investigate these associations through a systematic review and meta-analysis.
Methods
A systematic search was conducted in four online databases, including PubMed, Scopus, Embase, and the Web of Science. Relevant studies were retrieved, screened, and extracted. Random-effect meta-analysis was performed for the calculation of standardized mean difference (SMD) and 95% confidence interval (CI). Blood calprotectin levels were compared between CAD patients and controls, as well as CAD subtypes.
Results
A total of 20 studies were included in the systematic review and meta-analysis, comprising 3300 CAD patients and 1230 controls. Patients with CAD had significantly higher calprotectin levels (SMD 0.81, 95% CI 0.32−1.30, p < 0.01). Similarly, patients with ACS were reported to have higher levels compared to those with stable CAD. However, there was no significant difference in terms of blood calprotectin levels between stable CAD cases and healthy controls. Finally, studies have shown that calprotectin could be used as a diagnostic biomarker of CAD while also predicting major adverse events and mortality in these patients.
Conclusion
Based on our findings, calprotectin, as an inflammatory marker, could be used as a possible biomarker for patients with CAD and ACS. These suggest the possibility of pathophysiological pathways for this involvement and warrant further research on these associations as well as their clinical utility.