Faculty of Medicine, Alexandria University, Alexandria, Egypt.
Weill Cornell Medicine, New York, NY, USA.
Curr Probl Cardiol. 2023 Oct;48(10):101812. doi: 10.1016/j.cpcardiol.2023.101812. Epub 2023 May 19.
We aimed to perform a meta-analysis to investigate the value of Cyclophilin C as a diagnostic and prognostic biomarker in Coronary Artery Disease. PubMed, Web of Science, Scopus and Cochrane library databases were searched. The inclusion criteria were any randomized control trials or controlled observational studies that measured the levels of Cyclophilin C in Coronary Artery disease patients and healthy controls. We excluded case reports, case series, reviews, editorials and animal studies. After search of the literature, 4 studies were included in the meta-analysis with a total number of 454 individuals included in the study. The pooled analysis showed a significant association between CAD group and increased levels of Cyclophilin C (MD = 28.94, 95% confidence interval (CI) = 19.28-38.60, P-value < 0.00001). Subgroup analysis showed a significant association between acute and chronic CAD group with increased levels of cyclophilin c compared with the control group (MD = 35.98, 95% CI = 19.84-52.11, P-value < 0.0001) and (MD = 26.36, 95% CI = 21.87 to 30.85, P-value < 0.00001), respectively. The pooled effect estimate showed that the ROC area for the cyclophillin c as a diagnostic biomarker of CAD was (ROC= 0.880, 95% CI =0.844-0.917, P-value < 0.001). Our study revealed a significant association between acute and chronic coronary artery disease with increased levels of Cyclophilin C. Cyclophilin C could be used as a novel diagnostic and prognostic biomarker in acute and chronic CAD. More research is warranted to support our results.
我们旨在进行荟萃分析,以研究亲环素 C 作为冠心病诊断和预后生物标志物的价值。检索了 PubMed、Web of Science、Scopus 和 Cochrane 图书馆数据库。纳入标准为任何测量冠心病患者和健康对照者亲环素 C 水平的随机对照试验或对照观察性研究。我们排除了病例报告、病例系列、综述、社论和动物研究。文献检索后,共有 4 项研究纳入荟萃分析,共纳入 454 名研究对象。汇总分析显示 CAD 组与亲环素 C 水平升高之间存在显著相关性(MD=28.94,95%置信区间[CI]=19.28-38.60,P 值<0.00001)。亚组分析显示,与对照组相比,急性和慢性 CAD 组的亲环素 C 水平升高与急性和慢性 CAD 组存在显著相关性(MD=35.98,95%CI=19.84-52.11,P 值<0.0001)和(MD=26.36,95%CI=21.87-30.85,P 值<0.00001)。汇总效应估计显示,亲环素 c 作为 CAD 诊断生物标志物的 ROC 面积为(ROC=0.880,95%CI=0.844-0.917,P 值<0.001)。本研究显示,急性和慢性冠状动脉疾病与亲环素 C 水平升高之间存在显著相关性。亲环素 C 可作为急性和慢性 CAD 的新型诊断和预后生物标志物。需要更多的研究来支持我们的结果。