Assessment of Microvascular Function in Angina Pectoris by Angiography-Based Index of Microcirculation Resistance: A Meta-Analysis

基于血管造影的微循环阻力指数评估心绞痛患者的微血管功能:一项荟萃分析

阅读:2

Abstract

BACKGROUND: While the invasive index of microcirculation resistance (IMR) remains the gold standard for diagnosing coronary microvascular dysfunction (CMD), its clinical adoption is limited by procedural complexity and cost. Angiography-based IMR (Angio-IMR), a computational angiography-based method, offers a promising alternative. This study evaluates the diagnostic efficacy of Angio-IMR for CMD detection in angina pectoris (AP). METHODS: A comprehensive literature search was conducted across PubMed, Embase, Scopus, and the Cochrane Library to identify studies assessing Angio-IMR's diagnostic performance for CMD in AP populations. Primary outcomes included pooled sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and area under the receiver operating characteristic (ROC) curve (AUC). RESULTS: 11 studies involving 927 patients were included. Angio-IMR demonstrated robust diagnostic performance: sensitivity 86% (95% CI: 0.83-0.90), specificity 90% (95% CI: 0.87-0.92), PPV 82% (95% CI: 0.78-0.86), NPV 91% (95% CI: 0.88-0.94), and AUC 0.91 (95% CI: 0.89-0.94), with low heterogeneity. Subgroup analyses revealed no significant differences in diagnostic accuracy between obstructive (stenosis ≥50%) and non-obstructive coronary artery disease. Hyperemic Angio-IMR measurements (adenosine-induced) showed superior sensitivity (89% vs. 86%) and specificity (94% vs. 91%) compared to resting-state assessments by AccuFFR system. Additionally, the sensitivity (88% vs. 82%), specificity (92% vs. 86%), PPV (82% vs. 78%) and NPV (91% vs. 88%) calculated based on AccuFFR were higher than that of quantitative flow ratio (QFR). CONCLUSIONS: Angio-IMR is a reliable, non-invasive tool for CMD identification in angina patients, particularly under hyperemic conditions. Its diagnostic consistency across stenosis severity subgroups supports broad clinical applicability.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。