Prognostic impact of coronary microvascular dysfunction in patients with atrial fibrillation (prognosis of CMD in AF)

狼牙棒 医学 心脏病学 内科学 心房颤动 冠状动脉疾病 临床意义 导管消融 心肌梗塞 经皮冠状动脉介入治疗
作者
Ayman A. Mohammed,Siqi Li,Hengbin Zhang,Fuad A. Abdu,Abdul-Quddus Mohammed,Wen Zhang,Ekhlas Mahmoud Al-Hashedi,Yawei Xu,Wenliang Che
出处
期刊:Microvascular Research [Elsevier]
卷期号:154: 104685-104685
标识
DOI:10.1016/j.mvr.2024.104685
摘要

Coronary microvascular dysfunction (CMD) is frequently observed in atrial fibrillation (AF), the most commonly sustained arrhythmia. Nevertheless, an in-depth prognostic significance of CMD in AF is lacking. We aimed to provide insight into the predictive impact of CMD assessed by a novel non-invasive coronary angiography-derived index of microcirculatory resistance (caIMR) for major adverse events (MACE) in AF patients.This study included patients with AF who underwent invasive coronary angiography due to suspected cardiac ischemia and did not exhibit obstructive epicardial coronary artery disease (≤50 % stenosis). The caIMR was prospectively evaluated, and the optimal cutoff value for predicting MACE was determined through ROC analysis.A total of 463 patients with AF were enrolled. During a median of 33 months of follow-up, 111 (23.97 %) patients had MACE endpoints. The best caIMR cutoff value was 39.28. In patients with MACE, both the mean caIMR and the prevalence of elevated caIMR (caIMR>39.28) were significantly higher compared to those without MACE. An elevated caIMR was linked to a higher risk of MACE (log-rank P < 0.001) and emerged as an independent predictor of clinical outcomes (HR: 4.029; 95 % CI: 2.529-6.418; P < 0.001). In addition, the risk of MACE was higher in high caIMR patients with non-paroxysmal AF (log-rank P < 0.001) and no catheter ablation (log-rank P < 0.001).Elevated caIMR is common and showed a vital independent prognostic significance in AF patients. In addition to well-known risk factors, assessment of microvascular function can be a feasible approach for early prevention and a therapeutic target in AF patients.
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