Microvascular dysfunction in patients with heart failure with preserved ejection fraction: A meta‐analysis

Author:

Azuma Mai1,Kato Shingo2ORCID,Fukui Kazuki1,Horita Nobuyuki3,Utsunomiya Daisuke2

Affiliation:

1. Department of Cardiology Kanagawa Cardiovascular and Respiratory Center Yokohama Japan

2. Department of Diagnostic Radiology Yokohama City University Graduate School of Medicine Yokohama Japan

3. Chemotherapy Center Yokohama City University Hospital Yokohama Japan

Abstract

AbstractBackgroundAlthough microvascular dysfunction (MVD) is considered an essential pathophysiology in patients with heart failure with preserved ejection fraction (HFpEF), the frequency and prognostic impact of MVD are not fully understood. This meta‐analysis evaluated the frequency of MVD in patients with HFpEF and its utility in risk stratification.Materials and MethodsOn May 26, 2022, a literature search was performed on PubMed, Web of Science, the Cochrane library, and Embase using the search terms such as “Heart failure with preserved ejection fraction,” “HFpEF,” “microvascular dysfunction,” and “MVD.” The prevalence of MVD in patients with HFpEF was calculated using the general inverse variance method. A comprehensive literature review was conducted to examine the association between MVD and prognosis in patients with HFpEF.ResultsData pertaining to a total of 941 patients diagnosed with HFpEF were extracted from the collective pool of 9 studies. The results of the meta‐analysis revealed that the frequency of MVD among patients with HFpEF was found to be 55.5% (95% CI: 34.8%–76.2%), with a substantial degree of heterogeneity (I2 = 98%, p for heterogeneity <.001). Among the five studies that provided data on the association between MVD and prognosis, a significant statistical association was observed in four of them.ConclusionsThis meta‐analysis revealed that approximately 50% of patients diagnosed with HFpEF exhibited MVD. Moreover, the presence of MVD demonstrated significant prognostic implications in multiple studies conducted on patients with HFpEF. These findings strongly suggest that MVD plays a crucial role in the underlying pathophysiology of patients with HFpEF.

Publisher

Wiley

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Molecular Biology,Physiology

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