Metabolic dysfunction and incidence of heart failure subtypes among Black individuals: The Jackson Heart Study

Author:

Kaze Arnaud D.1,Bertoni Alain G.2,Fox Ervin R.3,Hall Michael E.3,Mentz Robert J.4,Echouffo‐Tcheugui Justin B.56ORCID

Affiliation:

1. Department of Medicine, Division of Cardiology Banner‐University Medical Center Phoenix, The University of Arizona College of Medicine Phoenix AZ USA

2. Department of Epidemiology and Prevention Wake Forest School of Medicine Winston‐Salem NC USA

3. Department of Medicine, Division of Cardiology University of Mississippi Medical Center Jackson Jackson MS USA

4. Duke University Medical Center and Duke Clinical Research Institute Durham NC USA

5. Department of Medicine, Division of Endocrinology, Diabetes & Metabolism Johns Hopkins School of Medicine Baltimore MD USA

6. Welch Prevention Center for Prevention, Epidemiology and Clinical Research Johns Hopkins University Baltimore MD USA

Abstract

AimsThe extent to which metabolic syndrome (MetS) severity influences subclinical myocardial remodelling, heart failure (HF) incidence and subtypes, remains unclear. We assessed the association of MetS with incident HF (including ejection fraction subtypes) among Black individuals.Methods and resultsWe included 4069 Jackson Heart Study participants (mean age 54.4 years, 63.8% women, 37.2% with MetS) without HF. We categorized participants based on MetS status and MetS severity scores (based on waist circumference [MetS‐Z‐WC] and body mass index [MetS‐Z‐BMI]). We assessed the associations of MetS indices with echocardiographic parameters, biomarkers of myocardial damage (high‐sensitivity cardiac troponin I [hs‐cTnI] and B‐type natriuretic peptide [BNP]) and incident HF hospitalizations including HF with preserved ejection fraction (HFpEF) and HF with reduced ejection fraction (HFrEF). MetS severity was associated with subclinical cardiac remodelling (assessed by echocardiographic measures and biomarkers of myocardial damage). Over a median of 12 years, 319 participants developed HF (157 HFpEF, 149 HFrEF and 13 HF of unknown type). MetS was associated with a twofold greater risk of HF (hazard ratio [HR] 2.07, 95% confidence interval [CI] 1.64–2.61). Compared to the lowest quartile (Q1) of MetS‐Z‐WC, the highest quartile (Q4) conferred a higher risk of HF (HR 2.35, 95% CI 1.67–3.30), with a stronger association for HFpEF (Q4 vs. Q1: HR 4.94, 95% CI 2.67–9.14) vs. HFrEF (HR 1.69, 95% CI 1.06–2.70).ConclusionsMetabolic syndrome severity was associated with both HF subtypes among Black individuals, highlighting the importance of optimal metabolic health for preventing HF.

Funder

National Heart, Lung, and Blood Institute

National Institute on Minority Health and Health Disparities

Publisher

Wiley

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