Dysglycemia and incident heart failure among blacks: The jackson heart study

Justin B Echouffo-Tcheugui, Stanford E Mwasongwe, Solomon K Musani, Michael E Hall, Adolfo Correa, Adrian F Hernandez, Sherita H Golden, Robert J Mentz, Alain G Bertoni, Justin B Echouffo-Tcheugui, Stanford E Mwasongwe, Solomon K Musani, Michael E Hall, Adolfo Correa, Adrian F Hernandez, Sherita H Golden, Robert J Mentz, Alain G Bertoni

Abstract

Background: We aimed to investigate the associations of glycemic markers (hemoglobin A1C [HbA1C], fasting plasma glucose [FPG] and glycemic status [normoglycemia, prediabetes and diabetes]) with incident heart failure (HF) and its subtypes, among Blacks.

Methods: We included 2,290 community-dwelling Blacks (64% women, mean age 58 years) without prevalent HF from the Jackson Heart Study who attended the second exam (2005 - 2008). The associations between glycemic markers and incident HF (and subtypes including HF with preserved ejection fraction [HFpEF] and reduced ejection fraction [HFrEF]) were evaluated using Cox proportional hazards regression models, adjusting for risk factors and coronary heart disease.

Results: There were 119 incident HF events (48 HFpEF, 58 HFrEF, and 13 unclassified HF events) over a median follow-up of 10.5 years. Higher levels of HbA1C (HR per SD increment, 1.30; 95% CI 1.12, 1.51) and FPG (HR per SD increment FPG: 1.32; 95% CI: 1.17, 1.48) were associated with a higher risk of incident HF. Compared to normal glycemia, diabetes status was associated with a higher risk of incident HF (HR: 1.24; 95%CI: 1.02, 2.05). HbA1C was significantly associated with higher risks of HFpEF (HR per SD increment: 1.41, 95% CI: 1.18, 1.69) and HFrEF (HR per SD increment: 1.32; 95% CI: 1.12, 1.56). FPG was significantly associated with higher risk of HFpEF (HR per SD increment: 1.35, 95% CI: 1.14, 1.62) but not HFrEF (HR per SD increment: 1.12; 95% CI: 0.53, 2.35).

Conclusions: Among community-dwelling Blacks, higher levels of glycemic markers were associated with higher risk of HF subtypes.

Trial registration: ClinicalTrials.gov NCT00005485.

Conflict of interest statement

Competing interests: Robert J. Mentz receives research support from Amgen, AstraZeneca, Bayer, GlaxoSmithKline, Gilead, InnoLife, Luitpold/American Regent, Medtronic, Merck, Novartis and Sanofi; honoraria from Abbott, Amgen, AstraZeneca, Bayer, Boston Scientific, Janssen, Luitpold Pharmaceuticals, Medtronic, Merck, Novartis, Roche, Sanofi and Vifor; and has served on an advisory board for Amgen, AstraZeneca, Luitpold, Merck, Novartis and Boehringer Ingelheim. All the other authors report no conflicts of interest.

Copyright © 2021 Elsevier Inc. All rights reserved.

Figures

Figure 1:
Figure 1:
Process of selecting eligible participants for the analyses
Figure 2:
Figure 2:
Survival plot comparing the risk of heart failure hospitalization across levels of glycemic markers. Panel A: by levels of glycosylated hemoglobin (HbA1C), Panel B: by levels of by levels of fasting plasma glucose (FPG), Panel C: by glycemic status categories

Source: PubMed

3
Suscribir