Natriuretic peptides, body mass index and heart failure risk: Pooled analyses of SAVOR‐TIMI 53, DECLARE‐TIMI 58 and CAMELLIA‐TIMI 61

Author:

Patel Siddharth M.1ORCID,Morrow David A.1,Bellavia Andrea1,Berg David D.1,Bhatt Deepak L.2,Jarolim Petr3,Leiter Lawrence A.4,McGuire Darren K.56,Raz Itamar78,Steg P. Gabriel910,Wilding John P.H.11,Sabatine Marc S.1,Wiviott Stephen D.1,Braunwald Eugene1,Scirica Benjamin M.1,Bohula Erin A.1

Affiliation:

1. TIMI Study Group, Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital Harvard Medical School Boston MA USA

2. Mount Sinai Heart, Icahn School of Medicine at Mount Sinai Health System New York NY USA

3. Department of Pathology, Brigham and Women's Hospital Harvard Medical School Boston MA USA

4. Li Ka Shing Knowledge Institute, St Michael's Hospital University of Toronto Toronto ON Canada

5. Division of Cardiology, Department of Internal Medicine University of Texas Southwestern Medical Center Dallas TX USA

6. Parkland Health and Hospital System Dallas TX USA

7. Diabetes Unit, Department of Endocrinology and Metabolism, Hadassah Medical Center, Faculty of Medicine Hebrew University of Jerusalem Jerusalem Israel

8. Faculty of Medicine, Hebrew University of Jerusalem Jerusalem Israel

9. Université Paris Cité, INSERM U‐1148, Hôpital Bichat Assistance Publique‐Hôpitaux de Paris Paris France

10. FACT (French Alliance for Cardiovascular Trials) Paris France

11. Department of Cardiovascular and Metabolic Medicine University of Liverpool Liverpool UK

Abstract

AbstractAimN‐terminal pro‐B‐type natriuretic peptide (NT‐proBNP) concentrations are lower in patients with obesity. The interaction between body mass index (BMI) and NT‐proBNP with respect to heart failure risk remains incompletely defined.Methods and resultsData were pooled across three randomized clinical trials enrolling predominantly patients who were overweight or obese with established cardiometabolic disease: SAVOR‐TIMI 53, DECLARE‐TIMI 58 and CAMELLIA‐TIMI 61. Hospitalization for heart failure (HHF) was examined across strata of baseline BMI and NT‐proBNP. The effect of dapagliflozin versus placebo was assessed for a treatment interaction across BMI categories in patients with or without an elevated baseline NT‐proBNP (≥125 pg/ml). Among 24 455 patients, the median NT‐proBNP was 96 (interquartile range [IQR]: 43–225) pg/ml and the median BMI was 33 (IQR 29–37) kg/m2, with 68% of patients having a BMI ≥30 kg/m2. There was a significant inverse association between NT‐proBNP and BMI which persisted after adjustment for all clinical variables (p < 0.001). Within any range of NT‐proBNP, those at higher BMI had higher risk of HHF at 2 years (comparing BMI <30 vs. ≥40 kg/m2 for NT‐proBNP ranges of <125, 125–<450 and ≥450 pg/ml: 0.0% vs. 0.6%, 1.3% vs. 4.0%, and 8.1% vs. 13.8%, respectively), which persisted after multivariable adjustment (adjusted hazard ratio [HRadj] 7.47, 95% confidence interval [CI] 3.16–17.66, HRadj 3.22 [95% CI 2.13–4.86], and HRadj 1.87 [95% CI 1.35–2.60], respectively). In DECLARE‐TIMI 58, dapagliflozin versus placebo consistently reduced HHF across BMI categories in those with an elevated NT‐proBNP (p‐trend for HR across BMI = 0.60), with a pattern of greater absolute risk reduction (ARR) at higher BMI (ARR for BMI <30 to ≥40 kg/m2: 2.2% to 4.7%; p‐trend = 0.059).ConclusionsThe risk of HHF varies across BMI categories for any given range of circulating NT‐proBNP. These findings showcase the importance of considering BMI when applying NT‐proBNP for heart failure risk stratification, particularly for patients with low‐level elevations in NT‐proBNP (125–<450 pg/ml) where there appears to be a clinically meaningful absolute and relative risk gradient.

Funder

National Heart, Lung, and Blood Institute

Bristol-Myers Squibb

Eisai

Roche Diagnostics

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine

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