Association of Long-term Change in N-Terminal Pro–B-Type Natriuretic Peptide With Incident Heart Failure and Death

Author:

Jia Xiaoming1,Al Rifai Mahmoud12,Hoogeveen Ron3,Echouffo-Tcheugui Justin B.4,Shah Amil M.5,Ndumele Chiadi E.6,Virani Salim S.137,Bozkurt Biykem17,Selvin Elizabeth8,Ballantyne Christie M.13,Nambi Vijay137

Affiliation:

1. Section of Cardiology, Department of Medicine, Baylor College of Medicine, Houston, Texas

2. now with Houston Methodist DeBakey Heart & Vascular Center, Houston, Texas

3. Division of Atherosclerosis and Vascular Medicine, Department of Medicine, Baylor College of Medicine, Houston, Texas

4. Division of Endocrinology, Diabetes and Metabolism, Johns Hopkins Bayview Medical Center, Baltimore, Maryland

5. Division of Cardiovascular Medicine, Brigham and Women’s Hospital, Boston, Massachusetts

6. Division of Cardiology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland

7. Section of Cardiology, Michael E. DeBakey Veterans Affairs Medical Center, Houston, Texas

8. Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland

Abstract

ImportanceMost studies, especially in primary prevention patients, have evaluated N-terminal B-type natriuretic peptide (NT-proBNP) at one time point. Evaluation of change in NT-proBNP may improve risk stratification for incident cardiovascular events.ObjectiveTo assess the association between change in NT-proBNP and risk for incident heart failure (HF) and death.Design, Setting, and ParticipantsParticipants were recruited from 4 US communities enrolled in the Atherosclerosis Risk in Community (ARIC) study. Individuals who attended ARIC visits 2 and 4 (approximately 6 years apart) with measurements of NT-proBNP and without prevalent HF were included. Assays of NT-proBNP were conducted between 2011 and 2013, and analysis took place between July 2021 and October 2022.ExposuresThe primary exposure variable was NT-proBNP change between visits 2 and 4, modeled as change categories (<125 pg/mL or ≥125 pg/mL) and as percent change.Main Outcomes and MeasuresThe primary outcome measures were incident HF hospitalization and all-cause death. The association between changes in cardiovascular risk factors with change in NT-proBNP was further assessed.ResultsA total of 9776 individuals (mean [SD] age, 57.1 [5.7] years at visit 2; 5523 [56.5%] women) were included in the study. Compared with participants with NT-proBNP level less than 125 pg/mL at both visits, participants with NT-proBNP level of 125 pg/mL or higher at both visits had an increase in incident HF (adjusted hazard ratio [HR], 2.40 [95% CI, 2.00-2.88]) and mortality risk (HR, 1.68 [95% CI, 1.47-1.91). Participants with NT-proBNP levels of 125 pg/mL or higher at visit 2 and less than 125 pg/mL at visit 4 had similar risk for HF and death (HR, 1.01 [95% CI, 0.71-1.43]; HR, 0.79 [95% CI, 0.61-1.01]) compared with the group with NT-proBNP levels of less than 125 pg/mL at both visits. The percent change in NT-proBNP was positively associated with HF and death (HR, 1.06 [95% CI, 1.02-1.10]; HR, 1.05 [95% CI, 1.03-1.08] per 1-SD increase, respectively). Change in systolic blood pressure, low-density lipoprotein cholesterol, triglyceride level, body mass index, and estimated glomerular filtration rate were significantly associated with change in NT-proBNP.Conclusions and RelevanceIn this study, 6-year change in NT-proBNP reflected dynamic change in risk for HF events and death among community-dwelling adults without prevalent clinical HF. These results support the utility of serial NT-proBNP measurements to improve risk stratification of patients with pre-HF.

Publisher

American Medical Association (AMA)

Subject

Cardiology and Cardiovascular Medicine

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