Abstract 4367184: Association of natriuretic peptide concentration with lifetime risk of heart failure in adults with diabetes mellitus: a pooled cohort analysis

M Matthew Segar (Texas Heart Institute, Houston, Texas, United States) K Kershaw Patel (Houston Methodist Hospital, Houston, Texas, United States) J James de Lemos (UT SOUTHWESTERN MEDICAL CTR, Dallas, Texas, United States) M Muthiah Vaduganathan (Division of Cardiovascular Medicine Brigham and Women’s Hospital, Harvard Medical School, Boston, MA (M.V.).) C Christie Ballantyne (BAYLOR COLLEGE MEDICINE, Houston, Texas, United States) C Chris deFilippi (University of maryland, Baltimore, Maryland, United States) C Colby Ayers (UT Southwestern Medical Center, Dallas, Texas, United States) J James Januzzi (Baim Institute for Clinical Research, Boston, Massachusetts, United States) R Robin Dullaart R Rodica Busui (UNIVERSITY MICHIGAN, Ann Arbor, Michigan, United States) J John Wilkins (Northwestern University, Chicago, Illinois, United States) M Mark Espeland (Wake Forest School of Medicine, Winston-Salem, North Carolina, United States) A Alain Bertoni A Antoni Bayés-Genís A Ambarish Pandey

Abstract

Background: Natriruetic peptide (NP) screening is recommended for HF prevention in diabetes mellitus (DM), with NT-proBNP >125 pg/mL considered abnormal. However, evidence supporting this threshold is derived primarily from shorter-term studies. Lifetime risk (LTR) estimates for HF across NT-proBNP concentrations in DM is unknown. Methods: Participant-level data from 6 prospective cohorts (ARIC, MESA, CHS, FOS, FHS Generation 3, CRIC) and the Look AHEAD trial control group were pooled excluding participants with prevalent HF or ASCVD at baseline. Participants were stratified according to well-established NP thresholds ( Figure) . LTR of HF was determined at different index ages using the pratical incidence estimator macro with modified Kaplan-Meier methods that uses age as a time scale and mortality as a competing risk. A positive control group of adults with DM and prevalent CVD was analyzed separately. Results: Among 5,986 participants (age 61 y, 45% male, 25% Black), 1,134 developed HF over 79,347 person-years (14.3 per 1,000 person-years). At index age 55 y, the LTR of HF through 90 years was 34.4%. Lifetime risk of HF increased progressively across increasing NT-proBNP categories at each index age ( Figure 1A and 1B ). At index age 55 y, the LTR estimate for the NT-proBNP >125 pg/mL category (48.7%) was comparable to the positive control group with prevalent CVD (n = 1,687; 51.7%). LTR of HF was higher in Black (vs. non-Black) adults at every category with detectable NT-proBNP and was comparable to prevalent CVD at lower thresholds (50-125 pg/ml) ( Figure 1B ). LTR of HF among adults with low short-term HF risk (based on WATCH-DM or 10-y HF PREVENT risk scores) and NT-proBNP >125 pg/mL was high and comparable with the prevalent CVD group. Adding NT-proBNP to 30-year PREVENT HF risk score substantially improved LTR prediction performance (AUROC for 30-year risk: 0.569 to 0.685, p<0.001). Conclusions: In adults with DM, higher NT-proBNP concentrations identify higher LTR of HF, with the highest risk noted among those with concentrations >125 pg/ml supporting the current guideline recommended screening thresholds to discriminate lifetime risk. Lifetime risk of HF associated with NT-proBNP concentrations vary by race with disporporationtely high risk observed among Black adults.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (15)

M

Matthew Segar

Texas Heart Institute, Houston, Texas, United States

K

Kershaw Patel

Houston Methodist Hospital, Houston, Texas, United States

J

James de Lemos

UT SOUTHWESTERN MEDICAL CTR, Dallas, Texas, United States

M

Muthiah Vaduganathan

Division of Cardiovascular Medicine Brigham and Women’s Hospital, Harvard Medical School, Boston, MA (M.V.).

C

Christie Ballantyne

BAYLOR COLLEGE MEDICINE, Houston, Texas, United States

C

Chris deFilippi

University of maryland, Baltimore, Maryland, United States

C

Colby Ayers

UT Southwestern Medical Center, Dallas, Texas, United States

J

James Januzzi

Baim Institute for Clinical Research, Boston, Massachusetts, United States

R

Robin Dullaart

R

Rodica Busui

UNIVERSITY MICHIGAN, Ann Arbor, Michigan, United States

J

John Wilkins

Northwestern University, Chicago, Illinois, United States

M

Mark Espeland

Wake Forest School of Medicine, Winston-Salem, North Carolina, United States

A

Alain Bertoni

A

Antoni Bayés-Genís

A

Ambarish Pandey