Abstract 4346854: Intensive Blood Pressure Control and SGLT2 Inhibitors for the PREVENTion of Heart Failure: The Multi-Ethnic Study of Atherosclerosis

A Alexander Razavi (Emory University School of Medicine, Atlanta, Georgia, United States) A Aditya Mehta (Inova Heart and Vascular Institute, Falls Church, Virginia, United States) O Omar Dzaye (JOHNS HOPKINS UNIVERSITY, Baltimore, Maryland, United States) W Wendy Post (JOHNS HOPKINS UNIVERSITY, Baltimore, Maryland, United States) D Darren McGuire (UT Southwestern, Dallas, Texas, United States) K Khurram Nasir V Viola Vaccarino (EMORY UNIV ROLLINS SCHL PUBLIC HLTH, Atlanta, Georgia, United States) Z Zeina Dardari (Johns Hopkins University, Baltimore, Maryland, United States) A Arshed Quyyumi (EMORY UNIVERSITY, Atlanta, Georgia, United States) M Michael Bancks (Wake Forest Univ School of Medicine, Winston-Salem, North Carolina, United States) R Roger Blumenthal (Johns Hopkins University School of Medicine, Baltimore, Maryland, United States) L Laurence Sperling M Michael Blaha (JOHNS HOPKINS HOSPITAL, Baltimore, Maryland, United States) M Matthew Budoff (The Lundquist Institute, Torrance, California, United States) S Seamus Whelton (Johns Hopkins School of Medicine, Baltimore, Maryland, United States)

Abstract

Background: Intensive systolic blood pressure (SBP) lowering and sodium-glucose cotransport-2 inhibitor (SGLT2i) treatment can reduce the risk of incident heart failure (HF). Research Question: Based on the American Heart Association Predicting Risk of Cardiovascular Disease Events (PREVENT) estimated risk, what is the modeled number needed to treat (NNT) to a SBP <120 mmHg or with a SGLT2i to prevent an incident diagnosis of HF? Goal: Estimate the 5-year number needed to treat (NNT 5 ) to prevent one HF event for intensive systolic blood pressure control and SGLT2i initiation according to PREVENT HF risk. Methods: Baseline (2000-02) data for 6,034 participants in the Multi-Ethnic Study of Atherosclerosis (MESA) were used to calculate PREVENT HF risk. Mean risk reduction estimates from randomized controlled trials targeting SBP <120 mmHg [38% relative risk reduction (RRR)] and with SGLT2i (31% RRR) were applied to observed HF incidence rates in MESA for NNT 5 calculations across baseline HF risk, as well as N-terminal prohormone of brain natriuretic peptide (NT-proBNP), and diabetes related risk. Low, intermediate, and high 10-year HF risk were defined as <5%, 5-14%, and > 15%, respectively. Results: Mean age was 62 years, 53% were female, 61% were non-white, and 12% had diabetes. The median 10-year PREVENT HF risk was 4%, distributed across individuals with low (52%), intermediate (39%), and high risk (9%). Over 10-year follow-up, there were 198 incident HF cases (3.6 per 1,000 person-years). In the overall sample, the estimated NNT 5 was 112 for intensive SBP control and 199 for SGLT2i. There were large differences in NNT 5 for intensive SBP control and SGLT2i among individuals with low PREVENT HF risk (537 and 768) versus high PREVENT HF risk (34 and 45) ( Figure ). Among individuals with an intermediate PREVENT HF risk, those with NT-proBNP > 125 pg/mL or diabetes had a lower NNT 5 for intensive SBP control (47 and 53) and SGLT2i (64 and 91) compared to those with NT-proBNP <125 pg/mL or without diabetes (intensive SBP control: 209 and 137; SGLT2i: 310 and 183). Conclusions: Both intensive SBP control and SGLT2i had a stepwise lower NNT 5 to prevent the incident diagnosis of HF across higher PREVENT risk scores, with a lower NNT 5 for intensive SBP control compared to SGLT2i. Incorporation of NTproBNP and DM assessment among intermediate risk persons may further guide allocation of therapies to reduce the risk of HF.

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)

A

Alexander Razavi

Emory University School of Medicine, Atlanta, Georgia, United States

A

Aditya Mehta

Inova Heart and Vascular Institute, Falls Church, Virginia, United States

O

Omar Dzaye

JOHNS HOPKINS UNIVERSITY, Baltimore, Maryland, United States

W

Wendy Post

JOHNS HOPKINS UNIVERSITY, Baltimore, Maryland, United States

D

Darren McGuire

UT Southwestern, Dallas, Texas, United States

K

Khurram Nasir

V

Viola Vaccarino

EMORY UNIV ROLLINS SCHL PUBLIC HLTH, Atlanta, Georgia, United States

Z

Zeina Dardari

Johns Hopkins University, Baltimore, Maryland, United States

A

Arshed Quyyumi

EMORY UNIVERSITY, Atlanta, Georgia, United States

M

Michael Bancks

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

R

Roger Blumenthal

Johns Hopkins University School of Medicine, Baltimore, Maryland, United States

L

Laurence Sperling

M

Michael Blaha

JOHNS HOPKINS HOSPITAL, Baltimore, Maryland, United States

M

Matthew Budoff

The Lundquist Institute, Torrance, California, United States

S

Seamus Whelton

Johns Hopkins School of Medicine, Baltimore, Maryland, United States