Evidence map›Paper›PMID 42150810›Full record

ArticleEuropean journal of preventive cardiology2026

Association of cardiometabolic disease with subclinical cardiac remodeling in men vs women in the Framingham Heart Study.

Rachel L Goldberg, Yunong Zhao, Joanne Murabito, Susan Cheng, Ramachandran S Vasan, Daniel Levy, Gary F Mitchell, Emelia J Benjamin, Emily S Lau

Abstract read
In one paragraph

Article in European journal of preventive cardiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Rachel L GoldbergDivision of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, MA.ORCID 0000-0003-1600-4471
Yunong ZhaoDivision of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, MA.
Joanne MurabitoFramingham Heart Study, Framingham, MA, USA; Department of Medicine.
Susan ChengDepartment of Cardiology, Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, CA.
Ramachandran S VasanFramingham Heart Study, Framingham, MA, USA; Department of Medicine.
Daniel LevyFramingham Heart Study, Framingham, MA, USA; Department of Medicine.
Gary F MitchellCardiovascular Engineering, Inc., Needham, MA.
Emelia J BenjaminFramingham Heart Study, Framingham, MA, USA; Department of Medicine.
Emily S LauDivision of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, MA.ORCID 0000-0001-9361-6397

Funding

FRAMINGHAM HEART STUDY - YEAR 5 EXAM75N92019D00031 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI RAMACHANDRAN, VASAN · 2019 to 2024
$29.8M
IDENTIFICATION OF COMMON GENETIC VARIANTS FOR ATRIAL FIBRILLATION AND PR INTERVALR01HL092577 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI BENJAMIN, EMELIA J., ELLINOR, PATRICK THOMAS · 2009 to 2025
$20.6M
FRAMINGHAM HEART STUDY (FHS), TASK AREA B - PROTOCOL DEVELOPMENT AND BASIC EXAMINATION75N92025D00012 · NHLBI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI LLOYD-JONES, DONALD · 2025 to 2025
$8.9M
Ventricular Vascular Coupling: Correlates and PrognosisR01HL080124 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI RAMACHANDRAN, VASAN S · 2005 to 2009
$3.4M
Ventricular-vascular coupling in the elderly: lifecourse determinants, trajectories, and prognostic significanceR01HL142983 · NHLBI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CHENG, SUSAN, MITCHELL, GARY FRANK · 2019 to 2022
$3.2M
Aortic Dysfunction, Pulsatile Stress and Target Organ Damage in FraminghamR01HL107385 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI MITCHELL, GARY FRANK, RAMACHANDRAN, VASAN S · 2011 to 2014
$2.6M
Vascular Function in the Framingham Third GenerationR01HL070100 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BENJAMIN, EMELIA J. · 2002 to 2005
$2.4M
Boston University BIRCWHK12AR085635 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI Emelia J. Benjamin, JOYCE Y WONG · 2025 to 2026
$2.2M
Menopause-related Vasomotor Symptoms and Cardiovascular HealthR01HL180648 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI Emily Lau · 2025 to 2026
$1.5M
HFpEF Susceptibility in Women: The Role of InflammationK23HL159243 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI Emily Lau · 2022 to 2026
$1.1M
THE FRAMINGHAM HEART STUDY-N01HC25195-268025195-268025195N01HC025195 · HC · TRUSTEES OF BOSTON UNIVERSITY · PI WOLF, PHILIP A · 2002 to 2006
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NHLBI NIH HHS 75N92019D00031NHLBI NIH HHS 75N92025D00012NHLBI NIH HHS HHSN268201500001CNHLBI NIH HHS HHSN268201500001INHLBI NIH HHS K23 HL159243NHLBI NIH HHS N01 HC025195NHLBI NIH HHS R01 HL070100NHLBI NIH HHS R01 HL080124NHLBI NIH HHS R01 HL092577NHLBI NIH HHS R01 HL107385NHLBI NIH HHS R01 HL142983NHLBI NIH HHS R01 HL180648NIAMS NIH HHS K12 AR085635
6 · The paper itself

Abstract

aimsAlthough the prevalence of cardiometabolic disease is greater in men vs women, the relative risk of cardiovascular disease (CVD) conferred by cardiometabolic conditions is higher in women than in men. We examined the sex-specific association of cardiometabolic risk factor burden with subclinical echocardiographic cardiac remodeling.

methodsIn this cross-sectional study, we examined whether sex modifies the association between cardiometabolic disease burden (measured as metabolic syndrome severity [MetSS] score) with echocardiographic markers of subclinical cardiac remodeling (including global longitudinal strain [GLS] and E/e' ratio) using multiplicative interaction terms in multivariable-adjusted linear regression models.

resultsAmong 6182 Framingham Heart Study participants (mean age 51 ± 15 years; 54% women), we observed that sex modifies the association between the MetSS score and subclinical markers of left ventricular systolic and diastolic function. Specifically, a higher MetSS score was associated with worse GLS and E/e' ratio in women versus men. For example, every 1-point increase in the MetSS score was associated with 0.35% higher (worse) GLS in women compared with 0.23% higher GLS in men (ß 0.35, SE 0.04 in women versus ß 0.23, SE 0.04 in men, pint 0.01). Similarly, the MetSS score was more strongly associated with a higher (worse) E/e' ratio in women versus men (ß 0.29, SE, 0.02 in women versus ß, 0.20, SE, 0.02 in men, pint <0.001).

conclusionWe observed that sex modifies the association of cardiometabolic disease burden with subclinical markers of cardiac dysfunction. Specifically, higher cardiometabolic disease burden was associated with worse GLS and E/e' ratio in women versus men.

Indexed as

CardiometabolicEchocardiographyRemodelingRiskSexStrainWomen

Identifiers

PMID42150810
PMCPMC13429261

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.