Moderate excess alcohol consumption and adverse cardiac remodelling in dilated cardiomyopathy

Author:

Tayal UpasanaORCID,Gregson John,Buchan Rachel,Whiffin Nicola,Halliday Brian P,Lota Amrit,Roberts Angharad M,Baksi A John,Voges Inga,Jarman Julian W E,Baruah Resham,Frenneaux Michael,Cleland John G F,Barton Paul,Pennell Dudley J,Ware James S,Cook Stuart A,Prasad Sanjay K

Abstract

ObjectiveThe effect of moderate excess alcohol consumption is widely debated and has not been well defined in dilated cardiomyopathy (DCM). There is need for a greater evidence base to help advise patients. We sought to evaluate the effect of moderate excess alcohol consumption on cardiovascular structure, function and outcomes in DCM.MethodsProspective longitudinal observational cohort study. Patients with DCM (n=604) were evaluated for a history of moderate excess alcohol consumption (UK government guidelines; >14 units/week for women, >21 units/week for men) at cohort enrolment, had cardiovascular magnetic resonance and were followed up for the composite endpoint of cardiovascular death, heart failure and arrhythmic events. Patients meeting criteria for alcoholic cardiomyopathy were not recruited.ResultsDCM patients with a history of moderate excess alcohol consumption (n=98, 16%) had lower biventricular function and increased chamber dilatation of the left ventricle, right ventricle and left atrium, as well as increased left ventricular hypertrophy compared with patients without moderate alcohol consumption. They were more likely to be male (alcohol excess group: n=92, 94% vs n=306, 61%, p=<0.001). After adjustment for biological sex, moderate excess alcohol was not associated with adverse cardiac structure. There was no difference in midwall myocardial fibrosis between groups. Prior moderate excess alcohol consumption did not affect prognosis (HR 1.29, 95% CI 0.73 to 2.26, p=0.38) during median follow-up of 3.9 years.ConclusionDCM patients with moderate excess alcohol consumption have adverse cardiac structure and function at presentation, but this is largely due to biological sex. Alcohol may contribute to sex-specific phenotypic differences in DCM. These findings help to inform lifestyle discussions for patients with DCM.

Funder

Novartis

Servier

Torrent Pharmaceuticals

PharmaNord

Medical Research Council

Sanofi

NIHR Imperial Biomedical Research Centre

Amgen

Rosetrees Trust

Wellcome Trust

Bristol Myers Squibb

GSK

AstraZeneca

Bayer

Imperial College

Biomedical Research Centre

Abbott

NIHR

Siemens

Philips

Pharmacosmos

Medtronic

Publisher

BMJ

Subject

Cardiology and Cardiovascular Medicine

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1. Alcoholic cardiomyopathy: aspects of pathogenesis and clinic;The Clinician;2024-06-23

2. Alcoholic cardiomyopathy: an update;European Heart Journal;2024-06-07

3. Cardiomyopathies – Inherited subtypes and phenocopies;Genomic and Molecular Cardiovascular Medicine;2024

4. Utilities and Limitations of Cardiac Magnetic Resonance Imaging in Dilated Cardiomyopathy;Korean Journal of Radiology;2023

5. Ethanol and Heart Failure: A Clinical Perspective;Alcohol and Alcohol-related Diseases;2023

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