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Moderate excess alcohol consumption and adverse cardiac remodelling in dilated cardiomyopathy
Upasana Tayal1,2, John Gregson3, Rachel Buchan4,2
1National Heart and Lung Institute, Imperial College London, London, UK u.tayal@rbht.nhs.uk.
Insights
Moderate excess alcohol consumption in dilated cardiomyopathy (DCM) patients shows adverse cardiac structure and function, but this is primarily linked to biological sex, not alcohol itself. Prognosis remains unaffected by alcohol intake.
Area of Science:
- Cardiology
- Cardiovascular Medicine
- Alcohol-related Heart Disease
Background:
- The impact of moderate excess alcohol consumption on dilated cardiomyopathy (DCM) is not well-defined.
- There is a need for more evidence to guide patient advice regarding alcohol intake in DCM.
- Previous studies have not clearly established the relationship between moderate alcohol excess and DCM outcomes.
Purpose of the Study:
- To evaluate the effect of moderate excess alcohol consumption on cardiovascular structure, function, and outcomes in patients with DCM.
- To investigate whether moderate excess alcohol consumption influences cardiac remodeling and prognosis in DCM.
- To clarify the role of alcohol in the pathophysiology of DCM.
Main Methods:
- Prospective longitudinal observational cohort study of 604 DCM patients.
- Assessment of moderate excess alcohol consumption based on UK government guidelines (>14 units/week for women, >21 units/week for men).
- Cardiovascular magnetic resonance imaging and follow-up for a composite endpoint of cardiovascular death, heart failure, and arrhythmic events.
Main Results:
- DCM patients with moderate excess alcohol consumption (16%) exhibited lower biventricular function and increased chamber dilatation compared to non-consumers.
- These differences were largely attributed to biological sex, with moderate excess alcohol not associated with adverse cardiac structure after adjustment.
- No significant difference in midwall myocardial fibrosis or prognosis was observed between groups after a median follow-up of 3.9 years.
Conclusions:
- Moderate excess alcohol consumption in DCM patients is associated with adverse cardiac structure and function at presentation, primarily driven by biological sex.
- Alcohol may contribute to sex-specific phenotypic variations within DCM.
- These findings support informed lifestyle discussions for patients diagnosed with DCM regarding alcohol consumption.
Objective:
The 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.
Methods:
Prospective 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.
Results:
DCM 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.
Conclusion:
DCM 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.
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