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Alcohol intake and long-term mortality risk after myocardial infarction in the Alpha Omega Cohort
Esther Cruijsen1, Anne J de Ruiter1, Leanne K Küpers1
1Division of Human Nutrition and Health, Wageningen University, Wageningen, The Netherlands.
Insights
Light to moderate alcohol consumption was linked to lower mortality risk in patients who had experienced a myocardial infarction (MI). This study highlights potential benefits but urges cautious interpretation due to observational data on alcohol and health.
Area of Science:
- Cardiology
- Epidemiology
- Public Health
Background:
- Population studies suggest J-shaped alcohol-CVD mortality curves.
- Limited data exists on alcohol's long-term impact post-myocardial infarction (MI).
Purpose of the Study:
- To investigate alcohol intake's association with all-cause, cardiovascular disease (CVD), and ischemic heart disease (IHD) mortality.
- To analyze mortality risks in Dutch patients following an MI within the Alpha Omega Cohort.
Main Methods:
- Analysis of 4365 post-MI patients (60-80 years; 79% male) using a 203-item food frequency questionnaire (FFQ).
- Categorization of patients into nondrinkers, very light, light, moderate, and heavy drinkers based on daily ethanol intake.
- Cox proportional hazards models adjusted for multiple covariates to determine mortality hazard ratios (HRs).
Main Results:
- During ~12 years follow-up, 2035 deaths occurred (903 CVD, 558 IHD).
- Light and moderate alcohol intake showed inverse associations with all-cause and CVD mortality compared to non-drinkers.
- HRs for all-cause mortality: 0.87 (light), 0.85 (moderate), 0.91 (heavy).
- HRs for CVD mortality: 0.80 (light), 0.82 (moderate), 0.87 (heavy).
Conclusions:
- Light and moderate alcohol consumption demonstrated an inverse association with mortality risk in stable post-MI patients.
- These observational findings warrant cautious interpretation considering the broader evidence on alcohol and health.
- The Alpha Omega Cohort study is registered (NCT03192410).
Background:
Population-based studies generally show J-shaped associations between alcohol intake and mortality from cardiovascular disease (CVD). Little is known about alcohol and long-term mortality risk after myocardial infarction (MI).
Objectives:
We examined alcohol intake in relation to all-cause, CVD, and ischemic heart disease (IHD) mortality in Dutch post-MI patients of the Alpha Omega Cohort.
Methods:
The analysis comprised 4365 patients (60-80 years; 79% male) with an MI ≤ 10 years before study enrolment. We used a 203-item FFQ to assess alcohol (total ethanol) and dietary intakes over the past month. Patients were classified as nondrinkers (0 g/d; n = 956) or very light (>0 to 2 g/d; n = 385), light (M: >2 to 10 g/d; F: >2 to 5 g/d; n = 1125), moderate (M: >10 to 30 g/d; F: >5 to 15 g/d; n = 1207), or heavy drinkers (M: >30 g/d; F: >15 g/d; n = 692). HRs of mortality for alcohol intake were obtained from Cox models, adjusting for age, sex, education, smoking, BMI, physical activity, and dietary factors.
Results:
Alcohol was consumed by 83% of males and 61% of females. During ∼12 years of follow-up, 2035 deaths occurred, of which 903 were from CVD and 558 were from IHD. Compared to the (combined) reference group of nondrinkers and very light drinkers, HRs for all-cause mortality were 0.87 (95% CI, 0.78-0.98), 0.85 (95% CI, 0.75-0.96), and 0.91 (95% CI, 0.79-1.04) for light, moderate, and heavy drinkers, respectively. For CVD mortality, corresponding HRs were 0.80 (95% CI, 0.67-0.96), 0.82 (95% CI, 0.69-0.98), and 0.87 (95% CI, 0.70-1.08) for light, moderate, and heavy drinkers, respectively. Findings for IHD mortality were similar. HRs did not materially change when nondrinkers or very light drinkers were taken as the reference, or after exclusion of former drinkers or patients with diabetes or poor/moderate self-rated health.
Conclusions:
Light and moderate alcohol intakes were inversely associated with mortality risk in stable post-MI patients. These observational findings should be cautiously interpreted in light of the total evidence on alcohol and health. The Alpha Omega Cohort is registered at clinicaltrials.gov as NCT03192410.
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