Target Trial Emulation of Alcohol Intake Interventions in Young Adults and Risk of CVD over 30 years: Data from the CARDIA study
AIM: This study uses a target trial emulation framework to estimate how different hypothetical sustained alcohol intake patterns affect 30-year cardiovascular disease risk in young adults.
METHODS: This target trial emulation used longitudinal data from the CARDIA study, a multi-site cohort of Black and White young adults aged 18-30 at baseline (1985-1986), followed for 35 years. The exposure of this study consisted of self-reported daily alcohol intake categorized by sex into abstainer, light, moderate, heavy, and very heavy use categories. The emulated intervention compared hypothetical scenarios in which participants maintained consistent levels of alcohol consumption over time (assigned each of the 5 categories above) to estimate their long-term cardiovascular risk. Using the parametric g-formula to account for time-varying confounding and treatment-confounder feedback, we then estimated the 30-year incident risk of the composite cardiovascular outcome.
RESULTS: Over 30 years, the overall CVD risk among all participants was 8.7%. Abstaining was associated with a slightly lower risk (8.3%; risk difference [RD] -0.4%; 95% CI, -0.6 to 0.1), while light (8.8%; RD 0.2%; 95% CI, -0.1 to 0.2) and moderate (9.4%; RD 0.7%; 95% CI, -0.1 to 0.9) drinking showed minimal risk differences. Heavy (RD 1.3%; 95% CI, -0.2 to 1.8) and very heavy drinking (RD 1.9%; 95% CI, -0.3 to 2.9) suggested modestly increased risks, though confidence intervals included no effect.
CONCLUSION: This hypothetical intervention indicates no meaningful difference in 30-year CVD risk among abstainers, light, or moderate drinkers in young adults. Heavy alcohol intake may modestly raise risk, but estimates are imprecise with a range from no effect to a modest increase. By addressing key biases and leveraging comprehensive longitudinal data, these findings offer valuable insights for clinical and public health guidance.
OVERVIEW: The long-term impact of alcohol consumption patterns starting in early adulthood on cardiovascular disease (CVD) risk remains unclear, partly due to the lack of randomized trials and limited inclusion of young adults in observational studies. Existing evidence suggests that sustained light to moderate drinking likely does not increase long-term CVD risk (with evidence suggesting that it is possibly beneficial), whereas heavy consumption may elevate it. This study utilizes a target trial emulation framework to assess the relationship between alcohol intake and CVD.
KEY FINDINGS: Using data of young adults of the CARDIA study, this target trial emulation study found no material difference in 30-year CVD risks among abstainers and those with light or moderate alcohol intake. Heavy and very heavy intake were associated with suggestive increases in risk but are imprecise. Estimates accounted for time-varying confounding and treatment-confounder feedback.
Additional Info
-
Authors
Li J.; Jiang L.; Timberlake D. S.; Wong N. D.; Jacobs D. R.; Odegaard A. O. -
Issue
Periodical: Eur J Prev Cardiol - Edition: 20260604 -
Published Date
4 june 2026
Related items
- Cardiovascular disease risk under low-fat, Mediterranean, and American Heart Association diets: a target trial emulation in United States adults
- Link between alcohol consumption and myocardial infarction, stroke, and all-cause mortality among Swedish male automotive workers over 30 years
- Global Geospatial Trends in Breast Cancer and Atrial Fibrillation/Flutter Among Older Women: Uncovering Shared Epidemiological Patterns and Etiological Links
- The interaction of age and total lifetime drinks is associated with regional cortical perfusion and thickness in healthy adults with low-level alcohol consumption
- Alcohol consumption and risk of atrial fibrillation: a pairwise and network meta-analysis