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Target trial emulation of alcohol intake interventions in young adults and risk of cardiovascular disease over 30 years: data from the CARDIA study

医学 混淆 年轻人 酒精摄入量 心理干预 置信区间 环境卫生 随机对照试验 饮酒量 队列 队列研究 情感(语言学) 物理疗法 人口学 前瞻性队列研究 低风险 风险评估 干预(咨询) 老年学 纵向研究 仿真 疾病 风险因素 优势比
作者
Jiarui Li,Luohua Jiang,David S. Timberlake,Nathan D. Wong,David R. Jacobs,Andrew Odegaard
出处
期刊:European Journal of Preventive Cardiology [Oxford University Press]
标识
DOI:10.1093/eurjpc/zwag302
摘要

Abstract Aims 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 and results 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 (1985–86), 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 five 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. Over 30 years, the overall cardiovascular disease (CVD) risk among all participants was 8.7%. Abstaining was associated with a slightly lower risk [8.3%; risk difference (RD), −0.4%; 95% confidence interval (CI), −0.6–0.1], while light (8.8%; RD, 0.2%; 95% CI, −0.1–0.2) and moderate (9.4%; RD, 0.7%; 95% CI, −0.1–0.9) drinking showed minimal risk differences. Heavy (RD, 1.3%; 95% CI, −0.2–1.8) and very heavy drinking (RD, 1.9%; 95% CI, −0.3–2.9) suggested modestly increased risks, though CIs 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. Lay summary 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 from 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 intakes were associated with suggestive increases in risk but are imprecise. Estimates accounted for time-varying confounding and treatment-confounder feedback.
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