Background: Long-term alcohol consumption patterns play a critical role in human health. Objectives: We aimed to identify alcohol consumption trajectories and analyze their associations with coronary heart disease (CHD) and all-cause mortality in the Framingham Heart Study (FHS). Methods: We used a growth mixture model to identify sex-specific alcohol consumption trajectories over 15 years and Cox regression to examine associations of these trajectories with incident events that occurred during an additional 10-year follow-up, adjusting for covariates. Results: We identified four distinct trajectory groups among 6,570 participants (mean age 52; 55% women): Group 1 (n=2,713, reference) consisted of low-level drinkers; Group 2 (n=1,818) mainly included abstainers; Groups 3 (n=805) and 4 (n=1,234) comprised drinkers with varying patterns, with Group 4 consuming the most. Over 10 years of follow-up, women in Groups 2 to 4 had hazard ratios (HR) for CHD of 1.57 (95% CI = 1.11-2.22), 1.57 (95% CI = 1.08-2.29), and 1.27 (95% CI = 1.05-1.55) compared to Group 1. Women in Groups 2 (HR = 1.26, 95% CI = 1.05-1.50) and 3 (HR = 1.27, 95% CI = 1.05-1.55) also had higher all-cause mortality risks. Men in Group 2 had higher mortality (HR = 1.18, 95% CI = 1.02-1.37, P = 0.030) and CHD (HR = 1.56, 95% CI = 1.07-1.52, P = 0.001) risks compared to Group 1, while men in Group 4 had the highest mortality risk (HR = 1.27, 95% CI = 1.02-1.37). Conclusion: This study identified four distinct alcohol consumption trajectories and demonstrated that maintaining low to moderate levels of alcohol drinking over time is likely associated with a lower risk of CHD and mortality in both women and men.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementData collection for FHS was supported by N01-HC-25195, HHSN268201500001, and grants (R01AG059727, R01AG016495, R01AG008122, RF1AG062109, U19AG068753, R01AA028263) from the National Institute on Aging. R01AA028263 supported YLeng, YLi, JM, and CL. HD was supported by the American Heart Association (20SFRN35360180).
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
All participants provided their written consent for genetic studies. The study protocol received approval from the Institutional Review Boards at Boston University Medical Center, Massachusetts General Hospital, and Beth Israel Deaconess Medical Center. The study adhered strictly to regulations and guidelines to ensure compliance.
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
留言 (0)