Association Between Alcohol Use Disorders and Dementia in 262,703 Dementia-free Finnish Adults: Is Cardiovascular Disease a Mediator?

Author:

Hu Yaoyue1ORCID,Korhonen Kaarina2ORCID,Li Peng3,Bobak Martin4ORCID,Martikainen Pekka23ORCID,Bijlsma Maarten J3

Affiliation:

1. School of Public Health, Chongqing Medical University , Chongqing , P.R. China

2. Population Research Unit, Faculty of Social Sciences, University of Helsinki , Helsinki , Finland

3. Laboratory of Population Health, Max Planck Institute for Demographic Research , Rostock , Germany

4. Research Department of Epidemiology and Public Health, University College London , London , UK

Abstract

Abstract Background The possible mediating role of cardiovascular disease (CVD) in the relationship between alcohol use disorders (AUD) and the risk of early-onset (<age 65) and late-onset (≥age 65) dementia lacks formal investigation. Methods Using linked Finnish national register data, a population-based cohort study of 262,703 dementia-free Finnish men and women aged 40 + at baseline (December 31, 1999) was established. AUD and CVD in 1988–2014, and incident dementia in 2000–2014 were identified from Finnish Hospital Discharge Register and/or Drug Reimbursement Register. Causal association and mediation were assessed using mediational g-formula. Results AUD was associated with a substantial increase in the risk of early-onset dementia in both men (hazard ratio: 5.67, 95% confidence interval: 4.37–7.46) and women (6.13, 4.20–8.94) after adjustments for confounding; but the elevated risk for late-onset dementia was smaller (men: 2.01, 1.80–2.25; women: 2.03, 1.71–2.40). Mediational g-formula results showed that these associations were causal in men with no mediation by CVD as the virtually identical total effect of AUD (early-onset: 5.26, 3.48–7.48; late-onset: 2.01, 1.41–2.87) and direct effect of AUD (early-onset: 5.24, 3.38–7.64; late-onset: 2.19, 1.61–2.96) were found with no indirect effect via CVD. In women, the results were similar for late-onset dementia (total effect: 2.80, 1.70–4.31; direct effect: 2.92, 1.86–4.62) but underpowered for early-onset dementia. Conclusion AUD increased dementia risk, particularly the risk of early-onset dementia. This elevated risk of dementia associated with AUD was not mediated by CVD. Clinicians should consider the increased risk of dementia in the management of middle-aged and older adults with a history and/or current AUD.

Funder

Academy of Finland

European Research Council under the European Union’s Horizon 2020 Research and Innovation Programme

Max Planck—University of Helsinki Center for Social Inequalities in Population Health

Publisher

Oxford University Press (OUP)

Subject

Geriatrics and Gerontology,Aging

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