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Influence of cognitive reserve on risk of depression and subsequent dementia: A large community-based longitudinal study

Published online by Cambridge University Press:  04 June 2024

Wenzhe Yang
Affiliation:
School of Public Health, Tianjin Medical University, Tianjin, China Tianjin Key Laboratory of Environment, Nutrition and Public Health, Tianjin, China
Jiao Wang
Affiliation:
Department of Epidemiology, College of Preventive Medicine, Army Medical University (Third Military Medical University), Chongqing, China
Abigail Dove
Affiliation:
Aging Research Center, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden
Yonghua Yang
Affiliation:
Department of Rehabilitation Medicine, Xiaogan Hospital of Traditional Chinese Medicine, Xiaogan, China
Xiuying Qi*
Affiliation:
School of Public Health, Tianjin Medical University, Tianjin, China Tianjin Key Laboratory of Environment, Nutrition and Public Health, Tianjin, China
Marc Guitart-Masip
Affiliation:
Aging Research Center, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden Center for Psychiatry Research, Region Stockholm, Stockholm, Sweden Center for Cognitive and Computational Neuropsychiatry (CCNP), Karolinska Institutet, Stockholm, Sweden
Goran Papenberg
Affiliation:
Aging Research Center, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden
Weili Xu*
Affiliation:
School of Public Health, Tianjin Medical University, Tianjin, China Tianjin Key Laboratory of Environment, Nutrition and Public Health, Tianjin, China Aging Research Center, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden
*
Corresponding authors: Xiuying Qi and Weili Xu; Emails: qixiuying@tmu.edu.cn; weili.xu@ki.se
Corresponding authors: Xiuying Qi and Weili Xu; Emails: qixiuying@tmu.edu.cn; weili.xu@ki.se

Abstract

Background

Cognitive reserve (CR) has been linked to dementia, yet its influence on the risk of depression and related outcomes remains unknown. We aimed to examine the association of CR with depression and subsequent dementia or death, and to assess the extent to which CR is related to depression-free survival.

Methods

Within the UK Biobank, 436,232 participants free of depression and dementia were followed. A comprehensive CR indicator (low, moderate, and high) was created using latent class analysis based on information on education, occupation, mentally passive sedentary behavior, social connection, confiding with others, and leisure activities. Depression, dementia, and survival status were ascertained through self-reported medical history and/or linkages to medical records. Data were analyzed using multi-state Markov model and Laplace regression.

Results

Over a median follow-up of 12.96 years, 16,560 individuals developed depression (including 617 with subsequent dementia) and 28,655 died. In multivariable multi-state models, compared with low CR, high CR was associated with lower risk of depression (hazard ratio 0.53 [95% confidence interval 0.51–0.56]) and lower risk of post-depression dementia (0.55 [0.34–0.88]) or death (0.69 [0.55–0.88]) in middle-aged adults (aged <60 years). In Laplace regression, the depression-free survival time was prolonged by 2.77 (2.58–2.96) years in participants with high compared to low CR.

Conclusions

High CR is associated with lower risks of depression and subsequent transitions to dementia and death, particularly in middle age. High CR may prolong depression-free survival. Our findings highlight the importance of enhancing CR in the prevention and prognosis of depression.

Information

Type
Research Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2024. Published by Cambridge University Press on behalf of European Psychiatric Association
Figure 0

Figure 1. Schematic representation of multistate model.State-specific numbers of participants were reported in boxes, and numbers (percentages) of participants in transitions from baseline to depression, subsequently to dementia, and ultimately to death were reported on arrows.

Figure 1

Table 1. Baseline characteristics of the study population by different levels of cognitive reserve

Figure 2

Table 2. Hazard ratios (HRs) and 95% confidence intervals (CIs) for associations between cognitive reserve and transitions from baseline to depression, post-depression dementia, and death

Figure 3

Table 3. Hazard ratios (HRs) from Cox models and 10th percentile differences (PDs) in time (years) to incident depression/death from Laplace regression, and 95% confidence intervals (CIs) in relation to cognitive reserve.

Figure 4

Figure 2. The 10th percentile differences in years of depression-free survival in relation to cognitive reserve (CR) among (A) all participants, (B) participants aged < 60, and (C) participants aged ≥ 60.Models were adjusted for age, sex, race, smoking status, alcohol consumption, physical activity, body mass index, hypertension, diabetes, heart disease, and stroke.

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