Dementia risk estimates associated with measures of depression: a systematic review and meta-analysis

被引:156
|
作者
Cherbuin, Nicolas [1 ]
Kim, Sarang [1 ]
Anstey, Kaarin J. [1 ]
机构
[1] Australian Natl Univ, Ctr Res Ageing Hlth & Wellbeing, Res Sch Populat Hlth, Canberra, ACT, Australia
来源
BMJ OPEN | 2015年 / 5卷 / 12期
基金
澳大利亚国家健康与医学研究理事会;
关键词
CES-D; Late-life depression; Alzheimer's disease; Vascular dementia; Meta-regression; DSM-IV; MILD COGNITIVE IMPAIRMENT; PRIMARY-CARE PATIENTS; ALZHEIMERS-DISEASE; LATE-LIFE; TEMPORAL RELATIONSHIP; INCIDENT DEMENTIA; SYMPTOMS; PREDICTORS; GENOTYPE; ATROPHY;
D O I
10.1136/bmjopen-2015-008853
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives To perform a systematic review of reported HRs of all cause dementia, Alzheimer's disease (AD) and vascular dementia (VaD) for late-life depression and depressive symptomatology on specific screening instruments at specific thresholds. Design Meta-analysis with meta-regression. Setting and participants PubMed, PsycInfo, and Cochrane databases were searched through 28 February 2014. Articles reporting HRs for incident all-cause dementia, AD and VaD based on published clinical criteria using validated measures of clinical depression or symptomatology from prospective studies of general population of adults were selected by consensus among multiple reviewers. Studies that did not use clinical dementia diagnoses or validated instruments for the assessment of depression were excluded. Data were extracted by two reviewers and reviewed by two other independent reviewers. The most specific analyses possible using continuous symptomatology ratings and categorical measures of clinical depression focusing on single instruments with defined reported cut-offs were conducted. Primary outcome measures HRs for all-cause dementia, AD, and VaD were computed where possible for continuous depression scores, or for major depression assessed with single or comparable validated instruments. Results Searches yielded 121301 articles, of which 36 (0.03%) were eligible. Included studies provided a combined sample size of 66532 individuals including 6593 cases of dementia, 2797 cases of AD and 585 cases of VaD. The increased risk associated with depression did not significantly differ by type of dementia and ranged from 83% to 104% for diagnostic thresholds consistent with major depression. Risk associated with continuous depression symptomatology measures were consistent with those for clinical thresholds. Conclusions Late-life depression is consistently and similarly associated with a twofold increased risk of dementia. The precise risk estimates produced in this study for specific instruments at specified thresholds will assist evidence-based medicine and inform policy on this important population health issue.
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页数:13
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