Cross-sectional and prospective inter-relationships between depressive symptoms, vascular disease and cognition in older adults

被引:4
|
作者
Mewton, Louise [1 ]
Reppermund, Simone [2 ,3 ]
Crawford, John [2 ]
Bunce, David [2 ,4 ]
Wenz, Wei [2 ,5 ]
Sachdev, Perminder [2 ,5 ]
机构
[1] Univ New South Wales, Ctr Res Excellence Mental Hlth & Subst Use, Natl Drug & Alcohol Res Ctr, Sydney, NSW, Australia
[2] Univ New South Wales, UNSW Med, Ctr Hlth Brain Ageing, Sch Psychiat, Sydney, NSW, Australia
[3] Univ New South Wales, Dept Dev Disabil Neuropsychiat, UNSW Med, Sydney, NSW, Australia
[4] Univ Leeds, Fac Med & Hlth, Sch Psychol, Leeds, W Yorkshire, England
[5] Prince Wales Hosp, Neuropsychiat Inst, Sydney, NSW, Australia
基金
英国医学研究理事会;
关键词
Cognition; cohort study; depression; vascular disease; LATE-LIFE DEPRESSION; PROBLEM-SOLVING THERAPY; SMALL-VESSEL DISEASE; EXECUTIVE DYSFUNCTION; GERIATRIC DEPRESSION; ANTIDEPRESSANT-TREATMENT; POSTSTROKE DEPRESSION; ELDERLY POPULATION; SUPPORTIVE THERAPY; TREATMENT RESPONSE;
D O I
10.1017/S0033291718002994
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Background It has been proposed that vascular disease is the mechanism linking depression and cognition, but prospective studies have not supported this hypothesis. This study aims to investigate the inter-relationships between depressive symptoms, cognition and cerebrovascular disease using a well-characterised prospective cohort. Method Data came from waves 1 (2005-2007) and 2 (2007-2009) of the Sydney Memory and Ageing Study (n = 462; mean age = 78.3 years). Results At wave 1, there was an association between depressive symptoms and white matter hyperintensity (WMH) volume [b = 0.016, t((414)) = 2.34, p = 0.020]. Both depressive symptoms [b = -0.058, t((413)) = -2.64, p = 0.009] and WMH volume [b = -0.011, t((413)) = -3.77, p < 0.001], but not stroke/transient ischaemic attack (TIA) [b = -0.328, t((413)) = -1.90, p = 0.058], were independently associated with lower cognition. Prospectively, cerebrovascular disease was not found to predict increasing depressive symptoms [stroke/TIA: b = -0.349, t((374.7)) = -0.76, p = 0.448; WMH volume: b = 0.007, t((376.3)) = 0.875, p = 0.382]. Depressive symptoms predicted increasing WMH severity [b = 0.012, t((265.9)) = -3.291, p = 0.001], but not incident stroke/TIA (odds ratio = 0.995; CI 0.949-1.043; p = 0.820). When examined in separate models, depressive symptoms [b = -0.027, t((373.5)) = -2.16, p = 0.032] and a history of stroke/TIA [b = -0.460, t((361.2)) = -4.45, p < 0.001], but not WMH volume [b = 0.001, t((362.3)) = -0.520, p = 0.603], predicted declines in cognition. When investigated in a combined model, a history of stroke/TIA remained a predictor of cognitive decline [b = -0.443, t((360.6)) = -4.28, p < 0.001], whilst depressive symptoms did not [b = -0.012, t((359.7)) = -0.96, p = 0.336]. Conclusions This study is contrasted with previous prospective studies which indicate that depressive symptoms predict cognitive decline independently of vascular disease. Future research should focus on further exploring the vascular mechanisms underpinning the relationship between depressive symptoms and cognition.
引用
收藏
页码:2168 / 2176
页数:9
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