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Temporal relation between depression and cognitive impairment in old age: prospective population based study
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     1 Section of Gerontology and Geriatrics, Department of General Internal Medicine, Leiden University Medical Centre, PO Box 9600, 2300 RC Leiden, Netherlands, 2 Department of Psychiatry, Leiden University Medical Centre, Netherlands

    Correspondence to: D J Vinkers d.j.vinkers@lumc.nl

    Abstract

    Depression and cognitive impairment are among the most important mental health problems in elderly people. Both conditions have severe consequences, including diminished quality of life, functional decline, increased use of services, and high mortality.1 Late onset depression and cognitive impairment often occur together, suggesting a close association between them.2-4 It is not known, however, whether depression leads to cognitive decline or vice versa.4 5

    Clinical practice and research evidence suggest that depression precedes cognitive decline in old age.5-10 However, inferring a relationship is hampered because most studies on this topic examined only the association between depression and the subsequent development of cognitive impairment.6-14 As depression may be an early sign rather than an independent risk factor for cognitive impairment, the temporal relation between depression and cognitive impairment in old age remains unclear.

    Hitherto, only one study has investigated the temporal relation between depression and cognitive impairment in people aged 65 years and older.15 The study is limited, however, by its use of the clinical diagnosis of depression and dementia as a dichotomous endpoint. We therefore followed up 500 elderly people living in the community with annual assessments of depressive symptoms and cognitive function in order to determine their temporal relation.

    Participants and methods

    The figure shows the annual follow up visits for the 500 participants included in our study. During 1459 person-years of follow up (mean per person, 2.9 years), 39 people (8%) refused to participate in the repeated annual measurements, most of them at the first follow up visit. Of the 334 participants without significant depressive symptoms at baseline (geriatric depression scale score 2 points), 97 (29%) died and 28 (8%) declined to participate during follow up. Of the 415 non-demented participants at baseline (mini-mental state examination score 24 points), 124 (30%) died and 32 (8%) declined to participate during follow up.

    Participant flow through study

    Table 1 shows the 500 participants' demographic and clinical characteristics at baseline. Of these participants, 184 (37%) were men, 303 (61%) had only a low level of education ( 6 years of schooling), 334 (67%) had no significant depressive symptoms (geriatric depression scale score 2 points), and 415 (83%) had no serious cognitive impairment (mini-mental state exam score 24 points).

    Table 1 Demographic and clinical characteristics of 500 people aged 85 years living in the community. Values are numbers (percentages) unless stated otherwise

    Table 2 shows the cross sectional correlation between depressive symptoms and cognitive function at baseline. Depressive symptoms were significantly correlated with lower scores for global cognitive function, attention, processing speed, and immediate and delayed recall and with higher test scores for attention (indicating reduced attention) (all P < 0.001).

    Table 2 Cross sectional correlation of depressive symptoms* with various measures of cognitive function in 500 people aged 85 years living in the community

    Table 3 shows the impact of cognitive function at baseline on the course of depressive symptoms in the 334 non-depressed participants at baseline (geriatric depression scale score 2 points). An accelerated annual increase of depressive symptoms during follow up was associated with impaired attention (0.08 points (95% confidence interval 0.01 to 0.16)), poorer immediate recall (0.17 points (0.09 to 0.25)), and poorer delayed recall (0.10 points (0.02 to 0.18)) at baseline. These estimates remained similar when we included participants with a geriatric depression scale score of 2 points (data not shown).

    Table 3 Impact of cognitive function at baseline on depressive symptoms from age 85 to 89 years in 334 people living in the community without depressive symptoms at baseline (GDS-15 score 2 points). Impact is additional annual increase of depressive symptoms score per SD of cognitive function test score at baseline (2.65 for global cognitive function, 31.59 for attention, 7.08 for processing, 5.72 for immediate recall, and 2.74 for delayed recall)

    Table 4 shows the impact of depressive symptoms at baseline on the course of cognitive function in the 415 non-demented participants at baseline (mini-mental state exam 24 points). Depressive symptoms at baseline were not associated with an accelerated cognitive decline during follow up (P > 0.05). These estimates remained similar when we included participants with a mini-mental state exam score 24 points (data not shown).

    Table 4 Impact of depressive symptoms at baseline (GDS-15 score) on cognitive decline from age 85 to 89 years in 415 people living in the community without cognitive impairment at baseline (MMSE score 24 points). Impact is additional annual impact on cognitive function per SD of mean GDS-15 score at baseline (2.11)

    Discussion

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