Prognosis of late life depression: a three-year cohort study of outcome and potential predictors

被引:34
作者
Baldwin, RC
Gallagley, A
Gourlay, M
Jackson, A
Burns, A
机构
[1] Manchester Royal Infirm, Manchester Mental Hlth & Social Care Trust, Manchester M13 9WL, Lancs, England
[2] Wythenshawe Hosp, Manchester M23 9LT, Lancs, England
[3] Univ Manchester, Dept Image Sci & Biomed Engn, Manchester M13 9PL, Lancs, England
[4] Wythenshawe Hosp, Sch Psychiat & Behav Sci, Manchester M23 9LT, Lancs, England
关键词
depression; geriatric; vascular risk; prognosis;
D O I
10.1002/gps.1424
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Background Late-onset depression (LOD) has a poor prognosis which may be worsened by the presence of cerebrovascular disease. Few studies have explored prospectively the influence of vascular risk factors on longer term prognosis. Methods The original study involved 50 patients with LOD and 35 healthy age matched controls. Follow-up was at three years. Baseline measures included clinical, neuroradiological and neuropsychological variables. Outcome was assessed by mortality, progression to dementia and clinical course of depressive disorder. Results Sixty-two (73%) of the original cohort agreed to be re-interviewed. Seven participants had died (all from the depressed group) and six developed dementia, all but one from the depressed group. Vascular dementia predominated (although not significantly so) among those with dementia at follow-up. For 28 depressed patients with complete follow-up data (56% of the original sample), poor outcome was predicted by lower High Density Lipoprotein (HDL), raised Erythrocyte Sedimentation Rate (ESR) and a higher score on the Hachinski Index scale and one test of immediate memory. Initial response to treatment was not associated with later outcome. Conclusion Late-onset depressive disorder is associated with a high rate of mortality and possibly dementia. Biochemical and inflammatory markers may be important in prognosis and their role should be confirmed in future studies. Copyright (c) 2005 John Wiley & Sons, Ltd.
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页码:57 / 63
页数:7
相关论文
共 47 条
[1]  
Abas M, 2002, BRIT J PSYCHIAT, V181, P123
[2]  
ALEXOPOULOS GS, 1993, AM J PSYCHIAT, V150, P1693
[3]  
Alexopoulos GS, 1997, ARCH GEN PSYCHIAT, V54, P915
[4]  
American Psychiatric Association (APA), 1994, DIAGN STAT MAN, V4th
[5]  
[Anonymous], 1979, Schedule for affective disorders and schizophrenia
[6]   Neurological findings in late-onset depressive disorder: comparison of individuals with and without depression [J].
Baldwin, R ;
Jeffries, S ;
Jackson, A ;
Sutcliffe, C ;
Thacker, N ;
Scott, M ;
Burns, A .
BRITISH JOURNAL OF PSYCHIATRY, 2005, 186 :308-313
[7]   Treatment response in late-onset depression: relationship to neuropsychological, neuroradiological and vascular risk factors [J].
Baldwin, R ;
Jeffries, S ;
Jackson, A ;
Sutcliffe, C ;
Thacker, N ;
Scott, M ;
Burns, A .
PSYCHOLOGICAL MEDICINE, 2004, 34 (01) :125-136
[8]  
Baldwin RC, 2000, INT J GERIATR PSYCH, V15, P1097, DOI 10.1002/1099-1166(200012)15:12<1097::AID-GPS251>3.0.CO
[9]  
2-N
[10]   THE PROGNOSIS OF DEPRESSION IN OLD-AGE [J].
BALDWIN, RC ;
JOLLEY, DJ .
BRITISH JOURNAL OF PSYCHIATRY, 1986, 149 :574-583