Late-onset major depression: clinical and treatment-response variability

被引:48
作者
Driscoll, HC
Basinski, J
Mulsant, BH
Butters, MA
Dew, MA
Houck, PR
Mazumdar, S
Miller, MD
Pollock, BG
Stack, JA
Schlernitzauer, MA
Reynolds, CR
机构
[1] Western Psychiat Inst & Clin, Intervent Res Ctr Late Life Mood Disorders, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Biostat, Pittsburgh, PA USA
关键词
major depression; late-onset; treatment outcome;
D O I
10.1002/gps.1334
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
Objective To explore clinical and treatment-response variability in late-onset vs early-onset non-bipolar, non-psychotic major depression. Methods We grouped patients from alate-life depression treatment study according to illness-course characteristics: those with early-onset, recurrent depression (n = 59), late-onset, recurrent depression (n = 27), and late-onset, single-episode depression (n = 95). Early-onset was defined as having a first lifetime episode of major depression at age 59 or earlier; late-onset was defined as having a first episode of major depression at age 60 or later. We characterized the three groups of patients with respect to baseline demographic, neuropsychological, and clinical characteristics, use of augmentation pharmacotherapy to achieve response, and treatment outcomes. Results Rates of response, remission, relapse, and termination were similar in all three groups; however, patients with late-onset, recurrent major depression took longer to respond to treatment than those with late-onset, single-episode depression (12 weeks vs 8 weeks) and had more cognitive and functional impairment. Additionally, patients with recurrent depression (whether early or late) were more likely to require pharmacotherapy augmentation to achieve response than patients with a single lifetime episode. Conclusion Late-onset, recurrent depression takes longer to respond to treatment than late-onset single-episode depression and is more strongly associated with cognitive and functional impairment. Further study of biological, neuropsychologic, and psychosocial correlates of late-onset, recurrent depression is needed. Copyright (c) 2005 John Wiley & Sons, Ltd.
引用
收藏
页码:661 / 667
页数:7
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