Support for the vascular depression hypothesis in late-life depression: results of a 2-site, prospective, antidepressant treatment trial.

Support for the vascular depression hypothesis in late-life depression: results of a 2-site, prospective, antidepressant treatment trial.
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DOI:
10.1001/archgenpsychiatry.2009.204
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发表时间:
2010-03
影响因子:
--
通讯作者:
Doraiswamy PM
Doraiswamy PM
中科院分区:
其他
文献类型:
--
作者:
Sheline YI;Pieper CF;Barch DM;Welsh-Bohmer K;McKinstry RC;MacFall JR;D'Angelo G;Garcia KS;Gersing K;Wilkins C;Taylor W;Steffens DC;Krishnan RR;Doraiswamy PM

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Research on “vascular depression” has used two approaches to subtype late life depression (LLD) based on executive dysfunction or white matter hyperintensity (WMH) severity. Evaluate the relationship of neuropsychological performance and WMH to clinical response in LLD. 2-site prospective nonrandomized controlled trial. Outpatient clinics at Washington University and Duke University. 217 subjects age ≥ 60 met DSM-IV criteria for major depression, scored ≥ 20 (MADRS), received vascular risk factor (VRF) scores, neuropsychological testing and MRI scan; were excluded for cognitive impairment or severe medical disorders. Fazekas rating was conducted to grade WMH lesions. 12 weeks of sertraline treatment, titrated by clinical response. Montgomery-Asberg Depression Rating Scale (MADRS) score over time. Baseline neuropsychological factor scores correlated negatively with baseline Fazekas scores. A mixed model examined effects of predictor variables on MADRS scores over time. Baseline episodic memory (p = 0.002); language (p = 0.007); working memory (p = 0.01); processing speed (p = 0.0001); executive function factor scores (p = 0.002), and categorical Fazekas ratings (p = 0.049) predicted MADRS scores, controlling for age, education, age of onset and race. Controlling for baseline MADRS scores these factors remained significant predictors of decrease in MADRS scores except working memory and Fazekas ratings. 33% of subjects achieved remission (MADRS ≤ 7). Remitters differed from non-remitters in baseline cognitive processing speed, executive function, language, episodic memory and VRF scores. Comprehensive neuropsychological function and WMH severity predicted MADRS scores prospectively over a 12 week SSRI treatment course in LLD. Baseline neuropsychological function differentiated remitters from non-remitters and predicted time to remission in a proportional hazards model. Predictor variables correlated highly with VRF severity. These data support the vascular depression hypothesis and highlight the importance of linking subtypes based on neuropsychological function and white matter integrity.
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