Patterns of memory impairment in bipolar disorder and unipolar major depression

被引:131
作者
Bearden, Carrie E.
Glahn, David C.
Monkul, E. Serap
Barrett, Jennifer
Najt, Pablo
Villarreal, Veronica
Soares, Jair C.
机构
[1] Univ Calif Los Angeles, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90095 USA
[2] Univ Texas, Hlth Sci Ctr, Dept Psychiat, Div Schizophrenia & Related Disorders, San Antonio, TX 78229 USA
[3] Dokuz Eylul Univ, Sch Med, Dept Psychiat, TR-35340 Izmir, Turkey
[4] Univ Texas, Hlth Sci Ctr, Div Mood & Anxiety Disorders, Dept Psychiat, San Antonio, TX 78229 USA
[5] S Texas Vet Hlth Care Syst, Audie L Murphy Div, San Antonio, TX 78229 USA
关键词
mood disorder; clinical state; declarative memory; cognition; bipolar depression; unipolar depression;
D O I
10.1016/j.psychres.2005.08.010
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Unipolar and bipolar depression are known to exert detrimental effects on learning and memory processes. However, few comparisons have been undertaken between bipolar and unipolar patients with comparable illness histories, and predictors of impairment are not well understood. Adult outpatients with unipolar major depressive illness (UP, n = 30) and bipolar disorder (BP, n = 30), group-matched for illness duration and severity of depressive symptomatology (16% clinically remitted, 42% partially remitted, 42% depressed), and 30 demographically matched controls completed measures of general cognitive functioning and declarative memory. Despite comparable general intellectual abilities, BP and UP patients exhibited significant memory deficits relative to healthy controls. A similar deficit profile was observed in both patient groups, involving poorer verbal recall and recognition. Impairments were not secondary to strategic processing deficits or rapid forgetting. Although depression severity was not associated with neurocognitive performance, number of hospitalizations and family history of mood disorder significantly affected memory function in BP, but not UP, patients. Results suggest qualitatively similar patterns of memory impairment in BP and UP patients, consistent with a primary encoding deficit. These impairments do not appear to be secondary to clinical state, but rather suggest a similar underlying pathophysiology involving medial temporal dysfunction. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:139 / 150
页数:12
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