Working memory functioning in schizophrenia patients and their first-degree relatives: cognitive functioning shedding light on etiology

被引:96
作者
Conklin, HA
Curtis, CE
Calkins, ME
Iacono, WG
机构
[1] Univ Minnesota, Dept Psychol, Minneapolis, MN 55455 USA
[2] Univ Penn, Dept Psychiat, Philadelphia, PA 19104 USA
[3] NYU, Dept Psychol, New York, NY 10003 USA
[4] Kennedy Krieger Inst, Dept Neuropsychol, Baltimore, MD 21231 USA
关键词
dorsolateral prefrontal cortex (DLPFC); endophenotype; domain-specific; process-specific; central executive; schizotypy;
D O I
10.1016/j.neuropsychologia.2004.09.013
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
There is accumulating evidence for involvement of the prefrontal cortex (PFC) in the pathophysiology of schizophrenia. A primary function supported by the PFC is working memory (WM). Findings from WM studies in schizophrenia can provide insight into the nature of clinical symptoms and cognitive deficits associated with this disorder, as well as begin to suggest areas of underlying neuropathology. To date, studies have not adequately investigated different WM domains (e.g., verbal, spatial, or object) or processing requirements (e.g., maintenance, monitoring, or manipulation), shown to be associated with distinct patterns of neural activation, in schizophrenia patients and their well relatives. Accordingly, this study evaluated the performance of schizophrenia patients, their first-degree biological relatives, and nonpsychiatric controls on a comprehensive battery of WM tasks and investigated the association among WM deficits and schizophrenia-spectrum psychopathology. The findings indicate that schizophrenia patients are consistently impaired on WM tasks, irrespective of WM domain or processing requirements. In contrast, their unaffected relatives are only impaired on WM tasks with higher central executive processing requirements. This pattern of WM performance may further implicate DLPFC dysfunction in the liability for schizophrenia and has implications for future cognitive, genetic, and neurodevelopmental research. (c) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:930 / 942
页数:13
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