Schizophrenic patients without neuropsychological deficits: subgroup, disease severity or cognitive compensation?

被引:66
作者
Holthausen, EAE
Wiersma, D
Sitskoorn, MM
Hijman, R
Dingemans, PM
Schene, AH
van den Bosch, RJ
机构
[1] Univ Groningen Hosp, Dept Psychiat, NL-9700 RB Groningen, Netherlands
[2] Univ Utrecht, Med Ctr, NL-3584 CX Utrecht, Netherlands
[3] Univ Hosp Amsterdam, NL-1105 BC Amsterdam, Netherlands
关键词
cognition; neuropsychology; schizophrenia;
D O I
10.1016/S0165-1781(02)00184-1
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Some schizophrenic patients do not show clinically relevant cognitive deficits. The question remains whether this represents the existence of an etiologically different subgroup, a general effect of disease severity or whether their cognitive deficits do not reach a clinical threshold due to a greater cognitive compensation ('brain reserve') capacity. A group of 23 out of 118 first onset patients was identified as cognitively normal (CN). The cognitive profile of these patients was compared with that of 45 healthy controls. Next these patients were compared with the cognitively impaired (0) patients on obstetric complications (OCs), premorbid adjustment, age at onset, Positive and Negative Syndrome Scale ratings, social functioning and substance abuse. In addition both groups were compared on intelligence and educational level as indirect indicators of cognitive compensation capacity. There were no differences in OCs, premorbid adjustment, age at onset, psychopathology or substance abuse between the two patient groups. There was a significant difference in social functioning, which is a consequence rather than a cause of cognitive deficits. However, the CN patients scored significantly higher on measures of intelligence and educational level than the CI patients. This suggests that a difference in cognitive compensation capacity could explain the existence of a CN patient group. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
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页码:1 / 11
页数:11
相关论文
共 50 条
[31]   IS SCHIZOPHRENIA A NEURODEVELOPMENTAL DISORDER [J].
MURRAY, RM ;
LEWIS, SW .
BRITISH MEDICAL JOURNAL, 1987, 295 (6600) :681-682
[32]   GENES, VIRUSES AND NEURODEVELOPMENTAL SCHIZOPHRENIA [J].
MURRAY, RM ;
JONES, P ;
OCALLAGHAN, E ;
TAKEI, N ;
SHAM, P .
JOURNAL OF PSYCHIATRIC RESEARCH, 1992, 26 (04) :225-235
[33]   Is it possible to be schizophrenic yet neuropsychologically normal? [J].
Palmer, BW ;
Heaton, RK ;
Paulsen, JS ;
Kuck, J ;
Braff, D ;
Harris, MJ ;
Zisook, S ;
Jeste, DV .
NEUROPSYCHOLOGY, 1997, 11 (03) :437-446
[34]   Cognitive and behavioural functioning in men with schizophrenia both before and shortly after first admission to hospital - Cross-sectional analysis [J].
Rabinowitz, J ;
Reichenberg, A ;
Weiser, M ;
Mark, M ;
Kaplan, Z ;
Davidson, M .
BRITISH JOURNAL OF PSYCHIATRY, 2000, 177 :26-32
[35]  
Rey A., 1964, L'examen Clinique en Psychologie
[36]  
Satz P., 1993, Neuropsychology, V7, P273, DOI [DOI 10.1037/0894-4105.7.3.273, 10.1037/0894-4105.7.3.273]
[37]  
SAYKIN AJ, 1994, ARCH GEN PSYCHIAT, V51, P124
[38]  
SAYKIN AJ, 1991, ARCH GEN PSYCHIAT, V48, P618
[39]   The effects of intelligence and education on the development of dementia. A test of the brain reserve hypothesis [J].
Schmand, B ;
Smit, JH ;
Geerlings, MI ;
Lindeboom, J .
PSYCHOLOGICAL MEDICINE, 1997, 27 (06) :1337-1344
[40]   Alzheimer's disease and brain reserve [J].
Schofield, P .
AUSTRALASIAN JOURNAL ON AGEING, 1999, 18 (01) :10-14