Journal
BRAIN BEHAVIOR AND IMMUNITY
Volume 32, Issue -, Pages 105-111Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbi.2013.03.001
Keywords
Schizophrenia; Cognition; Interleukin-18; Immune function; Psychopathology
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Funding
- Wenzhou Science and Technology Bureau [Y20100324]
- National Natural Science Foundation of China [81000509]
- Beijing Municipal Excellent Talents Foundation [2010D003034000032]
- Stanley Medical Research Institute [03T-459, 05T-726]
- United States National Institute of Health [K05-DA0454, P50-DA18827, U01-MH79639]
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Alterations in the inflammatory and immune systems have been documented to occur from the earliest stages of schizophrenia, and have been associated with neurodevelopmental changes. Cognitive impairment is a core feature in the pathology of schizophrenia, and recent studies showed a significant increase in serum IL-18 in schizophrenia, and a putative role of IL-18 in neuroprogression and thus neurocognitive defects. The purpose of this study was to examine the association of IL-18 with cognitive deficits in schizophrenia. We recruited 77 first episode and drug naive schizophrenic patients and 75 healthy control subjects and examined the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) and serum IL-18 in both groups. Schizophrenic symptoms were assessed using the positive and negative syndrome scale (PANSS). We found that IL-18 levels were non-significantly higher in patients than controls (206.0 +/- 92.9 pg/ml vs 193.2 +/- 41.8 pg/ml, p = 0.28). Cognitive scores on the RBANS and nearly all of its five subscales (all p < 0.05) except for the Visuospatial/Constructional index (p > 0.05) were significantly lower in schizophrenic patients than normal controls. For the patients, IL-18 was positively associated with the Visuospatial/Constructional domain of cognitive deficits in schizophrenia. Our findings suggest that cognitive deficits occur during the acute stage of a schizophrenic episode, and IL-18 may be involved in Visuospatial/Constructional deficits of these patients. (C) 2013 Elsevier Inc. All rights reserved.
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