Neuroinflammation in Schizophrenia-Related Psychosis: A PET Study

被引:463
作者
Doorduin, Janine [1 ]
de Vries, Erik F. J. [1 ]
Willemsen, Antoon T. M. [1 ]
de Groot, Jan Cees [2 ]
Dierckx, Rudi A. [1 ]
Klein, Hans C. [1 ,3 ]
机构
[1] Univ Groningen, Dept Nucl Med & Mol Imaging, Univ Med Ctr Groningen, NL-9700 RB Groningen, Netherlands
[2] Univ Groningen, Dept Radiol, Univ Med Ctr Groningen, NL-9700 RB Groningen, Netherlands
[3] Univ Groningen, Univ Ctr Psychiat, Univ Med Ctr Groningen, NL-9700 RB Groningen, Netherlands
关键词
schizophrenia; psychosis; neuroinflammation; microglia; PET; C-11-PK11195; 18 KDA TSPO; BENZODIAZEPINE-RECEPTORS; PERIPHERAL BENZODIAZEPINE; CULTURED ASTROCYTES; ADJUNCTIVE THERAPY; MICROGLIAL CELLS; ELDERLY-PATIENTS; BRAIN-INJURY; ACTIVATION; PROTEIN;
D O I
10.2967/jnumed.109.066647
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
100231 [临床病理学]; 100902 [航空航天医学];
摘要
Schizophrenia is a chronic and disabling brain disease characterized by psychotic episodes with unknown etiology. It is suggested that neuroinflammation plays a role in the pathophysiology of schizophrenia. Neuroinflammation is characterized by the activation of microglia cells, which show an increase in the expression of the peripheral benzodiazepine receptor. The isoquinoline (R)-N-C-11-methyl-N-(1-methylpropyl)-1-(2-chlorophenyl)isoquinoline-3-carboxamide (C-11-(R)-PK11195) is a peripheral benzodiazepine receptor ligand that can be used for the imaging of activated microglia cells, and thus neuroinflammation, with PET. We hypothesized that neuroinflammation would be more profound in schizophrenic patients during psychosis, and it was therefore investigated whether neuroinflammation was present in patients within the schizophrenia spectrum who were in a psychotic phase. Methods: Seven patients within the schizophrenia spectrum who were recovering from psychosis were included. Recovering psychosis was defined by a score of 5 or more on 1 item of the positive scale of the positive and negative symptoms scale (PANSS) or a score of 4 on 2 items. The patients were compared with 8 age-matched healthy volunteers. Dynamic 60-min PET scans were acquired after the injection of C-11-(R)-PK11195. All subjects underwent T1- and T2-weighted MRI, and the scans were visually examined for abnormalities and used for anatomic coregistration in data analysis. The PET data were analyzed with a 2-tissue-compartment model to calculate the binding potential, using the metabolite-corrected plasma curve as input. Results: A significantly higher binding potential of C-11-(R)-PK11195, indicative of neuroinflammation, was found in the hippocampus of schizophrenic patients than in healthy volunteers (2.07 +/- 0.42 vs. 1.37 +/- 0.30; P = 0.004). A nonsignificant 30% higher C-11-(R)-PK11195 binding potential was found in the whole-brain gray matter of schizophrenic patients. The MR images did not reveal any visual abnormalities. Conclusion: The present study suggests that focal neuroinflammation may play an important role in schizophrenia during psychosis.
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收藏
页码:1801 / 1807
页数:7
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