Association of catechol-O-methyltransferase Val(108/158) Met genetic polymorphism with schizophrenia, P50 sensory gating, and negative symptoms in a Chinese population

• Published in: Psychiatry research Vol. 242; p. 271
• Main Authors: Mao, Qiao, Tan, Yun-Long, Luo, Xing-Guang, Tian, Li, Wang, Zhi-Ren, Tan, Shu-Ping, Chen, Song, Yang, Gui-Gang, An, Hui-Mei, Yang, Fu-De, Zhang, Xiang-Yang
• Format: Journal Article
• Language: English
• Published: Ireland 30.08.2016
• Subjects: Adult; Alleles; Asian Continental Ancestry Group - genetics; Case-Control Studies; Catechol O-Methyltransferase - genetics; Catechol O-Methyltransferase - metabolism; China; Dopamine - metabolism; Female; Genotype; Humans; Male; Middle Aged; Polymorphism, Genetic; Prefrontal Cortex - metabolism; Schizophrenia - genetics; Schizophrenia - physiopathology; Schizophrenic Psychology; Sensory Gating - genetics; Schizophrenia; Biomarker; Sensory gating; COMT; Negative symptom
• ISSN: 1872-7123; 1872-7123
• DOI: 10.1016/j.psychres.2016.04.029

Catechol-O-methyltransferase (COMT), an enzyme involved in the degradation and inactivation of the neurotransmitter dopamine, is associated with the sensory gating phenomenon, protecting the cerebral cortex from information overload. The COMT Val(108/158)Met polymorphism is essential for prefrontal cortex processing capacity and efficiency. The current study was designed to investigate the role of COMT Val(108/158)Met polymorphism in development, sensory gating deficit, and symptoms of schizophrenia in Han Chinese population. P50 gating was determined in 139 schizophrenic patients and 165 healthy controls. Positive and Negative Syndrome Scale (PANSS) was used to assess the clinical symptomatology in 370 schizophrenic subjects. COMT Val(108/158)Met polymorphism was genotyped by PCR-restriction fragment length polymorphism (PCR-RFLP). No significant differences in COMT allele and genotype distributions were observed between schizophrenic patients and control groups. Although P50 deficits were present in patients, there was no evidence for an association between COMT Val(108/158)Met polymorphism and the P50 biomarker. Moreover, PANSS negative subscore was significantly higher in Val allele carriers than in Met/Met individuals. The present findings suggest that COMT Val(108/158)Met polymorphism may not contribute to the risk of schizophrenia and to the P50 deficits, but may contribute to the negative symptoms of schizophrenia among Han Chinese.