Association of AKT1 gene polymorphisms with risk of schizophrenia and with response to antipsychotics in the Chinese population

• Published in: The journal of clinical psychiatry Vol. 68; no. 9; p. 1358
• Main Authors: Xu, Ming-Qing, Xing, Qing-He, Zheng, Yong-Lan, Li, Sheng, Gao, Jian-Jun, He, Guang, Guo, Ting-Wei, Feng, Guo-Yin, Xu, Feng, He, Lin
• Format: Journal Article
• Language: English
• Published: United States 01.09.2007
• Subjects: Adult; Age of Onset; Antipsychotic Agents - adverse effects; Antipsychotic Agents - therapeutic use; Asian Continental Ancestry Group - genetics; Basal Ganglia Diseases - chemically induced; Basal Ganglia Diseases - ethnology; China; Chlorpromazine - adverse effects; Chlorpromazine - therapeutic use; Chromosomes, Human, Pair 14 - genetics; DNA Primers - genetics; Female; Gene Expression - genetics; Gene Frequency; Genotype; Haplotypes - genetics; Humans; Male; Neuronal Plasticity - physiology; Polymorphism, Genetic - genetics; Proto-Oncogene Proteins c-akt - genetics; Schizophrenia - drug therapy; Schizophrenia - ethnology; Schizophrenia - genetics; Signal Transduction - genetics; China
• ISSN: 1555-2101
• DOI: 10.4088/JCP.v68n0906

A number of studies have pointed to the involvement of AKT signaling pathways in the etiology of schizophrenia. The purpose of this study was to determine whether the AKT1 gene is involved in the etiology of schizophrenia and whether it affects therapeutic outcomes in the Chinese population. Five single nucleotide polymorphisms (SNPs) were genotyped among 384 schizophrenic patients (DSM-IV criteria) and 384 healthy controls from the Chinese population. We systematically analyzed the association of the AKT1 gene with schizophrenia on the basis of sex, age at onset, therapeutic response to typical antipsychotics and atypical antipsychotics, and presence or absence of extrapyramidal syndrome. The study was conducted from May 2004 to June 2006. We found a positive association of the G allele of the SNP marker rs3803300 with schizophrenia (p = .003), both in early-onset and late-onset subjects, and that a haplotype A-G-C-G-A constructed by the 5 SNPs showed significant association (p = .00004886). However, we found no relationship between any of the 5 SNP markers and therapeutic response to typical and atypical antipsychotics and chlorpromazine-induced extrapyramidal syndrome. Our study suggests that AKT1 is a susceptibility gene for schizophrenia in the Chinese population and that the AKT1 gene may play no major role in the therapeutic response to antipsychotics or in chlorpromazine-induced extrapyramidal syndrome.