Association study of polymorphisms in the neutral amino acid transporter genes SLC1A4, SLC1A5 and the glycine transporter genes SLC6A5, SLC6A9with schizophrenia

• Published in: BMC Psychiatry Vol. 8; no. 1
• Main Authors: Deng, Xiangdong, Sagata, Noriaki, Takeuchi, Naoko, Tanaka, Masami, Ninomiya, Hideaki, Iwata, Nakao, Ozaki, Norio, Shibata, Hiroki, Fukumaki, Yasuyuki
• Format: Journal Article
• Language: English; Japanese
• Published: London Springer Science and Business Media LLC 18.07.2008; BioMed Central
• Subjects: Alleles; Amino Acid Transport System ASC; Case-Control Studies; Exons; Female; Genotype; Glycine Plasma Membrane Transport Proteins; Haplotypes; Hartnup Disease; Humans; Male; Medicine; Medicine & Public Health; Middle Aged; Minor Histocompatibility Antigens; Polymorphism, Genetic; Psychiatry; Psychiatry and Mental health; Psychotherapy; RC435-571; Research Article; Schizophrenia; Schizophrenia; Neutral Amino Acid Transporter; Copy Number Variation; Haplotype Association; Linkage Disequilibrium
• ISSN: 1471-244X; 1471-244X
• DOI: 10.1186/1471-244x-8-58

Background Based on the glutamatergic dysfunction hypothesis for schizophrenia pathogenesis, we have been performing systematic association studies of schizophrenia with the genes involved in glutametergic transmission. We report here association studies of schizophrenia with SLC1A4 , SLC1A5 encoding neutral amino acid transporters ASCT1, ASCT2, and SLC6A5 , SLC6A9 encoding glycine transporters GLYT2, GLYT1, respectively. Methods We initially tested the association of 21 single nucleotide polymorphisms (SNPs) distributed in the four gene regions with schizophrenia using 100 Japanese cases-control pairs and examined allele, genotype and haplotype association with schizophrenia. The observed nominal significance were examined in the full-size samples (400 cases and 420 controls). Results We observed nominally significant single-marker associations with schizophrenia in SNP2 ( P = 0.021) and SNP3 ( P = 0.029) of SLC1A4 , SNP1 ( P = 0.009) and SNP2 ( P = 0.022) of SLC6A5 . We also observed nominally significant haplotype associations with schizophrenia in the combinations of SNP2-SNP7 ( P = 0.037) of SLC1A4 and SNP1-SNP4 ( P = 0.043) of SLC6A5 . We examined all of the nominal significance in the Full-size Sample Set, except one haplotype with insufficient LD. The significant association of SNP1 of SLC6A5 with schizophrenia was confirmed in the Full-size Sample Set ( P = 0.018). Conclusion We concluded that at least one susceptibility locus for schizophrenia may be located within or nearby SLC6A5 , whereas SLC1A4 , SLC1A5 and SLC6A9 are unlikely to be major susceptibility genes for schizophrenia in the Japanese population.