Association between glutamate receptor 2 polymorphisms and epilepsy in children
WANG Xian, ZHU Tian-Jiao, WAN Zhi-Ting, ZHU Xue-Mei
Department of Pediatrics, Xianning Central Hospital/First Affiliated Hospital of Hubei University of Science and Technology, Xianning, Hubei 437100, China
Abstract:Objective To investigate the association between two single nucleotide polymorphisms (SNPs), rs9390754 and rs4840200, in the glutamate receptor 2 (GRIK2) gene and the genetic susceptibility to epilepsy (EP) in the Han population in Central China. Methods A case-control study was performed in 284 EP children (including 132 children with refractory epilepsy) and 315 normal children from Central China. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was used to determine the genotypes of the two SNPs rs9390754 and rs4840200. The genotype frequency was compared between groups. Results The frequencies of GG, GA, and AA genotypes of SNP rs9390754 showed a significant difference between the EP and normal control groups (P = 0.016). The allele frequency also showed a significant difference between the two groups (P = 0.002). The frequencies of CC, CT, and TT genotypes of SNP rs4840200 and allele frequency showed no significant differences between the two groups. The C allele frequency of SNP rs4840200 in the refractory EP subgroup was significantly higher than in the non-refractory EP subgroup (OR = 1.435, 95% CI: 1.021-2.016, P = 0.037). Conclusions In the Han population in Central China, the polymorphisms of SNP rs9390754 in the GRIK2 gene may be associated with EP susceptibility, and the C allele of SNP rs4840200 may be a genetic risk factor for the development of drug resistance in children with EP.
WANG Xian,ZHU Tian-Jiao,WAN Zhi-Ting et al. Association between glutamate receptor 2 polymorphisms and epilepsy in children[J]. CJCP, 2016, 18(6): 492-495.
Guo YL, Larry W, Sham PC, et al. Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese[J]. Hum Mol Genet, 2012, 21(5): 1184-1189.
[5]
Fisher RS, van Emde Boas W, Blume W, et al. Epileptic seizures and epilepsy: definitions proposed by the International League Against Epilepsy (ILAE) and the International Bureau for Epilepsy (IBE) [J]. Epilepsia, 2005, 46(4): 470-472.
[6]
吴逊, 沈鼎烈. 难治性癫癎[J]. 中华神经科杂志, 1998, 31(1): 4.
[7]
Laqranha VL, Matte U, Carvalho TG, et al. Increased glutamate receptor and transporter expression in the cerebral cortex and striatum of gcdh-/- mice: possible implications for the neuropathology of glutaric acidemia type I[J]. PLoS One, 2014, 9(3): e90477.
[8]
Manuel M, Samuels JF, Wang Y, et al. Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS[J]. Mol Psychiatry, 2015, 20(3): 337-344.
[9]
Cordoba M, Rodiguez S, Gonzalez MD, et al. Expanding the spectrum of Grik2 mutations: intellectual disability, behavioural disorder, epilepsy and dystonia[J]. Clin Genet, 2015, 87(3): 293-295.
[10]
Lee JH, Lee JM, Ramos EM, et al. TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease[J]. Biochem Biophys Res Commun, 2012, 424(3): 404-408.
[11]
Griswold AJ, Ma D, Cukier HN, et al. Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways[J]. Hum Mol Genet, 2012, 21(15): 3513-3523.
[12]
Casey JP, Maqalhaes T, Conroy JM, et al. A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder[J]. Hum Genet, 2012, 131(4): 565-579.
[13]
Telfeian AE, Federoff HJ, Leone P, et al. Overexpression of GluR6 in rat hippocampus produces seizures and spontaneous nonsynaptic bursting in vitro[J]. Neurobiol Dis, 2000, 7(4): 362-374.