Investigation of autism and GABA receptor subunit genes in multiple ethnic groups

• Published in: Neurogenetics 2006-07, Vol.7 (3), p.167-174
• Main Authors: COLLINS, Ann L, DEQIONG MA, PERICAK-VANCE, Margaret A, WHITEHEAD, Patrice L, MARTIN, Eden R, WRIGHT, Harry H, ABRAMSON, Ruth K, HUSSMAN, John P, HAINES, Jonathan L, CUCCARO, Michael L, GILBERT, John R
• Format: Article
• Language: English
• Subjects: Autism; Autistic Disorder - genetics; Biological and medical sciences; Brain; Child clinical studies; Developmental disorders; Ethnic Groups; Ethnicity; Gene Frequency; General aspects. Genetic counseling; Genes; Genetic Predisposition to Disease; Genetic Testing; Genetic Variation; Genotype & phenotype; Haplotypes; Humans; Infantile autism; Linkage Disequilibrium; Medical genetics; Medical sciences; Original; Polymorphism, Single Nucleotide; Psychology. Psychoanalysis. Psychiatry; Psychopathology. Psychiatry; Receptors, GABA - genetics
• ISSN: 1364-6745; 1364-6753
• DOI: 10.1007/s10048-006-0045-1

Autism is a neurodevelopmental disorder of complex genetics, characterized by impairment in social interaction and communication, as well as repetitive behavior. Multiple lines of evidence, including alterations in levels of GABA and GABA receptors in autistic patients, indicate that the GABAergic system, which is responsible for synaptic inhibition in the adult brain, may be involved in autism. Previous studies in our lab indicated association of noncoding single nucleotide polymorphisms (SNPs) within a GABA receptor subunit gene on chromosome 4, GABRA4, and interaction between SNPs in GABRA4 and GABRB1 (also on chromosome 4), within Caucasian autism patients. Studies of genetic variation in African-American autism families are rare. Analysis of 557 Caucasian and an independent population of 54 African-American families with 35 SNPs within GABRB1 and GABRA4 strengthened the evidence for involvement of GABRA4 in autism risk in Caucasians (rs17599165, p=0.0015; rs1912960, p=0.0073; and rs17599416, p=0.0040) and gave evidence of significant association in African-Americans (rs2280073, p=0.0287 and rs16859788, p=0.0253). The GABRA4 and GABRB1 interaction was also confirmed in the Caucasian dataset (most significant pair, rs1912960 and rs2351299; p=0.004). Analysis of the subset of families with a positive history of seizure activity in at least one autism patient revealed no association to GABRA4; however, three SNPs within GABRB1 showed significant allelic association; rs2351299 (p=0.0163), rs4482737 (p=0.0339), and rs3832300 (p=0.0253). These results confirmed our earlier findings, indicating GABRA4 and GABRB1 as genes contributing to autism susceptibility, extending the effect to multiple ethnic groups and suggesting seizures as a stratifying phenotype.