The NRG1 exon 11 missense variant is not associated with autism in the Central Valley of Costa Rica

• Main Authors: Fallas Marietha, Esquivel Marcela, Jimenez Patricia, Nakamine Alisa, Ouchanov Leonid, McInnes Lynne A, Monge Silvia, Bondy Pamela, Manghi Elina R
• Format: Article
• Language: English
• Published: BMC 2007-05-01
• Series: BMC Psychiatry
• Online Access: http://www.biomedcentral.com/1471-244X/7/21

<p>Abstract</p> <p>Background</p> <p>We are conducting a genetic study of autism in the isolated population of the Central Valley of Costa Rica (CVCR). A novel Neuregulin 1 (NRG1) missense variant (exon 11 G>T) was recently associated with psychosis and schizophrenia (SCZ) in the same population isolate.</p> <p>Methods</p> <p>We genotyped the NRG1 exon 11 missense variant in 146 cases with autism, or autism spectrum disorder, with CVCR ancestry, and both parents when available (N = 267 parents) from 143 independent families. Additional microsatellites were genotyped to examine haplotypes bearing the exon 11 variant.</p> <p>Results</p> <p>The NRG1 exon 11 G>T variant was found in 4/146 cases including one de novo occurrence. The frequency of the variant in case chromosomes was 0.014 and 0.045 in the parental non-transmitted chromosomes. At least 6 haplotypes extending 0.229 Mb were associated with the T allele. Three independent individuals, with no personal or family history of psychiatric disorder, shared at least a 1 megabase haplotype 5' to the T allele.</p> <p>Conclusion</p> <p>The NRG1 exon 11 missense variant is not associated with autism in the CVCR.</p>