Polymorphisms in the GRIA1 gene region in psychotic bipolar disorder.

TitlePolymorphisms in the GRIA1 gene region in psychotic bipolar disorder.
Publication TypeJournal Article
Year of Publication2009
AuthorsKerner, B, Jasinska AJ, Deyoung J, Almonte M, Choi O-W, Freimer NB
JournalAmerican journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Volume150B
Issue1
Pagination24-32
Date Published2009 Jan 5
ISSN1552-485X
KeywordsBipolar disorder, Chromosomes, Human, Pair 5, Genotype, Humans, Polymorphism, Single Nucleotide, Receptors, AMPA
Abstract

We reported previously a significant linkage signal between psychotic bipolar disorder (BP) and microsatellite markers on chromosome 5q31-34 in the National Institute of Mental Health Bipolar Genetics Initiative (NIMH-BPGI) data set, Wave 1. In an attempt to fine-map this linkage signal we genotyped 1,134 single nucleotide polymorphisms (SNPs) under the linkage peak in 23 informative families (131 individuals) with evidence of linkage. We tested family based association in the presence of linkage with the computer software package FBAT. The most significant association in these families was with a SNP in the second intron of GRIA1 (alpha-amino-3-hydroxy-5-methyl-4-isoxazole proprionic acid (AMPA) subunit 1 receptor gene) (rs490922, Z-score = 3.3, P = 0.001). The analysis of 37 additional families with psychotic BP from NIMH-BPGI data sets, Waves 2, 3, and 4 revealed a signal at a SNP in intron 5 of the GRIA1 gene (rs4385264, Z-score = 3.2, P-value = 0.002). A combined analysis of all 60 families continued to support evidence for association of GRIA1 with psychotic BP; however, individual SNPs could not be replicated across datasets. The AMPA1 receptor has been shown to influence cognitive function, such as working memory and reward learning. Our findings suggest that variations in this receptor may contribute to the pathophysiology of BP with psychotic features in some families.

DOI10.1042/AN20110027
Alternate JournalAm. J. Med. Genet. B Neuropsychiatr. Genet.