Background: Pediatric bipolar I disorder (BP-I) and childhood schizophrenia (SZ) share certain symptoms (e.g., psychosis, aggression/irritability [A/I]), and the psychotic and A/I features are treated with neuroleptics in both disorders. Thus, it is of interest to examine the association of GAD1 to child BP-I because of its recently reported association to childhood SZ. Methods: Child BP-I probands were obtained by consecutive new case ascertainment, and the phenotype was defined as current DSM-IV BP-I (manic or mixed phase) with at least one of the cardinal symptoms of mania (i.e., elation and/or grandiosity) and a Children's Global Assessment Scale score ≤60 (clinical impairment). These child BP-I probands are part of a large, ongoing, longitudinal study in which the phenotype has been validated by unique symptoms, longitudinal stability, and 78 times greater family loading than adult BP-I probands. Genotyping was performed using a TaqMan® Validated SNP Genotyping Assay, and FBAT was used for analysis. Results: There were 48 families. The rs2241165 A allele was preferentially transmitted (FBAT χ2 = 5.2, df = 1, p = 0.022). No interaction between this GAD1 SNP and the Val66 BDNF allele was found. Conclusions: These data are consistent with some shared genetic vulnerability between child BP-I and SZ, which may be related to similar treatments. © 2008 Mary Ann Liebert, Inc.
CITATION STYLE
Geller, B., Tillman, R., Bolhofner, K., Hennessy, K., & Cook, E. H. (2008). GAD1 single nucleotide polymorphism is in linkage disequilibrium with a child bipolar I disorder phenotype. Journal of Child and Adolescent Psychopharmacology, 18(1), 25–29. https://doi.org/10.1089/cap.2007.0056
Mendeley helps you to discover research relevant for your work.