Evidence that putative ADHD low risk alleles at SNAP25 may increase the risk of schizophrenia

27Citations
Citations of this article
37Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Synaptosomal Associated Protein 25 kDa (SNAP25) has been implicated in the pathogenesis of schizophrenia by numerous neuropathological studies and genetic variation at SNAP25 has been reported to be associated with ADHD. Expression levels of the putative schizophrenia susceptibility gene DTNBP1 has been shown to influence the levels of SNAP25 in vitro. We undertook directed mutation screening of SNAP25 in UK schizophrenic cases followed by direct association analysis of all variants identified and identified known exonic SNPs that showed evidence for association (rs3746544 P=0.004 OR=1.26, rs8636 P=0.003 OR=1.27), although these SNPs are highly correlated (r2>0.99). We additionally genotyped a further 31 tag SNPs spanning the SNAP25 locus and identified several independent SNPs that were nominally associated with schizophrenia (strongest association at rs3787283, P=0.006, OR=1.25) however, due to the number of tests performed no SNP met experiment-wise significance (minimum permuted P-value=0.1). Post hoc analysis revealed that the SNPs nominally associated with schizophrenia (rs3787283, rs3746544) were the same as those previously demonstrated to be associated with ADHD but with the opposite alleles, allowing the intriguing hypothesis that genetic variation at SNAP25 maybe differentially associated with both schizophrenia and ADHD. © 2009 Wiley-Liss, Inc.

Author supplied keywords

Cite

CITATION STYLE

APA

Carroll, L. S., Kendall, K., O’Donovan, M. C., Owen, M. J., & Williams, N. M. (2009). Evidence that putative ADHD low risk alleles at SNAP25 may increase the risk of schizophrenia. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 150(7), 893–899. https://doi.org/10.1002/ajmg.b.30915

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free