Schizophrenia Bulletin Advance Access published online on November 20, 2008
Schizophrenia Bulletin, doi:10.1093/schbul/sbn155
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A Genome-Wide Association Study of Schizophrenia Using Brain Activation as a Quantitative Phenotype
2 Department of Psychiatry and Human Behavior, 5251 California Avenue, Suite 240, University of California, Irvine, CA 92617
3 Department of Sciences and Biomedical Technologies, University of Milan, Via Fratelli Cervi 93, 20090 Segrate (MI), Italy
4 University of California, San Francisco
5 Yale University, West Haven, CT (Yale)
6 Department of Psychiatry, University of New Mexico, Albuquerque, NM 87131
7 The Mind Research Network, Albuquerque, NM 87131
1 To whom correspondence should be addressed; tel: 949-824-8040, fax: 949-824-3324, e-mail: sgpotkin{at}uci.edu
Background: Genome-wide association studies (GWASs) are increasingly used to identify risk genes for complex illnesses including schizophrenia. These studies may require thousands of subjects to obtain sufficient power. We present an alternative strategy with increased statistical power over a case-control study that uses brain imaging as a quantitative trait (QT) in the context of a GWAS in schizophrenia. Methods: Sixty-four subjects with chronic schizophrenia and 74 matched controls were recruited from the Functional Biomedical Informatics Research Network (FBIRN) consortium. Subjects were genotyped using the Illumina HumanHap300 BeadArray and were scanned while performing a Sternberg Item Recognition Paradigm in which they learned and then recognized target sets of digits in an functional magnetic resonance imaging protocol. The QT was the mean blood oxygen level–dependent signal in the dorsolateral prefrontal cortex during the probe condition for a memory load of 3 items. Results: Three genes or chromosomal regions were identified by having 2 single-nucleotide polymorphisms (SNPs) each significant at P < 10–6 for the interaction between the imaging QT and the diagnosis (ROBO1-ROBO2, TNIK, and CTXN3-SLC12A2). Three other genes had a significant SNP at <10–6 (POU3F2, TRAF, and GPC1). Together, these 6 genes/regions identified pathways involved in neurodevelopment and response to stress. Conclusion: Combining imaging and genetic data from a GWAS identified genes related to forebrain development and stress response, already implicated in schizophrenic dysfunction, as affecting prefrontal efficiency. Although the identified genes require confirmation in an independent sample, our approach is a screening method over the whole genome to identify novel SNPs related to risk for schizophrenia.
Keywords: genome-wide scan / schizophrenia / working memory / genes / DLPFC / fMRI