Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS

• Published in: Molecular psychiatry Vol. 20; no. 3; pp. 337 - 344
• Main Authors: Mattheisen, M, Samuels, J F, Wang, Y, Greenberg, B D, Fyer, A J, McCracken, J T, Geller, D A, Murphy, D L, Knowles, J A, Grados, M A, Riddle, M A, Rasmussen, S A, McLaughlin, N C, Nurmi, E L, Askland, K D, Qin, H-D, Cullen, B A, Piacentini, J, Pauls, D L, Bienvenu, O J, Stewart, S E, Liang, K-Y, Goes, F S, Maher, B, Pulver, A E, Shugart, Y Y, Valle, D, Lange, C, Nestadt, G
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.03.2015; Nature Publishing Group
• Subjects: 45/43; 692/699/476; Adult; Behavioral Sciences; Biological Psychology; Care and treatment; Chromosome 9; Chromosomes, Human, Pair 9 - genetics; Cooperative Behavior; Family Health; Female; Follow-Up Studies; GABA; Gene Expression Profiling; Gene polymorphism; Genetic aspects; Genetic Predisposition to Disease - genetics; Genetics; Genome-wide association studies; Genome-Wide Association Study; Genomes; Genotype; Glutamatergic transmission; Humans; Male; Medicine; Medicine & Public Health; Neurosciences; Neuroses; Obsessive compulsive disorder; Obsessive-Compulsive Disorder - genetics; Oligonucleotide Array Sequence Analysis; original-article; Pharmacotherapy; Physiological aspects; Polymorphism, Single Nucleotide; Psychiatry; Quality control; Receptor-Like Protein Tyrosine Phosphatases, Class 2 - genetics; Risk factors; Single nucleotide polymorphisms; Single-nucleotide polymorphism; Synapses; Synaptogenesis; Young Adult; γ-Aminobutyric acid; United States
• ISSN: 1359-4184; 1476-5578
• DOI: 10.1038/mp.2014.43

Obsessive-compulsive disorder (OCD) is a psychiatric condition characterized by intrusive thoughts and urges and repetitive, intentional behaviors that cause significant distress and impair functioning. The OCD Collaborative Genetics Association Study (OCGAS) is comprised of comprehensively assessed OCD patients with an early age of OCD onset. After application of a stringent quality control protocol, a total of 1065 families (containing 1406 patients with OCD), combined with population-based samples (resulting in a total sample of 5061 individuals), were studied. An integrative analyses pipeline was utilized, involving association testing at single-nucleotide polymorphism (SNP) and gene levels (via a hybrid approach that allowed for combined analyses of the family- and population-based data). The smallest P -value was observed for a marker on chromosome 9 (near PTPRD , P =4.13 × 10 − 7 ). Pre-synaptic PTPRD promotes the differentiation of glutamatergic synapses and interacts with SLITRK3. Together, both proteins selectively regulate the development of inhibitory GABAergic synapses. Although no SNPs were identified as associated with OCD at genome-wide significance level, follow-up analyses of genome-wide association study (GWAS) signals from a previously published OCD study identified significant enrichment ( P =0.0176). Secondary analyses of high-confidence interaction partners of DLGAP1 and GRIK2 (both showing evidence for association in our follow-up and the original GWAS study) revealed a trend of association ( P =0.075) for a set of genes such as NEUROD6 , SV2A , GRIA4 , SLC1A2 and PTPRD . Analyses at the gene level revealed association of IQCK and C16orf88 (both P <1 × 10 − 6 , experiment-wide significant), as well as OFCC1 ( P =6.29 × 10 − 5 ). The suggestive findings in this study await replication in larger samples.