[go: up one dir, main page]
More Web Proxy on the site http://driver.im/
Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Original Article
  • Published:

Revealing the complex genetic architecture of obsessive–compulsive disorder using meta-analysis

Abstract

Two obsessive–compulsive disorder (OCD) genome-wide association studies (GWASs) have been published by independent OCD consortia, the International Obsessive-Compulsive Disorder Foundation Genetics Collaborative (IOCDF-GC) and the OCD Collaborative Genetics Association Study (OCGAS), but many of the top-ranked signals were supported in only one study. We therefore conducted a meta-analysis from the two consortia, investigating a total of 2688 individuals of European ancestry with OCD and 7037 genomically matched controls. No single-nucleotide polymorphisms (SNPs) reached genome-wide significance. However, in comparison with the two individual GWASs, the distribution of P-values shifted toward significance. The top haplotypic blocks were tagged with rs4733767 (P=7.1 × 10−7; odds ratio (OR)=1.21; confidence interval (CI): 1.12–1.31, CASC8/CASC11), rs1030757 (P=1.1 × 10−6; OR=1.18; CI: 1.10–1.26, GRID2) and rs12504244 (P=1.6 × 10−6; OR=1.18; CI: 1.11–1.27, KIT). Variants located in or near the genes ASB13, RSPO4, DLGAP1, PTPRD, GRIK2, FAIM2 and CDH20, identified in linkage peaks and the original GWASs, were among the top signals. Polygenic risk scores for each individual study predicted case–control status in the other by explaining 0.9% (P=0.003) and 0.3% (P=0.0009) of the phenotypic variance in OCGAS and the European IOCDF-GC target samples, respectively. The common SNP heritability in the combined OCGAS and IOCDF-GC sample was estimated to be 0.28 (s.e.=0.04). Strikingly, 65% of the SNP-based heritability in the OCGAS sample was accounted for by SNPs with minor allele frequencies of 40%. This joint analysis constituting the largest single OCD genome-wide study to date represents a major integrative step in elucidating the genetic causes of OCD.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1
Figure 2

Similar content being viewed by others

References

  1. American Psychiatric Association Diagnostic and Statistical Manual of Mental Disorders, 5th edn. American Psychiatric Association: Arlington, VA, 2013.

  2. Karno M, Golding JM. . Obsessive compulsive disorder. In: Robins LN, Regier DA (eds). Psychiatric Disorders in America: The Epidemiologic Catchment Area Study. Free Press; Collier Macmillan Canada; Maxwell Macmillan International: New York, Toronto, 1991, pp 204–219.

    Google Scholar 

  3. Pauls DL, Alsobrook JP 2nd, Goodman W, Rasmussen S, Leckman JF . A family study of obsessive-compulsive disorder. Am J Psychiatry 1995; 152: 76–84.

    Article  CAS  Google Scholar 

  4. Nestadt G, Samuels J, Riddle M, Bienvenu OJ 3rd, Liang KY, LaBuda M et al. A family study of obsessive-compulsive disorder. Arch Gen Psychiatry 2000; 57: 358–363.

    Article  CAS  Google Scholar 

  5. Grabe HJ, Ruhrmann S, Ettelt S, Buhtz F, Hochrein A, Schulze-Rauschenbach S et al. Familiality of obsessive-compulsive disorder in nonclinical and clinical subjects. Am J Psychiatry 2006; 163: 1986–1992.

    Article  Google Scholar 

  6. Fyer AJ, Lipsitz JD, Mannuzza S, Aronowitz B, Chapman TF . A direct interview family study of obsessive-compulsive disorder. I. Psychol Med 2005; 35: 1611–1621.

    Article  Google Scholar 

  7. Hanna GL, Himle JA, Curtis GC, Gillespie BW . A family study of obsessive-compulsive disorder with pediatric probands. Am J Med Genet B Neuropsychiatr Genet 2005; 134: 13–19.

    Article  Google Scholar 

  8. do Rosario-Campos MC, Leckman JF, Curi M, Quatrano S, Katsovitch L, Miguel EC et al. A family study of early-onset obsessive-compulsive disorder. Am J Med Genet B Neuropsychiatr Genet 2005; 136: 92–97.

    Article  Google Scholar 

  9. van Grootheest DS, Cath DC, Beekman AT, Boomsma DI . Twin studies on obsessive-compulsive disorder: a review. Twin Res Hum Genet 2005; 8: 450–458.

    Article  Google Scholar 

  10. Clifford CA, Murray RM, Fulker DW . Genetic and environmental influences on obsessional traits and symptoms. Psychol Med 1984; 14: 791–800.

    Article  CAS  Google Scholar 

  11. Jonnal AH, Gardner CO, Prescott CA, Kendler KS . Obsessive and compulsive symptoms in a general population sample of female twins. Am J Med Genet 2000; 96: 791–796.

    Article  CAS  Google Scholar 

  12. Eley TC, Bolton D, O'Connor TG, Perrin S, Smith P, Plomin R . A twin study of anxiety-related behaviours in pre-school children. J Child Psychol Psychiatry 2003; 44: 945–960.

    Article  Google Scholar 

  13. Hudziak JJ, Van Beijsterveldt CE, Althoff RR, Stanger C, Rettew DC, Nelson EC et al. Genetic and environmental contributions to the Child Behavior Checklist Obsessive-Compulsive Scale: a cross-cultural twin study. Arch Gen Psychiatry 2004; 61: 608–616.

    Article  Google Scholar 

  14. Taylor S . Etiology of obsessions and compulsions: a meta-analysis and narrative review of twin studies. Clin Psychol Rev 2011; 31: 1361–1372.

    Article  Google Scholar 

  15. Davis LK, Yu D, Keenan CL, Gamazon ER, Konkashbaev AI, Derks EM et al. Partitioning the heritability of tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. PLoS Genet 2013; 9: e1003864.

    Article  Google Scholar 

  16. Mathews CA, Badner JA, Andresen JM, Sheppard B, Himle JA, Grant JE et al. Genome-wide Linkage Analysis of Obsessive-Compulsive Disorder Implicates Chromosome 1p36. Biol Psychiatry 2012; 72: 629–636.

    Article  CAS  Google Scholar 

  17. Ross J, Badner J, Garrido H, Sheppard B, Chavira DA, Grados M et al. Genomewide linkage analysis in Costa Rican families implicates chromosome 15q14 as a candidate region for OCD. Hum Genet 2011; 130: 795–805.

    Article  Google Scholar 

  18. Hanna GL, Veenstra-Vanderweele J, Cox NJ, Van Etten M, Fischer DJ, Himle JA et al. Evidence for a susceptibility locus on chromosome 10p15 in early-onset obsessive-compulsive disorder. Biol Psychiatry 2007; 62: 856–862.

    Article  CAS  Google Scholar 

  19. Shugart YY, Samuels J, Willour VL, Grados MA, Greenberg BD, Knowles JA et al. Genomewide linkage scan for obsessive-compulsive disorder: evidence for susceptibility loci on chromosomes 3q, 7p, 1q, 15q, and 6q. Mol Psychiatry 2006; 11: 763–770.

    Article  CAS  Google Scholar 

  20. Hanna GL, Veenstra-VanderWeele J, Cox NJ, Boehnke M, Himle JA, Curtis GC et al. Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands. Am J Med Genet 2002; 114: 541–552.

    Article  Google Scholar 

  21. Wang Y, Samuels JF, Chang YC, Grados MA, Greenberg BD, Knowles JA et al. Gender differences in genetic linkage and association on 11p15 in obsessive-compulsive disorder families. Am J Med Genet B Neuropsychiatr Genet 2009; 150B: 33–40.

    Article  CAS  Google Scholar 

  22. Samuels J, Shugart YY, Grados MA, Willour VL, Bienvenu OJ, Greenberg BD et al. Significant linkage to compulsive hoarding on chromosome 14 in families with obsessive-compulsive disorder: results from the OCD Collaborative GeneticsStudy. Am J Psychiatry 2007; 164: 493–499.

    Article  Google Scholar 

  23. Mattheisen M, Samuels JF, Wang Y, Greenberg BD, Fyer AJ, McCracken JT et al. Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS. Mol Psychiatry 2015; 20: 337–344.

    Article  CAS  Google Scholar 

  24. Stewart SE, Yu D, Scharf JM, Neale BM, Fagerness JA, Mathews CA et al. Genome-wide association study of obsessive-compulsive disorder. Mol Psychiatry 2013; 18: 788–798.

    Article  CAS  Google Scholar 

  25. den Braber A, Zilhao NR, Fedko IO, Hottenga JJ, Pool R, Smit DJ et al. Obsessive-compulsive symptoms in a large population-based twin-family sample are predicted by clinically based polygenic scores and by genome-wide SNPs. Transl Psychiatry 2016; 6: e731.

    Article  CAS  Google Scholar 

  26. Stewart SE, Yu D, Scharf JM, Neale BM, Fagerness JA, Mathews CA et al. Genome-wide association study of obsessive-compulsive disorder. Mol Psychiatry 2013; 18: 788–798.

    Article  CAS  Google Scholar 

  27. Davis LK, Gamazon ER, Kistner-Griffin E, Badner JA, Liu C, Cook EH et al. Loci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitative trait loci. Mol Autism 2012; 3: 3.

    Article  CAS  Google Scholar 

  28. Below JE, Parra EJ, Gamazon ER, Torres J, Krithika S, Candille S et al. Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs. Sci Rep 2016; 6: 19429.

    Article  CAS  Google Scholar 

  29. Bulik-Sullivan BK, Loh PR, Finucane HK, Ripke S, Yang J, Schizophrenia Working Group of the Psychiatric Genomics Consortium. LD Score regression distinguishes confounding from polygenicity in genome-wide association studies. Nat Genet 2015; 47: 291–295.

    Article  CAS  Google Scholar 

  30. Pato MT, Sobell JL, Medeiros H, Abbott C, Sklar BM, Buckley PF et al. The genomic psychiatry cohort: partners in discovery. Am J Med Genet B Neuropsychiatr Genet 2013; 162B: 306–312.

    Article  Google Scholar 

  31. Howie B, Marchini J, Stephens M . Genotype imputation with thousands of genomes. G3 (Bethesda) 2011; 1: 457–470.

    Article  Google Scholar 

  32. Delaneau O, Howie B, Cox AJ, Zagury JF, Marchini J . Haplotype estimation using sequencing reads. Am J Hum Genet 2013; 93: 687–696.

    Article  CAS  Google Scholar 

  33. Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 2007; 81: 559–575.

    Article  CAS  Google Scholar 

  34. Willer CJ, Li Y, Abecasis GR . METAL: fast and efficient meta-analysis of genomewide association scans. Bioinformatics 2010; 26: 2190–2191.

    Article  CAS  Google Scholar 

  35. Khramtsova EA, Stranger BE . Assocplots: a python package for static and interactive visualization of multiple-group gwas results. Bioinformatics 2017; 33: 432–434.

    Article  CAS  Google Scholar 

  36. Yu D, Mathews CA, Scharf JM, Neale BM, Davis LK, Gamazon ER et al. Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. Am J Psychiatry 2015; 172: 82–93.

    Article  Google Scholar 

  37. Schizophrenia Working Group of the Psychiatric Genomics Consortium. Biological insights from 108 schizophrenia-associated genetic loci. Nature 2014; 511: 421–427.

    Article  Google Scholar 

  38. Klei L, Sanders SJ, Murtha MT, Hus V, Lowe JK, Willsey AJ et al. Common genetic variants, acting additively, are a major source of risk for autism. Mol Autism 2012; 3: 9.

    Article  Google Scholar 

  39. Malik AN, Vierbuchen T, Hemberg M, AA Rubin, Ling E, Couch CH et al. Genome-wide identification and characterization of functional neuronal activity-dependent enhancers. Nat Neurosci 2014; 17: 1330–1339.

    Article  CAS  Google Scholar 

  40. GTEx Consortium. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans. Science 2015; 348: 648–660, 40.

    Article  Google Scholar 

  41. Ng SY, Lin L, Soh BS, Stanton LW . Long noncoding RNAs in development and disease of the central nervous system. Trends Genet 2013; 29: 461–468.

    Article  CAS  Google Scholar 

  42. Ramasamy A, Trabzuni D, Guelfi S, Varghese V, Smith C, Walker R et al. Genetic variability in the regulation of gene expression in ten regions of the human brain. Nat Neurosci 2014; 17: 1418–28.

    Article  CAS  Google Scholar 

  43. Graybiel AM, Rauch SL . Toward a neurobiology of obsessive-compulsive disorder. Neuron 2000; 28: 343–7.

    Article  CAS  Google Scholar 

  44. Pittenger C, Bloch MH, Williams K . Glutamate abnormalities in obsessive compulsive disorder: neurobiology, pathophysiology, and treatment. Pharmacol Ther 2011; 132: 314–332.

    Article  CAS  Google Scholar 

  45. Coutelier M, Burglen L, Mundwiller E, Abada-Bendib M, Rodriguez D, Chantot-Bastaraud S et al. GRID2 mutations span from congenital to mild adult-onset cerebellar ataxia. Neurology 2015; 28: 1751–1759.

    Article  Google Scholar 

  46. Fernando J, Faber TW, Pullen NA, Falanga YT, Kolawole EM, Oskeritzian CA et al. Genotype-dependent effects of TGF-β1 on mast cell function: targeting the Stat5 pathway. J Immunol 2013; 191: 4505–4513.

    Article  CAS  Google Scholar 

  47. Kawakami T, Soma Y, Kawa Y, Ito M, Yamasaki E, Watabe H et al. Transforming growth factor beta1 regulates melanocyte proliferation and differentiation in mouse neural crest cells via stem cell factor/KIT signaling. J Invest Dermatol 2002; 118: 471–478.

    Article  CAS  Google Scholar 

  48. Cacheaux LP, Ivens S, David Y, Lakhter AJ, Bar-Klein G, Shapira M et al. Transcriptome profiling reveals TGF-beta signaling involvement in epileptogenesis. J Neurosci 2009; 29: 8927–8935.

    Article  CAS  Google Scholar 

  49. Arnold PD, Rosenberg DR, Mundo E, Tharmalingam S, Kennedy JL, Richter MA . Association of a glutamate (NMDA) subunit receptor gene (GRIN2B) with obsessive-compulsive disorder: a preliminary study. Psychopharmacology (Berl) 2004; 174: 530–538.

    Article  CAS  Google Scholar 

  50. Stewart SE, Mayerfeld C, Arnold PD, Crane JR, O'Dushlaine C, Fagerness JA et al. Meta-analysis of association between obsessive-compulsive disorder and the 3' region of neuronal glutamate transporter gene SLC1A1. Am J Med Genet B Neuropsychiatr Genet 2013; 162B: 367–379.

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The OCD Collaborative Genetics Association Study (OCGAS) is a collaborative research study and was funded by the following NIMH Grant Numbers: MH071507 (GN), MH079489 (DAG), MH079487 (JM), MH079488 (AF) and MH079494 (JK). Yao Shugart and Wei Guo were also supported by the Intramural Research Program of the NIMH (MH002930-06)

The International Obsessive Compulsive Foundation Genetics Collaborative (IOCDF-GC) was supported by a grant from the David Judah Foundation (a private, nonindustry-related foundation established by a family affected by OCD), MH079489 (DLP), MH073250 (DLP), S40024 (JMS), MH 085057 (JMS), and MH087748 (CAM).

We thank the Psychiatric Genomics Consortium (PGC) for the use of their servers for data integration and analysis, the many families who have participated in the study, as well as the clinicians, study managers and clinical interviewers at the respective study sites for their efforts in participant recruitment and clinical assessments.

The views expressed here do not reflect the view of the National Institutes of Health, the Department of Health and Human Services, or the United States government.

Author contributions

Analytic group: Wei Guo, Dongmei Yu, Lea Davis, Stephan Ripke and Yin Yao Shugart; interpretation of data and manuscript preparation: Paul Arnold, Lea Davis, E.M. Derks, Wei Guo, James Knowles, Carol A Mathews, Rainald Moessner, Gerald Nestadt, Jeremiah M Scharf, Yin Yao Shugart and Dongmei Yu.

Author information

Authors and Affiliations

Consortia

Corresponding authors

Correspondence to James A Knowles or Gerald Nestadt.

Ethics declarations

Competing interests

The authors declare no conflict of interest.

Additional information

Members of the IOCDF-GC and OCGAS consortia Paul D Arnold (IOCDF-GC), Kathleen D Askland (OCGAS and IOCDF-GC), Cristina Barlassina (IOCDF-GC), Laura Bellodi (IOCDF-GC), OJ Bienvenu (OCGAS and IOCDF-GC), Donald Black (IOCDF-GC), Michael Bloch (IOCDF-GC), Helena Brentani (IOCDF-GC), Christie L Burton (IOCDF-GC), Beatriz Camarena (IOCDF-GC), Carolina Cappi (IOCDF-GC), Danielle Cath (IOCDF-GC), Maria Cavallini (IOCDF-GC), David Conti (OCGAS), Edwin Cook (IOCDF-GC), Vladimir Coric (IOCDF-GC), Bernadette A Cullen (OCGAS and IOCDF-GC), Danielle Cusi (IOCDF-GC), Lea K Davis (IOCDF-GC), Richard Delorme (IOCDF-GC), Damiaan Denys (IOCDF-GC), Eske Derks (IOCDF-GC), Valsamma Eapen (IOCDF-GC), Christopher Edlund (IOCDF-GC), Lauren Erdman (IOCDF-GC), Peter Falkai (IOCDF-GC), Martijn Figee (IOCDF-GC), Abigail J Fyer (OCGAS and IOCDF-GC), Daniel A Geller (IOCDF-GC and OCGAS), Fernando S Goes (OCGAS), Hans Grabe (IOCDF-GC), Marcos A Grados (OCGAS and IOCDF-GC), Benjamin D Greenberg (OCGAS and IOCDF-GC), Edna Grünblatt (IOCDF-GC), Wei Guo (OCGAS), Gregory L Hanna (IOCDF-GC), Sian Hemmings (IOCDF-GC), Ana G Hounie (IOCDF-GC), Michael Jenicke (IOCDF-GC), Clare Keenan (IOCDF-GC), James Kennedy (IOCDF-GC), Ekaterina A Khramtsova (IOCDF-GC), Anuar Konkashbaev (IOCDF-GC), James A Knowles (IOCDF-GC and OCGAS), Janice Krasnow (IOCDF-GC and OCGAS), Cristophe Lange (OCGAS), Nuria Lanzagorta (IOCDF-GC), Marion Leboyer (IOCDF-GC), Leonhard Lennertz (IOCDF-GC), Bingbin Li (OCGAS), K-Y Liang (OCGAS and IOCDF-GC), Christine Lochner (IOCDF-GC), Fabio Macciardi (IOCDF-GC), Brion Maher (OCGAS), Wolfgang Maier (IOCDF-GC), Maurizio Marconi (IOCDF-GC), Carol A Mathews (IOCDF-GC), Manuel Matthesien (OCGAS), James T McCracken (OCGAS and IOCDF-GC), Nicole C McLaughlin (OCGAS and IOCDF-GC), Euripedes C Miguel (IOCDF-GC), Rainald Moessner (IOCDF-GC), Dennis L Murphy (OCGAS and IOCDF-GC), Benjamin Neale (IOCDF-GC), Gerald Nestadt (OCGAS and IOCDF-GC), Paul Nestadt (IOCDF-GC and OCGAS), Humberto Nicolini (OCDF-GC), Ericka Nurmi (OCGAS), Lisa Osiecki (IOCDF-GC), David L Pauls (IOCDF-GC and OCGAS), John Piacentini (OCGAS and IOCDF-GC), Danielle Posthuma (IOCDF-GC), Ann E Pulver (OCGAS), H-D Qin (OCGAS), Steven A Rasmussen (OCGAS and IOCDF-GC), Scott Rauch (IOCDF-GC), Margaret A Richter (IOCDF-GC), Mark A Riddle (OCGAS and IOCDF-GC), Stephan Ripke (Psychiatric Genomics Consortium), Stephan Ruhrmann (IOCDF-GC), Aline S Sampaio (IOCDF-GC), Jack F Samuels (OCGAS and IOCDF-GC), Jeremiah M Scharf (IOCDF-GC), Yin Yao Shugart (OCGAS and IOCDF-GC), Jan Smit (IOCDF-GC), Daniel Stein (IOCDF-GC), S Evelyn Stewart (IOCDF-GC and OCGAS), Maurizio Turiel (IOCDF-GC), Homero Vallada (IOCDF-GC), Jeremy Veenstra-VanderWeele (IOCDF-GC), Michael Wagner (IOCDF-GC), Susanne Walitza (IOCDF-GC), Y Wang (OCGAS and IOCDF-GC), Jens Wendland (IOCDF-GC), Nienke Vulink (IOCDF-GC), Dongmei Yu (IOCDF-GC), Gwyneth Zai (IOCF-GC).

Supplementary Information accompanies the paper on the Molecular Psychiatry website

Supplementary information

PowerPoint slides

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

International Obsessive Compulsive Disorder Foundation Genetics Collaborative (IOCDF-GC) and OCD Collaborative Genetics Association Studies (OCGAS). Revealing the complex genetic architecture of obsessive–compulsive disorder using meta-analysis. Mol Psychiatry 23, 1181–1188 (2018). https://doi.org/10.1038/mp.2017.154

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/mp.2017.154

This article is cited by

Search

Quick links