Polygenic Heterogeneity Across Obsessive-Compulsive Disorder Subgroups Defined by a Comorbid Diagnosis

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  • Nora I. Strom
  • Jakob Grove
  • Sandra M. Meier
  • Marie Bækvad-Hansen
  • Judith Becker Nissen
  • Thomas Damm Als
  • Matthew Halvorsen
  • Nordentoft, Merete
  • Preben B. Mortensen
  • David M. Hougaard
  • Werge, Thomas
  • Ole Mors
  • Anders D. Børglum
  • James J. Crowley
  • Jonas Bybjerg-Grauholm
  • Manuel Mattheisen

Among patients with obsessive-compulsive disorder (OCD), 65–85% manifest another psychiatric disorder concomitantly or at some other time point during their life. OCD is highly heritable, as are many of its comorbidities. A possible genetic heterogeneity of OCD in relation to its comorbid conditions, however, has not yet been exhaustively explored. We used a framework of different approaches to study the genetic relationship of OCD with three commonly observed comorbidities, namely major depressive disorder (MDD), attention-deficit hyperactivity disorder (ADHD), and autism spectrum disorder (ASD). First, using publicly available summary statistics from large-scale genome-wide association studies, we compared genetic correlation patterns for OCD, MDD, ADHD, and ASD with 861 somatic and mental health phenotypes. Secondly, we examined how polygenic risk scores (PRS) of eight traits that showed heterogeneous correlation patterns with OCD, MDD, ADHD, and ASD partitioned across comorbid subgroups in OCD using independent unpublished data from the Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH). The comorbid subgroups comprised of patients with only OCD (N = 366), OCD and MDD (N = 1,052), OCD and ADHD (N = 443), OCD and ASD (N = 388), and OCD with more than 1 comorbidity (N = 429). We found that PRS of all traits but BMI were significantly associated with OCD across all subgroups (neuroticism: p = 1.19 × 10−32, bipolar disorder: p = 7.51 × 10−8, anorexia nervosa: p = 3.52 × 10−20, age at first birth: p = 9.38 × 10−5, educational attainment: p = 1.56 × 10−4, OCD: p = 1.87 × 10−6, insomnia: p = 2.61 × 10−5, BMI: p = 0.15). For age at first birth, educational attainment, and insomnia PRS estimates significantly differed across comorbid subgroups (p = 2.29 × 10−4, p = 1.63 × 10−4, and p = 0.045, respectively). Especially for anorexia nervosa, age at first birth, educational attainment, insomnia, and neuroticism the correlation patterns that emerged from genetic correlation analysis of OCD, MDD, ADHD, and ASD were mirrored in the PRS associations with the respective comorbid OCD groups. Dissecting the polygenic architecture, we found both quantitative and qualitative polygenic heterogeneity across OCD comorbid subgroups.

OriginalsprogEngelsk
Artikelnummer711624
TidsskriftFrontiers in Genetics
Vol/bind12
ISSN1664-8021
DOI
StatusUdgivet - 2021

Bibliografisk note

Funding Information:
This research has been conducted using the Danish National Biobank resource, supported by the Novo Nordisk Foundation. High-performance computer capacity for handling and statistical analysis of iPSYCH data on the GenomeDK HPC facility was provided by the Center for Genomics and Personalized Medicine and the Centre for Integrative Sequencing, iSEQ, Aarhus University, Denmark. We acknowledge support by the German Research Foundation (DFG) and the Open Access Publication Fund of Humboldt-Universit?t zu Berlin. Funding. The iPSYCH team was funded by the Lundbeck Foundation (R102-A9118, R155-2014-1724, and R248-2017-2003), the EU H2020 Program (Grant No. 667302, CoCA), NIMH (1U01MH109514-01) and the universities and university hospitals of Aarhus and Copenhagen. This study was supported by NIH grants R01MH105500 and R01MH110427.

Publisher Copyright:
© Copyright © 2021 Strom, Grove, Meier, Bækvad-Hansen, Becker Nissen, Damm Als, Halvorsen, Nordentoft, Mortensen, Hougaard, Werge, Mors, Børglum, Crowley, Bybjerg-Grauholm and Mattheisen.

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