Abstract

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correlation patterns with OCD, MDD, ADHD, and ASD partitioned across comorbid subgroups in OCD using independent unpublished data from the Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH).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.

Highlights

  • Obsessive-Compulsive-Disorder (OCD) is a common, longlasting and disabling neuropsychiatric disorder with an estimated lifetime prevalence of 1–3% (Weissman, 1998; U.S International institutes of health (NIH), 2016)

  • Cross-Trait PRS Analyses To examine a possible polygenic heterogeneity of OCD, we further investigated how PRS trained on different phenotypes (OCD, neuroticism, EA, anorexia nervosa (AN), bipolar disorder (BP), body mass index (BMI), at first birth (AFB), and insomnia) distribute across the Integrative Psychiatric Research (iPSYCH) OCD subgroups defined by a comorbid diagnosis of either major depressive disorder (MDD), attentiondeficit hyperactivity-disorder (ADHD), and/or autism spectrum disorder (ASD)

  • OCD itself was included as a training dataset for the PRS analysis. With this selection of phenotypes we aimed to explore whether a heterogeneous genetic correlation pattern between a phenotype and OCD, MDD, ADHD, and ASD translates into heterogeneous PRS loadings in the OCD comorbid subgroups

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Summary

Introduction

Obsessive-Compulsive-Disorder (OCD) is a common, longlasting and disabling neuropsychiatric disorder with an estimated lifetime prevalence of 1–3% (Weissman, 1998; U.S International institutes of health (NIH), 2016). Genome-wide association studies (GWAS) in OCD have found suggestive evidence for some single nucleotide polymorphisms (SNPs) and genes that are potentially involved in its pathogenesis (International Obsessive Compulsive Disorder Foundation Genetics, 2017) Overall these findings remain rather inconclusive with no single genetic variant reliably replicating across individual studies (Sampaio et al, 2013; Bozorgmehr et al, 2017). These studies did, suggest that an increase in sample size will likely aid the identification of genome-wide significant loci, following the example of other psychiatric disorders like major depressive disorder (MDD) (Wray et al, 2018), attentiondeficit hyperactivity-disorder (ADHD) (Demontis et al, 2019), or autism spectrum disorder (ASD) (Grove et al, 2019). Dissecting OCD into more homogeneous and accurate sub-phenotypes based on comorbidity, may lead to the successful identification of genetic risk variants for OCD (MacRae and Vasan, 2011; Kulminski et al, 2016)

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