Abstract

Alterations in frontal and parietal neural activations during working memory task performance have been suggested as a candidate endophenotype of obsessive-compulsive disorder (OCD) in studies involving first-degree relatives. However, the direct link between genetic risk for OCD and neuro-functional alterations during working memory performance has not been investigated to date. Thus, the aim of the current functional magnetic resonance imaging (fMRI) study was to test the direct association between polygenic risk for OCD and neural activity during the performance of a numeric n-back task with four working memory load conditions in 128 participants, including patients with OCD, unaffected first-degree relatives of OCD patients, and healthy controls. Behavioral results show a significant performance deficit at high working memory load in both patients with OCD and first-degree relatives (p < 0.05). A whole-brain analysis of the fMRI data indicated decreased neural activity in bilateral inferior parietal lobule and dorsolateral prefrontal cortex in both patients and relatives. Most importantly, OCD polygenic risk scores predicted neural activity in orbitofrontal cortex. Results indicate that genetic risk for OCD can partly explain alterations in brain response during working memory performance, supporting the notion of a neuro-functional endophenotype for OCD.

Highlights

  • Post-hoc two-sample t tests of this analysis of covariance (ANCOVA) model indicated significant differences only in the 3-back condition between patients with obsessive-compulsive disorder (OCD) and healthy controls (HC) (t(94) = 2.14, p = 0.035); and between REL and HC (t(75) = 2.35, p = 0.021). These results show that, when age is taken into account, HC show a higher performance in 3-back compared to both patients with OCD and REL

  • Results reflect that patients with OCD and unaffected REL showed performance decrements in working memory updating as well as reduced blood oxygen level-dependent (BOLD) responses in right IPL, left SPL/IPL, bilateral dorsolateral prefrontal cortex (DLPFC), left premotor cortex (PMC), and left inferior frontal gyrus (IFG) during 2- and 3-back

  • OCD polygenic risk scores predicted BOLD response in medial orbitofrontal cortex (OFC), indicating that higher genetic risk for OCD led to increased activity in medial OFC during the performance of a demanding working memory task

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Summary

Introduction

Unaffected REL showed deviant brain activity in fronto-parietal regions (most pronounced in dorsolateral prefrontal cortex (DLPFC) and pre-supplementary motor area) compared to healthy controls (HC) during a working memory updating ­task[17]. This hypothesis would be supported, if (a) orbitofronto-striatal and/or fronto-parietal alterations in blood oxygen level-dependent (BOLD) response were found in both OCD and unaffected REL, and (b) OCD polygenic risk scores would predict these neuro-functional deviations

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