Abstract

Schizophrenia (SZ) is a psychiatric disorder with a convoluted etiology that includes cognitive symptoms, which arise from among others a dysfunctional dorsolateral prefrontal cortex (dlPFC). In our search for the molecular underpinnings of the cognitive deficits in SZ, we here performed RNA sequencing of gray matter from the dlPFC of SZ patients and controls. We found that the differentially expressed RNAs were enriched for mRNAs involved in the Liver X Receptor/Retinoid X Receptor (LXR/RXR) lipid metabolism pathway. Components of the LXR/RXR pathway were upregulated in gray matter but not in white matter of SZ dlPFC. Intriguingly, an analysis for shared genetic etiology, using two SZ genome-wide association studies (GWASs) and GWAS data for 514 metabolites, revealed genetic overlap between SZ and acylcarnitines, VLDL lipids, and fatty acid metabolites, which are all linked to the LXR/RXR signaling pathway. Furthermore, analysis of structural T1-weighted magnetic resonance imaging in combination with cognitive behavioral data showed that the lipid content of dlPFC gray matter is lower in SZ patients than in controls and correlates with a tendency towards reduced accuracy in the dlPFC-dependent task-switching test. We conclude that aberrations in LXR/RXR-regulated lipid metabolism lead to a decreased lipid content in SZ dlPFC that correlates with reduced cognitive performance.

Highlights

  • Schizophrenia (SZ) is a psychiatric disorder with a convoluted etiology and a lifetime prevalence of 0.84%

  • We investigated whether other mRNAs related to Liver X Receptor/Retinoid X Receptor (LXR/RXR) activation were differentially expressed in SZ dorsolateral prefrontal cortex (dlPFC) gray matter

  • SZ is a psychiatric disorder with an unknown etiology and its cognitive deficits are associated with the dlPFC

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Summary

Introduction

Schizophrenia (SZ) is a psychiatric disorder with a convoluted etiology and a lifetime prevalence of 0.84%. It is thought that an interplay between genetic, epigenetic, and environmental risk factors is involved in SZ etiology[1]. Symptoms of SZ include positive, negative, and cognitive symptoms[2]. The positive symptoms comprise delusions and hallucinations[3], the negative symptoms are a loss of typical affective functions[2], and the most prominent cognitive symptoms of SZ are deficits in attention[4] and executive functioning[5,6,7]. The majority of transcriptomic studies performed on SZ dlPFC

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