O4.1. GENETIC VULNERABILITY TO DUSP22 PROMOTOR HYPERMETHYLATION IS INVOLVED IN THE RELATION BETWEEN IN UTERO FAMINE EXPOSURE AND SCHIZOPHRENIA

Marco P Boks ,Gianluca Ursini,Schahram Akbarian,Prashanth Rajarajan,Andrew E Jaffe ,Je Kleinmann ,Bart P F Rutten ,Christiaan H Vinkers ,Adam X Maihofer ,Caroline M Nievergelt ,Yaqin Yu ,Elly M Hol ,Lotte C Houtepen ,Weinberger ,Witte Ld ,David Baker ,Zhida Xu ,H Pol Hulshoff ,Yujie He ,René S Kahn

doi:10.1093/schbul/sby015.207

Abstract

BackgroundEpigenetic changes may account for the doubled risk to develop schizophrenia in individuals exposed to famine in utero.MethodsWe therefore investigated DNA methylation in a unique sample of patients and healthy individuals conceived during the great famine in China. To further examine the causality of the identified DNA methylation differences we also exposed human fibroblasts to nutritional deprivation and analyzed changes in expression and DNA methylation.ResultsIn the famine exposed schizophrenia patients we found significant hypermethylation of the dual specificity phosphatase 22 (DUSP22) gene promoter (Chr6:291687–293285) (N=153, p=0.01). The presence of a direct link between famine exposure and DUSP22 transcription was supported by increased methylation (p=0.048) and expression (p=0.019) in response to nutritional deprivation in the cultured human fibroblasts (N=10). These findings are in line with previous research that implicated hypermethylation of DUSP22 in the environmental risk to neuropsychiatric disorders. In postmortem brain samples from schizophrenia patients, variation in DUSP22 methylation was genetically regulated across chromosomes by a region on chromosome 16. This cross chromosomal regulation of variability in DUSP22 methylation is consistent with new 3D genome interaction data obtained using Hi-C capture in brain and previously published data on lymphocytes.DiscussionTogether our results identify an epigenetic locus at which the response to prenatal famine exposure is genetically regulated across chromosomes and that is relevant for a major psychiatric disorder.

Highlights

Dorsolateral Prefrontal Cortex (DLPFC) has been identified as the seat of many synaptic changes in schizophrenia
There were no significant differences in CBF in the ACC (mean (SD) placebo = 47.22 (8.81); NAC = 46.83 (7.29); t(18) = .349, P = .73) or in the right caudate nucleus (mean (SD) placebo = 37.51 (7.48); NAC = 37.77 (6.71); t(18) -.310, P = .76) in the NAC compared to placebo condition
We aimed to isolate the brain regions showing abnormal variance of phase coherence (vPC) with right DLPFC in drug-naïve first episode schizophrenia compared to healthy controls

Summary

Introduction

Dorsolateral Prefrontal Cortex (DLPFC) has been identified as the seat of many synaptic changes in schizophrenia. Results: In the ACC, Glx/Cr was significantly reduced in the NAC compared to placebo condition (t(17) = 2.40; P = .03, d = 0.64). There were no significant differences in CBF in the ACC (mean (SD) placebo = 47.22 (8.81); NAC = 46.83 (7.29); t(18) = .349, P = .73) or in the right caudate nucleus (mean (SD) placebo = 37.51 (7.48); NAC = 37.77 (6.71); t(18) -.310, P = .76) in the NAC compared to placebo condition.

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