Evaluation of shared genetic susceptibility loci between autoimmune diseases and schizophrenia based on genome-wide association studies. (2nd January 2017)

• Record Type: Journal Article
• Authors: Hoeffding, Louise K.; Rosengren, Anders; Thygesen, Johan H.; Schmock, Henriette; Werge, Thomas; Hansen, Thomas
• Is Part Of: Nordic journal of psychiatry. Volume 71:Number 1(2017)
• Page Start: 20
• Page End: 25
• Publication Date: 2017-01-02
• Subjects: GWAS -- schizophrenia -- autoimmune diseases -- comorbidity; Psychopharmacology -- Periodicals; Psychotherapy -- Periodicals; Psychiatry -- Periodicals; Psychiatry -- Scandinavia -- Periodicals; 616.89
• DOI: 10.1080/08039488.2016.1198420
• Languages: English
• ISSNs: 0803-9488

Abstract

Abstract: Background: Epidemiological studies have documented higher than expected comorbidity (or, in some cases, inverse comorbidity) between schizophrenia and several autoimmune disorders. It remains unknown whether this comorbidity reflects shared genetic susceptibility loci. Aims: The present study aimed to investigate whether verified genome wide significant variants of autoimmune disorders confer risk of schizophrenia, which could suggest a common genetic basis. Methods: Seven hundred and fourteen genome wide significant risk variants of 25 autoimmune disorders were extracted from the NHGRI GWAS catalogue and examined for association to schizophrenia in the Psychiatric Genomics Consortium schizophrenia GWAS samples (36, 989 cases and 113, 075 controls). Results: Two independent loci at 4q24 and 6p21.32–33 originally identified from GWAS of autoimmune diseases were found genome wide associated with schizophrenia (1.7 × 10 −8 ≥ p ≥ 4.0 × 10 −21 ). While these observations confirm the existence of shared genetic susceptibility loci between schizophrenia and autoimmune diseases, the findings did not show a significant enrichment. Conclusion: The findings do not support a genetic overlap in common SNPs between autoimmune diseases and schizophrenia that in part could explain the observed comorbidity from epidemiological studies.