Identification of VIPR2 rare and common variants in the Chinese Han population with schizophrenia

IntroductionSchizophrenia is a severe and chronic psychiatric disorder with hereditary risk up to 80% as previous studies indicated. Several researches have demonstrated a significant association between schizophrenia and microduplications that overlap the vasoactive intestinal peptide receptor 2 gene (VIPR2). MethodsTo further investigate potential causal VIPR2 gene variants, all exons and un-translated portions of the VIPR2 gene were sequenced using amplicon targeted resequencing in 1804 Chinese Han patients with schizophrenia and 996 healthy counterparts in the present study. ResultsNineteen rare non-synonymous mutations and 1 frameshift deletion was identified for schizophrenia, among which 5 variants have never been reported so far. Frequencies of rare non-synonymous mutations were significantly different between the two groups. Specifically, the non-synonymous mutation rs78564798 (P-allele = 0.006) as well as two rare variations in the VIPR2 gene's introns (rs372544903, P-allele = 0.026 and a novel mutation, chr7:159034078, GRCh38, P-allele = 0.048) were significantly associated with schizophrenia. DiscussionOur findings add new evidence that the functional and probable causative variants of VIPR2 gene may play an important role in susceptibility to schizophrenia. Further studies on validations of VIPR2's function in the etiology of schizophrenia are warranted.

Automated summary

This study sequenced the exons and un-translated portions of the VIPR2 gene in 1804 Chinese Han patients with schizophrenia and 996 healthy counterparts, identifying 19 rare non-synonymous mutations and 1 frameshift deletion associated with schizophrenia. Among them, 5 variants have never been reported before. The study provides further evidence for the role of the VIPR2 gene in susceptibility to schizophrenia.