Frontiers in Pharmacology (Dec 2022)

Methylome-wide association study of different responses to risperidone in schizophrenia

  • Huihui Du,
  • Jingsong Ma,
  • Jingsong Ma,
  • Wei Zhou,
  • Mo Li,
  • Cong Huai,
  • Lu Shen,
  • Hao Wu,
  • Xianglong Zhao,
  • Na Zhang,
  • Songyin Gao,
  • Qi Wang,
  • Lin He,
  • Xuming Wu,
  • Shengying Qin,
  • Mingzhe Zhao,
  • Mingzhe Zhao

DOI
https://doi.org/10.3389/fphar.2022.1078464
Journal volume & issue
Vol. 13

Abstract

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Background: Accumulating evidence shows that DNA methylation plays a role in antipsychotic response. However, the mechanisms by which DNA methylation changes are associated with antipsychotic responses remain largely unknown.Methods: We performed a methylome-wide association study (MWAS) to evaluate the association between DNA methylation and the response to risperidone in schizophrenia. Genomic DNA methylation patterns were assessed using the Agilent Human DNA Methylation Microarray.Results: We identified numerous differentially methylated positions (DMPs) and regions (DMRs) associated with antipsychotic response. CYP46A1, SPATS2, and ATP6V1E1 had the most significant DMPs, with p values of 2.50 × 10–6, 3.53 × 10–6, and 5.71 × 10–6, respectively. The top-ranked DMR was located on chromosome 7, corresponding to the PTPRN2 gene with a Šidák-corrected p-value of 9.04 × 10–13. Additionally, a significant enrichment of synaptic function and neurotransmitters was found in the differentially methylated genes after gene ontology and pathway analysis.Conclusion: The identified DMP- and DMR-overlapping genes associated with antipsychotic response are related to synaptic function and neurotransmitters. These findings may improve understanding of the mechanisms underlying antipsychotic response and guide the choice of antipsychotic in schizophrenia.

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