AI Article Synopsis

  • The study explored how DNA methylation (DNAm) in a specific gene related to stress might connect genetic and environmental factors influencing schizophrenia symptoms.
  • Researchers analyzed blood samples from 66 schizophrenia patients and 63 controls using advanced sequencing techniques.
  • Results showed that while certain genetic variations (haplotype and VNTR) and environmental risk scores affected DNAm, the findings did not support the idea that this specific DNA region mediates the impact of these risk factors on schizophrenia symptoms.

Article Abstract

As genetic and environmental influences on schizophrenia might converge on DNA methylation (DNAm) within loci which are both associated with the disease and implicated in response to environmental stress, we examined whether DNAm within , a hypothalamus-pituitary-adrenal axis gene which is situated within the schizophrenia risk locus 10q24.32, would mediate genetic and environmental effects on stress-related schizophrenia symptoms. DNAm within an exonic-intronic fragment of was assessed in the blood of 66 schizophrenia patients and 63 controls using single-molecule real-time bisulfite sequencing. Additionally, the VNTR polymorphism of the gene, a plausible causal variant within the 10q24.32 locus, was genotyped in extended patient and control samples ( = 700). The effects of local haplotype, VNTR and a polyenviromic risk score (PERS) on DNAm, episodic verbal memory, executive functions, depression, and suicidality of patients were assessed. Haplotype and PERS differentially influenced DNAm at four variably methylated sites identified within the fragment, with stochastic, additive, and allele-specific effects being found. An allele-specific DNAm at CpG-SNP rs3781286 mediated the relationship between the local haplotype and verbal fluency. Our findings do not confirm that the interrogated DNA fragment is a place where genetic and environmental risk factors converge to influence schizophrenia symptoms through DNAm.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604497PMC
http://dx.doi.org/10.3390/ijms232012629DOI Listing

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