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Differential COMT DNA methylation in patients with Borderline Personality Disorder: Genotype matters. | LitMetric

AI Article Synopsis

  • Differential DNA methylation in peripheral tissues is linked to Borderline Personality Disorder (BPD), with notable alterations in the COMT gene.
  • The COMT gene has a variant (ValMet) that impacts protein function and is associated with various psychiatric disorders, including BPD.
  • This study highlights the importance of considering genotype when examining COMT DNA methylation, as significant differences were found between BPD patients and healthy controls, suggesting that genotype influences these alterations.

Article Abstract

Differential DNA methylation in peripheral tissues has been associated with Borderline Personality Disorder (BPD). Alterations have been found in several genes, among them the Catechol-O-methyltransferase (COMT) gene. COMT is a known neuropsychiatric candidate gene, which contains a genotype variant (ValMet) that affects protein function and has been found associated with several psychiatric disorders. In addition, this variant also affects COMT DNA methylation. However, in previous epigenetic studies, the DNA methylation results have not always been controlled for genotype, even though overrepresentation of the Met allele has been frequently reported in cohorts of BPD patients. Therefore, in the present study, we investigated whether alteration of COMT DNA methylation in BPD patients is indeed associated with mental health status or merely influenced by a differential distribution of the COMT genotype between BPD patients and healthy control individuals. We found significant group differences, as well as a strong effect of genotype on COMT DNA methylation. While the direction of effect was different compared to a previous study, our study supports the finding of altered COMT DNA methylation in patients with BPD and reinforces the need to include genotype information in future DNA methylation studies of COMT.

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Source
http://dx.doi.org/10.1016/j.euroneuro.2019.09.011DOI Listing

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