4.7 Article

A genome-wide methylation study reveals X chromosome and childhood trauma methylation alterations associated with borderline personality disorder

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TRANSLATIONAL PSYCHIATRY
卷 11, 期 1, 页码 -

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DOI: 10.1038/s41398-020-01139-z

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  1. Centro de Investigacion Biomedica en Red de Salud Mental (CIBERSAM)
  2. Instituto de Salud Carlos III [PI14/00214]
  3. European Regional Development Fund (ERDF)

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BPD patients exhibit significantly lower methylation levels in CpG sites on the X chromosome and chromosome 6 compared to healthy controls, with childhood trauma potentially exacerbating these differences. Epigenetic alterations are more frequently found in genes controlling estrogen regulation, neurogenesis, and cell differentiation, suggesting their potential contribution to BPD development and gender differences in presentation.
Borderline personality disorder (BPD) is a severe and highly prevalent psychiatric disorder, more common in females than in males and with notable differences in presentation between genders. Recent studies have shown that epigenetic modifications such as DNA methylation may modulate genexenvironment interactions and impact on neurodevelopment. We conducted an epigenome wide study (Illumina Infinium HumanMethylation450k beadchip) in a group of BPD patients with (N=49) and without (N=47) childhood traumas and in a control group (N=44). Results were confirmed in a replication cohort (N=293 BPD patients and N=114 controls) using EpiTYPER assays. Differentially methylated CpG sites were observed in several genes and intragenic regions in the X chromosome (PQBP1, ZNF41, RPL10, cg07810091 and cg24395855) and in chromosome 6 (TAP2). BPD patients showed significantly lower methylation levels in these CpG sites than healthy controls. These differences seemed to be increased by the existence of childhood trauma. Comparisons between BPD patients with childhood trauma and patients and controls without revealed significant differences in four genes (POU5F1, GGT6, TNFRSF13C and FAM113B), none of them in the X chromosome. Gene set enrichment analyses revealed that epigenetic alterations were more frequently found in genes controlling oestrogen regulation, neurogenesis and cell differentiation. These results suggest that epigenetic alterations in the X chromosome and oestrogen-regulation genes may contribute to the development of BPD and explain the differences in presentation between genders. Furthermore, childhood trauma events may modulate the magnitude of the epigenetic alterations contributing to BPD.

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