Borderline Personality Disorder Clinical Trial
Official title:
Neuropsychiatric Mechanisms of Change in Mentalization Based Treatment of Borderline Personality Disorder (MENTAB)
Purpose:
Borderline personality disorder (BPD) is a complex psychiatric disease of uncertain
aetiology and pathogenesis. A key mechanism of disease susceptibility and treatment response
could be epigenetic changes in DNA methylation patterns. However, no study has yet
demonstrated that psychotherapy can exert its therapeutic effect through epigenetic
mechanisms. The main aim of this study is to analyze the promoter methylation pattern of
genes considered to be related to the development and psychopathology of BPD, in particular
the brain-derived neurotrophic factor (BDNF) and glucocorticoid receptor genes, and the
effects of mentalization based treatment (MBT) on changes. Associations to changes in BDNF
serum levels and salivary cortisol levels, as well as key components of BPD aetiology and
core treatment targets in MBT, will also be investigated. Should epigenetic mechanisms have
importance for BPD pathology and effects of treatment, there is potential use of DNA
methylation patterns as valid biomarker measures of diagnosis, prognosis, and treatment
response.
Hypothesis:
The formation and maintenance of symptoms in BPD is mediated through neuropsychiatric
mechanisms that can be affected through psychological treatment. Specifically, aberrant
epigenetic regulation of neuropsychiatric genes related to behavioural control and affect
regulation, as well as BDNF and cortisol levels, is ameliorated by therapeutic processes.
Method:
Fifty female patients diagnosed with BPD will undergo a year of intensive MBT that is
designed to target domains of BPD pathology. The patients will be assessed at baseline and
every 6 months over the treatment period. Matched healthy control subjects will be assessed
at 6 month intervals to compare changes in DNA methylation, BDNF serum levels, salivary
cortisol levels, and neuropsychological test performance. To link components of the
neuropsychiatric mechanisms underlying the onset of illness, course, and response to
treatment, patients will undergo assessment of clinical symptoms, comorbidity patterns and
psychosocial impairment. Patients and control subjects will at baseline undergo assessment
for childhood trauma, self-harm, suicidal behavior, early maladaptive schemas, and
personality traits, and within the 1-year study period also undergo continuous assessment
for changes in symptoms of dissociation, depression, and personality dysfunction.
n/a
Observational Model: Case Control, Time Perspective: Prospective
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