Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT02134223 |
Other study ID # |
13MMHIS257 |
Secondary ID |
MMH103-80MOST 10 |
Status |
Completed |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
March 20, 2014 |
Est. completion date |
February 26, 2020 |
Study information
Verified date |
September 2021 |
Source |
Mackay Memorial Hospital |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
Borderline personality disorder (BPD) is a chronic and debilitating syndrome associated with
considerable morbidity, mortality, and high rates of medical and psychiatric utilization
services. Research focusing on finding a biological observable marker for the purpose of
monitoring treatment effects has started to draw attention. Recent research has implicated
that brain-derived neutrophilic factor (BDNF) might be a natural candidate for a biological
correlate of early life stress. The alterations in levels of BDNF or BDNF methylation in BPD
patients compared to general population, or pre- and post- psychotherapeutic treatment might
indicate the consequence of epigenetic modification associated with stressful experience or
suicide, and may later be able to explain the psychopathology or neuro-development of BPD.
Method: The investigators therefore propose this current randomized control trial to test
whether epigenetic changes happen during and after DBT treatments, and not TAU. Proportions
having suicide or non-suicidal self injurious behaviors will be followed and tested against
changes in BDNF methylation levels. Other clinical symptoms will as be assessed, including
suicidality, depression, hopelessness, quality of life, disability, service utilization, and
function.
In the first to third years of this study, the investigators will aim to recruit 180 study
and control subjects, to gather information, to collect biological samples, to give out
one-year of psychotherapy per subject, to evaluate results before, during, and after
treatment. In addition, the investigators also hope to explore the effects of known or
unknown drugs associated with the change of DNA methylation at cell level.
Hypothesis:
Responders of participants who receive DBT will show greater decrease in BDNF methylation
levels than patients receiving TAU.
Description:
Background: Borderline personality disorder (BPD) is a chronic and debilitating syndrome
associated with considerable morbidity, mortality, and high rates of medical and psychiatric
utilization services. The prevalence of BPD is around 1%-2% in general population. However,
suicidality and self-injury are common, an estimated 69-80% of patients with BPD attempt
suicide and a higher percentage engage in nonsuicidal self-injurious behavior. The rate of
completed suicide in this group is appropriately 10%. Several Western literature have
demonstrated the therapeutic effects of dialectical behavior therapy (DBT) in patients with
BPD. However, research focusing on finding a biological observable marker for the purpose of
monitoring treatment effects has started to draw attention. Recent research has implicated
that brain-derived neutrophilic factor (BDNF) might be a natural candidate for a biological
correlate of early life stress. The alterations in levels of BDNF or BDNF methylation in BPD
patients compared to general population, or pre- and post- psychotherapeutic treatment might
indicate the consequence of epigenetic modification associated with stressful experience or
suicide, and may later be able to explain the psychopathology or neurodevelopment of BPD.
Such studies investigating associations of changes in methylation levels, with changes in
depressive scores, hopelessness scores, impulsivity, or effects of psychotherapy have never
been done in Asian countries. Little is known about the possible epigenetic changes related
to Western psychological therapies for BPD patients in Asia.
Method: The investigators therefore propose this current randomized control trial to test
whether epigenetic changes happen during and after DBT treatments, and not treatment as usual
(TAU). Proportions having suicide or non-suicidal self injurious behaviors will be followed
and tested against changes in BDNF methylation levels. Other clinical symptoms will as be
assessed, including suicidality, depression, hopelessness, quality of life, disability,
service utilization, and function. Inclusion criteria will be subjects who fulfill the
Diagnostic Statistic Manual-IV (DSM-IV) criteria for BPD, 20-60 years of age, sign the
informed consent, have had at least two episodes of suicidal or non-suicidal self-injurious
episodes in the past 5 years, and at least one of which is in the 3 months preceding
enrollment. The exclusion criteria include psychotic disorder, bipolar I disorder, severe
physical illness, and mental retardation. Outcome measures and blood samples will be obtained
at pre-treatment, 4-month, 8-month and post-treatment (12-month) during 1-year protocol.
Using semi-structured interview and a battery of self-report forms, a range of symptoms and
behaviors associated with BPD will be assessed. Outcome variables will be evaluated by
blinded assessors.
In the first to third years of this study, the investigators will aim to recruit 180 study
and control subjects, to gather information, to collect biological samples, to give out
one-year of psychotherapy per subject, to evaluate results before, during, and after
treatment. The TAU group would receive any therapy the patient could get excluding DBT. In
addition, we also hope to explore the effects of known or unknown drugs associated with this
project (such as decitabine, azacitidine, trichostatin A, valproic acid) on the change of DNA
methylation at cell level. As a consequence, considering potential developments of biological
correlates or medications as future evidences of treatments for BPD, this research is
expected to take at least three years of investment.
Primary hypothesis:
Responders of participants who receive DBT will show greater decrease in BDNF methylation
levels than patients receiving TAU.
Secondary Hypotheses:
1. Participants who receive DBT and have greater reductions in the frequency and severity
of suicidal and non-suicidal self-injurious behaviors will have different levels in BDNF
methylations compared to those who didn't have as much improvement.
2. Changes in scores or frequencies of borderline personality symptoms, depression,
psychological symptoms, suicidal ideation, hopelessness, disability, and quality of life
measures will be associated with changes in levels of BDNF proteins or BDNF
methylations.
3. Known or unknown epigenetic drugs are also associated with alterations in methylation
status in patient with BPD at cell level.