Depression Clinical Trial
Official title:
Predicting Effects and Risk of Relapse Into Depression - The Danish ECT/MRI Project
The main purpose of this study is to determine whether electroconvulsive therapy (ECT) causes any structural or functional brain changes and thus indicating its mechanism of action. The second aim is to find predictors of an immediate response, sustained remission, relapse and side-effects. Thirdly, this study aims to explore whether ECT causes any changes in blood-brain barriers permeability and whether these changes correlate to memory problems. The fourth objective is to examine whether ECT causes any brain tissue damage.
ECT has been the most effective treatment of depression for decades. Despite of this, neither
the mechanism of action or side-effects are fully elucidated. The reason why some patients
relapse shortly after remission is still not completely understood. Thus, there is a need to
find predictors of the favourable clinical effect, relapse and side-effects. ECT is
considered by professionals to be a safe procedure. However, this view is based on rather old
and small studies. Additionally, many patients do not consent to this treatment because they
fear a permanent loss of memory or that they will contract a brain damage after the completed
ECT series. Therefore, it is very important to examine whether ECT might have negative
effects on the structure or function of the brain, using state of the art Magnetic Resonance
Imaging (MRI) techniques on a greater study population.
The study consists of 60 inpatients, diagnosed with depression, admitted to one of the
recruiting Mental Health Centres, and scheduled to ECT. The most modern MRI sequences
examining brain structure and function are used at 3 time points: at baseline (just before
ECT series), the second examination (just after ECT series) and the third (follow-up)
examination (6 months after ECT series). Blood samples (measurements of Brain-Derived
Neurotrophic Factor - BDNF, Vascular Endothelial Growth Factor - VEGF along with the marker
of brain injury - S100B-protein) and the evaluation of clinical effect and side-effects to
ECT are performed at the same time points.
The study has 4 main hypotheses. The first hypothesis assumes that the immediate and
sustained response to ECT can be predicted by combining neuroimaging findings and
blood-samples results. The second hypothesis is based on the assumption that ECT modulates
the microstructure and connectivity in the fronto-limbic pathways (FLPs) and that this
modulation correlates with the clinical effect. Thus, the altered microstructure of the FLPs
in depression is normalised by an ECT series. Furthermore, the depression-associated
increased resting state connectivity in FLPs is normalised by ECT. The third hypothesis is
that ECT will induce changes in blood-brain barrier (BBB) permeability, which will correlate
with the severity of memory problems. The last hypothesis assumes that ECT does not cause any
brain tissue damage (including brain atrophy and white matter lesions - WMLs).
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