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    A meta-analysis of randomized placebo-controlled treatment trials for depression and anxiety in Parkinson’s disease

    193600_98250_journal.pone.0079510.pdf (683.0Kb)
    Access Status
    Open access
    Authors
    Troeung, L.
    Egan, Sarah
    Gasson, Natalie
    Date
    2013
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Troeung, Lakkhina and Egan, Sarah J. and Gasson, Natalie. 2013. A meta-analysis of randomized placebo-controlled treatment trials for depression and anxiety in Parkinson’s disease. PLoS ONE. 8 (11): pp. e79510.
    Source Title
    PLoS ONE
    DOI
    10.1371/journal.pone.0079510
    ISSN
    19326203
    Remarks

    This article is published under the Open Access publishing model and distributed under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/. Please refer to the licence to obtain terms for any further reuse or distribution of this work.

    URI
    http://hdl.handle.net/20.500.11937/2764
    Collection
    • Curtin Research Publications
    Abstract

    Background: Psychopharmacotherapy currently constitutes the first-line treatment for depression and anxiety in Parkinson’s disease (PD) however the efficacy of antidepressant treatments in PD is unclear. Several alternative treatments have been suggested as potentially more viable alternatives including dopamine agonists, repetitive transcranial magnetic stimulation, and cognitive behavioural therapy (CBT). Method: A meta-analysis of randomised placebo-controlled trials for depression and/or anxiety in PD was conducted to systematically examine the efficacy of current treatments for depression and anxiety in PD. Results: Nine trials were included. There was only sufficient data to calculate a pooled effect for antidepressant therapies. The pooled effect of antidepressants for depression in PD was moderate but non-significant (d = .71, 95% CI = −1.33 to 3.08). The secondary effect of antidepressants on anxiety in PD was large but also non-significant (d = 1.13, 95% CI = −.67 to 2.94). Two single-trials of non-pharmacological treatments for depression in PD resulted in significant large effects; Omega-3 supplementation (d = .92, 95% CI = .15 to 1.69) and CBT (d = 1.57, 95% CI = 1.06 to 2.07), and warrant further exploration. Conclusions: There remains a lack of controlled trials for both pharmacological and non-pharmacological treatments for depression and anxiety in PD which limits the conclusions which can be drawn. While the pooled effects of antidepressant therapies in PD were non-significant, the moderate to large magnitude of each pooled effect is promising. Non-pharmacological approaches show potential for depression in PD however more research is required.

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