Is the efficacy of antidepressants in panic disorder mediated by adverse events? A mediational analysis.

It has been hypothesised that the perception of adverse events in placebo-controlled antidepressant clinical trials may induce patients to conclude that they have been randomized to the active arm of the trial, leading to the breaking of blind. This may enhance the expectancies for improvement and t...

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Main Authors: Irene Bighelli, Anna Borghesani, Corrado Barbui
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5456299?pdf=render
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spelling doaj-4041b5a6660944389d13c8929259937e2020-11-25T02:47:45ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01126e017861710.1371/journal.pone.0178617Is the efficacy of antidepressants in panic disorder mediated by adverse events? A mediational analysis.Irene BighelliAnna BorghesaniCorrado BarbuiIt has been hypothesised that the perception of adverse events in placebo-controlled antidepressant clinical trials may induce patients to conclude that they have been randomized to the active arm of the trial, leading to the breaking of blind. This may enhance the expectancies for improvement and the therapeutic response. The main objective of this study is to test the hypothesis that the efficacy of antidepressants in panic disorder is mediated by the perception of adverse events. The present analysis is based on a systematic review of published and unpublished randomised trials comparing antidepressants with placebo for panic disorder. The Baron and Kenny approach was applied to investigate the mediational role of adverse events in the relationship between antidepressants treatment and efficacy. Fourteen placebo-controlled antidepressants trials were included in the analysis. We found that: (a) antidepressants treatment was significantly associated with better treatment response (ß = 0.127, 95% CI 0.04 to 0.21, p = 0.003); (b) antidepressants treatment was not associated with adverse events (ß = 0.094, 95% CI -0.05 to 0.24, p = 0.221); (c) adverse events were negatively associated with treatment response (ß = 0.035, 95% CI -0.06 to -0.05, p = 0.022). Finally, after adjustment for adverse events, the relationship between antidepressants treatment and treatment response remained statistically significant (ß = 0.122, 95% CI 0.01 to 0.23, p = 0.039). These findings do not support the hypothesis that the perception of adverse events in placebo-controlled antidepressant clinical trials may lead to the breaking of blind and to an artificial inflation of the efficacy measures. Based on these results, we argue that the moderate therapeutic effect of antidepressants in individuals with panic disorder is not an artefact, therefore reflecting a genuine effect that doctors can expect to replicate under real-world conditions.http://europepmc.org/articles/PMC5456299?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Irene Bighelli
Anna Borghesani
Corrado Barbui
spellingShingle Irene Bighelli
Anna Borghesani
Corrado Barbui
Is the efficacy of antidepressants in panic disorder mediated by adverse events? A mediational analysis.
PLoS ONE
author_facet Irene Bighelli
Anna Borghesani
Corrado Barbui
author_sort Irene Bighelli
title Is the efficacy of antidepressants in panic disorder mediated by adverse events? A mediational analysis.
title_short Is the efficacy of antidepressants in panic disorder mediated by adverse events? A mediational analysis.
title_full Is the efficacy of antidepressants in panic disorder mediated by adverse events? A mediational analysis.
title_fullStr Is the efficacy of antidepressants in panic disorder mediated by adverse events? A mediational analysis.
title_full_unstemmed Is the efficacy of antidepressants in panic disorder mediated by adverse events? A mediational analysis.
title_sort is the efficacy of antidepressants in panic disorder mediated by adverse events? a mediational analysis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description It has been hypothesised that the perception of adverse events in placebo-controlled antidepressant clinical trials may induce patients to conclude that they have been randomized to the active arm of the trial, leading to the breaking of blind. This may enhance the expectancies for improvement and the therapeutic response. The main objective of this study is to test the hypothesis that the efficacy of antidepressants in panic disorder is mediated by the perception of adverse events. The present analysis is based on a systematic review of published and unpublished randomised trials comparing antidepressants with placebo for panic disorder. The Baron and Kenny approach was applied to investigate the mediational role of adverse events in the relationship between antidepressants treatment and efficacy. Fourteen placebo-controlled antidepressants trials were included in the analysis. We found that: (a) antidepressants treatment was significantly associated with better treatment response (ß = 0.127, 95% CI 0.04 to 0.21, p = 0.003); (b) antidepressants treatment was not associated with adverse events (ß = 0.094, 95% CI -0.05 to 0.24, p = 0.221); (c) adverse events were negatively associated with treatment response (ß = 0.035, 95% CI -0.06 to -0.05, p = 0.022). Finally, after adjustment for adverse events, the relationship between antidepressants treatment and treatment response remained statistically significant (ß = 0.122, 95% CI 0.01 to 0.23, p = 0.039). These findings do not support the hypothesis that the perception of adverse events in placebo-controlled antidepressant clinical trials may lead to the breaking of blind and to an artificial inflation of the efficacy measures. Based on these results, we argue that the moderate therapeutic effect of antidepressants in individuals with panic disorder is not an artefact, therefore reflecting a genuine effect that doctors can expect to replicate under real-world conditions.
url http://europepmc.org/articles/PMC5456299?pdf=render
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