Does Early Improvement in Anxiety Symptoms in Patients with Major Depressive Disorder Affect Remission Rates? A Post-Hoc Analysis of Pooled Duloxetine Clinic Trials
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Author(s)
Eli Lilly-Turkey, Istanbul, Turkey.
Lilly Research Laboratories Japan, Eli Lilly Japan K.K., Kobe, Japan.
Eli Lilly and Company, Health Technology Appraisal Group, Bad Homburg, Germany.
Eli Lilly and Company, Health Technology Appraisal Group, Bad Homburg, Germany.
Lilly USA, LLC, Indianapolis, USA.
Eli Lilly de México, Mexico City, Mexico.
Lilly Research Laboratories Japan, Eli Lilly Japan K.K., Kobe, Japan.
Eli Lilly and Company, Health Technology Appraisal Group, Bad Homburg, Germany.
Eli Lilly and Company, Health Technology Appraisal Group, Bad Homburg, Germany.
Lilly USA, LLC, Indianapolis, USA.
Eli Lilly de México, Mexico City, Mexico.
Objectives: Patients with major depressive disorder
(MDD) and a comorbid anxiety disorder or significant anxiety symptoms
have decreased functioning, increased risk of suicidality, and worse
post-treatment outcomes. This pooled analysis of 8 duloxetine MDD trials
was designed to determine whether early improvement in anxiety symptoms
predicts MDD remission. Methods: Eight trials were pooled. Patients
with a baseline 17-item Hamilton Rating Scale for Depression (HA-MD17)
anxiety/somatization factor score ≥7 were considered to have anxious
depression. Early response on the HAMD17 total score was defined as a
20% reduction at weeks 2 or 4, a 30% reduction at weeks 2 or 4, or a 50%
reduction at weeks 2 or 4 in the HAMD17 anxiety subscale. Each category
was analyzed separately for all patients. MDD remission is a score of
≤7 on the HAMD17 total score at study endpoint. Results: The early
responder group in each analysis showed greater numerical improvement at
endpoint on the HAMD17 total score than the nonresponder group.
Duloxetine showed statistically significantly greater improvement than
placebo in most nonresponder and responder subgroups. There were no
statistically significant interaction effects for the difference between
duloxetine and placebo for any of the anxious categories. Conclusion:
Although patients who responded in the various response categories had
greater numerical improvement and greater remission rates than
nonresponding patients, the response and nonresponse groups did not
differ statistically regarding the treatment effect of duloxetine.
Therefore, early improvement in anxiety symptoms was not a predictor of
greater endpoint remission of depressive symptoms for duloxetine
treatment.
Cite this paper
Altin, M. , Harada, E. , Schacht, A. , Berggren, L. ,
Walker, D. and Dueñas, H. (2014) Does Early Improvement in Anxiety
Symptoms in Patients with Major Depressive Disorder Affect Remission
Rates? A Post-Hoc Analysis of Pooled Duloxetine Clinic Trials. Open Journal of Depression, 3, 112-123. doi: 10.4236/ojd.2014.33015.
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