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Randomized Controlled Trial
. 2009;26(3):266-72.
doi: 10.1002/da.20544.

High worry severity is associated with poorer acute and maintenance efficacy of antidepressants in late-life depression

Affiliations
Randomized Controlled Trial

High worry severity is associated with poorer acute and maintenance efficacy of antidepressants in late-life depression

Carmen Andreescu et al. Depress Anxiety. 2009.

Abstract

Background: Co-morbid anxiety symptoms are common in late-life depression (LLD) and predict poorer treatment outcomes. No research has delineated the impact of different dimensions of anxiety (such as worry/anxious apprehension and panic/anxious arousal) on treatment response in LLD. We explored the impact of the dimensions of worry and panic on acute and maintenance treatment outcomes in LLD.

Methods: We measured anxiety symptoms in 170 LLD subjects receiving protocolized treatment. Exploratory principal component analysis was used to delineate dimensions of anxiety symptoms. We defined sub-groups based on factor scores. We used survival analysis to test the association of pretreatment anxiety dimensions with time to response and time to recurrence of LLD.

Results: The principal component analysis found two factors: "worry" and "panic." Three sub-groups were defined: low panic-low worry, low panic-high worry, and high panic-high worry. The low panic-high worry and high panic-high worry sub-groups had longer time to response than the low panic-low worry sub-group. Time to recurrence was longer in low panic-low worry subjects randomized to drug. Among subjects with high worry, there was no difference between those with low versus high panic regarding both time to response and time to recurrence of LLD.

Conclusion: High levels of worry were associated with longer time to response and earlier recurrence with pharmacotherapy for LLD. There was no additional effect of panic symptoms on treatment outcomes when accounting for the effects of excessive worry. These results suggest that worry symptoms should be a focus of strategies to improve acute and maintenance treatment response in LLD.

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Conflict of interest statement

Conflict of Interest: Carmen Andreescu and Amy Begley have no conflict of interest to report. Eric J. Lenze has received research support from OrthoMcNeill, Novartis and Forest Pharmaceuticals. Benoit H. Mulsant has received research support or honoraria from Astra-Zeneca, Bristol-Myers Squibb, Eli Lilly, Forest Laboratories, GlaxoSmithKline, Janssen, Lundbeck, and Pfizer; he holds stock (all less than $10,000) in Akzo-Nobel, Alkermes, AstraZeneca, Biogen Idec, Celsion, Elan, Eli Lilly, Forest and Orchestra Therapeutics. Dr. Wetherell has received research support from Forest Pharmaceuticals. Sati Mazumdar directly purchased stocks from Forest (less than $10,000). Charles F. Reynolds III has received pharmaceutical supplies for his NIH-sponsored research from GlaxoSmithKline, Pfizer Inc., Eli Lilly and Co., Bristol Meyers Squibb, Wyeth Pharmaceuticals and Forest Pharmaceuticals.

Figures

Figure 1
Figure 1
Co-morbid dimensions of anxiety and time to response. Subjects with high worry-high panic and subjects with high worry-low panic had a median time to response significantly longer than those with low worry-low panic (Wilcoxon chi-square = 9.81, df = 2, p=0.007)
Figure 2
Figure 2
Co-morbid dimensions of anxiety symptoms and time to recurrence. The mean time to recurrence was significantly longer in low worry-low panic subjects randomized to drug (log-rank p=0.038). There was no difference between subjects with high worry-low panic and high worry-high panic with regard to time to recurrence of late-life depression.

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