Which aspects of anhedonia predict response to pharmacotherapy in major depressive disorder?

作者
Rudolf Uher,Sakina Rizvi,Lena C. Quilty,Barbara Pavlova,Abraham Vas Nunes,Jane A. Foster,Raymond W. Lam,Roumen Milev,Daniel J. Müller,Valerie Taylor,Claudio N. Soares,Susan Rotzinger,Sidney H. Kennedy,Benício N. Frey
出处
期刊:Psychological Medicine [Cambridge University Press]
卷期号:56
标识
DOI:10.1017/s0033291725102894
摘要

Abstract Background Anhedonia is a multidimensional concept, and it is not known which aspects of it are linked to the heterogeneity of treatment responses in major depressive disorder (MDD). We examine the role of anhedonia dimensions in predicting response to antidepressant medication and adjunctive pharmacotherapy. Methods In CAN-BIND-1, 187 adults with MDD completed the Dimensional Anhedonia Rating Scale (DARS) and the Snaith–Hamilton Pleasure Scale (SHAPS) before undergoing 8 weeks of treatment with escitalopram. At week 8, 90 nonresponders received adjunctive treatment with aripiprazole for an additional 8 weeks. Mixed-effects models tested the hobbies, food, social, and sensory subscales and items of DARS and SHAPS as predictors of change in the Montgomery-Åsberg Depression Rating Scale (MADRS). Results Of the four DARS subscales, sensory anhedonia predicted a worse treatment outcome with escitalopram ( b = 1.14, 95%CI 0.08 to 2.20, p = 0.034) as did a three-item SHAPS sensory anhedonia subscale ( b = 1.50, 95%CI 0.43 to 2.57, p = 0.006). A combined DARS–SHAPS sensory anhedonia subscale complemented the previously reported interest–activity symptom dimension to improve treatment outcome prediction. In contrast, food and social anhedonia dimensions predicted worse outcomes with adjunctive aripiprazole ( b = 2.52, 95%CI 1.25 to 3.80, p < 0.001; b = 2.56, 95%CI 1.16 to 3.96, p < 0.001). Corresponding SHAPS items showed similar results. Conclusions The inability to enjoy sensory experiences and the lack of interest in food and social activities distinctly predict outcomes with serotonergic versus dopaminergic pharmacotherapy. These findings require replication and extension to other treatments.

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