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Published on: August 11, 2015
Treatment Response Prediction in Major Depressive Disorder Using Multimodal MRI and Clinical Data: Secondary Analysis
Maarten G Poirot1, Henricus G Ruhe1, Henk-Jan M M Mutsaerts1
1Department of Radiology and Nuclear Medicine (Poirot, Ruhe, Marquering, Reneman) and Department of Biomedical Engineering and Physics (Poirot, Marquering, Reneman, Caan), Amsterdam UMC Location AMC, University of Amsterdam, Amsterdam; Brain Imaging, Amsterdam Neuroscience, Amsterdam (Poirot, Mutsaerts, Reneman, Caan); Department of Psychiatry, Radboudumc, Nijmegen, the Netherlands (Ruhe); Donders Institute for Brain, Cognition, and Behavior, Radboud University, Nijmegen, the Netherlands (Ruhe); Department of Radiology and Nuclear Medicine, Amsterdam UMC location, Vrije Universiteit Amsterdam, Amsterdam (Mutsaerts); Department of Health and Functioning, Western Norway University of Applied Sciences, Bergen (Maximov, Bjørnerud); Division of Radiology, Vestfold Hospital Trust, Tønsberg, Norway (Groote, Caan); Computational Radiology and Artificial Intelligence, Division of Radiology and Nuclear Medicine, Oslo University Hospital, Oslo (Groote, Bjørnerud); Department of Psychology, University of Oslo, Oslo (Bjørnerud).
Objective:
Response to antidepressant treatment in major depressive disorder varies substantially between individuals, which lengthens the process of finding effective treatment. The authors sought to determine whether a multimodal machine learning approach could predict early sertraline response in patients with major depressive disorder. They assessed the predictive contribution of MR neuroimaging and clinical assessments at baseline and after 1 week of treatment.
Methods:
This was a preregistered secondary analysis of data from the Establishing Moderators and Biosignatures of Antidepressant Response in Clinical Care (EMBARC) study, a multisite double-blind, placebo-controlled randomized clinical trial that included 296 adult outpatients with unmedicated recurrent or chronic major depressive disorder. MR neuroimaging and clinical data were collected before and after 1 week of treatment. Performance in predicting response and remission, collected after 8 weeks, was quantified using balanced accuracy (bAcc) and area under the receiver operating characteristic curve (AUROC) scores.
Results:
A total of 229 patients were included in the analyses (mean age, 38 years [SD=13]; 66% female). Internal cross-validation performance in predicting response to sertraline (bAcc=68% [SD=10], AUROC=0.73 [SD=0.03]) was significantly better than chance. External cross-validation on data from placebo nonresponders (bAcc=62%, AUROC=0.66) and placebo nonresponders who were switched to sertraline (bAcc=65%, AUROC=0.68) resulted in differences that suggest specificity for sertraline treatment compared with placebo treatment. Finally, multimodal models outperformed unimodal models.
Conclusions:
The study results confirm that early sertraline treatment response can be predicted; that the models are sertraline specific compared with placebo; that prediction benefits from integrating multimodal MRI data with clinical data; and that perfusion imaging contributes most to these predictions. Using this approach, a lean and effective protocol could individualize sertraline treatment planning to improve psychiatric care.
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