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Multicenter Study
. 2025 Sep:98:26-34.
doi: 10.1016/j.euroneuro.2025.06.011. Epub 2025 Jul 11.

Clinical predictors of treatment resistant depression

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Free article
Multicenter Study

Clinical predictors of treatment resistant depression

Alessandro Serretti et al. Eur Neuropsychopharmacol. 2025 Sep.
Free article

Abstract

Despite advances in the treatment of major depressive disorder (MDD) yet a substantial proportion of patients fail to achieve remission and instead develop treatment-resistant depression (TRD). Identifying robust clinical predictors of response is essential for early, personalized interventions. We analyzed a large, multicenter sample (N = 2953) from the Group for the Study of Resistant Depression (GSRD) project, which included previously studied cohorts (TRD I-III) and a newly recruited cohort (TRD IV, N = 294). Patients were categorized as responders, non-responders, or TRD. Sociodemographic and clinical variables, including current and retrospective MADRS items, were used to train an XGBoost classifier. Primary outcomes were the multi-class metrics area under the curve (AUC), accuracy, and F1-scores. Previously reported predictors were mainly confirmed in the new TRD IV sample. The XGBoost model showed a mean ROC AUC of 0.80 and an accuracy of 61 %, significantly above chance. Misclassification was more frequent among responders versus non-responders, while TRD was predicted most accurately (precision=0.73; recall=0.73). Measures of illness chronicity, such as duration of current episode, duration of disease lifetime, number of hospitalizations, and number of depressive episodes, as well as severity features, BMI and level of functioning were among the most important predictors. Secondary analyses using earlier cohorts to train and the new TRD IV sample to test confirmed stable performance metrics. Our findings highlight the central role of chronicity indicators, severity measures and functioning in predicting antidepressant response and TRD. Future work should include prospective validation and integration of biomarker data to further enhance predictive power.

Keywords: Antidepressants; Machine learning; Major depression; Predictive models; Treatment resistant depression.

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Conflict of interest statement

Declaration of competing interest Dr. Rujescu served as consultant for Janssen, received honoraria from Boehringer-Ingelheim, Gerot Lannacher, Janssen and Pharmagenetix, received research/ travel support from Angelini, Boehringer-Ingelheim, Janssen and Schwabe, and served on advisory boards of AC Immune, Boehringer-Ingelheim, Roche and Rovi. Dr. Souery has received grant/research support from GlaxoSmithKline and Lundbeck; and he has served as a consultant or on advisory boards for AstraZeneca, Bristol-Myers Squibb, Eli Lilly, Janssen, and Lundbeck. Dr. Mendlewicz is a member of the board of the Lundbeck International Neuroscience Foundation and of the advisory board of Servier. Dr. Zohar has received grant/research support from Lundbeck, Servier, and Pfizer; he has served as a consultant or on the advisory boards for Servier, Pfizer, Solvay, and Actelion; and he has served on speakers’ bureaus for Lundbeck, GlaxoSmithKline, Jazz, and Solvay. Dr. Montgomery has served as a consultant or on advisory boards for AstraZeneca, Bionevia, Bristol-Myers Squibb, Forest, GlaxoSmithKline, Grunenthal, Intellect Pharma, Johnson & Johnson, Lilly, Lundbeck, Merck, Merz, M's Science, Neurim, Otsuka, Pierre Fabre, Pfizer, Pharmaneuroboost, Richter, Roche, Sanofi, Sepracor, Servier, Shire, Synosis, Takeda, Theracos, Targacept, Transcept, UBC, Xytis, and Wyeth. Dr. Serretti has served as a consultant or speaker for Abbott, Abbvie, Angelini, AstraZeneca, Clinical Data, Boehringer, Bristol-Myers Squibb, Eli Lilly, GlaxoSmithKline, Innovapharma, Italfarmaco, Janssen, Lundbeck, Naurex, Pfizer, Polifarma, Sanofi, and Servier and Taliaz. Dr. Kasper has received grant/research support from Lundbeck; he has served as a consultant or on advisory boards for Angelini, Biogen, Boehringer-Ingelheim, Esai, Janssen, IQVIA, Lundbeck, Mylan, Recordati, Rovi, Sage and Schwabe; and he has served on speakers bureaus for Aspen Farmaceutica S.A., Angelini, Biogen, Janssen, Lundbeck, Neuraxpharma, Recordati, Sage, Sanofi, Schwabe, Servier and Sun Pharma. Dr. Baune received honoraria for serving as a consultant or on advisory boards unrelated to the present work for Angelini, AstraZeneca, Biogen, Boehringer Ingelheim, Bristol-Meyers Squibb, Janssen, LivaNova, Lundbeck, Medscape, Neurotorium, Novartis, Otsuka, Pfizer, Recordati, Roche, Rovi, Sanofi, Servier, Teva. Dr. Bartova has received travel grants and/or consultant/speaker honoraria from Market Access Transformation, Alpine Market Research, Medizin Medien Austria, Universimed, Vertretungsnetz, Diagnosia, Dialectica, EQT, IQVIA, AOP Orphan, Schwabe, Janssen (Johnson & Johnson), Angelini, Lundbeck, Novartis, Biogen, Takeda. The other authors declare no potential conflicts of interest.

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