Clinical predictors of treatment resistant depression.

Journal: European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology
Published Date:

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.

Authors

  • Alessandro Serretti
    Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
  • Siegfried Kasper
    Department of Psychiatry and Psychotherapy, Medical University of Vienna, Währinger Gürtel 18-20, A-1090 Vienna, Austria. sci-biolpsy@meduniwien.ac.at.
  • Lucie Bartova
    Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna, Austria.
  • Joseph Zohar
    Psychiatric Division, Chaim Sheba Medical Center, Ramat Gan, Israel.
  • Daniel Souery
    Université Libre de Bruxelles and Psy Pluriel Centre Europèen de Psychologie Medicale, Brussels, Belgium.
  • Stuart Montgomery
    Imperial College, University of London, London, United Kingdom.
  • Panagiotis Ferentinos
    Department of Psychiatry, Athens University Medical School, Athens, Greece.
  • Dan Rujescu
    Department of Psychiatry and Psychotherapy, Medical University Vienna, Vienna, Austria.
  • Alexander Kautzky
    Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna, Austria.
  • Francesco Attanasio
    Vita-Salute San Raffaele University, Milan, Italy.
  • Raffaella Zanardi
    Department of Clinical Neurosciences, IRCCS San Raffaele Scientific Institute, Milan, Italy.
  • Chiara Fabbri
    Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
  • Bernhard T Baune
    Discipline of Psychiatry, Adelaide Medical School, The University of Adelaide.
  • Raffaele Ferri
    Units of Psychology I.C. and Unit of Bioinformatics and Statistics, Oasi Research Institute-IRCCS, 94018 Troina, Italy.
  • Julien Mendlewicz
    School of Medicine, Free University of Brussels, Brussels, Belgium.