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Predicting prognosis for adults with depression using individual symptom data: a comparison of modelling approaches.
Buckman, J E J; Cohen, Z D; O'Driscoll, C; Fried, E I; Saunders, R; Ambler, G; DeRubeis, R J; Gilbody, S; Hollon, S D; Kendrick, T; Watkins, E; Eley, T C; Peel, A J; Rayner, C; Kessler, D; Wiles, N; Lewis, G; Pilling, S.
Afiliação
  • Buckman JEJ; Research Department of Clinical, Educational & Health Psychology, Centre for Outcomes Research and Effectiveness (CORE), University College London, 1-19 Torrington Place, London, UK.
  • Cohen ZD; iCope - Camden & Islington Psychological Therapies Services - Camden & Islington NHS Foundation Trust, St Pancras Hospital, London, UK.
  • O'Driscoll C; Department of Psychiatry, University of California, Los Angeles, Los Angeles, CA, USA.
  • Fried EI; Research Department of Clinical, Educational & Health Psychology, Centre for Outcomes Research and Effectiveness (CORE), University College London, 1-19 Torrington Place, London, UK.
  • Saunders R; Department of Clinical Psychology, Leiden University, Leiden, The Netherlands.
  • Ambler G; Research Department of Clinical, Educational & Health Psychology, Centre for Outcomes Research and Effectiveness (CORE), University College London, 1-19 Torrington Place, London, UK.
  • DeRubeis RJ; Statistical Science, University College London, 1-19 Torrington Place, London, UK.
  • Gilbody S; Department of Psychology, School of Arts and Sciences, 425 S. University Avenue, Philadelphia PA, USA.
  • Hollon SD; Department of Health Sciences, University of York, Seebohm Rowntree Building, Heslington, York, UK.
  • Kendrick T; Department of Psychology, Vanderbilt University, Nashville, TN, USA.
  • Watkins E; Primary Care, Population Sciences and Medical Education, Faculty of Medicine, University of Southampton, Aldermoor Health Centre, Southampton, UK.
  • Eley TC; Department of Psychology, University of Exeter, Sir Henry Wellcome Building for Mood Disorders Research, Perry Road, Exeter, UK.
  • Peel AJ; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.
  • Rayner C; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.
  • Kessler D; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.
  • Wiles N; Centre for Academic Primary Care, Population Health Sciences, Bristol Medical School, University of Bristol, Canynge Hall, Bristol, UK.
  • Lewis G; Centre for Academic Mental Health, Population Health Sciences, Bristol Medical School, University of Bristol, Oakfield House, Bristol, UK.
  • Pilling S; Division of Psychiatry, University College London, Maple House, London, UK.
Psychol Med ; 53(2): 408-418, 2023 01.
Article em En | MEDLINE | ID: mdl-33952358
BACKGROUND: This study aimed to develop, validate and compare the performance of models predicting post-treatment outcomes for depressed adults based on pre-treatment data. METHODS: Individual patient data from all six eligible randomised controlled trials were used to develop (k = 3, n = 1722) and test (k = 3, n = 918) nine models. Predictors included depressive and anxiety symptoms, social support, life events and alcohol use. Weighted sum scores were developed using coefficient weights derived from network centrality statistics (models 1-3) and factor loadings from a confirmatory factor analysis (model 4). Unweighted sum score models were tested using elastic net regularised (ENR) and ordinary least squares (OLS) regression (models 5 and 6). Individual items were then included in ENR and OLS (models 7 and 8). All models were compared to one another and to a null model (mean post-baseline Beck Depression Inventory Second Edition (BDI-II) score in the training data: model 9). Primary outcome: BDI-II scores at 3-4 months. RESULTS: Models 1-7 all outperformed the null model and model 8. Model performance was very similar across models 1-6, meaning that differential weights applied to the baseline sum scores had little impact. CONCLUSIONS: Any of the modelling techniques (models 1-7) could be used to inform prognostic predictions for depressed adults with differences in the proportions of patients reaching remission based on the predicted severity of depressive symptoms post-treatment. However, the majority of variance in prognosis remained unexplained. It may be necessary to include a broader range of biopsychosocial variables to better adjudicate between competing models, and to derive models with greater clinical utility for treatment-seeking adults with depression.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ansiedade / Depressão Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans Idioma: En Revista: Psychol Med Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ansiedade / Depressão Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Humans Idioma: En Revista: Psychol Med Ano de publicação: 2023 Tipo de documento: Article