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Clinical factors predicting treatment resistant depression: affirmative results from the European multicenter study

OBJECTIVES: Clinical variables were investigated in the ‘treatment resistant depression (TRD)‐ III’ sample to replicate earlier findings by the European research consortium ‘Group for the Study of Resistant Depression’ (GSRD) and enable cross‐sample prediction of treatment outcome in TRD. EXPERIMENT...

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Autores principales: Kautzky, A., Dold, M., Bartova, L., Spies, M., Kranz, G. S., Souery, D., Montgomery, S., Mendlewicz, J., Zohar, J., Fabbri, C., Serretti, A., Lanzenberger, R., Dikeos, D., Rujescu, D., Kasper, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6586002/
https://www.ncbi.nlm.nih.gov/pubmed/30291625
http://dx.doi.org/10.1111/acps.12959
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author Kautzky, A.
Dold, M.
Bartova, L.
Spies, M.
Kranz, G. S.
Souery, D.
Montgomery, S.
Mendlewicz, J.
Zohar, J.
Fabbri, C.
Serretti, A.
Lanzenberger, R.
Dikeos, D.
Rujescu, D.
Kasper, S.
author_facet Kautzky, A.
Dold, M.
Bartova, L.
Spies, M.
Kranz, G. S.
Souery, D.
Montgomery, S.
Mendlewicz, J.
Zohar, J.
Fabbri, C.
Serretti, A.
Lanzenberger, R.
Dikeos, D.
Rujescu, D.
Kasper, S.
author_sort Kautzky, A.
collection PubMed
description OBJECTIVES: Clinical variables were investigated in the ‘treatment resistant depression (TRD)‐ III’ sample to replicate earlier findings by the European research consortium ‘Group for the Study of Resistant Depression’ (GSRD) and enable cross‐sample prediction of treatment outcome in TRD. EXPERIMENTAL PROCEDURES: TRD was defined by a Montgomery and Åsberg Depression Rating Scale (MADRS) score ≥22 after at least two antidepressive trials. Response was defined by a decline in MADRS score by ≥50% and below a threshold of 22. Logistic regression was applied to replicate predictors for TRD among 16 clinical variables in 916 patients. Elastic net regression was applied for prediction of treatment outcome. RESULTS: Symptom severity (odds ratio (OR) = 3.31), psychotic symptoms (OR = 2.52), suicidal risk (OR = 1.74), generalized anxiety disorder (OR = 1.68), inpatient status (OR = 1.65), higher number of antidepressants administered previously (OR = 1.23), and lifetime depressive episodes (OR = 1.15) as well as longer duration of the current episode (OR = 1.022) increased the risk of TRD. Prediction of TRD reached an accuracy of 0.86 in the independent validation set, TRD‐I. CONCLUSION: Symptom severity, suicidal risk, higher number of lifetime depressive episodes, and comorbid anxiety disorder were replicated as the most prominent risk factors for TRD. Significant predictors in TRD‐III enabled robust prediction of treatment outcome in TRD‐I.
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spelling pubmed-65860022019-06-27 Clinical factors predicting treatment resistant depression: affirmative results from the European multicenter study Kautzky, A. Dold, M. Bartova, L. Spies, M. Kranz, G. S. Souery, D. Montgomery, S. Mendlewicz, J. Zohar, J. Fabbri, C. Serretti, A. Lanzenberger, R. Dikeos, D. Rujescu, D. Kasper, S. Acta Psychiatr Scand Original Articles OBJECTIVES: Clinical variables were investigated in the ‘treatment resistant depression (TRD)‐ III’ sample to replicate earlier findings by the European research consortium ‘Group for the Study of Resistant Depression’ (GSRD) and enable cross‐sample prediction of treatment outcome in TRD. EXPERIMENTAL PROCEDURES: TRD was defined by a Montgomery and Åsberg Depression Rating Scale (MADRS) score ≥22 after at least two antidepressive trials. Response was defined by a decline in MADRS score by ≥50% and below a threshold of 22. Logistic regression was applied to replicate predictors for TRD among 16 clinical variables in 916 patients. Elastic net regression was applied for prediction of treatment outcome. RESULTS: Symptom severity (odds ratio (OR) = 3.31), psychotic symptoms (OR = 2.52), suicidal risk (OR = 1.74), generalized anxiety disorder (OR = 1.68), inpatient status (OR = 1.65), higher number of antidepressants administered previously (OR = 1.23), and lifetime depressive episodes (OR = 1.15) as well as longer duration of the current episode (OR = 1.022) increased the risk of TRD. Prediction of TRD reached an accuracy of 0.86 in the independent validation set, TRD‐I. CONCLUSION: Symptom severity, suicidal risk, higher number of lifetime depressive episodes, and comorbid anxiety disorder were replicated as the most prominent risk factors for TRD. Significant predictors in TRD‐III enabled robust prediction of treatment outcome in TRD‐I. John Wiley and Sons Inc. 2018-10-05 2019-01 /pmc/articles/PMC6586002/ /pubmed/30291625 http://dx.doi.org/10.1111/acps.12959 Text en © 2018 The Authors Acta Psychiatrica Scandinavica Published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Kautzky, A.
Dold, M.
Bartova, L.
Spies, M.
Kranz, G. S.
Souery, D.
Montgomery, S.
Mendlewicz, J.
Zohar, J.
Fabbri, C.
Serretti, A.
Lanzenberger, R.
Dikeos, D.
Rujescu, D.
Kasper, S.
Clinical factors predicting treatment resistant depression: affirmative results from the European multicenter study
title Clinical factors predicting treatment resistant depression: affirmative results from the European multicenter study
title_full Clinical factors predicting treatment resistant depression: affirmative results from the European multicenter study
title_fullStr Clinical factors predicting treatment resistant depression: affirmative results from the European multicenter study
title_full_unstemmed Clinical factors predicting treatment resistant depression: affirmative results from the European multicenter study
title_short Clinical factors predicting treatment resistant depression: affirmative results from the European multicenter study
title_sort clinical factors predicting treatment resistant depression: affirmative results from the european multicenter study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6586002/
https://www.ncbi.nlm.nih.gov/pubmed/30291625
http://dx.doi.org/10.1111/acps.12959
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