Combining clinical variables to optimize prediction of antidepressant treatment outcomes

Raquel Iniesta, Karim Malki, Wolfgang Maier, Marcella Rietschel, Ole Mors, Joanna Hauser, Neven Henigsberg, Mojca Zvezdana Dernovsek, Daniel Souery, Daniel Stahl, Richard Dobson, Katherine J. Aitchison, Anne Farmer, Cathryn M. Lewis, Peter McGuffin, Rudolf Uher

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126 Citas (Scopus)

Resumen

The outcome of treatment with antidepressants varies markedly across people with the same diagnosis. A clinically significant prediction of outcomes could spare the frustration of trial and error approach and improve the outcomes of major depressive disorder through individualized treatment selection. It is likely that a combination of multiple predictors is needed to achieve such prediction. We used elastic net regularized regression to optimize prediction of symptom improvement and remission during treatment with escitalopram or nortriptyline and to identify contributing predictors from a range of demographic and clinical variables in 793 adults with major depressive disorder. A combination of demographic and clinical variables, with strong contributions from symptoms of depressed mood, reduced interest, decreased activity, indecisiveness, pessimism and anxiety significantly predicted treatment outcomes, explaining 5-10% of variance in symptom improvement with escitalopram. Similar combinations of variables predicted remission with area under the curve 0.72, explaining approximately 15% of variance (pseudo R2) in who achieves remission, with strong contributions from body mass index, appetite, interest-activity symptom dimension and anxious-somatizing depression subtype. Escitalopram-specific outcome prediction was more accurate than generic outcome prediction, and reached effect sizes that were near or above a previously established benchmark for clinical significance. Outcome prediction on the nortriptyline arm did not significantly differ from chance. These results suggest that easily obtained demographic and clinical variables can predict therapeutic response to escitalopram with clinically meaningful accuracy, suggesting a potential for individualized prescription of this antidepressant drug.

Idioma originalEnglish
Páginas (desde-hasta)94-102
Número de páginas9
PublicaciónJournal of Psychiatric Research
Volumen78
DOI
EstadoPublished - jul. 1 2016

Nota bibliográfica

Funding Information:
Open access for this article was funded by King’s College London.

Funding Information:
Iniesta, McGuffin, Farmer, Maier, Stahl, Rietschel, Dernovsek, Souery, Hauser, Mors, Dobson and Malki have no conflicts of interest. Lewis and Uher reports grants from European Commission, during the conduct of the study. Henigsberg reports grant from European Commission (through Institute of Psychiatry, King's College, London), and participation in clinical trials sponsored by pharmaceutical companies, including Lundbeck outside the submitted work. Aitchison reports grants and personal fees from Lundbeck/GlaxoSmithKline, outside the submitted work.

Funding Information:
This work has been funded by the European Commission Framework 6 grant, EC Contract LSHB-CT-2003-503428 and an Innovative Medicine Initiative Joint Undertaking (IMI-JU) grant n° 115008 of which resources are composed of European Union and the European Federation of Pharmaceutical Industries and Associations (EFPIA) in-kind contribution and financial contribution from the European Union's Seventh Framework Programme (FP7/2007-2013).

Funding Information:
Funding was also received from the European Community's FP7 Marie Curie Industry-Academia Partnership and Pathways, grant agreement n° 286213 (PsychDPC).

Funding Information:
This article represents independent research part funded by the National Institute for Health Research (NIHR) Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King’s College London. The views expressed are those of the authors and not necessarily those of the NHS, the NIHR or the Department of Health.

Publisher Copyright:
© 2016 The Authors.

ASJC Scopus Subject Areas

  • Psychiatry and Mental health
  • Biological Psychiatry

PubMed: MeSH publication types

  • Comparative Study
  • Journal Article
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

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