Clinical predictors of antipsychotic treatment resistance: Development and internal validation of a prognostic prediction model by the STRATA-G consortium.

Détails

Ressource 1Télécharger: S092099.pdf (622.93 [Ko])
Etat: Public
Version: Final published version
Licence: CC BY 4.0
ID Serval
serval:BIB_FD83206AB9D6
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Clinical predictors of antipsychotic treatment resistance: Development and internal validation of a prognostic prediction model by the STRATA-G consortium.
Périodique
Schizophrenia research
Auteur⸱e⸱s
Smart S.E., Agbedjro D., Pardiñas A.F., Ajnakina O., Alameda L., Andreassen O.A., Barnes TRE, Berardi D., Camporesi S., Cleusix M., Conus P., Crespo-Facorro B., D'Andrea G., Demjaha A., Di Forti M., Do K., Doody G., Eap C.B., Ferchiou A., Guidi L., Homman L., Jenni R., Joyce E., Kassoumeri L., Lastrina O., Melle I., Morgan C., O'Neill F.A., Pignon B., Restellini R., Richard J.R., Simonsen C., Španiel F., Szöke A., Tarricone I., Tortelli A., Üçok A., Vázquez-Bourgon J., Murray R.M., Walters JTR, Stahl D., MacCabe J.H.
ISSN
1573-2509 (Electronic)
ISSN-L
0920-9964
Statut éditorial
Publié
Date de publication
12/2022
Peer-reviewed
Oui
Volume
250
Pages
1-9
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: ppublish
Résumé
Our aim was to, firstly, identify characteristics at first-episode of psychosis that are associated with later antipsychotic treatment resistance (TR) and, secondly, to develop a parsimonious prediction model for TR.
We combined data from ten prospective, first-episode psychosis cohorts from across Europe and categorised patients as TR or non-treatment resistant (NTR) after a mean follow up of 4.18 years (s.d. = 3.20) for secondary data analysis. We identified a list of potential predictors from clinical and demographic data recorded at first-episode. These potential predictors were entered in two models: a multivariable logistic regression to identify which were independently associated with TR and a penalised logistic regression, which performed variable selection, to produce a parsimonious prediction model. This model was internally validated using a 5-fold, 50-repeat cross-validation optimism-correction.
Our sample consisted of N = 2216 participants of which 385 (17 %) developed TR. Younger age of psychosis onset and fewer years in education were independently associated with increased odds of developing TR. The prediction model selected 7 out of 17 variables that, when combined, could quantify the risk of being TR better than chance. These included age of onset, years in education, gender, BMI, relationship status, alcohol use, and positive symptoms. The optimism-corrected area under the curve was 0.59 (accuracy = 64 %, sensitivity = 48 %, and specificity = 76 %).
Our findings show that treatment resistance can be predicted, at first-episode of psychosis. Pending a model update and external validation, we demonstrate the potential value of prediction models for TR.
Mots-clé
Humans, Antipsychotic Agents/therapeutic use, Prognosis, Prospective Studies, Psychotic Disorders/diagnosis, Educational Status, First episode psychosis, Machine learning, Prediction modelling, Prospective longitudinal cohort, Stratification, Treatment resistant schizophrenia
Pubmed
Web of science
Open Access
Oui
Création de la notice
27/12/2022 14:58
Dernière modification de la notice
16/04/2024 6:25
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