Predicting the individual risk of psychosis conversion in at-risk mental state (ARMS): a multivariate model reveals the influence of nonpsychotic prodromal symptoms.


Journal

European child & adolescent psychiatry
ISSN: 1435-165X
Titre abrégé: Eur Child Adolesc Psychiatry
Pays: Germany
ID NLM: 9212296

Informations de publication

Date de publication:
Nov 2020
Historique:
received: 16 07 2018
accepted: 16 11 2019
pubmed: 25 12 2019
medline: 1 12 2020
entrez: 25 12 2019
Statut: ppublish

Résumé

To improve the prediction of the individual risk of conversion to psychosis in UHR subjects, by considering all CAARMS' symptoms at first presentation and using a multivariate machine learning method known as logistic regression with Elastic-net shrinkage. 46 young individuals who sought help from the specialized outpatient unit at Sainte-Anne hospital and who met CAARMS criteria for UHR were assessed, among whom 27 were reassessed at follow-up (22.4 ± 6.54 months) and included in the analysis. Elastic net logistic regression was trained, using CAARMS items at baseline to predict individual evolution between converters (UHR-P) and non-converters (UHR-NP). Elastic-net was used to select the few CAARMS items that best predict the clinical evolution. All validations and significances of predictive models were computed with non-parametric re-sampling strategies that provide robust estimators even when the distributional assumption cannot be guaranteed. Among the 25 CAARMS items, the Elastic net selected 'obsessive-compulsive symptoms' and 'aggression/dangerous behavior' as risk factors for conversion while 'anhedonia' and 'mood swings/lability' were associated with non-conversion at follow-up. In the ten-fold stratified cross-validation, the classification achieved 81.8% of sensitivity (P = 0.035) and 93.7% of specificity (P = 0.0016). Non-psychotic prodromal symptoms bring valuable information to improve the prediction of conversion to psychosis. Elastic net logistic regression applied to clinical data is a promising way to switch from group prediction to an individualized prediction.

Identifiants

pubmed: 31872289
doi: 10.1007/s00787-019-01461-y
pii: 10.1007/s00787-019-01461-y
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1525-1535

Auteurs

Julie Bourgin (J)

INSERM, Laboratoire Physiopathologie Des Maladies Psychiatriques, IPNP, UMR 1266, Institut de Psychiatrie (CNRS GDR 3557), Paris, France. julie.bourgin@gmail.com.
GHNE, Site de Orsay. Domaine du Grand Mesnil, Voie Kastler, 91440, Bures sur Yvette, France. julie.bourgin@gmail.com.

Edouard Duchesnay (E)

NeuroSpin, CEA, Paris-Saclay, Gif-sur-Yvette, France.

Emilie Magaud (E)

Hotchkiss Brain Institute, Mathison Centre for Mental Health Research and Education, Calgary, AB, Canada.

Raphaël Gaillard (R)

INSERM, Laboratoire Physiopathologie Des Maladies Psychiatriques, IPNP, UMR 1266, Institut de Psychiatrie (CNRS GDR 3557), Paris, France.
GHU Paris Sainte-Anne, Service Hospitalo-Universitaire, University Paris Descartes, Paris, France.

Mathilde Kazes (M)

INSERM, Laboratoire Physiopathologie Des Maladies Psychiatriques, IPNP, UMR 1266, Institut de Psychiatrie (CNRS GDR 3557), Paris, France.
GHU Paris Sainte-Anne, Service Hospitalo-Universitaire, University Paris Descartes, Paris, France.

Marie-Odile Krebs (MO)

INSERM, Laboratoire Physiopathologie Des Maladies Psychiatriques, IPNP, UMR 1266, Institut de Psychiatrie (CNRS GDR 3557), Paris, France.
GHU Paris Sainte-Anne, Service Hospitalo-Universitaire, University Paris Descartes, Paris, France.

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