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Machine-learning-based prediction of disability progression in multiple sclerosis: An observational, international, multi-center study.
De Brouwer, Edward; Becker, Thijs; Werthen-Brabants, Lorin; Dewulf, Pieter; Iliadis, Dimitrios; Dekeyser, Cathérine; Laureys, Guy; Van Wijmeersch, Bart; Popescu, Veronica; Dhaene, Tom; Deschrijver, Dirk; Waegeman, Willem; De Baets, Bernard; Stock, Michiel; Horakova, Dana; Patti, Francesco; Izquierdo, Guillermo; Eichau, Sara; Girard, Marc; Prat, Alexandre; Lugaresi, Alessandra; Grammond, Pierre; Kalincik, Tomas; Alroughani, Raed; Grand'Maison, Francois; Skibina, Olga; Terzi, Murat; Lechner-Scott, Jeannette; Gerlach, Oliver; Khoury, Samia J; Cartechini, Elisabetta; Van Pesch, Vincent; Sà, Maria José; Weinstock-Guttman, Bianca; Blanco, Yolanda; Ampapa, Radek; Spitaleri, Daniele; Solaro, Claudio; Maimone, Davide; Soysal, Aysun; Iuliano, Gerardo; Gouider, Riadh; Castillo-Triviño, Tamara; Sánchez-Menoyo, José Luis; Laureys, Guy; van der Walt, Anneke; Oh, Jiwon; Aguera-Morales, Eduardo; Altintas, Ayse; Al-Asmi, Abdullah.
Afiliação
  • De Brouwer E; ESAT-STADIUS, KU Leuven, Belgium.
  • Becker T; I-Biostat, Hasselt University, Belgium.
  • Werthen-Brabants L; Data Science Institute, Hasselt University, Belgium.
  • Dewulf P; SUMO, IDLAB, Ghent University - imec, Belgium.
  • Iliadis D; KERMIT, Department of Data Analysis and Mathematical Modelling, Ghent University, Belgium.
  • Dekeyser C; KERMIT, Department of Data Analysis and Mathematical Modelling, Ghent University, Belgium.
  • Laureys G; Department of Neurology, Ghent University, Belgium.
  • Van Wijmeersch B; 4 Brain, Ghent University, Belgium.
  • Popescu V; Biomedical Research Institute, Hasselt University, Belgium.
  • Dhaene T; Department of Neurology, Ghent University, Belgium.
  • Deschrijver D; 4 Brain, Ghent University, Belgium.
  • Waegeman W; Noorderhart ziekenhuizen Pelt, Belgium.
  • De Baets B; Universitair MS Centrum Hasselt-Pelt, Belgium.
  • Stock M; Noorderhart ziekenhuizen Pelt, Belgium.
  • Horakova D; Universitair MS Centrum Hasselt-Pelt, Belgium.
  • Patti F; SUMO, IDLAB, Ghent University - imec, Belgium.
  • Izquierdo G; SUMO, IDLAB, Ghent University - imec, Belgium.
  • Eichau S; KERMIT, Department of Data Analysis and Mathematical Modelling, Ghent University, Belgium.
  • Girard M; KERMIT, Department of Data Analysis and Mathematical Modelling, Ghent University, Belgium.
  • Prat A; KERMIT, Department of Data Analysis and Mathematical Modelling, Ghent University, Belgium.
  • Lugaresi A; Biobix, Department of Data Analysis and Mathematical Modelling, Ghent University, Belgium.
  • Grammond P; Charles University in Prague and General University Hospital, Prague, Czech Republic.
  • Kalincik T; Department of Medical and Surgical Sciences and Advanced Technologies, GF Ingrassia, Catania, Italy.
  • Alroughani R; Hospital Universitario Virgen Macarena, Sevilla, Spain.
  • Grand'Maison F; Hospital Universitario Virgen Macarena, Sevilla, Spain.
  • Skibina O; CHUM and Université de Montreal, Montreal, Canada.
  • Terzi M; CHUM and Université de Montreal, Montreal, Canada.
  • Lechner-Scott J; IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna, Italia and Dipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, Bologna, Italia.
  • Gerlach O; CISSS Chaudière-Appalache, Levis, Canada.
  • Khoury SJ; Melbourne MS Centre, Department of Neurology, Royal Melbourne Hospital, Melbourne, Australia.
  • Cartechini E; CORe, Department of Medicine, University of Melbourne, Melbourne, Australia.
  • Van Pesch V; Amiri Hospital, Sharq, Kuwait.
  • Sà MJ; Neuro Rive-Sud, Quebec, Canada.
  • Weinstock-Guttman B; Box Hill Hospital, Melbourne, Australia.
  • Blanco Y; 19 Mayis University, Samsun, Turkey.
  • Ampapa R; University Newcastle, Newcastle, Australia.
  • Spitaleri D; Academic MS Center Zuyderland, Department of Neurology, Zuyderland Medical Center, Sittard-Geleen, The Netherlands.
  • Solaro C; School for Mental Health and Neuroscience, Maastricht University, Maastricht, The Netherlands.
  • Maimone D; American University of Beirut Medical Center, Beirut, Lebanon.
  • Soysal A; Azienda Sanitaria Unica Regionale Marche - AV3, Macerata, Italy.
  • Iuliano G; Cliniques Universitaires Saint-Luc, Brussels, Belgium.
  • Gouider R; Centro Hospitalar Universitario de Sao Joao, Porto, Portugal.
  • Castillo-Triviño T; Department of Neurology, Buffalo General Medical Center, Buffalo, United States of America.
  • Sánchez-Menoyo JL; Hospital Clinic de Barcelona, Barcelona, Spain.
  • Laureys G; Nemocnice Jihlava, Jihlava, Czech Republic.
  • van der Walt A; Azienda Ospedaliera di Rilievo Nazionale San Giuseppe Moscati Avellino, Avellino, Italy.
  • Oh J; Dept. of Rehabilitation, CRFF Mons. Luigi Novarese, Moncrivello, Italy.
  • Aguera-Morales E; MS center, UOC Neurologia, ARNAS Garibaldi, Catania, Italy.
  • Altintas A; Bakirkoy Education and Research Hospital for Psychiatric and Neurological Diseases, Istanbul, Turkey.
  • Al-Asmi A; Ospedali Riuniti di Salerno, Salerno, Italy.
PLOS Digit Health ; 3(7): e0000533, 2024 Jul.
Article em En | MEDLINE | ID: mdl-39052668
ABSTRACT

BACKGROUND:

Disability progression is a key milestone in the disease evolution of people with multiple sclerosis (PwMS). Prediction models of the probability of disability progression have not yet reached the level of trust needed to be adopted in the clinic. A common benchmark to assess model development in multiple sclerosis is also currently lacking.

METHODS:

Data of adult PwMS with a follow-up of at least three years from 146 MS centers, spread over 40 countries and collected by the MSBase consortium was used. With basic inclusion criteria for quality requirements, it represents a total of 15, 240 PwMS. External validation was performed and repeated five times to assess the significance of the results. Transparent Reporting for Individual Prognosis Or Diagnosis (TRIPOD) guidelines were followed. Confirmed disability progression after two years was predicted, with a confirmation window of six months. Only routinely collected variables were used such as the expanded disability status scale, treatment, relapse information, and MS course. To learn the probability of disability progression, state-of-the-art machine learning models were investigated. The discrimination performance of the models is evaluated with the area under the receiver operator curve (ROC-AUC) and under the precision recall curve (AUC-PR), and their calibration via the Brier score and the expected calibration error. All our preprocessing and model code are available at https//gitlab.com/edebrouwer/ms_benchmark, making this task an ideal benchmark for predicting disability progression in MS.

FINDINGS:

Machine learning models achieved a ROC-AUC of 0⋅71 ± 0⋅01, an AUC-PR of 0⋅26 ± 0⋅02, a Brier score of 0⋅1 ± 0⋅01 and an expected calibration error of 0⋅07 ± 0⋅04. The history of disability progression was identified as being more predictive for future disability progression than the treatment or relapses history.

CONCLUSIONS:

Good discrimination and calibration performance on an external validation set is achieved, using only routinely collected variables. This suggests machine-learning models can reliably inform clinicians about the future occurrence of progression and are mature for a clinical impact study.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: PLOS Digit Health Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Bélgica

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: PLOS Digit Health Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Bélgica