External validation of a clinical prediction model in multiple sclerosis

dc.contributor.authorMoradi, Nahid
dc.contributor.authorSharmin, Sifat
dc.contributor.authorMalpas, Charles B.
dc.contributor.authorShaygannejad, Vahid
dc.contributor.authorTerzi, Murat
dc.contributor.authorBoz, Cavit
dc.contributor.authorYamout, Bassem I.
dc.contributor.authorKhoury, Samia J.
dc.contributor.authorTürkoǧlu, Recai
dc.contributor.authorKarabudak, Rana
dc.contributor.authorShalaby, Nevin Mohieldin
dc.contributor.authorSoysal, Aysun
dc.contributor.authorAltintaş, Ayşe
dc.contributor.authorInshasi, Jihad Said
dc.contributor.authorAl-Harbi, Talal M.
dc.contributor.authorAlroughani, Raed A.
dc.contributor.authorKalincik, Tomas
dc.contributor.departmentNeurology
dc.contributor.departmentNehme and Therese Tohme Multiple Sclerosis (MS) Center
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T12:07:46Z
dc.date.available2025-01-24T12:07:46Z
dc.date.issued2023
dc.description.abstractBackground: Timely initiation of disease modifying therapy is crucial for managing multiple sclerosis (MS). Objective: We aimed to validate a previously published predictive model of individual treatment response using a non-overlapping cohort from the Middle East. Methods: We interrogated the MSBase registry for patients who were not included in the initial model development. These patients had relapsing MS or clinically isolated syndrome, a recorded date of disease onset, disability and dates of disease modifying therapy, with sufficient follow-up pre- and post-baseline. Baseline was the visit at which a new disease modifying therapy was initiated, and which served as the start of the predicted period. The original models were used to translate clinical information into three principal components and to predict probability of relapses, disability worsening or improvement, conversion to secondary progressive MS and treatment discontinuation as well as changes in the area under disability-time curve (ΔAUC). Prediction accuracy was assessed using the criteria published previously. Results: The models performed well for predicting the risk of disability worsening and improvement (accuracy: 81%–96%) and performed moderately well for predicting the risk of relapses (accuracy: 73%–91%). The predictions for ΔAUC and risk of treatment discontinuation were suboptimal (accuracy < 44%). Accuracy for predicting the risk of conversion to secondary progressive MS ranged from 50% to 98%. Conclusion: The previously published models are generalisable to patients with a broad range of baseline characteristics in different geographic regions. © The Author(s), 2022.
dc.identifier.doihttps://doi.org/10.1177/13524585221136036
dc.identifier.eid2-s2.0-85143590924
dc.identifier.pmid36448727
dc.identifier.urihttp://hdl.handle.net/10938/31636
dc.language.isoen
dc.publisherSAGE Publications Ltd
dc.relation.ispartofMultiple Sclerosis Journal
dc.sourceScopus
dc.subjectExternal validation
dc.subjectIndividual therapy response
dc.subjectMultiple sclerosis
dc.subjectOutcome prediction
dc.subjectDisease progression
dc.subjectHumans
dc.subjectModels, statistical
dc.subjectMultiple sclerosis, chronic progressive
dc.subjectMultiple sclerosis, relapsing-remitting
dc.subjectPrognosis
dc.subjectRecurrence
dc.subjectAciclovir
dc.subjectFingolimod
dc.subjectGlatiramer
dc.subjectMitoxantrone
dc.subjectNatalizumab
dc.subjectAdult
dc.subjectArea under the curve
dc.subjectArticle
dc.subjectClinical article
dc.subjectCohort analysis
dc.subjectDecision making
dc.subjectDisease activity
dc.subjectDrug safety
dc.subjectExpanded disability status scale
dc.subjectFemale
dc.subjectFollow up
dc.subjectHuman
dc.subjectLinear regression analysis
dc.subjectMale
dc.subjectMiddle east
dc.subjectPredictive model
dc.subjectPredictive value
dc.subjectTarget lesion revascularization
dc.subjectTreatment response
dc.subjectDisease exacerbation
dc.subjectRecurrent disease
dc.subjectStatistical model
dc.titleExternal validation of a clinical prediction model in multiple sclerosis
dc.typeArticle

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