Accurate classification of secondary progression in multiple sclerosis using a decision tree

The BeAMS study group

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

Background: The absence of reliable imaging or biological markers of phenotype transition in multiple sclerosis (MS) makes assignment of current phenotype status difficult. Objective: The authors sought to determine whether clinical information can be used to accurately assign current disease phenotypes. Methods: Data from the clinical visits of 14,387 MS patients in Sweden were collected. Classifying algorithms based on several demographic and clinical factors were examined. Results obtained from the best classifier when predicting neurologist recorded disease classification were replicated in an independent cohort from British Columbia and were compared to a previously published algorithm and clinical judgment of three neurologists. Results: A decision tree (the classifier) containing only most recently available expanded disability scale status score and age obtained 89.3% (95% confidence intervals (CIs): 88.8–89.8) classification accuracy, defined as concordance with the latest reported status. Validation in the independent cohort resulted in 82.0% (95% CI: 81.0–83.1) accuracy. A previously published classification algorithm with slight modifications achieved 77.8% (95% CI: 77.1–78.4) accuracy. With complete patient history of 100 patients, three neurologists obtained 84.3% accuracy compared with 85% for the classifier using the same data. Conclusion: The classifier can be used to standardize definitions of disease phenotype across different cohorts. Clinically, this model could assist neurologists by providing additional information.

Original languageEnglish (US)
Pages (from-to)1240-1249
Number of pages10
JournalMultiple Sclerosis Journal
Volume27
Issue number8
DOIs
StatePublished - Jul 2021

Keywords

  • Multiple sclerosis
  • classification
  • decision tree
  • secondary progressive

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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