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Multicenter Study
. 2017 Sep;23(10):1346-1357.
doi: 10.1177/1352458516679893. Epub 2016 Nov 25.

Quantifying risk of early relapse in patients with first demyelinating events: Prediction in clinical practice

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Free article
Multicenter Study

Quantifying risk of early relapse in patients with first demyelinating events: Prediction in clinical practice

Tim Spelman et al. Mult Scler. 2017 Sep.
Free article

Abstract

Background: Characteristics at clinically isolated syndrome (CIS) examination assist in identification of patient at highest risk of early second attack and could benefit the most from early disease-modifying drugs (DMDs).

Objective: To examine determinants of second attack and validate a prognostic nomogram for individualised risk assessment of clinical conversion.

Methods: Patients with CIS were prospectively followed up in the MSBase Incident Study. Predictors of clinical conversion were analysed using Cox proportional hazards regression. Prognostic nomograms were derived to calculate conversion probability and validated using concordance indices.

Results: A total of 3296 patients from 50 clinics in 22 countries were followed up for a median (inter-quartile range (IQR)) of 1.92 years (0.90, 3.71). In all, 1953 (59.3%) patients recorded a second attack. Higher Expanded Disability Status Scale (EDSS) at baseline, first symptom location, oligoclonal bands and various brain and spinal magnetic resonance imaging (MRI) metrics were all predictors of conversion. Conversely, older age and DMD exposure post-CIS were associated with reduced rates. Prognostic nomograms demonstrated high concordance between estimated and observed conversion probabilities.

Conclusion: This multinational study shows that age at CIS onset, DMD exposure, EDSS, multiple brain and spinal MRI criteria and oligoclonal bands are associated with shorter time to relapse. Nomogram assessment may be useful in clinical practice for estimating future clinical conversion.

Keywords: CIS; CSF; MRI; MS; Nomogram; clinically definite multiple sclerosis; clinically isolated syndrome; disease-modifying drugs; second attack.

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