External validation of a clinical prediction model in multiple sclerosis

Author:

Moradi Nahid1ORCID,Sharmin Sifat1,Malpas Charles B2,Shaygannejad Vahid3,Terzi Murat4,Boz Cavit5,Yamout Bassem6,Khoury Samia J6,Turkoglu Recai7,Karabudak Rana8,Shalaby Nevin9,Soysal Aysun10,Altıntaş Ayşe11,Inshasi Jihad12ORCID,Al-Harbi Talal13,Alroughani Raed14ORCID,Kalincik Tomas2ORCID

Affiliation:

1. Clinical Outcomes Research Unit (CORe), Department of Medicine, University of Melbourne, Parkville, VIC, Australia

2. Clinical Outcomes Research Unit (CORe), Department of Medicine, University of Melbourne, Parkville, VIC, Australia/MS Centre, Department of Neurology, The Royal Melbourne Hospital, Melbourne, VIC, Australia

3. Isfahan University of Medical Sciences, Isfahan, Iran

4. Faculty of Medicine, Ondokuz Mayis University, Samsun, Turkey

5. KTU Faculty of Medicine, Farabi Hospital, Trabzon, Turkey

6. Nehme and Therese Tohme Multiple Sclerosis Center, American University of Beirut Medical Center, Beirut, Lebanon

7. Haydarpasa Numune Training and Research Hospital, Istanbul, Turkey

8. Department of Neurology, Faculty of Medicine, Hacettepe University, Ankara, Turkey

9. Department of Neurology, Kasr Al-Ainy MS Research Unit (KAMSU), Cairo University, Cairo, Egypt

10. Bakirkoy Education and Research Hospital for Psychiatric and Neurological Diseases, Istanbul, Turkey

11. Department of Neurology, School of Medicine, Koç University, Istanbul, Turkey

12. Rashid Hospital, Dubai, United Arab Emirates

13. Department of Neurology, King Fahad Specialist Hospital, Dammam, Saudi Arabia

14. Division of Neurology, Department of Medicine, Amiri Hospital, Sharq, Kuwait

Abstract

Background: 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.

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

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