Signori, A and Izquierdo, G and Lugaresi, A and Hupperts, R and Grand'Maison, F and Sola, P and Horakova, D and Havrdova, E and Prat, A and Girard, M and Duquette, P and Boz, C and Grammond, P and Terzi, M and Singhal, B and Alroughani, R and Petersen, T and Ramo, C and Oreja-Guevara, C and Spitaleri, D and Shaygannejad, V and Butzkueven, H and Kalincik, T and Jokubaitis, V and Slee, M and Fernandez Bolanos, R and Sanchez-Menoyo, JL and Pucci, E and Granella, F and Lechner-Scott, J and Iuliano, G and Hughes, S and Bergamaschi, R and Taylor, B and Verheul, F and Edite Rio, M and Amato, MP and Sajedi, SA and Majdinasab, N and Van Pesch, V and Sormani, MP and Trojano, M, Long-term disability trajectories in primary progressive MS patients: A latent class growth analysis, Multiple Sclerosis Journal pp. 1-11. ISSN 1352-4585 (2017) [Refereed Article]
Copyright 2017 the authors
Objectives: To identify subgroups of PPMS patients with similar longitudinal trajectories of Expanded Disability Status Scale (EDSS) over time.
Methods: All PPMS patients collected within the MSBase registry, who had their first EDSS assessment within 5 years from onset, were included in the analysis. Longitudinal EDSS scores were modeled by a latent class mixed model (LCMM), using a nonlinear function of time from onset. LCMM is an advanced statistical approach that models heterogeneity between patients by classifying them into unobserved groups showing similar characteristics.
Results: A total of 853 PPMS (51.7% females) from 24 countries with a mean age at onset of 42.4 years (standard deviation (SD): 10.8 years), a median baseline EDSS of 4 (interquartile range (IQR): 2.5-5.5), and 2.4 years of disease duration (SD: 1.5 years) were included. LCMM detected three different subgroups of patients with a mild (n = 143; 16.8%), moderate (n = 378; 44.3%), or severe (n = 332; 38.9%) disability trajectory. The probability of reaching EDSS 6 at 10 years was 0%, 46.4%, and 81.9% respectively.
Conclusion: Applying an LCMM modeling approach to long-term EDSS data, it is possible to identify groups of PPMS patients with different prognosis.
|Item Type:||Refereed Article|
|Keywords:||primary progressive multiple sclerosis, clinical trials, disability, heterogeneity, long-term, trajectories|
|Research Division:||Medical and Health Sciences|
|Research Field:||Central Nervous System|
|Objective Group:||Clinical Health (Organs, Diseases and Abnormal Conditions)|
|Objective Field:||Nervous System and Disorders|
|Author:||Taylor, B (Professor Bruce Taylor)|
|Web of Science® Times Cited:||2|
|Deposited By:||Menzies Institute for Medical Research|
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