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059  Secondary progressive MS in the UK: a prospective cohort study

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BackgroundAlthough most people with relapsing onset multiple sclerosis (R-MS) eventually transition to secondary progressive multiple sclerosis (SPMS), little is known about disability progression in SPMS.MethodsAll R-MS patients in the Cardiff MS registry were included. Cox proportional hazards regression was used to examine a) hazard of converting to SPMS and b) hazard of attaining EDSS 6.0 and 8.0 in SPMS.Results1611 R-MS patients were included. Older age at MS onset (hazard ratio [HR] 1.02, 95%CI 1.01–1.03), male sex (HR 1.71, 95%CI 1.41–2.08), and residual disability after onset (HR 1.38, 95%CI 1.11–1.71) were asso- ciated with increased hazard of SPMS. Male sex (EDSS 6.0 HR 1.41 [1.04–1.90], EDSS 8.0 HR 1.75 [1.14–2.69]) and higher EDSS at SPMS onset (EDSS 6.0 HR 1.31 [1.17–1.46]; EDSS 8.0 HR 1.38 [1.19–1.61]) were associated with increased hazard of reaching disability milestones, while older age at SPMS was associated with a lower hazard of progression (EDSS 6.0 HR 0.94 [0.92–0.96]; EDSS 8.0: HR 0.92 [0.90–0.95]).ConclusionsDifferent factors are associated with hazard of SPMS compared to hazard of disability progres- sion after SPMS onset. These data may be used to plan services, and provide a baseline for comparison for future interventional studies and has relevance for new treatments for SPMSRobertsonNP@cardiff.ac.uk
Title: 059  Secondary progressive MS in the UK: a prospective cohort study
Description:
BackgroundAlthough most people with relapsing onset multiple sclerosis (R-MS) eventually transition to secondary progressive multiple sclerosis (SPMS), little is known about disability progression in SPMS.
MethodsAll R-MS patients in the Cardiff MS registry were included.
Cox proportional hazards regression was used to examine a) hazard of converting to SPMS and b) hazard of attaining EDSS 6.
0 and 8.
0 in SPMS.
Results1611 R-MS patients were included.
Older age at MS onset (hazard ratio [HR] 1.
02, 95%CI 1.
01–1.
03), male sex (HR 1.
71, 95%CI 1.
41–2.
08), and residual disability after onset (HR 1.
38, 95%CI 1.
11–1.
71) were asso- ciated with increased hazard of SPMS.
Male sex (EDSS 6.
0 HR 1.
41 [1.
04–1.
90], EDSS 8.
0 HR 1.
75 [1.
14–2.
69]) and higher EDSS at SPMS onset (EDSS 6.
0 HR 1.
31 [1.
17–1.
46]; EDSS 8.
0 HR 1.
38 [1.
19–1.
61]) were associated with increased hazard of reaching disability milestones, while older age at SPMS was associated with a lower hazard of progression (EDSS 6.
0 HR 0.
94 [0.
92–0.
96]; EDSS 8.
0: HR 0.
92 [0.
90–0.
95]).
ConclusionsDifferent factors are associated with hazard of SPMS compared to hazard of disability progres- sion after SPMS onset.
These data may be used to plan services, and provide a baseline for comparison for future interventional studies and has relevance for new treatments for SPMSRobertsonNP@cardiff.
ac.
uk.

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