Age Related Multiple Sclerosis Severity Score: Disability ranked by age

被引:95
|
作者
Manouchehrinia, Ali [1 ]
Westerlind, Helga [2 ]
Kingwell, Elaine [3 ]
Zhu, Feng [3 ]
Carruthers, Robert [3 ]
Ramanujam, Ryan [1 ]
Ban, Maria [4 ]
Glaser, Anna [1 ]
Sawcer, Stephen [4 ]
Tremlett, Helen [3 ]
Hillert, Jan [1 ]
机构
[1] Karolinska Inst, Dept Clin Neurosci CNS, Tomtebodavagen 18A Pl 5, S-17177 Stockholm, Sweden
[2] Karolinska Inst, Inst Environm Med IMM, Stockholm, Sweden
[3] Univ British Columbia, UBC Hosp, Div Neurol, Fac Med, Vancouver, BC, Canada
[4] Univ Cambridge, Dept Clin Neurosci, Cambridge, England
关键词
MSSS; EDSS; multiple sclerosis; disease severity; disability; AFRICAN-AMERICANS; DISEASE SEVERITY; PROGRESSION; MSSS; ASSOCIATION; COHORT; TIME;
D O I
10.1177/1352458517690618
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: The Multiple Sclerosis Severity Score (MSSS) is obtained by normalising the Expanded Disability Status Scale (EDSS) score for disease duration and has been a valuable tool in cross-sectional studies. Objective: To assess whether use of age rather than the inherently ambiguous disease duration was a feasible approach. Method: We pooled disability data from three population-based cohorts and developed an Age Related Multiple Sclerosis Severity (ARMSS) score by ranking EDSS scores based on the patient's age at the time of assessment. We established the power to detect a difference between groups afforded by the ARMSS score and assessed its relative consistency over time. Results: The study population included 26058 patients from Sweden (n=11846), Canada (n=6179) and the United Kingdom (n=8033). There was a moderate correlation between EDSS and disease duration (r=0.46, 95% confidence interval (CI): 0.45-0.47) and between EDSS and age (r=0.44, 95% CI: 0.43-0.45). The ARMSS scores showed comparable power to detect disability differences between groups to the updated and original MSSS. Conclusion: Since age is typically unbiased and readily obtained, and the ARMSS and MSSS were comparable, the ARMSS may provide a more versatile tool and could minimise study biases and loss of statistical power caused by inaccurate or missing onset dates.
引用
收藏
页码:1938 / 1946
页数:9
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