Comparison of the King's and MiToS staging systems for ALS

被引:64
作者
Fang, Ton [1 ]
Al Khleifat, Ahmad [1 ]
Stahl, Daniel R. [2 ]
La Torre, Claudia Lazo [3 ]
Murphy, Caroline [2 ]
Young, Carolyn [4 ]
Shaw, Pamela J. [5 ]
Leigh, P. Nigel [6 ]
Al-Chalabi, Ammar [1 ]
机构
[1] Kings Coll London, Dept Basic & Clin Neurosci, Maurice Wohl Clin Neurosci Inst, London, England
[2] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Biostat, London, England
[3] Univ Lleida, Dept Neurol, Lerida, Spain
[4] Walton Ctr NHS Fdn Trust, Liverpool, Merseyside, England
[5] Univ Sheffield, Dept Neurosci, Sheffield, S Yorkshire, England
[6] Brighton & Sussex Med Sch, Dept Neurol, Brighton, E Sussex, England
基金
英国医学研究理事会; 英国经济与社会研究理事会;
关键词
Clinical stage; MiToS stage; King's stage; prognosis; clinical trials; AMYOTROPHIC-LATERAL-SCLEROSIS;
D O I
10.1080/21678421.2016.1265565
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To investigate and compare two ALS staging systems, King's clinical staging and Milano-Torino (MiToS) functional staging, using data from the LiCALS phase III clinical trial (EudraCT 2008-006891-31). Methods: Disease stage was derived retrospectively for each system from the ALS Functional Rating Scale-Revised subscores using standard methods. The two staging methods were then compared for timing of stages using box plots, correspondence using chi-square tests, agreement using a linearly weighted kappa coefficient and concordance using Spearman's rank correlation. Results: For both systems, progressively higher stages occurred at progressively later proportions of the disease course, but the distribution differed between the two methods. King's stage 3 corresponded to MiToS stage 1 most frequently, with earlier King's stages 1 and 2 largely corresponding to MiToS stage 0 or 1. The Spearman correlation was 0.54. There was fair agreement between the two systems with kappa coefficient of 0.21. Conclusion: The distribution of timings shows that the two systems are complementary, with King's staging showing greatest resolution in early to mid-disease corresponding to clinical or disease burden, and MiToS staging having higher resolution for late disease, corresponding to functional involvement. We therefore propose using both staging systems when describing ALS.
引用
收藏
页码:227 / 232
页数:6
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