Investigation of heterogeneity in the association between interferon beta and disability progression in multiple sclerosis: an observational

被引:11
作者
Shirani, A. [1 ,2 ]
Zhao, Y. [3 ]
Karim, M. E. [4 ]
Petkau, J. [4 ]
Gustafson, P. [4 ]
Evans, C. [1 ,2 ]
Kingwell, E. [1 ,2 ]
van der Kop, M. L. [1 ,2 ]
Oger, J. [1 ,2 ]
Tremlett, H. [1 ,2 ]
机构
[1] Univ British Columbia, Div Neurol, Dept Med, Vancouver, BC V6T 2B5, Canada
[2] Univ British Columbia, Brain Res Ctr, Vancouver, BC V6T 2B5, Canada
[3] Univ British Columbia, Div Neurol, Dept Med, MS MRI Res Grp, Vancouver, BC V6T 2B5, Canada
[4] Univ British Columbia, Dept Stat, Vancouver, BC V6T 2B5, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
British Columbia; disability progression; interferon beta; multiple sclerosis; observational studies; SUBGROUP ANALYSIS; NATURAL-HISTORY; RELAPSES; TRIALS; CHALLENGE;
D O I
10.1111/ene.12324
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and purposeIt was recently reported that there was no significant overall association between interferon beta exposure and disability progression in relapsing-remitting multiple sclerosis (RRMS) patients in an observational study from Canada. In the current study, the potential for heterogeneity in the association between exposure to interferon beta and disability progression across patients' baseline characteristics was investigated. MethodsRRMS patients treated with interferon beta (n=868) and two cohorts of untreated patients (829 contemporary and 959 historical controls) were included. The main outcome was time from interferon beta treatment eligibility (baseline) to a confirmed and sustained Expanded Disability Status Scale (EDSS) score 6 using a multivariable Cox model, with treatment as a time-varying predictor, testing interaction effects for five pre-specified baseline characteristics: sex, age, disease duration, EDSS and annualized relapse rate (ARR) based on the previous 2years. ResultsSignificant heterogeneity was found in the association of interferon beta exposure and disability progression only across ARR, and only when treated patients were compared with historical controls (P=0.005 at a Bonferroni-adjusted alpha of 0.01). For patients with ARR>1, treatment-exposed time was associated with a hazard ratio of 0.38 (95%CI 0.20-0.75) for disability progression compared with the unexposed time. ConclusionsRRMS patients with more frequent relapses at baseline may be more likely to benefit from interferon beta treatment with respect to long-term disability progression.
引用
收藏
页码:835 / 844
页数:10
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