Impact of a switch to fingolimod on depressive symptoms in patients with relapsing multiple sclerosis: An analysis from the EPOC (Evaluate Patient OutComes) trial

被引:26
作者
Hunter, Samuel F. [1 ]
Agius, Mark [2 ]
Miller, Deborah M. [3 ]
Cutter, Gary [4 ]
Barbato, Luigi [5 ]
McCague, Kevin [5 ]
Meng, Xiangyi [5 ]
Agashivala, Neetu [5 ]
Chin, Peter [5 ]
Hollander, Eric [6 ,7 ]
机构
[1] Adv Neurosci Inst, 101 Forrest Crossing Blvd,Suite 103, Franklin, TN 37064 USA
[2] Barrow Neurol Inst, Dept Neurol, Phoenix, AZ 85013 USA
[3] Cleveland Clin Fdn, Mellen Ctr, 1950 East 89th St, Cleveland, OH 44195 USA
[4] Univ Alabama Birmingham, 1400 Univ Blvd, Birmingham, AL 35223 USA
[5] Novartis Pharmaceut, 1 Hlth Plz, E Hanover, NJ 07936 USA
[6] Albert Einstein Coll Med, 111 E 210th St, New York, NY 10467 USA
[7] Montefiore Med Ctr, 111 E 210th St, New York, NY 10467 USA
关键词
BDI-II; Depression; Fingolimod; Multiple sclerosis; Patient-reported outcomes; Satisfaction; QUALITY-OF-LIFE; RANDOMIZED CROSS-OVER; SIDE-EFFECT PROFILE; ORAL FINGOLIMOD; OPEN-LABEL; INTERFERON; PREFERENCE; INVENTORY; EDITION;
D O I
10.1016/j.jns.2016.03.024
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Depression is common in patients with multiple sclerosis (MS), may confound evaluation of therapeutic effectiveness and may be impacted by MS-specific treatments. Objective: First, to assess the impact on depressive symptoms of a switch to fingolimod versus remaining on an injectable disease-modifying therapy (iDMT) in a post-hoc analysis of prospectively collected data from the EPOC study. Secondly, to investigate the underlying Beck Depression Inventory-II (BDI-II) factor structure in patients with MS, and estimate treatment differences using the resulting subscales. Methods: EPOC was a 6-month, open-label study assessing patient-reported outcomes after switch from iDMT to oral fingolimod 0.5 mg versus remaining on iDMT in 1053 patients with relapsing-remitting MS. Results: At end of study (EOS), a greater proportion of patients on fingolimod versus iDMT no longer had BDI-II scores indicating depression (p < 0.001). Fewer mildly and moderately symptomatic patients developed severe depressive symptoms, and fewer severely symptomatic patients continued to have scores indicating severe depression at EOS on fingolimod versus iDMT (p = 0.027, p = 0.038, p = 0.030, respectively). Two BDI-II subscales were identified and labelled Somatic and Affective; fingolimod demonstrated more reduction on both subscales at EOS versus iDMT5 (p < 0.0001 and p = 0.0001, respectively). Conclusion: A switch to fingolimod versus remaining on/switching to another iDMT was associated with an improvement in depressive symptoms in patients with relapsing-remitting MS. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:190 / 198
页数:9
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