TY - JOUR
T1 - Impact of a switch to fingolimod on depressive symptoms in patients with relapsing multiple sclerosis
T2 - An analysis from the EPOC (Evaluate Patient OutComes) trial
AU - Hunter, Samuel F.
AU - Agius, Mark
AU - Miller, Deborah M.
AU - Cutter, Gary
AU - Barbato, Luigi
AU - McCague, Kevin
AU - Meng, Xiangyi
AU - Agashivala, Neetu
AU - Chin, Peter
AU - Hollander, Eric
PY - 2016/6/15
Y1 - 2016/6/15
N2 - 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 iDMTs (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.
AB - 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 iDMTs (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.
KW - BDI-II
KW - Depression
KW - Fingolimod
KW - Multiple sclerosis
KW - Patient-reported outcomes
KW - Satisfaction
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U2 - 10.1016/j.jns.2016.03.024
DO - 10.1016/j.jns.2016.03.024
M3 - Article
C2 - 27206905
AN - SCOPUS:84964466784
SN - 0022-510X
VL - 365
SP - 190
EP - 198
JO - Journal of the Neurological Sciences
JF - Journal of the Neurological Sciences
ER -