Fingolimod effect on gray matter, thalamus, and white matter in patients with multiple sclerosis

被引:47
作者
Gaetano, Laura [1 ,2 ,3 ,4 ,5 ]
Haering, Dieter A. [6 ]
Radue, Ernst-Wilhelm [1 ]
Mueller-Lenke, Nicole [1 ]
Thakur, Avinash [7 ]
Tomic, Davorka [6 ]
Kappos, Ludwig [2 ,3 ,4 ,5 ]
Sprenger, Till [1 ,2 ,3 ,4 ,5 ,8 ]
机构
[1] Univ Hosp Basel, Med Image Anal Ctr, Basel, Switzerland
[2] Univ Hosp, Dept Med, Neurol Clin & Policlin, Basel, Switzerland
[3] Univ Hosp, Dept Clin Res, Neurol Clin & Policlin, Basel, Switzerland
[4] Univ Hosp, Dept Biomed, Neurol Clin & Policlin, Basel, Switzerland
[5] Univ Hosp, Dept Biomed Engn, Neurol Clin & Policlin, Basel, Switzerland
[6] Novartis Pharma AG, Basel, Switzerland
[7] Novartis Healthcare Pvt Ltd, Hyderabad, Telangana, India
[8] DKD HELIOS Klin Wiesbaden, Dept Neurol, Wiesbaden, Germany
关键词
D O I
10.1212/WNL.0000000000005292
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective To study the effect of fingolimod on deep gray matter (dGM), thalamus, cortical GM (cGM), white matter (WM), and ventricular volume (VV) in patients with relapsing-remitting multiple sclerosis (RRMS). Methods Data were pooled from 2 phase III studies. A total of 2,064 of 2,355 (88%) contributed to the analysis: fingolimod 0.5 mg n = 783, fingolimod 1.25 mg n = 799, or placebo n = 773. Percentage change from baseline in dGM and thalamic volumes was evaluated with FMRIB's Integrated Registration & Segmentation Tool; WM, cGM, and VV were evaluated with structural image evaluation using normalization of atrophy cross-sectional version (SIENAX) at months 12 and 24. Results At baseline, compound brain volume (brain volume in the z block [BVz] = cGM + dGM + WM) correlated with SIENAX-normalized brain volume (r = 0.938, p < 0.001); percentage change from baseline in BVz over 2 years correlated with structural image evaluation using normalization of atrophy percentage brain volume change (r = 0.713, p < 0.001). For placebo, volume reductions were most pronounced in cGM, and relative changes from baseline were strongest in dGM. Over 24 months, there were significant reductions with fingolimod vs placebo for dGM (0.5 mg -14.5%, p = 0.017; 1.25 mg -26.6%, p < 0.01) and thalamus (0.5 mg -26.1%, p = 0.006; 1.25 mg -49.7%, p < 0.001). Reduction of cGM volume loss was not significant. Significantly less WM loss and VV enlargement were seen with fingolimod vs placebo (all p < 0.001). A high T2 lesion volume at baseline predicted on-study cGM, dGM, and thalamic volume loss (p < 0.0001) but not WM loss. Patients taking placebo with high dGM (hazard ratio [HR] 0.54, p = 0.0323) or thalamic (HR 0.58, p = 0.0663) volume at baseline were less likely to show future disability worsening. Conclusions Fingolimod significantly reduced dGM volume loss (including thalamus) vs placebo in patients with RRMS. Reducing dGM and thalamic volume loss might improve long-term outcome.
引用
收藏
页码:E1324 / E1332
页数:9
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