Effect of disease-modifying therapies on brain volume in relapsing-remitting multiple sclerosis: Results of a five-year brain MRI study

被引:33
作者
Khan, Omar [1 ,2 ]
Bao, Fen [1 ]
Shah, Megha [1 ]
Caon, Christina [2 ]
Tselis, Alexandros [2 ]
Bailey, Ronald [4 ]
Silverman, Bruce [5 ]
Zak, Imad [3 ]
机构
[1] Wayne State Univ, Sch Med, Dept Neurol, MR Image Anal Lab, Detroit, MI 48202 USA
[2] Wayne State Univ, Sch Med, Dept Neurol, Multiple Sclerosis Ctr, Detroit, MI 48202 USA
[3] Wayne State Univ, Sch Med, Dept Radiol, Detroit, MI 48202 USA
[4] Riverside Med Ctr, Riverside, CA USA
[5] Providence Hosp, Southfield, MI 48037 USA
关键词
Brain atrophy; Relapsing-remitting MS; Disease-modifying therapies; Neurodegeneration; Interferon beta; Glatiramer acetate; GLATIRAMER ACETATE; CEREBRAL ATROPHY; OPEN-LABEL; LONG-TERM; DOUBLE-BLIND; FOLLOW-UP; MS; LESIONS; INTERFERON-BETA-1A; MULTICENTER;
D O I
10.1016/j.jns.2011.08.034
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To compare the long-term effect of disease-modifying therapies (DMT) on brain volume loss in relapsing-remitting MS (RRMS) patients. Methods: We conducted a study to examine the effect of daily glatiramer acetate (GA), weekly low dose interferon beta (LD-IFNB), and high-dose high-frequency interferon beta disease (HD-IFNB) on brain volume loss over 5 years in RRMS patients. All patients were previously treatment nave, had disease duration <= 5 years at the time of initiating DMT, and subsequently received the same DMT for 5 years continuously. The percentage change in brain volume (PCBV) was measured using fully automated software. MRI analysis was performed blinded to treatment allocation. Results: The adjusted PCBV from baseline to year 5 was -2.27% in GA, -2.62% in LD-IFNB, and -3.21% in the HD-IFNB groups (-2.27 vs -2.62, p = 0.0036; -2.27 vs -3.21, p<0.0001; -2.62 vs -3.21, p<0.0001). These data remained unchanged from year 1 to year 5, after adjusting for pseudoatrophy in the first year. A group of RRMS patients that remained untreated for a period ranging from 8 to 24 months, served as controls. All treatment groups were significantly better than the rate of projected brain volume loss in the untreated group over 5 years (p<0.0001). Conclusions: Global brain volume loss is a dynamic process even in relatively early RRMS patients that occurs despite intervention with therapy. However, all DMT significantly reduced the loss of brain volume compared to no treatment. The GA-treated group experienced the least reduction in brain volume over 5 years, compared to the LD-IFNB and HD-IFNB treated groups. These differences could be partly related to the immunologic consequences of GA therapy in RRMS. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:7 / 12
页数:6
相关论文
共 35 条
[1]   Detecting treatment effects on brain atrophy in relapsing remitting multiple sclerosis: Sample size estimates [J].
Anderson, Valerie M. ;
Bartlett, Jonathan W. ;
Fox, Nick C. ;
Fisniku, Leonora ;
Miller, David H. .
JOURNAL OF NEUROLOGY, 2007, 254 (11) :1588-1594
[2]   The measurement and clinical relevance of brain atrophy in multiple sclerosis [J].
Bermel, RA ;
Bakshi, R .
LANCET NEUROLOGY, 2006, 5 (02) :158-170
[3]   Cervical cord and brain grey matter atrophy independently associate with long-term MS disability [J].
Bonati, U. ;
Fisniku, L. K. ;
Altmann, D. R. ;
Yiannakas, M. C. ;
Furby, J. ;
Thompson, A. J. ;
Miller, D. H. ;
Chard, D. T. .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2011, 82 (04) :471-472
[4]   Brain atrophy after immunoablation and stem cell transplantation in multiple sclerosis [J].
Chen, J. T. ;
Collins, D. L. ;
Atkins, H. L. ;
Freedman, M. S. ;
Galal, A. ;
Arnold, D. L. .
NEUROLOGY, 2006, 66 (12) :1935-1937
[5]   European/Canadian multicenter, double-blind, randomized, placebo-controlled study of the effects of glatiramer acetate on magnetic resonance imaging-measured disease activity and burden in patients with relapsing multiple sclerosis [J].
Comi, G ;
Filippi, M ;
Wolinsky, JS .
ANNALS OF NEUROLOGY, 2001, 49 (03) :290-297
[6]   Brain atrophy and lesion load measures over 1 year relate to clinical status after 6 years in patients with clinically isolated syndromes [J].
Di Filippo, M. ;
Anderson, V. M. ;
Altmann, D. R. ;
Swanton, J. K. ;
Plant, G. T. ;
Thompson, A. J. ;
Miller, D. H. .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2010, 81 (02) :204-208
[7]   Interferon beta-1a for brain tissue loss in patients at presentation with syndromes suggestive of multiple sclerosis: a randomised, double-blind, placebo-controlled trial [J].
Filippi, M ;
Rovaris, M ;
Inglese, M ;
Barkhof, F ;
De Stefano, N ;
Smith, S ;
Comi, G .
LANCET, 2004, 364 (9444) :1489-1496
[8]   Glatiramer acetate reduces the proportion of new MS lesions evolving into "black holes" [J].
Filippi, M ;
Rovaris, M ;
Rocca, MA ;
Sormani, MP ;
Wolinsky, JS ;
Comi, G .
NEUROLOGY, 2001, 57 (04) :731-733
[9]   Eight-year follow-up study of brain atrophy in patients with MS [J].
Fisher, E ;
Rudick, RA ;
Simon, JH ;
Cutter, G ;
Baier, M ;
Lee, JC ;
Miller, D ;
Weinstock-Guttman, B ;
Mass, MK ;
Dougherty, DS ;
Simonian, NA .
NEUROLOGY, 2002, 59 (09) :1412-1420
[10]   A prospective open-label study of glatiramer acetate: over a decade of continuous use in multiple sclerosis patients [J].
Ford, CC ;
Johnson, KP ;
Lisak, RP ;
Panitch, HS ;
Shifroni, G ;
Wolinsky, JS .
MULTIPLE SCLEROSIS JOURNAL, 2006, 12 (03) :309-320