The effect of disease-modifying therapies on brain atrophy in patients with clinically isolated syndrome: a systematic review and meta-analysis

被引:22
作者
Tsivgoulis, Georgios [1 ]
Katsanos, Aristeidis H. [2 ]
Grigoriadis, Nikolaos [3 ]
Hadjigeorgiou, Georgios M. [4 ]
Heliopoulos, Ioannis [5 ]
Papathanasopoulos, Panagiotis [6 ]
Dardiotis, Efthimios [4 ]
Kilidireas, Constantinos [7 ]
Voumvourakis, Konstantinos [2 ]
机构
[1] Univ Athens, Sch Med, Dept Neurol 2, Athens 15344, Greece
[2] Univ Athens, Sch Med, Attikon Hosp, Dept Neurol 2, Athens 15344, Greece
[3] Aristotle Univ Thessaloniki, AHEPA Univ Hosp, Dept Neurol 2, GR-54006 Thessaloniki, Greece
[4] Univ Thessaly, Univ Hosp Larissa, Dept Neurol, Larisa, Greece
[5] Democritus Univ Thrace, Alexandroupolis Univ Hosp, Dept Neurol, Alexandroupolis, Greece
[6] Univ Patras, Sch Med, Dept Neurol, GR-26110 Patras, Greece
[7] Univ Athens, Sch Med, Eginit Hosp, Dept Neurol 1, Athens 15344, Greece
关键词
brain atrophy; brain volume; clinically isolated syndrome; disease modifying therapy; REMITTING MULTIPLE-SCLEROSIS; GLATIRAMER ACETATE; DISABILITY PROGRESSION; DEMYELINATING EVENT; INTERFERON BETA-1A; VOLUME CHANGE; DOUBLE-BLIND; GREY-MATTER; PHASE-3; NEUROPROTECTION;
D O I
10.1177/1756285615600381
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: Brain atrophy is associated with cognitive deficits in patients with clinically isolated syndrome (CIS) and can predict conversion to clinical definite multiple sclerosis. The aim of the present meta-analysis was to evaluate the effect of disease-modifying drugs (DMDs) on brain atrophy in patients with CIS. Methods: Eligible placebo-control randomized clinical trials of patients with CIS that had reported changes in brain volume during the study period were identified by searching the MEDLINE, SCOPUS, and Cochrane Central Register of Controlled Trials (CENTRAL) databases. This meta-analysis adopted the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines for systematic reviews and meta-analyses. Results: Three eligible studies were identified, comprising 1362 patients. The mean percentage change in brain volume was found to be significantly lower in DMD-treated patients versus placebo-treated subgroups (standardized mean difference [SMD]: = -0.13, 95% confidence interval [CI]: -0.25, 0.01; p = 0.04). In the subgroup analysis of the two studies that provided data on brain-volume changes for the first (0-12 months) and second (13-24 months) year of treatment, DMD attenuated brain-volume loss in comparison with placebo during the second year (SMD = -0.25; 95% CI: -0.43, -0.07; p < 0.001), but not during the first year of treatment (SMD = -0.01; 95% CI: -0.27, 0.24; p = 0.93). No evidence of heterogeneity was found between estimates, while funnel-plot inspection revealed no evidence of publication bias. Conclusions: DMDs appear to attenuate brain atrophy over time in patients with CIS. The effect of DMDs on brain-volume loss is evident after the first year of treatment.
引用
收藏
页码:193 / 202
页数:10
相关论文
共 39 条
[1]   Neuroprotection with glatiramer acetate: evidence from the PreCISe trial [J].
Arnold, Douglas L. ;
Narayanan, Sridar ;
Antel, Samson .
JOURNAL OF NEUROLOGY, 2013, 260 (07) :1901-1906
[2]   Atrophy mainly affects the limbic system and the deep grey matter at the first stage of multiple sclerosis [J].
Audoin, Bertrand ;
Zaaraoui, Wafaa ;
Reuter, Francoise ;
Rico, Audrey ;
Malikova, Irina ;
Confort-Gouny, Sylviane ;
Cozzone, Patrick J. ;
Pelletier, Jean ;
Ranjeva, Jean-Philippe .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2010, 81 (06) :690-695
[3]   Measurement of brain and spinal cord atrophy by magnetic resonance imaging as a tool to monitor multiple sclerosis [J].
Bakshi, R ;
Dandamudi, VSR ;
Neema, M ;
De, C ;
Bermel, RA .
JOURNAL OF NEUROIMAGING, 2005, 15 (04) :30S-45S
[4]   The influence of patient demographics, disease characteristics and treatment on brain volume loss in Trial Assessing Injectable Interferon vs FTY720 Oral in Relapsing-Remitting Multiple Sclerosis (TRANSFORMS), a phase 3 study of fingolimod in multiple sclerosis [J].
Barkhof, Frederik ;
de Jong, Remko ;
Sfikas, Nikolaos ;
de Vera, Ana ;
Francis, Gordon ;
Cohen, Jeffrey .
MULTIPLE SCLEROSIS JOURNAL, 2014, 20 (13) :1704-1713
[5]   Imaging outcomes for neuroprotection and repair in multiple sclerosis trials [J].
Barkhof, Frederik ;
Calabresi, Peter A. ;
Miller, David H. ;
Reingold, Stephen C. .
NATURE REVIEWS NEUROLOGY, 2009, 5 (05) :256-266
[6]   Correlating brain atrophy with cognitive dysfunction, mood disturbances, and personality disorder in multiple sclerosis [J].
Benedict, RHB ;
Carone, DA ;
Bakshi, R .
JOURNAL OF NEUROIMAGING, 2004, 14 (03) :36S-45S
[7]   Subcortical and Cortical Gray Matter Atrophy in a Large Sample of Patients with Clinically Isolated Syndrome and Early Relapsing-Remitting Multiple Sclerosis [J].
Bergsland, N. ;
Horakova, D. ;
Dwyer, M. G. ;
Dolezal, O. ;
Seidl, Z. K. ;
Vaneckova, M. ;
Krasensky, J. ;
Havrdova, E. ;
Zivadinov, R. .
AMERICAN JOURNAL OF NEURORADIOLOGY, 2012, 33 (08) :1573-1578
[8]   The measurement and clinical relevance of brain atrophy in multiple sclerosis [J].
Bermel, RA ;
Bakshi, R .
LANCET NEUROLOGY, 2006, 5 (02) :158-170
[9]   WHY THE COCHRANE RISK OF BIAS TOOL SHOULD INCLUDE FUNDING SOURCE AS A STANDARD ITEM [J].
Bero, Lisa A. .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2013, (12)
[10]   Brain atrophy in clinically early relapsing-remitting multiple sclerosis [J].
Chard, DT ;
Griffin, CM ;
Parker, GJM ;
Kapoor, R ;
Thompson, AJ ;
Miller, DH .
BRAIN, 2002, 125 :327-337