Multiple sclerosis progression: time for a new mechanism-driven framework

被引:340
作者
Kuhlmann, Tanja [1 ,2 ]
Moccia, Marcello [3 ]
Coetzee, Timothy [4 ]
Cohen, Jeffrey A. [5 ]
Correale, Jorge [6 ,7 ]
Graves, Jennifer [8 ]
Marrie, Ruth Ann [9 ]
Montalban, Xavier [10 ,11 ]
Yong, V. Wee [12 ,13 ]
Thompson, Alan J. [14 ]
Reich, Daniel S. [15 ]
机构
[1] Univ Hosp Munster, Inst Neuropathol, Munster, Germany
[2] McGill Univ, Montreal Neurol Inst, Neuroimmunol Unit, Montreal, PQ, Canada
[3] Univ Naples Federico II, Dept Neurosci, Multiple Sclerosis Clin Care & Res Ctr, Naples, Italy
[4] Natl Multiple Sclerosis Soc USA, New York, NY USA
[5] Cleveland Clin, Neurol Inst, Dept Neurol, Mellen Ctr Multiple SclerosisTreatment & Res, Cleveland, OH USA
[6] Dept Neurol, Buenos Aires, DF, Argentina
[7] CONICET UBA, Biol Chem & Biophys IQUIFIB, Buenos Aires, DF, Argentina
[8] Univ Calif San Diego, Dept Neurosci, San Diego, CA USA
[9] Univ Manitoba, Rady Fac Hlth Sci, Max Rady Coll Med, Winnipeg, MB, Canada
[10] Univ Autonoma Barcelona, Hosp Univ Vall Hebron, Multiple Sclerosis Ctr Catalonia, Barcelona, Spain
[11] Univ Autonoma Barcelona, Hosp Univ Vall Hebron, Dept Neurol Neuroimmunol, Barcelona, Spain
[12] Univ Calgary, Hotchkiss Brain Inst, Calgary, AB, Canada
[13] Univ Calgary, Dept Clin Neurosci, Calgary, AB, Canada
[14] UCL, Fac Brain Sci, NIHR Univ Coll London Hosp Biomed Res Ctr, UCL Queen Sq Inst Neurol,Dept Neuroinflammation, London, England
[15] Natl Inst Neurol Disorders & Stroke, Natl Inst Hlth, Translat Neuroradiol Sect, Bethesda, MD USA
关键词
IRON RIM LESIONS; MENINGEAL INFLAMMATION; CLINICAL-COURSE; DOUBLE-BLIND; MATTER; MS; DEMYELINATION; DISEASE; WHITE; MRI;
D O I
10.1016/S1474-4422(22)00289-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Traditionally, multiple sclerosis has been categorised by distinct clinical descriptors-relapsing-remitting, secondary progressive, and primary progressive-for patient care, research, and regulatory approval of medications. Accumulating evidence suggests that the clinical course of multiple sclerosis is better considered as a continuum, with contributions from concurrent pathophysiological processes that vary across individuals and over time. The apparent evolution to a progressive course reflects a partial shift from predominantly localised acute injury to widespread inflammation and neurodegeneration, coupled with failure of compensatory mechanisms, such as neuroplasticity and remyelination. Ageing increases neural susceptibility to injury and decreases resilience. These observations encourage a new consideration of the course of multiple sclerosis as a spectrum defined by the relative contributions of overlapping pathological and reparative or compensatory processes. New understanding of key mechanisms underlying progression and measures to quantify progressive pathology will potentially have important and beneficial implications for clinical care, treatment targets, and regulatory decision-making.
引用
收藏
页码:78 / 88
页数:11
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