Therapeutic Advances and Challenges in the Treatment of Progressive Multiple Sclerosis

被引:0
作者
Laura E. Baldassari
Robert J. Fox
机构
[1] Neurological Institute,Mellen Center for Multiple Sclerosis Treatment and Research
[2] Cleveland Clinic,undefined
来源
Drugs | 2018年 / 78卷
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摘要
Despite the fact that majority of patients with multiple sclerosis (MS) have relapsing-remitting disease, many transition to secondary progressive disease (SPMS) over time. This transition is thought to be related to neurodegenerative processes increasingly predominating over inflammatory processes as the driving forces of disability. However, some patients initially present with primary progressive disease (PPMS) that is characterized by a gradual accumulation of neurological symptoms and subsequent disability accumulation. The treatment of both PPMS and SPMS, collectively referred to as progressive MS, has proven quite challenging due to the multifactorial and poorly understood pathophysiology of multiple sclerosis in general, specifically that of progressive disease. The purpose of this article is to discuss important clinical and pathophysiologic differences between relapsing and progressive forms of MS, review previous notable trials of drugs in progressive MS, examine current literature regarding recent and promising progressive MS treatments, and discuss future considerations for progressive MS therapeutics and management. Specifically, the current evidence regarding treatment of progressive MS with ocrelizumab, simvastatin, ibudilast, alpha-lipoic acid, high-dose biotin, siponimod, and cell-based therapies are discussed.
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页码:1549 / 1566
页数:17
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  • [1] Lublin FD(2014)Defining the clinical course of multiple sclerosis: the 2013 revisions Neurology 83 278-286
  • [2] Reingold SC(2018)Diagnosis of multiple sclerosis: 2017 revisions of the McDonald criteria Lancet Neurol 17 162-173
  • [3] Cohen JA(2011)Diagnostic criteria for multiple sclerosis: 2010 revisions to the McDonald criteria Ann Neurol 69 292-302
  • [4] Cutter GR(1998)Axonal transection in the lesions of multiple sclerosis N Engl J Med 338 278-285
  • [5] Sorensen PS(2015)Pathological mechanisms in progressive multiple sclerosis Lancet Neurol 14 183-193
  • [6] Thompson AJ(2009)Virtual hypoxia and chronic necrosis of demyelinated axons in multiple sclerosis Lancet Neurol 8 280-291
  • [7] Thompson AJ(2013)Iron and neurodegeneration in the multiple sclerosis brain Ann Neurol 74 848-861
  • [8] Banwell BL(2017)Metabolic pathways as possible therapeutic targets for progressive multiple sclerosis Neural Regen Res 12 1262-1267
  • [9] Barkhof F(2012)Cortical lesion load associates with progression of disability in multiple sclerosis Brain 135 2952-2961
  • [10] Carroll WM(2001)Transected neurites, apoptotic neurons, and reduced inflammation in cortical multiple sclerosis lesions Ann Neurol 50 389-400