» Articles » PMID: 30255442

Therapeutic Advances and Challenges in the Treatment of Progressive Multiple Sclerosis

Overview
Journal Drugs
Specialty Pharmacology
Date 2018 Sep 27
PMID 30255442
Citations 26
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

Kynurenines and Inflammation: A Remarkable Axis for Multiple Sclerosis Treatment.

Carrillo-Mora P, Landa-Solis C, Valle-Garcia D, Luna-Angulo A, Aviles-Arnaut H, Robles-Banuelos B Pharmaceuticals (Basel). 2024; 17(8).

PMID: 39204088 PMC: 11356993. DOI: 10.3390/ph17080983.


The Role of Cobalamin in Multiple Sclerosis: An Update.

Golabi M, Kazemi D, Chadeganipour A, Fouladseresht H, Sullman M, Ghezelbash B Inflammation. 2024; .

PMID: 38902541 DOI: 10.1007/s10753-024-02075-6.


BTK inhibition limits microglia-perpetuated CNS inflammation and promotes myelin repair.

Geladaris A, Torke S, Saberi D, Alankus Y, Streit F, Zechel S Acta Neuropathol. 2024; 147(1):75.

PMID: 38656399 PMC: 11043151. DOI: 10.1007/s00401-024-02730-0.


A Promising Drug Candidate as Potent Therapeutic Approach for Neuroinflammation and Its In Silico Justification of Chalcone Congeners: a Comprehensive Review.

Karati D, Mukherjee S, Roy S Mol Neurobiol. 2023; 61(4):1873-1891.

PMID: 37801205 DOI: 10.1007/s12035-023-03632-0.


Glucocorticoid-dependent multiple sclerosis overlapping anti-NMDA receptor encephalitis: a case report and literature review update.

Yang B, Yu N Neurol Sci. 2023; 45(1):83-92.

PMID: 37721572 PMC: 10761549. DOI: 10.1007/s10072-023-07034-x.


References
1.
Kieseier B . The mechanism of action of interferon-β in relapsing multiple sclerosis. CNS Drugs. 2011; 25(6):491-502. DOI: 10.2165/11591110-000000000-00000. View

2.
Chaudhary P, Marracci G, Galipeau D, Pocius E, Morris B, Bourdette D . Lipoic acid reduces inflammation in a mouse focal cortical experimental autoimmune encephalomyelitis model. J Neuroimmunol. 2015; 289:68-74. PMC: 4664888. DOI: 10.1016/j.jneuroim.2015.10.011. View

3.
Vergo S, Craner M, Etzensperger R, Attfield K, Friese M, Newcombe J . Acid-sensing ion channel 1 is involved in both axonal injury and demyelination in multiple sclerosis and its animal model. Brain. 2011; 134(Pt 2):571-84. DOI: 10.1093/brain/awq337. View

4.
Rommer P, Stuve O . Management of secondary progressive multiple sclerosis: prophylactic treatment-past, present, and future aspects. Curr Treat Options Neurol. 2013; 15(3):241-58. DOI: 10.1007/s11940-013-0233-x. View

5.
Wolinsky J . The PROMiSe trial: baseline data review and progress report. Mult Scler. 2004; 10 Suppl 1:S65-71. DOI: 10.1177/135245850401000112. View