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Recent advances in the treatment of primary and secondary progressive Multiple Sclerosis.
Sriwastava, Shitiz; Elkhooly, Mahmoud; Amatya, Suban; Shrestha, Kriti; Kagzi, Yusuf; Bhatia, Dipika; Gupta, Rajesh; Jaiswal, Shruti; Lisak, Robert P.
Afiliação
  • Sriwastava S; Division of Multiple Sclerosis and Neuroimmunology Department of Neurology, McGovern Medical School (UT Health), University of Texas Health Science Center at Houston, Houston, TX,USA. Electronic address: shitiz.k.sriastava@uth.tmc.edu.
  • Elkhooly M; Department of Neurology, Southern Illinois university, Springfield, IL, USA; Department of Neuropsychiatry, Minia University, Egypt.
  • Amatya S; Department of Medicine, Patan Academy of Health Sciences, Kathmandu, Nepal.
  • Shrestha K; Department of Medicine, Patan Academy of Health Sciences, Kathmandu, Nepal.
  • Kagzi Y; Mahatma Gandhi Memorial Medical College, Indore, India.
  • Bhatia D; Division of Multiple Sclerosis and Neuroimmunology Department of Neurology, McGovern Medical School (UT Health), University of Texas Health Science Center at Houston, Houston, TX,USA.
  • Gupta R; Division of Multiple Sclerosis and Neuroimmunology Department of Neurology, McGovern Medical School (UT Health), University of Texas Health Science Center at Houston, Houston, TX,USA.
  • Jaiswal S; Department of Neuro-Oncology, MD Anderson Cancer Center, Houston, TX, USA.
  • Lisak RP; Department of Neurology, Wayne state University, Detroit, MI, USA.
J Neuroimmunol ; 390: 578315, 2024 05 15.
Article em En | MEDLINE | ID: mdl-38554666
ABSTRACT

BACKGROUND:

The article highlights upcoming potential treatments, which target different phases of inflammation and offer remyelinating strategies as well as direct and indirect neuroprotective and oligodendrocyte protective effects, providing a hopeful outlook for patients with primary and secondary progressive multiple sclerosis (PPMS and SPMS).

OBJECTIVES:

The review aims to identify potential treatments and ongoing clinical trials for PPMS and SPMS, and compare their mechanisms of action, efficacy, and side effects with current treatments.

METHODS:

We reviewed ongoing clinical trials for PPMS and SPMS on the NIH website, as well as articles from PubMed, Embase, and clinicaltrails.gov since 2010.

RESULTS:

BTKIs like, tolebrutinib, and fenebrutinib are being explored as potential PMS treatments. Vidofludimus calcium, an orally available treatment, has shown a reduction of active and new MRI lesions. Other treatments like simvastatin, N-acetylcysteine (NAC), and alpha-lipoic acid are being explored for their antioxidant properties. AHSCT and mesenchymal stem cell therapy are experimental options for younger patients with high inflammatory activity.

CONCLUSIONS:

SPMS and PPMS are being studied for new treatments and future trials should consider combination therapies targeting inflammation, demyelination, and neuronal death, as the pathogenesis of PMS involves complex factors.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esclerose Múltipla Crônica Progressiva / Tirosina Quinase da Agamaglobulinemia Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esclerose Múltipla Crônica Progressiva / Tirosina Quinase da Agamaglobulinemia Idioma: En Ano de publicação: 2024 Tipo de documento: Article