Your browser doesn't support javascript.
loading
The Impact of Aging on Multiple Sclerosis.
Goyne, Christopher E; Fair, Ashley E; Sumowski, Paige E; Graves, Jennifer S.
Afiliación
  • Goyne CE; Department of Neurosciences, University of California San Diego, 9452 Medical Center Drive, Ste 4W-222, La Jolla, San Diego, CA, 92037, USA.
  • Fair AE; Department of Neurosciences, University of California San Diego, 9452 Medical Center Drive, Ste 4W-222, La Jolla, San Diego, CA, 92037, USA.
  • Sumowski PE; Department of Neurosciences, University of California San Diego, 9452 Medical Center Drive, Ste 4W-222, La Jolla, San Diego, CA, 92037, USA.
  • Graves JS; Department of Neurosciences, University of California San Diego, 9452 Medical Center Drive, Ste 4W-222, La Jolla, San Diego, CA, 92037, USA. Jgraves@health.ucsd.edu.
Curr Neurol Neurosci Rep ; 24(4): 83-93, 2024 04.
Article en En | MEDLINE | ID: mdl-38416310
ABSTRACT
PURPOSE OF REVIEW Multiple sclerosis (MS) is a chronic, immune-mediated demyelinating disorder of the central nervous system. Age is one of the most important factors in determining MS phenotype. This review provides an overview of how age influences MS clinical characteristics, pathology, and treatment. RECENT

FINDINGS:

New methods for measuring aging have improved our understanding of the aging process in MS. New studies have characterized the molecular and cellular composition of chronic active or smoldering plaques in MS. These lesions are important contributors to disability progression in MS. These studies highlight the important role of immunosenescence and the innate immune system in sustaining chronic inflammation. Given these changes in immune function, several studies have assessed optimal treatment strategies in aging individuals with MS. MS phenotype is intimately linked with chronologic age and immunosenescence. While there are many unanswered questions, there has been much progress in understanding this relationship which may lead to more effective treatments for progressive disease.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Inmunosenescencia / Esclerosis Múltiple Límite: Humans Idioma: En Revista: Curr Neurol Neurosci Rep / Curr. neurol. neurosci. rep / Current neurology and neuroscience reports Asunto de la revista: NEUROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Inmunosenescencia / Esclerosis Múltiple Límite: Humans Idioma: En Revista: Curr Neurol Neurosci Rep / Curr. neurol. neurosci. rep / Current neurology and neuroscience reports Asunto de la revista: NEUROLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos