Immune-mediated CNS diseases: a review on nosological classification and clinical features
- PMID: 21619943
- DOI: 10.1016/j.autrev.2011.05.008
Immune-mediated CNS diseases: a review on nosological classification and clinical features
Abstract
The immune-mediated diseases of the central nervous system (CNS) cover a wide range of clinical manifestations. Over the last years, considerable efforts have been made to establish a nosologic concept based upon distinctive pathophysiological characteristics of the single diseases. We describe the historically defined entities of immune-mediated diseases that primarily, but not exclusively, are affecting myelin structures. These include very rare entities as Schilder's, Balo's and Marburg's disease or the chronic and relapsing types of optic neuritis, for which evidence based paradigms still are virtually missing. In other, slightly more frequent diseases as neuromyelitis optica (NMO), advances in the concepts of specific biological features have been achieved and are beginning to transform into changes in clinical concepts. Acute disseminated encephalomyelitis (ADEM) and multiple sclerosis (MS) are by far the most frequent entities in this group and thus the only ones for which extensive empirical data on disease biology and evidence based clinical management strategies exist by now. For the most important entities, clinical features and therapeutic approaches are reviewed on the basis of current evidence. The results of basic science studies are assessed for their implications in nosological classification.
Copyright © 2011. Published by Elsevier B.V.
Similar articles
-
Comparative immunopathogenesis of acute disseminated encephalomyelitis, neuromyelitis optica, and multiple sclerosis.Curr Opin Neurol. 2007 Jun;20(3):343-50. doi: 10.1097/WCO.0b013e3280be58d8. Curr Opin Neurol. 2007. PMID: 17495631 Review.
-
[Diagnostic criteria of borderline forms of multiple sclerosis].Rev Neurol (Paris). 2001 Sep;157(8-9 Pt 2):935-43. Rev Neurol (Paris). 2001. PMID: 11787358 Review. French.
-
Neuromyelitis optica-IgG in childhood inflammatory demyelinating CNS disorders.Neurology. 2008 Jan 29;70(5):344-52. doi: 10.1212/01.wnl.0000284600.80782.d5. Epub 2007 Dec 19. Neurology. 2008. PMID: 18094334
-
The diagnosis of multiple sclerosis and the various related demyelinating syndromes: a critical review.J Autoimmun. 2014 Feb-Mar;48-49:134-42. doi: 10.1016/j.jaut.2014.01.022. Epub 2014 Feb 10. J Autoimmun. 2014. PMID: 24524923 Review.
-
Acute disseminated encephalomyelitis, transverse myelitis, and neuromyelitis optica.Continuum (Minneap Minn). 2013 Aug;19(4 Multiple Sclerosis):944-67. doi: 10.1212/01.CON.0000433289.38339.a2. Continuum (Minneap Minn). 2013. PMID: 23917095 Review.
Cited by
-
Genetic risk variants for multiple sclerosis are linked to differences in alternative pre-mRNA splicing.Front Immunol. 2022 Oct 28;13:931831. doi: 10.3389/fimmu.2022.931831. eCollection 2022. Front Immunol. 2022. PMID: 36405756 Free PMC article.
-
Whole Exome Sequencing in Multi-Incident Families Identifies Novel Candidate Genes for Multiple Sclerosis.Int J Mol Sci. 2022 Sep 28;23(19):11461. doi: 10.3390/ijms231911461. Int J Mol Sci. 2022. PMID: 36232761 Free PMC article.
-
Screening for severe drug-drug interactions in patients with multiple sclerosis: A comparison of three drug interaction databases.Front Pharmacol. 2022 Aug 5;13:946351. doi: 10.3389/fphar.2022.946351. eCollection 2022. Front Pharmacol. 2022. PMID: 36034780 Free PMC article.
-
Associated factors of potential drug-drug interactions and drug-food interactions in patients with multiple sclerosis.Ther Adv Chronic Dis. 2022 Aug 4;13:20406223221108391. doi: 10.1177/20406223221108391. eCollection 2022. Ther Adv Chronic Dis. 2022. PMID: 35959503 Free PMC article.
-
Implication of genetic variants in primary microRNA processing sites in the risk of multiple sclerosis.EBioMedicine. 2022 Jun;80:104052. doi: 10.1016/j.ebiom.2022.104052. Epub 2022 May 10. EBioMedicine. 2022. PMID: 35561450 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
