Myelin-oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is a recently identified autoimmune disorder that presents in both adults and children as CNS demyelination. Although there are clinical phenotypic overlaps between MOGAD, multiple sclerosis, and aquaporin-4 antibody-associated neuromyelitis optica spectrum disorder (NMOSD) cumulative biological, clinical, and pathological evidence discriminates between these conditions. Patients should not be diagnosed with multiple sclerosis or NMOSD if they have anti-MOG antibodies in their serum. However, many questions related to the clinical characterisation of MOGAD and pathogenetic role of MOG antibodies are still unanswered. Furthermore, therapy is mainly based on standard protocols for aquaporin-4 antibody-associated NMOSD and multiple sclerosis, and more evidence is needed regarding how and when to treat patients with MOGAD.

Myelin-oligodendrocyte glycoprotein antibody-associated disease / Marignier R.; Hacohen Y.; Cobo-Calvo A.; Probstel A.-K.; Aktas O.; Alexopoulos H.; Amato M.-P.; Asgari N.; Banwell B.; Bennett J.; Brilot F.; Capobianco M.; Chitnis T.; Ciccarelli O.; Deiva K.; De Seze J.; Fujihara K.; Jacob A.; Kim H.J.; Kleiter I.; Lassmann H.; Leite M.-I.; Linington C.; Meinl E.; Palace J.; Paul F.; Petzold A.; Pittock S.; Reindl M.; Sato D.K.; Selmaj K.; Siva A.; Stankoff B.; Tintore M.; Traboulsee A.; Waters P.; Waubant E.; Weinshenker B.; Derfuss T.; Vukusic S.; Hemmer B.. - In: LANCET NEUROLOGY. - ISSN 1474-4422. - ELETTRONICO. - 20:(2021), pp. 762-772. [10.1016/S1474-4422(21)00218-0]

Myelin-oligodendrocyte glycoprotein antibody-associated disease

Amato M. -P.;
2021

Abstract

Myelin-oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is a recently identified autoimmune disorder that presents in both adults and children as CNS demyelination. Although there are clinical phenotypic overlaps between MOGAD, multiple sclerosis, and aquaporin-4 antibody-associated neuromyelitis optica spectrum disorder (NMOSD) cumulative biological, clinical, and pathological evidence discriminates between these conditions. Patients should not be diagnosed with multiple sclerosis or NMOSD if they have anti-MOG antibodies in their serum. However, many questions related to the clinical characterisation of MOGAD and pathogenetic role of MOG antibodies are still unanswered. Furthermore, therapy is mainly based on standard protocols for aquaporin-4 antibody-associated NMOSD and multiple sclerosis, and more evidence is needed regarding how and when to treat patients with MOGAD.
2021
20
762
772
Goal 3: Good health and well-being for people
Marignier R.; Hacohen Y.; Cobo-Calvo A.; Probstel A.-K.; Aktas O.; Alexopoulos H.; Amato M.-P.; Asgari N.; Banwell B.; Bennett J.; Brilot F.; Capobian...espandi
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1262886
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