Patients with this phenotype generally appear to do better than those with aquaporin-4-antibody disease.
Several syndromes have been described with associated myelin oligodendrocyte glycoprotein (MOG) antibodies (Abs). The studies evaluating prognosis in patients with neuromyelitis optica spectrum disorder (NMOSD) with MOG Abs have conflicting findings (NEJM JW Neurol Feb 2018 and Brain 2017 Dec 1; 140:3128).
Investigators identified 197 MOG-Ab-positive patients (median age at presentation, 36; 1:1 sex ratio). Optic neuritis (ON) was the most frequent clinical syndrome (61%), followed by transverse myelitis (TM; 22.3%), combined ON/TM (8%), isolated brainstem syndrome (4%), and encephalopathy (3%). A positive immune profile in the cerebrospinal fluid was not common, present in less than 10%.
Immunosuppressants were used in 54%, which included 67…
Reviewing Author
DisclosuresConsultant/Advisory BoardAlexion Pharmaceuticals; Amgen; Astoria; Biogen; Bristol Myers Squibb; Celltrion; Genentech; Hoffmann-La Roche; Genzyme; EMD Serono; Immpact-Bio; Immunic Therapeutics; Kyverna; Lundbeck; Novartis; Sandoz; TG Therapeutics
Grant/Research SupportNational Institutes of Health; National Multiple Sclerosis Society; U.S. Department of Defense
Leadership Positions in Professional SocietiesConsortium of Multiple Sclerosis Centers (Treasurer)
DisclosuresConsultant/Advisory BoardAlexion Pharmaceuticals; Amgen; Astoria; Biogen; Bristol Myers Squibb; Celltrion; Genentech; Hoffmann-La Roche; Genzyme; EMD Serono; Immpact-Bio; Immunic Therapeutics; Kyverna; Lundbeck; Novartis; Sandoz; TG Therapeutics
Grant/Research SupportNational Institutes of Health; National Multiple Sclerosis Society; U.S. Department of Defense
Leadership Positions in Professional SocietiesConsortium of Multiple Sclerosis Centers (Treasurer)