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DOI 10.1093/brain/awx276

Медицинская библиотека · Brain : a journal of neurology · 2017

Clinical presentation and prognosis in MOG-antibody disease: a UK study.

Jurynczyk Maciej, Messina Silvia, Woodhall Mark R, Raza Naheed, Everett Rosie, Roca-Fernandez Adriana, Tackley George, Hamid Shahd, Sheard Angela, Reynolds Gavin, Chandratre Saleel, Hemingway Cheryl, Jacob Anu, Vincent Angela, Leite M Isabel, Waters Patrick, Palace Jacqueline

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Аннотация

See de Seze (doi:10.1093/brain/awx292) for a scientific commentary on this article. A condition associated with an autoantibody against MOG has been recently recognized as a new inflammatory disease of the central nervous system, but the disease course and disability outcomes are largely unknown. In this study we investigated clinical characteristics of MOG-antibody disease on a large cohort of patients from the UK. We obtained demographic and clinical data on 252 UK patients positive for serum immunoglobulin G1 MOG antibodies as tested by the Autoimmune Neurology Group in Oxford. Disability outcomes and disease course were analysed in more detail in a cohort followed in the Neuromyelitis Optica Oxford Service (n = 75), and this included an incident cohort who were diagnosed at disease onset (n = 44). MOG-antibody disease affects females (57%) slightly more often than males, shows no ethnic bias and typically presents with isolated optic neuritis (55%, bilateral in almost half), transverse myelitis (18%) or acute disseminated encephalomyelitis-like presentations (18%). In the total Oxford cohort after a median disease duration of 28 months, 47% of patients were left with permanent disability in at least one of the following: 16% patients had visual acuity ≤6/36 in at least one eye, mobility was limited in 7% (i.e. Expanded Disability Status Scale ≥ 4.0), 5% had Expanded Disability Status Scale ≥ 6.0, 28% had permanent bladder issues, 20% had bowel dysfunction, and 21% of males had erectile dysfunction. Transverse myelitis at onset was a significant predictor of long-term disability. In the incident cohort 36% relapsed after median disease duration of 16 months. The annualized relapse rate was 0.2. Immunosuppression longer than 3 months following the onset attack was associated with a lower risk of a second relapse. MOG-antibody disease has a moderate relapse risk, which might be mitigated by medium term immunosuppression at onset. Permanent disability occurs in about half of patients and more often involves sphincter and erectile functions than vision or mobility.

Для цитирования: Jurynczyk Maciej, Messina Silvia, Woodhall Mark R, Raza Naheed, Everett Rosie, Roca-Fernandez Adriana, Tackley George, Hamid Shahd, Sheard Angela, Reynolds Gavin, Chandratre Saleel, Hemingway Cheryl, Jacob Anu, Vincent Angela, Leite M Isabel, Waters Patrick, Palace Jacqueline. Clinical presentation and prognosis in MOG-antibody disease: a UK study.. Brain : a journal of neurology. 2017. DOI: 10.1093/brain/awx276.

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