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DOI 10.1212/nxi.0000000000000924

Медицинская библиотека · Neurology(R) neuroimmunology & neuroinflammation · 2020

Overlapping central and peripheral nervous system syndromes in MOG antibody-associated disorders.

Rinaldi Simon, Davies Alexander, Fehmi Janev, Beadnall Heidi N, Wang Justine, Hardy Todd A, Barnett Michael H, Broadley Simon A, Waters Patrick, Reddel Stephen W, Irani Sarosh R, Brilot Fabienne, Dale Russell C, Ramanathan Sudarshini, Australian and New Zealand MOG Study Group

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVE

Antibodies to myelin oligodendrocyte glycoprotein (MOG) are associated with CNS demyelination inclusive of optic neuritis (ON) and transverse myelitis (TM). To examine whether peripheral nervous system (PNS) involvement is associated with MOG antibody-associated disorders (MOGAD), we performed detailed characterization of an Australasian MOGAD cohort.

METHODS

Using a live cell-based assay, we diagnosed 271 adults with MOGAD (2013-2018) and performed detailed clinical and immunologic characterization on those with likely PNS involvement.

RESULTS

We identified 19 adults with MOGAD and PNS involvement without prior TM. All patients had CNS involvement including ON (bilateral [n = 3], unilateral [n = 3], and recurrent [n = 7]), a cortical lesion (n = 1), meningoencephalitis (n = 1), and subsequent TM (n = 4). Clinical phenotyping and neurophysiology were consistent with acute inflammatory demyelinating polyneuropathy (n = 1), myeloradiculitis (n = 3), multifocal motor neuropathy (n = 1), brachial neuritis (n = 2), migrant sensory neuritis (n = 3), and paresthesia and/or radicular limb pain (n = 10). Onset MRI spine was consistent with myeloradiculitis with nerve root enhancement in 3/19 and normal in 16/19. Immunotherapy resulted in partial/complete PNS symptom resolution in 12/15 (80%) (steroids and/or IV immunoglobulin n = 9, rituximab n = 2, and plasmapheresis n = 1). We identified serum antibodies targeting neurofascin 155, contactin-associated protein 2, or GM1 in 4/16 patients with MOGAD PNS compared with 0/30 controls (p = 0.01). There was no binding to novel cell surface antigens using an in vitro myelinating sensory neuronal coculture model.

CONCLUSIONS

Myeloradiculitis, combined central and peripheral demyelination syndromes, and inflammatory neuropathies may be associated with MOGAD and may be immunotherapy responsive. We identified a subgroup who may have pathology mediated by coexistent autoantibodies.

Для цитирования: Rinaldi Simon, Davies Alexander, Fehmi Janev, Beadnall Heidi N, Wang Justine, Hardy Todd A, Barnett Michael H, Broadley Simon A, Waters Patrick, Reddel Stephen W, Irani Sarosh R, Brilot Fabienne, Dale Russell C, Ramanathan Sudarshini, Australian and New Zealand MOG Study Group. Overlapping central and peripheral nervous system syndromes in MOG antibody-associated disorders.. Neurology(R) neuroimmunology & neuroinflammation. 2020. DOI: 10.1212/nxi.0000000000000924.

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