Trial of Minocycline in a Clinically Isolated Syndrome of Multiple Sclerosis

The risk of conversion from a first demyelinating event to MS was lower with minocycline than with placebo over 6 months but not over 24 months. Changes of demyelination on MRI favored minocycline over placebo. Adverse events were more frequent with minocycline. After a first focal clinical demyelin...

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Veröffentlicht in:The New England journal of medicine 2017-06, Vol.376 (22), p.2122-2133
Hauptverfasser: Metz, Luanne M, Li, David K.B, Traboulsee, Anthony L, Duquette, Pierre, Eliasziw, Misha, Cerchiaro, Graziela, Greenfield, Jamie, Riddehough, Andrew, Yeung, Michael, Kremenchutzky, Marcelo, Vorobeychik, Galina, Freedman, Mark S, Bhan, Virender, Blevins, Gregg, Marriott, James J, Grand’Maison, Francois, Lee, Liesly, Thibault, Manon, Hill, Michael D, Yong, V. Wee
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Sprache:eng
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Zusammenfassung:The risk of conversion from a first demyelinating event to MS was lower with minocycline than with placebo over 6 months but not over 24 months. Changes of demyelination on MRI favored minocycline over placebo. Adverse events were more frequent with minocycline. After a first focal clinical demyelinating event (also called a clinically isolated syndrome), the risk of conversion to multiple sclerosis is high. Minocycline is a tetracycline antibiotic agent that has immune-modulating properties; preliminary data have shown activity of minocycline in patients with multiple sclerosis. 1 – 4 Minocycline has a good safety profile, 5 although rash, headache, dizziness, and photosensitivity are common side effects. Pseudotumor cerebri and hypersensitivity syndromes are rare but serious complications, and hyperpigmentation may occur with long-term use. Antibiotic resistance is infrequently associated with minocycline therapy. 6 In one small clinical trial involving patients with relapsing–remitting multiple sclerosis, minocycline therapy reduced . . .
ISSN:0028-4793
1533-4406
DOI:10.1056/NEJMoa1608889