A placebo-controlled study of memantine for the treatment of human immunodeficiency virus-associated sensory neuropathy

Journal of NeuroVirology - Tập 12 - Trang 328-331 - 2006
Giovanni Schifitto1, Constantin T. Yiannoutsos2,3, David M. Simpson4, Christina M. Marra5, Elyse J. Singer6, Dennis L. Kolson7, Avindra Nath8, Joseph R. Berger9, Bradford Navia10
1Department of Neurology, University of Rochester, Rochester, USA.
2Harvard School of Public Health, Boston, USA
3Indiana University School of Medicine, Indianapolis, USA
4Mt Sinai Medical Center, New York, USA
5University of Washington, Seattle, USA
6UCLA Medical Center, Los Angeles, USA
7University of Pennsylvania, Philadelphia, USA
8Johns Hopkins Medical Center, Baltimore, USA
9University of Kentucky, Lexington, USA
10Departments of Neurology and Psychiatry, Tufts-New England Medical Center, Boston, USA

Tóm tắt

Distal sensory polyneuropathy (DSP) is the most frequent neurological complication of HIV infection. Neuropathic symptoms vary from mild paresthesias to severe pain that respond only partially to symptomatic treatment. Forty-five subjects with human immunodeficiency virus (HIV)-associated symptomatic DSP (SDSP) were enrolled in a randomized, multicenter, 16-week placebo-controlled study of memantine, an N-methyl-d-aspartate (NMDA) uncompetitive antagonist. Although memantine was well tolerated, no trend toward clinical benefit was observed. Results were similar to those of other pilot studies of memantine for neuropathic pain unrelated to HIV, suggesting that memantine is ineffective for the symptomatic treatment of HIV-associated SDSP.

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