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Effects of Cannabidiol in Huntington's Disease
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Neurology 36 (Suppl 1) April 1986 p. 342
By Reuven Sandyk, Paul Consroe, Lawrence Z.
Stern, and Stuart R. Snider, Tucson, AZ
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Abstract: Cannabidiol (CBD) is a major
nonpsychoactive cannabinoid of marijuana. Based on reports
indicating possible efficacy of CBD in dystonic movements
(Neurology 1984; 34 [Suppl 1]: 147 and 1985; 35 [Suppl 1]:
201), we tried CBD in three patients with Huntington's
disease (HD). The patients;, aged 30 to 56, had HD of 7 to
12 years' duration. Their condition has been slowly
progressive and unresponsive to prior therapy with
neuroleptics. Orally administered CBD was initiated at 300
mg/d and increased 1 week later to 600 mg/d for the next 3
weeks. Mild improvement (5 to 15%) in the choreic movements
was documented using the tongue protrusion test (Neurology
[Minneap} 1972; 22: 929-33) and a chorea severity
evaluation scale (Br J Clin Pharmacol 1981; 11: 129-51)
after the first week. Further improvement (20 to 40%) was
noticed after the second week of CBD, and this remained
stable for the following 2 weeks. Except for transient,
mild hypotension, no side effects were recorded, and
laboratory tests were normal. Withdrawal of CBD after 48
hours resulted in return of choreic movements to the
pre-CBD state.
(Supported in part by NINCDS grant #NS15441)
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