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Methanesulfonyl Fluoride (MSF): A Double-Blind, Placebo-Controlled Study of Safety and Efficacy in the Treatment of Senile Dementia of the Alzheimer Type

 

作者: D E Moss,   P Berlanga,   M M Hagan,   H Sandoval,   C Ishida,  

 

期刊: Alzheimer Disease and Associated Disorders  (OVID Available online 1999)
卷期: Volume 13, issue 1  

页码: 20-25

 

ISSN:0893-0341

 

年代: 1999

 

出版商: OVID

 

关键词: Alzheimer disease;Methanesulfonyl fluoride (MSF);Dementia;Acetylcholinesterase;ChEI

 

数据来源: OVID

 

摘要:

Summary:The purpose of the present study was to evaluate methanesulfonyl fluoride (MSF), a very long-acting CNS-selective acetylcholinesterase (AChE) inhibitor, as a palliative treatment for senile dementia of the Alzheimer type (SDAT). In experiment I, MSF (0.03-0.18 mg/ kg) was administered orally to 10 normal volunteers to measure toxicity and establish dose/ response function in erythrocyte AChE. MSF produced a dose-response function of % inhibition=(40)(Logl0[MSF mg/ kg] + 51.7) with no toxicity at these doses. Experiment II was a 16-week double-blind, placebo-controlled study of the safety and efficacy of MSF in doses of up to 0.18 mg/Kg given three times per week in 5 men and 10 women (60-82 years), with Mini-Mental State Examination (MMSE) scores of 9-24, who had SDAT. MSF produced a mean of 89.5% inhibition of erythrocyte AChE in patients and improved cognitive performance as measured by the MMSE, Alzheimer Disease Assessment Scale-Cognitive Subscale (ADAS-COG), Global Deterioration Scale, and the Clinical Interview Based Impression of Change (CIBIC). Most of the improvement on the ADAS-COG was maintained 8 weeks after ending MSF. No patients left the study because of drug-related adverse events and there were no toxic effects. MSF may be a safe and effective palliative treatment for SDAT and further clinical trials in larger groups of patients are warranted.

 

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