TY - JOUR
T1 - Current treatment of mild cognitive impairment and Alzheimer's disease
AU - Knopman, David S.
N1 - Funding Information:
Supported in part by grants U01 AG06786 (Mayo Alzheimer’s Disease Patient Registry) and P50 AG16574 (Mayo Alzheimer’s Disease Research Center) from the National Institute on Aging, and the Robert H. and Cla-rice Smith and Abigail Van Buren Alzheimer’s Disease Research Program of the Mayo Foundation.
Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2006/9
Y1 - 2006/9
N2 - Current therapy for Alzheimer's disease (AD) consists of two classes of drugs: the cholinesterase inhibitors, of which there are three currently available medications; and the glutamate modulators, of which there is one. There has been no new information regarding efficacy of the cholinesterase inhibitors or memantine in AD over the past year, but a large, randomized trial concerning mild cognitive impairment was reported. Donepezil delayed conversion to dementia for 12 months but not longer in that trial, whereas vitamin E had no impact on outcomes. The results of the first immunization therapy for AD were released in 2005. Adverse events forced the premature discontinuation of the trial, but there were some grounds for optimism about the basic approach. Several new agents targeted . directly at amyloid β peptide production are currently in clinical trials, but no large studies have been reported over the past year.
AB - Current therapy for Alzheimer's disease (AD) consists of two classes of drugs: the cholinesterase inhibitors, of which there are three currently available medications; and the glutamate modulators, of which there is one. There has been no new information regarding efficacy of the cholinesterase inhibitors or memantine in AD over the past year, but a large, randomized trial concerning mild cognitive impairment was reported. Donepezil delayed conversion to dementia for 12 months but not longer in that trial, whereas vitamin E had no impact on outcomes. The results of the first immunization therapy for AD were released in 2005. Adverse events forced the premature discontinuation of the trial, but there were some grounds for optimism about the basic approach. Several new agents targeted . directly at amyloid β peptide production are currently in clinical trials, but no large studies have been reported over the past year.
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U2 - 10.1007/s11910-996-0016-9
DO - 10.1007/s11910-996-0016-9
M3 - Review article
C2 - 16928345
AN - SCOPUS:33749028978
SN - 1528-4042
VL - 6
SP - 365
EP - 371
JO - Current Neurology and Neuroscience Reports
JF - Current Neurology and Neuroscience Reports
IS - 5
ER -