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The Importance of Alzheimer Disease Assessment Scale-cognitive Part in Predicting Progress for Amnestic Mild Cognitive Impairment to Alzheimer DiseaseDepartment of Neurology, University of Brescia, Italy, Geriatric Research Group, via Romanino 1, 25100 Brescia, Italy, lrozzini{at}iol.it
Department of Neurology, University of Brescia, Italy, Geriatric Research Group, via Romanino 1, 25100 Brescia, Italy
Department of Neurology, University of Brescia, Italy
Department of Neurology, University of Brescia, Italy
Department of Neurology, University of Brescia, Italy
Geriatric Research Group, via Romanino 1, 25100 Brescia, Italy
Department of Neurology, University of Brescia, Italy The aim of this study was to verify the usefulness of Alzheimer Disease Assessment Scale-cognitive subscale (ADAS-Cog), in screening participants at risk of developing Alzheimer disease (AD) among populations with amnestic mild cognitive impairment(aMCI). 98 outpatients with aMCI were recruited. Participants were revaluated after 1 year: 44 (44.9%) were progressed to AD (progressors), while 54 (55.1%) did not convert (nonprogressors MCI). At baseline, cognitive performances were more impaired in progressors assessed by MMSE and by a neuropsychological battery. When tested with the ADAS-Cog subscale, the 2 groups of participants at baseline, progressors, and nonprogressors MCI, were significantly different regarding total score, memory, and nonmemory subitems. Considering a cutoff of 9.5 total score, adjusted for education, ADAS-Cog subscale showed a good performance (area under the curve = 0.67; sensitivity = 0.62%; specificity = 0.73%) in predicting conversion from aMCI to AD. Progressors aMCI were characterized at baseline by a greater cognitive impairment. ADAS-Cog subscale is a useful and brief cognitive assessment tool to screen aMCI participants converting to AD within 1 year.
Key Words: mild cognitive impairment MCI Alzheimer Disease Assessment Scale-cognitive part ADAS-Cog Alzheimer disease AD dementia
Journal of Geriatric Psychiatry and Neurology, Vol. 21, No. 4,
261-267 (2008) |
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