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ABSTRACT: Aim
To characterize progression of Alzheimer's disease (AD) using proton magnetic resonance spectroscopy ((1)H MRS).Methods
Eleven subjects with mild to moderate AD underwent neurocognitive testing and single-voxel (1)H MRS from the precuneus and posterior cingulate region at baseline, after 24 weeks of monotherapy with a cholinesterase inhibitor, and after another 24 weeks of combination therapy with open-label memantine and a cholinesterase inhibitor. Baseline metabolites [N-acetylaspartate (NAA), myo-inositol (mI), choline (Cho), and creatine (Cr)] and their ratios in AD subjects were compared with those of an age-matched control group of 28 cognitively normal subjects.Results
AD subjects had significantly higher mI/Cr and lower NAA, NAA/Cr, NAA/Cho, and NAA/mI. Baseline Alzheimer's Disease Cooperative Study Activities of Daily Living (ADCS-ADL) scores significantly correlated with NAA/Cr, mI/Cr, and NAA/mI. There was an increase in mI and a decrease in NAA/mI, but no significant change in other metabolites or ratios, or neurocognitive measures, when memantine was added to a cholinesterase inhibitor.Conclusion
Metabolite ratios significantly differed between AD and control subjects. Baseline metabolite ratios correlated with function (ADCS-ADL). There was an increase in mI and a decrease in NAA/mI, but no changes in other metabolites, ratios, or cognitive measures, when memantine was added to a cholinesterase inhibitor.
SUBMITTER: Gordon ML
PROVIDER: S-EPMC3435529 | biostudies-literature | 2012 Jan
REPOSITORIES: biostudies-literature
Gordon Marc L ML Kingsley Peter B PB Goldberg Terry E TE Koppel Jeremy J Christen Erica E Keehlisen Lynda L Kohn Nina N Davies Peter P
Dementia and geriatric cognitive disorders extra 20120101 1
<h4>Aim</h4>To characterize progression of Alzheimer's disease (AD) using proton magnetic resonance spectroscopy ((1)H MRS).<h4>Methods</h4>Eleven subjects with mild to moderate AD underwent neurocognitive testing and single-voxel (1)H MRS from the precuneus and posterior cingulate region at baseline, after 24 weeks of monotherapy with a cholinesterase inhibitor, and after another 24 weeks of combination therapy with open-label memantine and a cholinesterase inhibitor. Baseline metabolites [N-ac ...[more]