Cerebral glucose metabolism, cerebrospinal fluid-β-amyloid1-42 (CSF-Aβ42), tau and apolipoprotein E genotype in long-term rivastigmine and tacrine treated Alzheimer disease (AD) patients
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作者:
Stefanova, E
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机构:Huddinge Univ Hosp, Karolinska Inst, Dept NEUROTEC, Div Mol Neuropharmacol, S-14186 Huddinge, Sweden
Stefanova, E
Blennow, K
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机构:Huddinge Univ Hosp, Karolinska Inst, Dept NEUROTEC, Div Mol Neuropharmacol, S-14186 Huddinge, Sweden
Blennow, K
Almkvist, O
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机构:Huddinge Univ Hosp, Karolinska Inst, Dept NEUROTEC, Div Mol Neuropharmacol, S-14186 Huddinge, Sweden
Almkvist, O
Hellström-Lindahl, E
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机构:Huddinge Univ Hosp, Karolinska Inst, Dept NEUROTEC, Div Mol Neuropharmacol, S-14186 Huddinge, Sweden
Hellström-Lindahl, E
Nordberg, A
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机构:Huddinge Univ Hosp, Karolinska Inst, Dept NEUROTEC, Div Mol Neuropharmacol, S-14186 Huddinge, Sweden
Nordberg, A
机构:
[1] Huddinge Univ Hosp, Karolinska Inst, Dept NEUROTEC, Div Mol Neuropharmacol, S-14186 Huddinge, Sweden
[2] Univ Gothenburg, Molndal Hosp, Dept Clin Neurosci, Gothenburg, Sweden
We evaluated cerebral glucose metabolism (CMRglc) and cerebrospinal fluid (CSF) levels of tau and beta-amyloid(1-42)(Abeta42), in relation to apolipoprotein E (ApoE) genotype, in patients with mild Alzheimer disease (AD) treated with rivastigmine (n = 11) and tacrine (n = 16) for 1 year; and two untreated AD groups. The rivastigmine-treated AD patients showed a significant increase in CMRglc as compared to both tacrine-treated and untreated AD subjects. The rivastigmine-treated AD group showed no change in CSF-tau levels after 1 year, while in contrast a significant increase as seen in tacrine-treated and untreated AD patients. The CSF-tau changes were mainly seen in ApoE epsilon4 carriers. There was no significant change in Abeta42 after 1-year treatment with either rivastigmine or tacrine. This study shows that the two long-term cholinesterase inhibitor treatments exert different effects on biological markers for AD. (C) 2002 Published by Elsevier Science Ireland Ltd.