Cortical cholinergic function is more severely affected in parkinsonian dementia than in Alzheimer disease - An in vivo positron emission tomographic study
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Bohnen, NI
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机构:Univ Pittsburgh, Sch Med, Dept Neurol, Pittsburgh, PA 15213 USA
Bohnen, NI
Kaufer, DI
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机构:Univ Pittsburgh, Sch Med, Dept Neurol, Pittsburgh, PA 15213 USA
Kaufer, DI
Ivanco, LS
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机构:Univ Pittsburgh, Sch Med, Dept Neurol, Pittsburgh, PA 15213 USA
Ivanco, LS
Lopresti, B
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机构:Univ Pittsburgh, Sch Med, Dept Neurol, Pittsburgh, PA 15213 USA
Lopresti, B
Koeppe, RA
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机构:Univ Pittsburgh, Sch Med, Dept Neurol, Pittsburgh, PA 15213 USA
Koeppe, RA
Davis, JG
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机构:Univ Pittsburgh, Sch Med, Dept Neurol, Pittsburgh, PA 15213 USA
Davis, JG
Mathis, CA
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机构:Univ Pittsburgh, Sch Med, Dept Neurol, Pittsburgh, PA 15213 USA
Mathis, CA
Moore, RY
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机构:Univ Pittsburgh, Sch Med, Dept Neurol, Pittsburgh, PA 15213 USA
Moore, RY
DeKosky, ST
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机构:Univ Pittsburgh, Sch Med, Dept Neurol, Pittsburgh, PA 15213 USA
DeKosky, ST
机构:
[1] Univ Pittsburgh, Sch Med, Dept Neurol, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Sch Med, Dept Radiol, Pittsburgh, PA 15213 USA
[3] Vet Adm Pittsburgh Healthcare Syst, Pittsburgh, PA USA
[4] Univ Michigan, Dept Radiol, Ann Arbor, MI 48109 USA
Background: Pathology reports have shown that cholinergic forebrain neuronal losses in parkinsonian dementia. (PDem) are equal to or greater than those in Alzheimer disease (AD). We hypothesized that patients with PDem would have cholinergic deficits that were similar to or greater than those of patients with AD. Objective: To determine in vivo cortical acetylcholinesterase (AChE) activity in healthy control subjects and in patients with mild AD, PDem, and Parkinson disease, without dementia using AChE positron emission tomography. Setting: University and Veterans' Administration medical center. Design and Patients: Group comparison design of patients with AD (n = 12), PDem (n = 14), and Parkinson disease without dementia (n = 11), and controls (n = 10) who underwent AChE imaging between July 1, 2000, and January 31, 2003. Patients with AD and PDem had approximately equal dementia severity. Main Outcome Measures: Cerebral AChE activity. Results: Compared with controls, mean cortical AChE activity was lowest in patients with PDem (-20.0%), followed by patients with Parkinson disease without dementia (-12.9%; P < .001). Mean cortical AChE activity was relatively preserved in patients with AD (-9.1%), except for regionally selective involvement of the lateral temporal cortex (-15%; P < .001). Conclusion: Reduced cortical AChE activity is more characteristic of patients with PDem than of patients with mild AD.
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NATL HOSP, INST NEUROL, MIRIAM MARKS DEPT NEUROCHEM, LONDON WC1N 3BG, ENGLANDNATL HOSP, INST NEUROL, MIRIAM MARKS DEPT NEUROCHEM, LONDON WC1N 3BG, ENGLAND
BOWEN, DM
SMITH, CB
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NATL HOSP, INST NEUROL, MIRIAM MARKS DEPT NEUROCHEM, LONDON WC1N 3BG, ENGLANDNATL HOSP, INST NEUROL, MIRIAM MARKS DEPT NEUROCHEM, LONDON WC1N 3BG, ENGLAND
SMITH, CB
WHITE, P
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NATL HOSP, INST NEUROL, MIRIAM MARKS DEPT NEUROCHEM, LONDON WC1N 3BG, ENGLANDNATL HOSP, INST NEUROL, MIRIAM MARKS DEPT NEUROCHEM, LONDON WC1N 3BG, ENGLAND
WHITE, P
DAVISON, AN
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NATL HOSP, INST NEUROL, MIRIAM MARKS DEPT NEUROCHEM, LONDON WC1N 3BG, ENGLANDNATL HOSP, INST NEUROL, MIRIAM MARKS DEPT NEUROCHEM, LONDON WC1N 3BG, ENGLAND
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NATL HOSP, INST NEUROL, MIRIAM MARKS DEPT NEUROCHEM, LONDON WC1N 3BG, ENGLANDNATL HOSP, INST NEUROL, MIRIAM MARKS DEPT NEUROCHEM, LONDON WC1N 3BG, ENGLAND
BOWEN, DM
SMITH, CB
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NATL HOSP, INST NEUROL, MIRIAM MARKS DEPT NEUROCHEM, LONDON WC1N 3BG, ENGLANDNATL HOSP, INST NEUROL, MIRIAM MARKS DEPT NEUROCHEM, LONDON WC1N 3BG, ENGLAND
SMITH, CB
WHITE, P
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NATL HOSP, INST NEUROL, MIRIAM MARKS DEPT NEUROCHEM, LONDON WC1N 3BG, ENGLANDNATL HOSP, INST NEUROL, MIRIAM MARKS DEPT NEUROCHEM, LONDON WC1N 3BG, ENGLAND
WHITE, P
DAVISON, AN
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NATL HOSP, INST NEUROL, MIRIAM MARKS DEPT NEUROCHEM, LONDON WC1N 3BG, ENGLANDNATL HOSP, INST NEUROL, MIRIAM MARKS DEPT NEUROCHEM, LONDON WC1N 3BG, ENGLAND