PET imaging of the in vivo brain acetylcholinesterase activity and nicotine binding in galantamine-treated patients with AD
2008 (English)In: Neurobiology of Aging, ISSN 0197-4580, E-ISSN 1558-1497, Vol. 29, no 8, 1204-1217 p.Article in journal (Refereed) Published
The effect of galantamine treatment on cortical acetylcholinesterase (AChE) activity and nicotinic receptor binding was investigated by positron emission tomography (PET) in 18 patients with mild Alzheimer's disease (AD) in relation to galantamine concentration and the patients' cognitive performances. The first 3 months of the study was of a randomized double-blind placebo-controlled design, during which 12 patients received galantamine (16-24 mg/day) and 6 patients the placebo, and this was followed by 9 months' galantamine treatment in all patients. The patients underwent PET examinations to measure cortical AChE activity (C-11-PMP) and C-11-nicotine binding. Neuropsychological tests were performed throughout the study. Inhibition (30-40%) of cortical AChE activity was observed after 3 weeks to 12 months of galantamine treatment. No significant change in mean cortical C-11-nicotine binding was observed during the study. C-11-Nicotine binding, however, positively correlated with plasma galantamine concentration. Both the changes of AChE activity and C-11-nicotine binding correlated positively with the results of a cognitive test of attention. In conclusion, galantamine caused sustained AChE inhibition for up to 12 months. At the individual level, the in vivo cortical AChE inhibition and C-11-nicotine binding were associated with changes in the attention domain of cognition rather than episodic memory.
Place, publisher, year, edition, pages
2008. Vol. 29, no 8, 1204-1217 p.
Alzheimer's disease, acetylcholinesterase, C-11-nicotine binding, positron emission tomography (PET), cerebrospinal fluid, plasma, cognitive function, attention, galantamine
Medical and Health Sciences
IdentifiersURN: urn:nbn:se:uu:diva-110000DOI: 10.1016/j.neurobiolaging.2007.02.020ISI: 000257302900011PubMedID: 17379359OAI: oai:DiVA.org:uu-110000DiVA: diva2:274999