A distinct [F-18]MPPF PET profile in amnestic mild cognitive impairment compared to mild Alzheimer's disease

作者:Truchot L*; Costes N; Zimmer L; Laurent B; Le Bars D; Thomas Anterion C; Mercier B; Hermier M; Vighetto A; Krolak Salmon P
来源:NeuroImage, 2008, 40(3): 1251-1256.
DOI:10.1016/j.neuroimage.2008.01.030

摘要

To date, two positron emission tomography ( PET) studies have explored 5-HT1A receptor density in the hippocampus of Alzheimer's disease (AD) patients. They showed early changes of 5-HT1A receptors in this brain region, known to have a dense serotonergic innervation. These studies only reported measurements in hippocampus. In the present PET study, we used an antagonist of 5-HT1A receptors, the [F-18] MPPF (1) to explore 5-HT1A receptor density in the whole brain of AD patients at a mild stage of dementia and amnestic mild cognitive impairment (aMCI) patients compared to a control population; (2) to explore more precisely the 5-HT1A receptor density in the limbic brain regions of AD patients and aMCI patients compared to controls. Voxel-based analyses were performed to assess differences in the [F-18] MPPF binding potential ( BP) between AD patients and aMCI patients compared to controls. Analyses of whole-brain [F-18] MPPF BP showed a global decrease in AD brains in contrast with a global increase in aMCI brains. In AD brains, a significant decrease of BP was detected in hippocampus and parahippocampal gyrus, whereas a significant increase of BP was observed in the inferior occipital gyrus in aMCI brains. These whole brain results are in accordance to hippocampal data reported in a previous study, showing an increase of [F-18] MPPF binding in the aMCI group contrasting with a decrease in the AD group. Altogether, these results suggest the implication of a compensatory mechanism illustrated by an up regulation of serotonergic metabolism at the aMCI stage before a breakdown of this mechanism at the AD stage. This difference of serotonergic receptor labeling allows to distinguish the groups of aMCI patients from mild AD patients with specific [F-18] MPPF PET profiles for each patient group.

  • 出版日期2008-4-15