Cognition and Amyloid Load in Alzheimer Disease Imaged With Florbetapir F 18(AV-45) Positron Emission Tomography
Objective To examine the association between regional brain uptake of a novel amyloid positron emission tomography (PET) tracer florbetapir F 18 ([18 F]-AV-45) and cognitive performance in a pilot study. Design Cross-sectional comparison of [18 F]-AV-45 in AD patients versus controls. Setting Three...
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Veröffentlicht in: | The American journal of geriatric psychiatry 2013-03, Vol.21 (3), p.272-278 |
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Zusammenfassung: | Objective To examine the association between regional brain uptake of a novel amyloid positron emission tomography (PET) tracer florbetapir F 18 ([18 F]-AV-45) and cognitive performance in a pilot study. Design Cross-sectional comparison of [18 F]-AV-45 in AD patients versus controls. Setting Three specialty memory clinics. Participants Eleven participants with probable Alzheimer disease (AD) by NINDS/ADRDA criteria and 15 healthy comparison (HC) participants. Measurements Participants underwent PET imaging following a 370 MBq (10 mCi) intravenous administration of [18 F]-AV-45. Regional/cerebellar standardized uptake value ratios (SUVRs) were calculated. Cognition was assessed using Mini-Mental State Examination, Alzheimer's Disease Assessment Scale-Cognitive subscale (ADAS-Cog), Wechsler Logical Memory IA (immediate recall) test (LMIA), and verbal category fluency. Results Greater [18 F]-AV-45 SUVR was associated with poorer performance on all cognitive tests. In the HC group, occipital, parietal, precuneus, temporal, and cortical average SUVR was associated with greater ADAS-Cog, and greater anterior cingulate SUVR was associated with lower LMIA. Two HC participants had [18 F]-AV-45 cortical/cerebellar SUVR greater than 1.5, one of whom had deficits in episodic recall and on follow-up met criteria for amnestic mild cognitive impairment. Conclusion [18 F]-AV-45 SUVR in several brain regions was associated with worse global cognitive performance particularly in HC, suggesting its potential as a marker of preclinical AD. |
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ISSN: | 1064-7481 1545-7214 |
DOI: | 10.1016/j.jagp.2012.11.016 |