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|Title:||Aβ imaging with 18F-florbetaben in prodromal Alzheimer's disease: a prospective outcome study.|
|Authors:||Ong, Kevin T;Villemagne, Victor L;Bahar-Fuchs, Alex;Lamb, Fiona;Langdon, Narelle;Catafau, Ana M;Stephens, Andrew W;Seibyl, John;Dinkelborg, Ludger M;Reininger, Cornelia B;Putz, Barbara;Rohde, Beate;Masters, Colin L;Rowe, Christopher C|
|Affiliation:||The Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, Victoria, Australia|
Molecular NeuroImaging, L.L.C., New Haven, Connecticut, USA
Department of Nuclear Medicine, Centre for PET, Austin Health, Heidelberg, Victoria, Australia The Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, Victoria, Australia
Department of Nuclear Medicine, Centre for PET, Austin Health, Heidelberg, Victoria, Australia Centre for Research on Aging, Health, and Wellbeing, The Australian National University, Acton, Australian Capital Territory, Australia
Department of Nuclear Medicine, Centre for PET, Austin Health, Heidelberg, Victoria, Australia
Piramal Imaging GmbH, Berlin, Germany.
Bayer Healthcare, Berlin, Germany.
|Citation:||Journal of Neurology, Neurosurgery, and Psychiatry 2014; 86(4): 431-6|
|Abstract:||We assessed the clinical utility of β-amyloid (Aβ) imaging with (18)F-florbetaben (FBB) in mild cognitive impairment (MCI) by evaluating its prognostic accuracy for progression to Alzheimer's disease (AD), comparing semiquantitative with visual scan assessment, and exploring the relationships among Aβ, hippocampal volume (HV) and memory over time.45 MCI underwent FBB positron emission tomography, MRI and neuropsychological assessment at baseline and 2 years and clinical follow-up at 4 years. Positive FBB (FBB+), defined by a cortical to cerebellar cortex standardised uptake value ratio (SUVR) ≥ 1.45, was compared with visual assessment by five readers. Amnestic MCI (aMCI) was defined by a composite episodic memory (EM) Z-score of <-1.5.At baseline, 24 (53%) MCI were FBB+. Majority reads agreed with SUVR classification (κ 0.96). In 2 years, 18 (75%) FBB+ progressed to AD compared with 2 (9.5%) FBB-, yielding a predictive accuracy of 83% (95% CI 61% to 94%). Four FBB- developed non-AD dementia. Predictive accuracies of HV (58% (95% CI 42% to 73%)) and aMCI status (73% (95% CI 58% to 81%)) were lower. Combinations did not improve accuracy. By 4 years, 21 (87.5%) FBB+ had AD whereas 5 (24%) FBB- had non-AD dementia yielding a predictive accuracy of 94% (95% CI 74% to 99%). While the strong baseline association between FBB SUVR and EM declined over 2 years, the association between EM and HV became stronger. FBB SUVR increased 2.2%/year in FBB+ with no change in FBB-.(18)F-florbetaben Aβ imaging facilitates accurate detection of prodromal AD. As neurodegeneration progresses, and in contrast with the early stages of the disease, hippocampal atrophy and not Aβ, seems to drive memory decline.NCT01138111.|
|Internal ID Number:||24970906|
Alzheimer Disease.metabolism.radionuclide imaging
Aniline Compounds.diagnostic use
Magnetic Resonance Imaging
Memory Disorders.radionuclide imaging
Mild Cognitive Impairment.radionuclide imaging
|Appears in Collections:||Journal articles|
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