Florbetapir (F18-AV-45) PET to assess amyloid burden in Alzheimer's disease dementia, mild cognitive impairment, and normal aging

Abstract Objective To evaluate the performance characteristics of florbetapir F18 positron emission tomography (PET) in patients with Alzheimer's disease (AD), mild cognitive impairment (MCI), and healthy control subjects (HCs). Methods Florbetapir PET was acquired in 184 subjects (45 AD patien...

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Published inAlzheimer's & dementia Vol. 9; no. 5; pp. S72 - S83
Main Authors Johnson, Keith A, Sperling, Reisa A, Gidicsin, Christopher M, Carmasin, Jeremy S, Maye, Jacqueline E, Coleman, Ralph E, Reiman, Eric M, Sabbagh, Marwan N, Sadowsky, Carl H, Fleisher, Adam S, Murali Doraiswamy, P, Carpenter, Alan P, Clark, Christopher M, Joshi, Abhinay D, Lu, Ming, Grundman, Michel, Mintun, Mark A, Pontecorvo, Michel J, Skovronsky, Daniel M
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.10.2013
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Summary:Abstract Objective To evaluate the performance characteristics of florbetapir F18 positron emission tomography (PET) in patients with Alzheimer's disease (AD), mild cognitive impairment (MCI), and healthy control subjects (HCs). Methods Florbetapir PET was acquired in 184 subjects (45 AD patients, 60 MCI patients, and 79 HCs) within a multicenter phase 2 study. Amyloid burden was assessed visually and quantitatively, and was classified as positive or negative. Results Florbetapir PET was rated visually amyloid positive in 76% of AD patients, 38% of MCI patients, and 14% of HCs. Eighty-four percent of AD patients, 45% of MCI patients, and 23% of HCs were classified as amyloid positive using a quantitative threshold. Amyloid positivity and mean cortical amyloid burden were associated with age and apolipoprotein E ε4 carrier status. Conclusions: The data are consistent with expected rates of amyloid positivity among individuals with clinical diagnoses of AD and MCI, and indicate the potential value of florbetapir F18 PET as an adjunct to clinical diagnosis.
Bibliography:Deceased.
K.J. has served as a site investigator for Avid, Pfizer, Janssen, and Bristol‐Myers‐Squibb; as a consultant to Bristol‐Myers‐Squibb, Siemens, Pfizer, Genzyme, GEHC, and Bayer; and as an unpaid consultant to Avid. R.A.S. has served as a site investigator for Avid, Bristol‐Myers‐Squibb, Elan, Janssen, Pfizer, and Wyeth; a consultant to Bayer, Bristol‐Myers‐Squibb, Elan, Eisai, Janssen, Pfizer, and Wyeth; and as an unpaid consultant to Avid. She has received speaking honoraria from Pfizer, Janssen, Eli Lilly, and Bayer. R.E.C. was a site principal investigator for the clinical study and served on an advisory board to Avid and Lilly. P.M.D. has served as a paid advisor/speaker and/or received research grants from Avid/Lilly and several pharmaceutical companies. He owns stock in Sonexa and Clarimedix. A.S.F. is a consultant for Lilly SAB and has received grant funding from Avid. M.N.S. has served as a site investigator for Avid, BMS, Elan, Janssen, Pfizer, Wyeth, Baxter, Bayer, GE, Lilly, Genentech, Eisai, Ceregene, and Celgene, and as a consultant to BMS, Bayer, Lilly, Avid, Amerisciences, Eisai, and Takeda. C.H.S. is on the speaker's bureau for Novartis, Forest, and Axona, and is a site investigator for Avid. M.G. is a paid consultant to Avid, Eli Lilly, and other pharmaceutical companies. A.P.C., C.M.C., A.D.J., M.L., M.A.M., M.J.P., and D.M.S. are employees of Avid Radiopharmaceuticals.
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ISSN:1552-5260
1552-5279
1552-5279
DOI:10.1016/j.jalz.2012.10.007