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Florbetapir positron emission tomography and cerebrospinal fluid biomarkers.
Hake, Ann; Trzepacz, Paula T; Wang, Shufang; Yu, Peng; Case, Michael; Hochstetler, Helen; Witte, Michael M; Degenhardt, Elisabeth K; Dean, Robert A.
Affiliation
  • Hake A; Eli Lilly and Company, Indianapolis, IN, USA; Department of Neurology Indiana University School of Medicine, Indianapolis, IN, USA. Electronic address: hakean@lilly.com.
  • Trzepacz PT; Eli Lilly and Company, Indianapolis, IN, USA; Department of Psychiatry, Indiana University School of Medicine, Indianapolis, IN, USA.
  • Wang S; Eli Lilly and Company, Indianapolis, IN, USA.
  • Yu P; Eli Lilly and Company, Indianapolis, IN, USA.
  • Case M; Eli Lilly and Company, Indianapolis, IN, USA.
  • Hochstetler H; Eli Lilly and Company, Indianapolis, IN, USA.
  • Witte MM; Eli Lilly and Company, Indianapolis, IN, USA.
  • Degenhardt EK; Eli Lilly and Company, Indianapolis, IN, USA; Department of Psychiatry, Indiana University School of Medicine, Indianapolis, IN, USA; Indiana University Health Physicians Group, Indiana University Health, Indianapolis, IN, USA.
  • Dean RA; Eli Lilly and Company, Indianapolis, IN, USA.
Alzheimers Dement ; 11(8): 986-93, 2015 Aug.
Article in En | MEDLINE | ID: mdl-25916563
BACKGROUND: We evaluated the relationship between florbetapir-F18 positron emission tomography (FBP PET) and cerebrospinal fluid (CSF) biomarkers. METHODS: Alzheimer's Disease Neuroimaging Initiative-Grand Opportunity and Alzheimer's Disease Neuroimaging Initiative 2 (GO/2) healthy control (HC), mild cognitive impairment (MCI), and Alzheimer's disease (AD) dementia subjects with clinical measures and CSF collected ±90 days of FBP PET data were analyzed using correlation and logistic regression. RESULTS: In HC and MCI subjects, FBP PET anterior and posterior cingulate and composite standard uptake value ratios correlated with CSF amyloid beta (Aß1-42) and tau/Aß1-42 ratios. Using logistic regression, Aß1-42, total tau (t-tau), phosphorylated tau181P (p-tau), and FBP PET composite each differentiated HC versus AD. Aß1-42 and t-tau distinguished MCI versus AD, without additional contribution by FBP PET. Total tau and p-tau added discriminative power to FBP PET when classifying HC versus AD. CONCLUSION: Based on cross-sectional diagnostic groups, both amyloid and tau measures distinguish healthy from demented subjects. Longitudinal analyses are needed.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peptide Fragments / Brain / Amyloid beta-Peptides / Tau Proteins / Ethylene Glycols / Alzheimer Disease / Aniline Compounds Type of study: Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Alzheimers Dement Year: 2015 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peptide Fragments / Brain / Amyloid beta-Peptides / Tau Proteins / Ethylene Glycols / Alzheimer Disease / Aniline Compounds Type of study: Observational_studies / Prevalence_studies / Risk_factors_studies Limits: Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Alzheimers Dement Year: 2015 Document type: Article Country of publication: United States