Volume 55, Issue 3 pp. 306-319
Original Articles

Imaging brain amyloid in Alzheimer's disease with Pittsburgh Compound-B

William E. Klunk MD, PhD

William E. Klunk MD, PhD

Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA

Search for more papers by this author
Henry Engler MD

Henry Engler MD

Uppsala University, PET Centre/Uppsala Imanet AB, Uppsala

Search for more papers by this author
Agneta Nordberg MD, PhD

Agneta Nordberg MD, PhD

Neurotec Department, Karolinska Institute, Huddinge University Hospital, Stockholm

Department of Geriatric Medicine, Huddinge University Hospital, Stockholm, Sweden

Search for more papers by this author
Yanming Wang PhD

Yanming Wang PhD

Department of Radiology, PET Facility, University of Pittsburgh, Pittsburgh, PA

Search for more papers by this author
Gunnar Blomqvist PhD

Gunnar Blomqvist PhD

Uppsala University, PET Centre/Uppsala Imanet AB, Uppsala

Search for more papers by this author
Daniel P. Holt BS

Daniel P. Holt BS

Department of Radiology, PET Facility, University of Pittsburgh, Pittsburgh, PA

Search for more papers by this author
Mats Bergström PhD

Mats Bergström PhD

Uppsala University, PET Centre/Uppsala Imanet AB, Uppsala

Search for more papers by this author
Irina Savitcheva MD

Irina Savitcheva MD

Uppsala University, PET Centre/Uppsala Imanet AB, Uppsala

Search for more papers by this author
Guo-Feng Huang PhD

Guo-Feng Huang PhD

Department of Radiology, PET Facility, University of Pittsburgh, Pittsburgh, PA

Search for more papers by this author
Sergio Estrada PhD

Sergio Estrada PhD

Uppsala University, PET Centre/Uppsala Imanet AB, Uppsala

Search for more papers by this author
Birgitta Ausén MSCI

Birgitta Ausén MSCI

Department of Geriatric Medicine, Huddinge University Hospital, Stockholm, Sweden

Search for more papers by this author
Manik L. Debnath MS

Manik L. Debnath MS

Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA

Search for more papers by this author
Julien Barletta BS

Julien Barletta BS

Department of Organic Chemistry, Uppsala University, Uppsala, Sweden

Search for more papers by this author
Julie C. Price PhD

Julie C. Price PhD

Department of Radiology, PET Facility, University of Pittsburgh, Pittsburgh, PA

Search for more papers by this author
Johan Sandell PhD

Johan Sandell PhD

Uppsala University, PET Centre/Uppsala Imanet AB, Uppsala

Search for more papers by this author
Brian J. Lopresti BS

Brian J. Lopresti BS

Department of Radiology, PET Facility, University of Pittsburgh, Pittsburgh, PA

Search for more papers by this author
Anders Wall PhD

Anders Wall PhD

Uppsala University, PET Centre/Uppsala Imanet AB, Uppsala

Search for more papers by this author
Pernilla Koivisto PhD

Pernilla Koivisto PhD

Uppsala University, PET Centre/Uppsala Imanet AB, Uppsala

Search for more papers by this author
Gunnar Antoni PhD

Gunnar Antoni PhD

Uppsala University, PET Centre/Uppsala Imanet AB, Uppsala

Search for more papers by this author
Chester A. Mathis PhD

Corresponding Author

Chester A. Mathis PhD

Department of Radiology, PET Facility, University of Pittsburgh, Pittsburgh, PA

PET Facility, B-938 UPMC Presbyterian, 200 Lothrop Street, Pittsburgh, PA 15213-2582Search for more papers by this author
Bengt Långström PhD

Bengt Långström PhD

Uppsala University, PET Centre/Uppsala Imanet AB, Uppsala

Department of Organic Chemistry, Uppsala University, Uppsala, Sweden

Search for more papers by this author
First published: 21 January 2004
Citations: 160

Abstract

This report describes the first human study of a novel amyloid-imaging positron emission tomography (PET) tracer, termed Pittsburgh Compound-B (PIB), in 16 patients with diagnosed mild AD and 9 controls. Compared with controls, AD patients typically showed marked retention of PIB in areas of association cortex known to contain large amounts of amyloid deposits in AD. In the AD patient group, PIB retention was increased most prominently in frontal cortex (1.94-fold, p = 0.0001). Large increases also were observed in parietal (1.71-fold, p = 0.0002), temporal (1.52-fold, p = 0.002), and occipital (1.54-fold, p = 0.002) cortex and the striatum (1.76-fold, p = 0.0001). PIB retention was equivalent in AD patients and controls in areas known to be relatively unaffected by amyloid deposition (such as subcortical white matter, pons, and cerebellum). Studies in three young (21 years) and six older healthy controls (69.5 ± 11 years) showed low PIB retention in cortical areas and no significant group differences between young and older controls. In cortical areas, PIB retention correlated inversely with cerebral glucose metabolism determined with 18F-fluorodeoxyglucose. This relationship was most robust in the parietal cortex (r = −0.72; p = 0.0001). The results suggest that PET imaging with the novel tracer, PIB, can provide quantitative information on amyloid deposits in living subjects.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.

click me