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PMID: 16330558 Published · ppublish English Comparative Study Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Simplified quantification of Pittsburgh Compound B amyloid imaging PET studies: a comparative analysis.

Lopresti BJ, Klunk WE, Mathis CA, Hoge JA, Ziolko SK, Lu X, Meltzer CC, Schimmel K, Tsopelas ND, DeKosky ST, Price JC

Abstract

PET studies have been performed using the amyloid binding radiotracer Pittsburgh Compound B (PIB). Previous quantitative analyses using arterial blood showed that the Logan graphical analysis using 90 min of emission data (ART90) provided a reliable measure of PIB retention. This work reports on simplified methods of analysis for human PIB imaging. PIB PET scans were conducted in 24 subjects (6 Alzheimer's disease [AD], 10 mild cognitive impairment [MCI], 8 controls) with arterial blood sampling. Retest scans were performed on 8 subjects (3 AD, 1 MCI, 4 controls) within 28 d. Data were analyzed over 60 and 90 min using the Logan analysis and (a) metabolite-corrected input functions based on arterial plasma (ART60, ART90), (b) carotid artery time-activity data with a population average metabolite correction (CAR60, CAR90); and (c) cerebellar reference tissue (CER60, CER90). Data also were analyzed using the simplified reference tissue method (SRTM60, SRTM90) and a single-scan method based on late-scan ratios of standardized uptake values (SUVR60, SUVR90). All methods of analysis examined effectively discerned regional differences between AD and control subjects in amyloid-laden cortical regions, although the performance of the simplified methods varied in terms of bias, test-retest variability, intersubject variability, and effect size. CAR90 best agreed with ART90 distribution volume ratio (DVR) measures across brain regions and subject groups and demonstrated satisfactory test-retest variability (+/-7.1% across regions). CER90 and CER60 showed negative biases relative to ART90 in high-DVR subjects but had the lowest test-retest variability. The single-scan SUV-based methods showed the largest effect sizes for AD and control group differences and performed well in terms of intersubject and test-retest variability. Of the simplified methods for PIB analysis examined, CAR90 provided DVR measures that were most comparable to ART90; CER90 was the most reproducible and SUVR90 produced the largest effect size. All simplified methods were effective at distinguishing AD and control differences and may be effectively used in the analysis of PIB. SUVR60 data can be obtained with as little as 20 min of PET emission data collection. The relative strengths and limitations of each method must be considered for each experimental design.

MeSH Terms
Alzheimer Disease/diagnostic imaging,pathology Amyloid/chemistry Aniline Compounds/pharmacology Brain/pathology Carotid Arteries/pathology Female Humans Image Interpretation, Computer-Assisted/methods Image Processing, Computer-Assisted Kinetics Male Positron-Emission Tomography/methods Radiopharmaceuticals/pharmacology Thiazoles/pharmacology Time Factors
Chemicals
2-(4'-(methylamino)phenyl)-6-hydroxybenzothiazole Amyloid Aniline Compounds Radiopharmaceuticals Thiazoles
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Lopresti Brian J
Department of Radiology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213, USA. [email protected]
Klunk William E
Mathis Chester A
Hoge Jessica A
Ziolko Scott K
Lu Xueling
Meltzer Carolyn C
Schimmel Kurt
Tsopelas Nicholas D
DeKosky Steven T
Price Julie C
Article Info
Journal
Journal of nuclear medicine : official publication, Society of Nuclear Medicine
Abbr.
J Nucl Med
ISSN
0161-5505
Published
2005-12-00
Pages
1959-72
Language
English
Region
United States
NLM ID
0217410
Subset
IM
Grants
NIMH NIH HHS · K01MH001976 · United States
NIA NIH HHS · K02AG001039 · United States
NIA NIH HHS · P50AG005133 · United States
NIA NIH HHS · R01AG018402 · United States
NIA NIH HHS · R01AG020226 · United States
NIMH NIH HHS · R01MH070729 · United States
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