TY - JOUR
T1 - Evaluation of18F-RO-948 PET for quantitative assessment of tau accumulation in the human brain
AU - Kuwabara, Hiroto
AU - Comley, Robert A.
AU - Borroni, Edilio
AU - Honer, Michael
AU - Kitmiller, Kelly
AU - Roberts, Joshua
AU - Gapasin, Lorena
AU - Mathur, Anil
AU - Klein, Gregory
AU - Wong, Dean F.
N1 - Funding Information:
Johns Hopkins University faculties receive salary support through several sponsored research sources, including NIH career award K24 DA000412 to Dean Wong, and none receive direct funding from Roche except via sponsored Johns Hopkins University contracts. This study was funded by a F. Hoffmann-La Roche Ltd. contract to Johns Hopkins University. No other potential conflict of interest relevant to this article was reported.
Publisher Copyright:
COPYRIGHT © 2018 by the Society of Nuclear Medicine and Molecular Imaging.
PY - 2018/12/1
Y1 - 2018/12/1
N2 - The availability of tau PET radioligands enables quantitative assessment of tau density and distribution in the human brain. We evaluated the kinetics of a novel radioligand,18F-RO-948 (previously referred to as18F-RO6958948), and its ability to identify tau positivity in individual patients with mild Alzheimer disease (AD). Methods: Eleven subjects with amyloid-positive mild AD, 5 amyloid-negative older control subjects (OC), and 5 younger control subjects (YC) completed 1 or 2 (4 AD and 5 OC) PET scans with18F-RO-948 for 90, 120, or 200 min. The kinetics of the radioligand was evaluated with standard compartmental and noncompartmental models (with plasma data in 70% of cases), tissue-reference methods, and SUV ratio. These approaches were applied to assess the ability of18F-RO-948 to discriminate AD subjects from OC subjects. Results: The plasma reference graphical analysis appeared to be the optimal method of quantification for18F-RO-948, yielding strictly time-consistent values of distribution volume and distribution volume ratio at 90 min against the analyses at 120 and 200 min. The reference tissue graphical analysis and SUV ratio were cross-validated against plasma reference graphical analysis. Test–retest evaluation showed excellent reproducibility. A proposed novel index of tau load, the regional tau-positive fraction, showed high values in the medial and lateral temporal and parietal regions in AD and successfully separated AD subjects from OC and YC subjects with a significant margin. Conclusion:18F-RO-948 appears to be a promising radioligand for quantitative imaging of tau in the brain of AD patients.
AB - The availability of tau PET radioligands enables quantitative assessment of tau density and distribution in the human brain. We evaluated the kinetics of a novel radioligand,18F-RO-948 (previously referred to as18F-RO6958948), and its ability to identify tau positivity in individual patients with mild Alzheimer disease (AD). Methods: Eleven subjects with amyloid-positive mild AD, 5 amyloid-negative older control subjects (OC), and 5 younger control subjects (YC) completed 1 or 2 (4 AD and 5 OC) PET scans with18F-RO-948 for 90, 120, or 200 min. The kinetics of the radioligand was evaluated with standard compartmental and noncompartmental models (with plasma data in 70% of cases), tissue-reference methods, and SUV ratio. These approaches were applied to assess the ability of18F-RO-948 to discriminate AD subjects from OC subjects. Results: The plasma reference graphical analysis appeared to be the optimal method of quantification for18F-RO-948, yielding strictly time-consistent values of distribution volume and distribution volume ratio at 90 min against the analyses at 120 and 200 min. The reference tissue graphical analysis and SUV ratio were cross-validated against plasma reference graphical analysis. Test–retest evaluation showed excellent reproducibility. A proposed novel index of tau load, the regional tau-positive fraction, showed high values in the medial and lateral temporal and parietal regions in AD and successfully separated AD subjects from OC and YC subjects with a significant margin. Conclusion:18F-RO-948 appears to be a promising radioligand for quantitative imaging of tau in the brain of AD patients.
KW - Alzheimer disease
KW - F-RO6958948 for tau imaging
KW - Neurology
KW - PET
KW - Radiotracer tissue kinetics
KW - Radiotracer tissue kinetics
UR - http://www.scopus.com/inward/record.url?scp=85057585024&partnerID=8YFLogxK
U2 - 10.2967/jnumed.118.214437
DO - 10.2967/jnumed.118.214437
M3 - Article
C2 - 30097505
AN - SCOPUS:85057585024
SN - 0161-5505
VL - 59
SP - 1877
EP - 1884
JO - Journal of Nuclear Medicine
JF - Journal of Nuclear Medicine
IS - 12
ER -