In vivo comparison of tau radioligands 18F-THK-5351 and 18F-THK-5317

Tobey J. Betthauser, Patrick J. Lao, Dhanabalan Murali, Todd E. Barnhart, Shozo Furumoto, Nobuyuki Okamura, Charles K. Stone, Sterling C. Johnson, Bradley T. Christian

研究成果: Article査読

40 被引用数 (Scopus)

抄録

This study compared the in vivo imaging characteristics of tau PET ligands 18F-THK-5351 and 18F-THK-5317 in the context of Alzheimer disease (AD). Additionally, reference tissue distribution volume ratio (DVR) estimation methods and SUV ratio (SUVR) timing windows were evaluated to determine the optimal strategy for specific binding quantification. Methods: Twenty-eight subjects (mean age 6 SD, 71 6 7 y) underwent either dynamic 90-min 18F-THK-5317 or 18F-THK-5351 PET scans. Bland-Altman plots were used to compare the simplified reference tissue method, multilinear reference tissue method (MRTM2), and Logan reference tissue DVR estimates and to assess temporal stability of SUVR windows using cerebellar gray matter as a reference region. In vivo kinetics and DVR estimates were directly compared for 10 subjects who underwent both 18F-THK-5317 and 18F-THK-5351 PET scans. Results: THK-5351 exhibited faster cerebellar gray matter clearance, faster cortical white matter clearance, and higher DVR estimates in AD tau-associated regions of interest than THK-5317. The MRTM2 method produced the most reliable DVR estimates for both tracers, particularly when scan duration was shortened to 60min. SUVR stability was observed 50-70min after injection for both tracers. Parametric images revealed differences between MRTM2, Logan, and SUVR binding in white matter regions for THK-5317. Conclusion: THK-5317 and THK-5351 show promise for in vivo detection of AD tau. THK-5351 has more favorable pharmacokinetics and imaging characteristics than THK-5317.

本文言語English
ページ(範囲)996-1002
ページ数7
ジャーナルJournal of Nuclear Medicine
58
6
DOI
出版ステータスPublished - 2017 6月 1
外部発表はい

ASJC Scopus subject areas

  • 放射線学、核医学およびイメージング

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