4.7 Article

In Vivo Comparison of Tau Radioligands 18F-THK-5351 and 18F-THK-5317

期刊

JOURNAL OF NUCLEAR MEDICINE
卷 58, 期 6, 页码 996-1002

出版社

SOC NUCLEAR MEDICINE INC
DOI: 10.2967/jnumed.116.182980

关键词

Alzheimer's disease; positron emission tomography; quantitation; tau; THK

资金

  1. National Institutes of Health [R01 AG021155, R01 AG027161]
  2. Alzheimer's Disease Research Center [P50 AG033514]
  3. National Institute on Child Health and Human Development [P30 HD03352]
  4. National Cancer Institute of the National Institutes of Health [T32 CA009206]
  5. GE Healthcare
  6. Grants-in-Aid for Scientific Research [26117003] Funding Source: KAKEN

向作者/读者索取更多资源

This study compared the in vivo imaging characteristics of tau PET ligands F-18-THK-5351 and F-18-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 +/- SD, 71 +/- 7 y) underwent either dynamic 90-min F-18-THK-5317 or F-18-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 F-18-THK-5317 and F-18-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 THK5317. 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.

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