Quantification of PET infusion studies without true equilibrium: A tissue clearance correction

J Cereb Blood Flow Metab. 2020 Apr;40(4):860-874. doi: 10.1177/0271678X19850000. Epub 2019 May 14.

Abstract

In some positron emission tomography (PET) studies, a reversibly binding radioligand is administered as a constant infusion to establish true equilibrium for quantification. This approach reduces scanning time and simplifies data analysis, but assumes similar behavior of the radioligand in plasma across the study population to establish true equilibrium in all subjects. Bias in outcome measurements can result if this assumption is not met. This work developed and validated a correction that reduces bias in total distribution volume (VT) estimates when true equilibrium is not present. This correction, termed tissue clearance correction (TCC), took the form VT=VT(A)/(1+βγVT(A)), where β is the radioligand clearance rate in tissue, γ is a radiotracer-specific constant, and VT(A) is the apparent VT. Simulations characterized the robustness of TCC across imperfect values of γ and β and demonstrated reduction to false positive rates. This approach was validated with human infusion data for three radiotracers: [18F]FPEB, (-)-[18F]flubatine, and [11C]UCB-J. TCC reduced bias in VT estimates for all radiotracers and significantly reduced intersubject variance in VT for [18F]FPEB data in some brain regions. Thus, TCC improves quantification of data acquired from PET infusion studies.

Keywords: Equilibrium; infusion; modeling; positron emission tomography; volume of distribution.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Biological Availability
  • Brain / diagnostic imaging*
  • Brain / metabolism
  • Computer Simulation
  • Healthy Volunteers
  • Humans
  • Kinetics
  • Male
  • Metabolic Clearance Rate
  • Models, Biological*
  • Positron-Emission Tomography / methods*
  • Radiopharmaceuticals / administration & dosage
  • Radiopharmaceuticals / blood*
  • Radiopharmaceuticals / metabolism*
  • Tissue Distribution

Substances

  • Radiopharmaceuticals