Test-retest stability of cerebral A1 adenosine receptor quantification using [18F]CPFPX and PET

Eur J Nucl Med Mol Imaging. 2007 Jul;34(7):1061-70. doi: 10.1007/s00259-006-0309-x. Epub 2007 Jan 23.

Abstract

Purpose: The goal of the present study was to evaluate the reproducibility of cerebral A1 adenosine receptor (A1AR) quantification using [18F]CPFPX and PET in a test-retest design.

Methods: Eleven healthy volunteers were studied twice. Eight brain regions ranging from high to low receptor binding were examined. [18F]CPFPX was injected as a bolus with subsequent infusion over 120 min. Various outcome parameters were compared based on either metabolite-corrected venous blood sampling [e.g. apparent equilibrium total distribution volume (DVt')] or a reference region [ratio of specific to non-specific distribution volume (BP2)].

Results: Test-retest variability was low in the outcome measure BP2 (on average 5.9%) and moderate in DVt' (on average 13.2%). Regarding reproducibility, the outcome parameter BP2 showed an intra-class correlation coefficient (ICC) of 0.94 +/- 0.1. For DVt' the between-subject coefficient of variation (%CV) was similar to the within-subject %CV (around 10%), resulting in a poor ICC of 0.06 +/- 0.2.

Conclusion: Our results suggest that quantification of [18F]CPFPX imaging is reproducible and reliable for PET studies of the cerebral A1AR. Among the outcome parameters the non-invasive measures were of superior test-retest stability over the invasive.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Brain / diagnostic imaging*
  • Brain / metabolism*
  • Humans
  • Image Interpretation, Computer-Assisted / methods*
  • Male
  • Positron-Emission Tomography / methods*
  • Radiopharmaceuticals / pharmacokinetics
  • Receptor, Adenosine A1 / metabolism*
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Tissue Distribution
  • Xanthines / pharmacokinetics*

Substances

  • 8-cyclopenta-3-(3-fluoropropyl)-1-propylxanthine
  • Radiopharmaceuticals
  • Receptor, Adenosine A1
  • Xanthines