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Publication Detail
Validation of a combined image derived input function and venous sampling approach for the quantification of [18F]GE-179 PET binding in the brain.
  • Publication Type:
    Journal article
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  • Authors:
    Galovic M, Erlandsson K, Fryer TD, Hong YT, Manavaki R, Sari H, Chetcuti S, Thomas BA, Fisher M, Sephton S, Canales R, Russell JJ, Sander K, Arstad E, Aigbirhio FI, Groves AM, Duncan JS, Thielemans K, Hutton B, Coles JP, Koepp MJ, NEST investigators
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  • Country:
    United States
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  • Keywords:
    NMDA receptor, Positron emission tomography, input function
Blood-based kinetic analysis of PET data relies on an accurate estimate of the arterial plasma input function (PIF). An alternative to invasive measurements from arterial sampling is an image-derived input function (IDIF). However, an IDIF provides the whole blood radioactivity concentration, rather than the required free tracer radioactivity concentration in plasma. To estimate the tracer PIF, we corrected an IDIF from the carotid artery with estimates of plasma parent fraction (PF) and plasma-to-whole blood (PWB) ratio obtained from five venous samples. We compared the combined IDIF+venous approach to gold standard data from arterial sampling in 10 healthy volunteers undergoing [18F]GE-179 brain PET imaging of the NMDA receptor. Arterial and venous PF and PWB ratio estimates determined from 7 patients with traumatic brain injury (TBI) were also compared to assess the potential effect of medication. There was high agreement between areas under the curves of the estimates of PF (r=0.99, p<0.001), PWB ratio (r=0.93, p<0.001), and the PIF (r=0.92, p<0.001) as well as total distribution volume (VT) in 11 regions across the brain (r=0.95, p<0.001). IDIF+venous VT had a mean bias of -1.7% and a comparable regional coefficient of variation (arterial: 21.3±2.5%, IDIF+venous: 21.5±2.0%). Simplification of the IDIF+venous method to use only one venous sample provided less accurate VT estimates (mean bias 9.9%; r=0.71, p<0.001). A version of the method that avoids the need for blood sampling by combining the IDIF with population-based PF and PWB ratio estimates systematically underestimated VT (mean bias -20.9%), and produced VT estimates with a poor correlation to those obtained using arterial data (r=0.45, p<0.001). Arterial and venous blood data from 7 TBI patients showed high correlations for PF (r=0.92, p=0.003) and PWB ratio (r=0.93, p=0.003). In conclusion, the IDIF+venous method with five venous samples provides a viable alternative to arterial sampling for quantification of [18F]GE-179 VT.
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Department of Imaging
Clinical & Experimental Epilepsy
Department of Imaging
Experimental & Translational Medicine
Div of Medicine
Clinical & Experimental Epilepsy
Dept of Chemistry
Department of Imaging
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