期刊
NEUROIMAGE
卷 237, 期 -, 页码 -出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2021.118194
关键词
Positron emission tomography; Input function; NMDA receptor
资金
- MRC PET Neuroscience programme grant (Training and Novel Probes Programme in PET Neurochemistry) [MR/K02308X/1]
- MRC Developmental Pathway Funding Scheme grant [MR/L013215/1]
- MRC [MR/L013215/1] Funding Source: UKRI
Blood-based kinetic analysis of PET data relies on an accurate estimation of the arterial plasma input function. An alternative is the image-derived input function (IDIF), which can be corrected for the required free tracer concentration in plasma. The IDIF + venous method provides comparable results to arterial sampling, making it a viable alternative for quantification of V-T.
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 [F-18]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 (V-T) in 11 regions across the brain (r = 0.95, p < 0.001). IDIF + venous V-T 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 V-T 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 V-T (mean bias - 20.9%), and produced V-T 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 [F-18]GE-179 V-T.
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