Imaging the blood-brain barrier (BBB) permeability of molecular PET tracers may allow pathway-specific assessment of the diverse transport mechanisms expressed at the BBB. However, PET quantification of BBB permeability typically requires dual-tracer protocols involving a flow tracer, increasing methodological complexity and clinical burden. We evaluated a single-tracer dynamic PET method for quantifying the BBB permeability-surface area (PS) of 18 fluorodeoxyglucose (FDG) against the conventional dual-tracer method. Our method uses high-temporal resolution imaging (1 s/frame), an image-derived arterial input function, and distributed kinetic modeling to simultaneously estimate cerebral blood flow (CBF) and transvascular transport rate K 1 , from which BBB PS is calculated via the Renkin-Crone equation. Single-tracer and conventional dual-tracer PS estimates were compared in 18 volunteers scanned with the flow-tracer 11 Cbutanol and 18 FDG PET. Single-tracer 18 FDG PS estimates had 3.7% mean bias and 4.2% standard deviation of differences compared to dual-tracer estimates. This was enabled by strong agreement between 18 FDG and 11 Cbutanol CBF estimates (Pearson R=0.85, P<0.001; mean difference: -0.057±0.078 mL/min/cm3). These results demonstrate that high-temporal resolution dynamic PET enables single-tracer quantification of both CBF and BBB PS without a dedicated flow tracer, expanding opportunities for quantitative studies of molecular BBB transport across a broad range of tracers and disorders.
Chung et al. (Sun,) studied this question.