In pCASL a well-defined, box-shaped bolus is created at the labeling plane and for quantification this shape is assumed to be preserved, however, in reality this shape will be dispersed. With multi-timepoint data, the effects of dispersion can be observed in the macrovascular component, which can be separated from the tissue component using a two-component model. In this study the combined estimation of dispersion and macrovascular signal was investigated. When a gamma distribution dispersion kernel was incorporated into the two-component model, a significant decrease in CBF values was found, while a significant increase in macrovascular signal was observed.
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