We identified abnormally long mean transit time (MTT) and large capillary transit time heterogeneity (CTH) in the basal ganglia of ten individuals with Huntington’s disease (HD) as compared to ten healthy control subjects. Since iron is elevated in the putamen and globus pallidus in HD [1], which can lead to an underestimation of relative cerebral blood flow (CBF) and cerebral blood volume (CBV), excessively prolonged MTT and CTH, which are ratios of CBV and CBF, could be utilized as relatively intact parameters for the estimation of perfusion deficits or breakdown in blood-brain barrier.
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