2014
DOI: 10.1016/j.nicl.2014.07.014
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Arterial spin labelling reveals prolonged arterial arrival time in idiopathic Parkinson's disease

Abstract: Idiopathic Parkinson's disease (IPD) is the second most common neurodegenerative disease, yet effective disease modifying treatments are still lacking. Neurodegeneration involves multiple interacting pathological pathways. The extent to which neurovascular mechanisms are involved is not well defined in IPD. We aimed to determine whether novel magnetic resonance imaging (MRI) techniques, including arterial spin labelling (ASL) quantification of cerebral perfusion, can reveal altered neurovascular status (NVS) i… Show more

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Cited by 65 publications
(80 citation statements)
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References 58 publications
(62 reference statements)
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“…[45][46][47] These findings suggest a common involvement of the neurovascular mechanism in neurodegenerative diseases of the CNS. Dysregulated cerebrovascular reactivity may lead to unstable oxygen supply to local neurons, and may actively participate in the acceleration of neurodegeneration in the brain of the patients.…”
Section: Discussionmentioning
confidence: 74%
“…[45][46][47] These findings suggest a common involvement of the neurovascular mechanism in neurodegenerative diseases of the CNS. Dysregulated cerebrovascular reactivity may lead to unstable oxygen supply to local neurons, and may actively participate in the acceleration of neurodegeneration in the brain of the patients.…”
Section: Discussionmentioning
confidence: 74%
“…Al-Bachari et al (2014) examined neurovascular status in PD through ASL measures of arterial arrival time (AAT). Widespread regions of the brain showed prolongation of AAT.…”
Section: Neuroimaging Of Pdmentioning
confidence: 99%
“…13 A previous work in PBTs has used a more complex model, providing measures of pre-capillary and capillary arrival time. 8 We felt that the lower temporal resolution of our ASL data (370 ms compared with 200 ms in Ref.…”
Section: Discussionmentioning
confidence: 99%
“…Control and label images were subtracted and averaged to provide difference images at each timepoint. A single blood compartment model, 12 adapted for the Look–Locker readout, 13 was fit to the averaged images on a voxel-by-voxel basis, producing maps of CBF and AAT (without vascular crushing) and CBF with vascular crushing (CBF VC ) and AAT with vascular crushing (AAT VC ) (with vascular crushing). This model assumes that labelled water remains in the blood and that no labelled water leaves the voxel, an approach that has been shown to be reasonably accurate.…”
Section: Methodsmentioning
confidence: 99%