Conan Chen, Ryan A Barnes, Katherine J Bangen, Fei Han, Josef Pfeuffer, Eric C Wong, Thomas T Liu, Divya S Bolar
{"title":"MVP-VSASL: measuring MicroVascular Pulsatility using Velocity-Selective Arterial Spin Labeling","authors":"Conan Chen, Ryan A Barnes, Katherine J Bangen, Fei Han, Josef Pfeuffer, Eric C Wong, Thomas T Liu, Divya S Bolar","doi":"10.1101/2024.06.21.24309261","DOIUrl":null,"url":null,"abstract":"<strong>Purpose:</strong> By leveraging the small-vessel specificity of velocity-selective arterial spin labeling (VSASL), we present a novel technique for measuring cerebral MicroVascular Pulsatility named MVP-VSASL.\n<strong>Theory and Methods:</strong> We present a theoretical model relating the pulsatile, cerebral blood flow-driven VSASL signal to the microvascular pulsatility index (PI), a widely used metric for quantifying cardiac-dependent fluctuations. The model describes the dependence of PI on bolus duration τ (an adjustable VSASL sequence parameter) and provides guidance for selecting a value of τ that maximizes the SNR of the PI measurement. The model predictions were assessed in humans using data acquired with retrospectively cardiac-gated VSASL sequences over a broad range of τ values. In vivo measurements were also used to demonstrate the feasibility of whole-brain voxel-wise PI mapping, assess intrasession repeatability of the PI measurement, and illustrate the potential of this method to explore an association with age.\n<strong>Results:</strong> The theoretical model showed excellent agreement to the empirical data in a gray matter region of interest (average R<sup>2</sup> value of 0.898 ± 0.107 across six subjects). We further showed excellent intrasession repeatability of the pulsatility measurement (ICC = 0.960, p < 0.001) and the potential to characterize associations with age (r = 0.554, p = 0.021).\n<strong>Conclusion:</strong> We have introduced a novel, VSASL-based cerebral microvascular pulsatility technique, which may facilitate investigation of cognitive disorders where damage to the microvasculature has been implicated.","PeriodicalId":501358,"journal":{"name":"medRxiv - Radiology and Imaging","volume":"22 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-06-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"medRxiv - Radiology and Imaging","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.06.21.24309261","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: By leveraging the small-vessel specificity of velocity-selective arterial spin labeling (VSASL), we present a novel technique for measuring cerebral MicroVascular Pulsatility named MVP-VSASL.
Theory and Methods: We present a theoretical model relating the pulsatile, cerebral blood flow-driven VSASL signal to the microvascular pulsatility index (PI), a widely used metric for quantifying cardiac-dependent fluctuations. The model describes the dependence of PI on bolus duration τ (an adjustable VSASL sequence parameter) and provides guidance for selecting a value of τ that maximizes the SNR of the PI measurement. The model predictions were assessed in humans using data acquired with retrospectively cardiac-gated VSASL sequences over a broad range of τ values. In vivo measurements were also used to demonstrate the feasibility of whole-brain voxel-wise PI mapping, assess intrasession repeatability of the PI measurement, and illustrate the potential of this method to explore an association with age.
Results: The theoretical model showed excellent agreement to the empirical data in a gray matter region of interest (average R2 value of 0.898 ± 0.107 across six subjects). We further showed excellent intrasession repeatability of the pulsatility measurement (ICC = 0.960, p < 0.001) and the potential to characterize associations with age (r = 0.554, p = 0.021).
Conclusion: We have introduced a novel, VSASL-based cerebral microvascular pulsatility technique, which may facilitate investigation of cognitive disorders where damage to the microvasculature has been implicated.