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Related Concept Videos

Peripheral Arterial Disease II: Clinical Manifestations and Diagnostic Evaluation01:21

Peripheral Arterial Disease II: Clinical Manifestations and Diagnostic Evaluation

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Clinical manifestationsPeripheral Arterial Disease (PAD) manifests through a range of symptoms, from the characteristic intermittent claudication to atypical presentations and severe complications in advanced stages. Intermittent claudication, a hallmark symptom of PAD, presents as exercise-induced muscle pain that typically resolves within minutes of rest. This pain is reproducible and stems from inadequate blood flow, leading to the accumulation of lactic acid produced during anaerobic...
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Magnetic Resonance Imaging Quantification of Pulmonary Perfusion using Calibrated Arterial Spin Labeling
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MVP-VSASL: measuring MicroVascular Pulsatility using velocity-selective arterial spin labeling.

Conan Chen1,2,3, Ryan A Barnes1,2, Katherine J Bangen4,5

  • 1Center for Functional MRI, University of California San Diego, La Jolla, California, USA.

Magnetic Resonance in Medicine
|January 31, 2025
PubMed
Summary
This summary is machine-generated.

We developed MVP-VSASL, a new method using velocity-selective arterial spin labeling to measure cerebral microvascular pulsatility. This technique shows promise for studying age-related changes and cognitive disorders.

Keywords:
VSASL ASLmicrovascularpulsatilityvelocity selective arterial spin labeling

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Area of Science:

  • Neuroimaging
  • Biomedical Engineering
  • Cardiovascular Physiology

Background:

  • Cerebral microvascular pulsatility reflects cardiac-dependent blood flow fluctuations.
  • Assessing microvascular pulsatility is crucial for understanding cerebrovascular health.
  • Existing methods may have limitations in specificity and resolution.

Purpose of the Study:

  • Introduce MVP-VSASL, a novel technique for measuring cerebral microvascular pulsatility.
  • Leverage the small-vessel specificity of velocity-selective arterial spin labeling (VSASL).
  • Establish a method for quantifying microvascular pulsatility index (MPI) using VSASL.

Main Methods:

  • Developed a theoretical model linking VSASL signal to MPI.
  • Guided selection of VSASL bolus duration for optimal signal-to-noise ratio (SNR).
  • Validated the model in humans using cardiac-gated VSASL and assessed repeatability and age association.

Main Results:

  • Theoretical model demonstrated excellent agreement with empirical data (R²=0.898).
  • Demonstrated excellent intrasession repeatability of pulsatility measurements.
  • Showcased potential for voxel-wise pulsatility mapping and age association studies.

Conclusions:

  • Introduced MVP-VSASL, a novel VSASL-based technique for cerebral microvascular pulsatility.
  • This method facilitates investigation of microvascular damage in cognitive disorders.
  • MVP-VSASL offers a promising tool for advancing cerebrovascular research.