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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

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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Related Experiment Video

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Magnetic Resonance Imaging Quantification of Pulmonary Perfusion using Calibrated Arterial Spin Labeling
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Perfusion Signal Analysis Using Multi-pulsed Arterial Spin Labeling (mPASL) with Multiple Post-labeling Delays:

Vadim Malis1, Yoshiki Kuwatsuru1, Mitsue Miyazaki1

  • 1Department of Radiology, University of California-San Diego, La Jolla CA, USA.

Magnetic Resonance in Medical Sciences : MRMS : an Official Journal of Japan Society of Magnetic Resonance in Medicine
|September 3, 2025
PubMed
Summary

This study extends the general kinetic model (GKM) for multi-pulsed arterial spin labeling (mPASL) to improve perfusion analysis. While accurate in phantoms, in-vivo results show potential model limitations for complex physiological flows.

Keywords:
arterial spin labelingfoot perfusiongeneral kinetic modelmulti-pulsed arterial spin labelingperfusion

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Area of Science:

  • Magnetic Resonance Imaging
  • Biomedical Engineering
  • Physiology

Background:

  • Accurate perfusion quantification is crucial for diagnosing and monitoring various medical conditions.
  • Arterial spin labeling (ASL) is a non-invasive MRI technique for measuring tissue perfusion.
  • Multi-pulsed ASL (mPASL) offers potential advantages in signal-to-noise ratio and temporal resolution.

Purpose of the Study:

  • To extend the general kinetic model (GKM) for perfusion signal analysis.
  • To adapt GKM for multi-pulsed arterial spin labeling (mPASL) with multiple post-labeling delays (mPLD).
  • To enhance accuracy and applicability of mPASL in experimental and clinical settings.

Main Methods:

  • Analyzed mPASL magnetization vector evolution using sequence diagrams and numerical simulation.
  • Adapted GKM for "dark" and "bright" mPASL configurations.
  • Validated the approach using constant-flow phantom experiments and in-vivo foot perfusion measurements in healthy subjects.

Main Results:

  • Simulations revealed "dark"/"bright" mPASL ratio depends on fluid T1 relaxation, pulse number, and labeling efficiency.
  • GKM with mPASL enabled semi-quantitative perfusion analysis with high temporal resolution in phantoms.
  • Phantom perfusion coefficients showed high consistency (5.1% variation), confirming GKM extension robustness.
  • In-vivo results deviated from simulations and phantom data, indicating physiological complexities and model limitations.

Conclusions:

  • The extended GKM for mPASL demonstrates reliable performance in controlled constant flow conditions.
  • Phantom validation confirmed the accuracy of the GKM extension for mPASL.
  • In-vivo foot perfusion measurements highlighted deviations, suggesting the need to incorporate physiological factors and pulsatile flow into the model.