Abstract

In this study, we evaluated an MRI fingerprinting approach (MRvF) designed to provide high-resolution parametric maps of the microvascular architecture (i.e., blood volume fraction, vessel diameter) and function (blood oxygenation) simultaneously. The method was tested in rats (n = 115), divided in 3 models: brain tumors (9 L, C6, F98), permanent stroke, and a control group of healthy animals. We showed that fingerprinting can robustly distinguish between healthy and pathological brain tissues with different behaviors in tumor and stroke models. In particular, fingerprinting revealed that C6 and F98 glioma models have similar signatures while 9 L present a distinct evolution. We also showed that it is possible to improve the results of MRvF and obtain supplemental information by changing the numerical representation of the vascular network. Finally, good agreement was found between MRvF and conventional MR approaches in healthy tissues and in the C6, F98, and permanent stroke models. For the 9 L glioma model, fingerprinting showed blood oxygenation measurements that contradict results obtained with a quantitative BOLD approach. In conclusion, MR vascular fingerprinting seems to be an efficient technique to study microvascular properties in vivo. Multiple technical improvements are feasible and might improve diagnosis and management of brain diseases.

Highlights

  • While the spatial resolution of MRI does not allow for direct depiction of small cerebrovascular structures (

  • In the first study proposed by Ma et al, pseudorandom MR acquisitions that lead to complicated signal evolutions or ‘fingerprints’ in every voxel are compared to a database obtained from numerical simulations of the same experiment

  • After the pattern matching procedure, we found that the method enabled the creation of high-resolution parametric maps in the human brain showing expected contrast, fine details, and numerical values in gray matter that were consistent with literature reports

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Summary

Introduction

While the spatial resolution of MRI does not allow for direct depiction of small cerebrovascular structures (

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