MR Angiography: Translational Potential to Combine High-Resolution MRA with single-vessel BOLD, CBV and CBF-velocity fMRI
Xin Yu1 and David Hike1
1Massachusetts General Hospital and Harvard Medical School, United States

Synopsis

There are two ongoing challenges when specifying vascular function underlying vascular cognitive impairment in patients. One issue is the size of vessels that altered anatomy and function can be detected in the brain. The other issue is the location of the affected vessels to be detected, e.g. gray matter vs. white matter, or cortical vs. subcortical cerebral vasculature. MR Angiography(MRA) provides the key anatomical vasculature measurement when studying cerebrovascular diseases or impaired cerebral blood flow related to vascular dementia. Here, we will discuss the linkage of high-resolution MRA with single-vessel fMRI to characterize vessel-specific oxygenation(BOLD), cerebral volume, and flow changes.

Abstract

MR angiography can be used to map the penetrating vessels in the cortex of animals with ultra-high resolution, e.g. in-plane resolution 50x50 µm. This method has been lately applied in a multi-gradient echo sequence with a large flip angle but shorter TR to identify micro-vessels with 20-70um diameter. By specifying the MR contrasts at different echoes, the arterioles and venules can be easily identified through the whole cortex. This MRA-based arteriole-venule (A-V) map can be used to guide the high-resolution fMRI studies in both deep layer cortex and hippocampus. One critical insight of MRA-based single-vessel fMRI is to identify the venule-specific BOLD signal vs. arteriole-specific CBV signals of the brain with tasks or during rest. Furthermore, the MRA-based A-V map can be compared with a phase-contrast MR-based flow velocity map to measure the vessel-specific velocity changes coupled with neuronal activation, e.g. functional CBF-velocity mapping. This unique advantage of the MRA-based single-vessel mapping scheme shows a great potential to measure altered vascular function in diseased stages. We will go over several potential clinical applications to apply MRA-based single-vessel functional mapping. Also, we will go over the ongoing challenges and perspectives to applying high field MR scanners to push the high-resolution vascular anatomical and functional mapping limits. In the end, we will highlight the pros and cons of the high resolution MRA-coupled vascular functional mapping methods when compared with the emerging cutting-edge method, e.g. functional ultrasounds.

Acknowledgements

This work was supported by NIH grant RF1NS113278, R01NS120594, R01MH111438, S10MH124733, R21NS121642, U19NS123717 and NSF grant 2123971.

References

No reference found.
Proc. Intl. Soc. Mag. Reson. Med. 30 (2022)