Using saturation bands to null signal from inflowing blood in single-slice fMRI: Toward a rapidly sampled black-blood functional contrast
Motivation: Magnetization-preparation schemes using inversion recovery measure aspects of hemodynamics like perfusion and blood volume, but their temporal resolution is limited by physiology, i.e., long blood arrival/transit times. Goal(s): To study brain hemodynamics at high temporal resolutions with novel inflow saturation. Approach: We applied saturation bands on both sides of a rapidly-sampled single imaging slice to suppress inflow-related signal and produce black-blood functional contrast sensitive to macrovascular blood volume. Results: Phantom experiments show successful suppression of inflow signal with flow-velocity-dependence at low- and high-velocity regimes but independence at mid-regime. Human brain vessels exhibited partial signal suppression, with more functional suppression seen in larger vessels. Impact: Fast blood nulling may be achievable using local saturation bands contiguous to an imaging slice rather than a global inversion slab, enabling functional contrasts sensitive to macrovascular blood flow-velocity and volume suitable for studying fast hemodynamics in specific vascular compartments.
Authors
- Sébastien Proulx (ORCID: https://orcid.org/0000-0003-1709-3277)
- Shota Hodono (ORCID: https://orcid.org/0000-0002-8107-5682)
- Martijn A. Cloos (ORCID: https://orcid.org/0000-0002-0636-234X)
- Jon̈athan R. Polimeni (ORCID: https://orcid.org/0000-0002-1348-1179)
- Zhangxuan Hu (ORCID: https://orcid.org/0000-0002-6534-4299)
- Divya Naradarajan
Publication Details
- Journal
- Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
- Published
- 2024-11-26
- DOI
- https://doi.org/10.58530/2024/3409
- Citations
- 1
- Primary Topic
- Functional Brain Connectivity Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.34