## Purpose: To evaluate reproducibility of total cerebral blood flow (cbf) measurements with phase contrast magnetic resonance imaging (pcmri). ## Materials and methods: We repeated total cbf measurements in 15 healthy volunteers with and without cardiac triggering, and with and without repositio
Assessment of cerebral blood flow reserve using functional magnetic resonance imaging
โ Scribed by Peter Hedera; Song Lai; Jonathan S. Lewin; E. Mark Haacke; Dee Wu; Alan J. Lerner; Robert P. Friedland
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 963 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1053-1807
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
Imaging of activated brain areas based on changes of blood deoxyhemoglobin levels is now possible with MRI. Acetazolamide (ACZ) increases cerebral blood flow (CBF) without changing cerebral oxygen consumption; this results in signal changes observed in gradient echo MR images from the areas with an increase in CBF. We assessed signal changes after ACZ application in seven healthy subjects with a conventional 1.5โT MRI scanner. The susceptibilityโsensitized threeโdimensional fast lowโangle shot (FLASH) sequence was used to visualize signal changes induced by ACZ. We analyzed anatomic localization of different ranges of detected signal changes. ACZ caused significant signal changes in the gray matter and at the edge of the cerebral cortex, the latter corresponding to draining surface veins. No significant differences were seen among different brain areas within the same slice. Using the maximum intensity projection technique, we were able to partially separate signal changes originating in draining veins from signal originating in the gray matter microvasculature. Signal changes from the microvessels reflect cerebrovascular reserve. Bloodโoxygenโlevelโdependent (BOLD) based MRI can evaluate CBF reserve with high spatial and temporal resolution. To assess cerebrovascular reserve, it is necessary to separate signal changes originating in large vessels from signal from brain microvasculature.
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