| Literature DB >> 30344364 |
Julie Coloigner1,2, Chau Vu1,2, Adam Bush3, Matt Borzage1,4,3, Vidya Rajagopalan1,2,5, Natasha Lepore1,2, John Wood3.
Abstract
Sickle cell disease (SCD) is an inherited blood disorder that effects red blood cells, which can lead to vasoocclusion, ischemia and infarct. This disease often results in neurological damage and strokes, leading to morbidity and mortality. Functional Magnetic Resonance Imaging (fMRI) is a non-invasive technique for measuring and mapping the brain activity. Blood Oxygenation Level-Dependent (BOLD) signals contain also information about the neurovascular coupling, vascular reactivity, oxygenation and blood propagation. Temporal relationship between BOLD fluctuations in different parts of the brain provides also a mean to investigate the blood delay information. We used the induced desaturation as a label to profile transit times through different brain areas, reflecting oxygen utilization of tissue. In this study, we aimed to compare blood flow propagation delay times between these patients and healthy subjects in areas vascularized by anterior, middle and posterior cerebral arteries. In a group comparison analysis with control subjects, BOLD changes in these areas were found to be almost simultaneous and shorter in the SCD patients, because of their increased brain blood flow. Secondly, the analysis of a patient with a stenosis on the anterior cerebral artery indicated that signal of the area vascularized by this artery lagged the MCA signal. These findings suggest that sickle cell disease causes blood propagation modifications, and that these changes could be used as a biomarker of vascular damage.Entities:
Keywords: Functional magnetic resonance imaging; desaturation; group delay; sickle cell disease
Year: 2016 PMID: 30344364 PMCID: PMC6192015 DOI: 10.1117/12.2217263
Source DB: PubMed Journal: Proc SPIE Int Soc Opt Eng ISSN: 0277-786X