Purpose: We propose a new method, displacement spectrum (DiSpect) imaging, for probing in vivo complex tissue dynamics such as motion, flow, diffusion, and perfusion. Based on stimulated echoes and image phase, our flexible approach enables observations of the spin dynamics over short (milliseconds) to long (seconds) evolution times.
Methods: The DiSpect method is a Fourier-encoded variant of displacement encoding with stimulated echoes, which encodes bulk displacement of spins that occurs between tagging and imaging in the image phase. However, this method fails to capture partial volume effects as well as blood flow. The DiSpect variant mitigates this by performing multiple scans with increasing displacement-encoding steps. Fourier analysis can then resolve the multidimensional spectrum of displacements that spins exhibit over the mixing time. In addition, repeated imaging following tagging can capture dynamic displacement spectra with increasing mixing times.
Results: We demonstrate properties of DiSpect MRI using flow phantom experiments as well as in vivo brain scans. Specifically, the ability of DiSpect to perform retrospective vessel-selective perfusion imaging at multiple mixing times is highlighted.
Conclusion: The DiSpect variant is a new tool in the arsenal of MRI techniques for probing complex tissue dynamics. The flexibility and the rich information it provides open the possibility of alternative ways to quantitatively measure numerous complex spin dynamics, such as flow and perfusion within a single exam.
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http://dx.doi.org/10.1002/mrm.28882 | DOI Listing |
Diagnostics (Basel)
November 2024
Department of Radiology, Stanford University, Palo Alto, CA 94305, USA.
In boys with Duchenne muscular dystrophy (DMD), cardiomyopathy has become the primary cause of death. Although both positive late gadolinium enhancement (LGE) and reduced left ventricular ejection fraction (LVEF) are late findings in a DMD cohort, LV end-systolic circumferential strain at middle wall (E) serves as a biomarker for detecting early impairment in cardiac function associated with DMD. However, E derived from cine Displacement Encoding with Stimulated Echoes (DENSE) has not been quantified in boys with DMD.
View Article and Find Full Text PDFJ Acoust Soc Am
December 2024
Department of Psychology, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093, USA.
A primary feature of bat and dolphin biosonar is the ability to measure echo-delay, both to determine absolute target range and to resolve range differences between targets. Measurements of range (i.e.
View Article and Find Full Text PDFInterface Focus
December 2024
Translational Neuroimaging Group, Center for Image Sciences, University Medical Center Utrecht, Utrecht, The Netherlands.
Intracerebral blood volume changes along the cardiac cycle cause volumetric strain in brain tissue, measurable with displacement encoding with stimulated echoes (DENSE) magnetic resonance imaging. Individual volumetric strain maps show compressing and expanding voxels, raising the question whether systolic compressions reflect a physiological phenomenon. In DENSE data from nine healthy volunteers, voxels were grouped into three clusters according to volumetric strain in a tissue mask excluding extracerebral blood vessels and cerebrospinal fluid using a two-stage clustering approach.
View Article and Find Full Text PDFJ Neurophysiol
December 2024
Department of Neuroscience, Brown University, Providence, Rhode Island, United States.
Echolocating big brown bats () detect changes in ultrasonic echo delay with an acuity as sharp as 1 µs or less. How this perceptual feat is accomplished in the nervous system remains unresolved. Here, we examined the precision of latency registration (latency jitter) in neural population responses as a possible mechanism underlying the bat's hyperacuity.
View Article and Find Full Text PDFJ Magn Reson Imaging
October 2024
Department of Radiology, Stanford University, Stanford, California, USA.
Background: The Osteoarthritis Initiative (OAI) collected extensive imaging data, including Multi-Echo Spin-Echo (MESE) sequences for measuring knee cartilage T relaxation times. Mono-exponential models are used in the OAI for T fitting, which neglects stimulated echoes and B inhomogeneities. Extended Phase Graph (EPG) modeling addresses these limitations but has not been applied to the OAI dataset.
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