462 research outputs found
Axon diameters and myelin content modulate microscopic fractional anisotropy at short diffusion times in fixed rat spinal cord
Mapping tissue microstructure accurately and noninvasively is one of the
frontiers of biomedical imaging. Diffusion Magnetic Resonance Imaging (MRI) is
at the forefront of such efforts, as it is capable of reporting on microscopic
structures orders of magnitude smaller than the voxel size by probing
restricted diffusion. Double Diffusion Encoding (DDE) and Double Oscillating
Diffusion Encoding (DODE) in particular, are highly promising for their ability
to report on microscopic fractional anisotropy ({\mu}FA), a measure of the pore
anisotropy in its own eigenframe, irrespective of orientation distribution.
However, the underlying correlates of {\mu}FA have insofar not been studied.
Here, we extract {\mu}FA from DDE and DODE measurements at ultrahigh magnetic
field of 16.4T in the aim to probe fixed rat spinal cord microstructure. We
further endeavor to correlate {\mu}FA with Myelin Water Fraction (MWF) derived
from multiexponential T2 relaxometry, as well as with literature-based
spatially varying axonal diameters. In addition, a simple new method is
presented for extracting unbiased {\mu}FA from three measurements at different
b-values. Our findings reveal strong anticorrelations between {\mu}FA (derived
from DODE) and axon diameter in the distinct spinal cord tracts; a moderate
correlation was also observed between {\mu}FA derived from DODE and MWF. These
findings suggest that axonal membranes strongly modulate {\mu}FA, which - owing
to its robustness towards orientation dispersion effects - reflects axon
diameter much better than its typical FA counterpart. The {\mu}FA exhibited
modulations when measured via oscillating or blocked gradients, suggesting
selective probing of different parallel path lengths and providing insight into
how those modulate {\mu}FA metrics. Our findings thus shed light into the
underlying microstructural correlates of {\mu}FA and are (...
Combined Diffusion-Relaxometry MRI to Identify Dysfunction in the Human Placenta
Purpose: A combined diffusion-relaxometry MR acquisition and analysis
pipeline for in-vivo human placenta, which allows for exploration of coupling
between T2* and apparent diffusion coefficient (ADC) measurements in a sub 10
minute scan time.
Methods: We present a novel acquisition combining a diffusion prepared
spin-echo with subsequent gradient echoes. The placentas of 17 pregnant women
were scanned in-vivo, including both healthy controls and participants with
various pregnancy complications. We estimate the joint T2*-ADC spectra using an
inverse Laplace transform.
Results: T2*-ADC spectra demonstrate clear quantitative separation between
normal and dysfunctional placentas.
Conclusions: Combined T2*-diffusivity MRI is promising for assessing fetal
and maternal health during pregnancy. The T2*-ADC spectrum potentially provides
additional information on tissue microstructure, compared to measuring these
two contrasts separately. The presented method is immediately applicable to the
study of other organs
Quantitative MRI in leukodystrophies
Leukodystrophies constitute a large and heterogeneous group of genetic diseases primarily affecting the white matter of the central nervous system. Different disorders target different white matter structural components. Leukodystrophies are most often progressive and fatal. In recent years, novel therapies are emerging and for an increasing number of leukodystrophies trials are being developed. Objective and quantitative metrics are needed to serve as outcome measures in trials. Quantitative MRI yields information on microstructural properties, such as myelin or axonal content and condition, and on the chemical composition of white matter, in a noninvasive fashion. By providing information on white matter microstructural involvement, quantitative MRI may contribute to the evaluation and monitoring of leukodystrophies. Many distinct MR techniques are available at different stages of development. While some are already clinically applicable, others are less far developed and have only or mainly been applied in healthy subjects. In this review, we explore the background, current status, potential and challenges of available quantitative MR techniques in the context of leukodystrophies
Early detection of human glioma sphere xenografts in mouse brain using diffusion MRI at 14.1 T.
Glioma models have provided important insights into human brain cancers. Among the investigative tools, MRI has allowed their characterization and diagnosis. In this study, we investigated whether diffusion MRI might be a useful technique for early detection and characterization of slow-growing and diffuse infiltrative gliomas, such as the proposed new models, LN-2669GS and LN-2540GS glioma sphere xenografts. Tumours grown in these models are not visible in conventional T2 -weighted or contrast-enhanced T1 -weighted MRI at 14.1 T. Diffusion-weighted imaging and diffusion tensor imaging protocols were optimized for contrast by exploring long diffusion times sensitive for probing the microstructural alterations induced in the normal brain by the slow infiltration of glioma sphere cells. Compared with T2 -weighted images, tumours were properly identified in their early stage of growth using diffusion MRI, and confirmed by localized proton MR spectroscopy as well as immunohistochemistry. The first evidence of tumour presence was revealed for both glioma sphere xenograft models three months after tumour implantation, while no necrosis, oedema or haemorrhage were detected either by MRI or by histology. Moreover, different values of diffusion indices, such as mean diffusivity and fractional anisotropy, were obtained in tumours grown from LN-2669GS and LN-2540GS glioma sphere lines. These observations highlighted diverse tumour microstructures for both xenograft models, which were reflected in histology. This study demonstrates the ability of diffusion MRI techniques to identify and investigate early stages of slow-growing, invasive tumours in the mouse brain, thus providing a potential imaging biomarker for early detection of tumours in humans
In vivo myelin water quantification using diffusion–relaxation correlation MRI: A comparison of 1D and 2D methods
Multidimensional Magnetic Resonance Imaging (MRI) is a versatile tool for microstructure mapping. We use a diffusion weighted inversion recovery spin echo (DW-IR-SE) sequence with spiral readouts at ultra-strong gradients to acquire a rich diffusion–relaxation data set with sensitivity to myelin water. We reconstruct 1D and 2D spectra with a two-step convex optimization approach and investigate a variety of multidimensional MRI methods, including 1D multi-component relaxometry, 1D multi-component diffusometry, 2D relaxation correlation imaging, and 2D diffusion-relaxation correlation spectroscopic imaging (DR-CSI), in terms of their potential to quantify tissue microstructure, including the myelin water fraction (MWF). We observe a distinct spectral peak that we attribute to myelin water in multi-component T1 relaxometry, T1-T2 correlation, T1-D correlation, and T2-D correlation imaging. Due to lower achievable echo times compared to diffusometry, MWF maps from relaxometry have higher quality. Whilst 1D multi-component T1 data allows much faster myelin mapping, 2D approaches could offer unique insights into tissue microstructure and especially myelin diffusion
Integrated and efficient diffusion-relaxometry using ZEBRA
The emergence of multiparametric diffusion models combining diffusion and
relaxometry measurements provide powerful new ways to explore tissue
microstructure with the potential to provide new insights into tissue structure
and function. However, their ability to provide rich analyses and the potential
for clinical translation critically depends on the availability of efficient,
integrated, multi-dimensional acquisitions. We propose a fully integrated
sequence simultaneously sampling the acquisition parameter spaces required for
T1 and T2* relaxometry and diffusion MRI. Slice-level interleaved diffusion
encoding, multiple spin/gradient echoes and slice-shuffling are combined for
higher efficiency, sampling flexibility and enhanced internal consistency.
In-vivo data was successfully acquired on healthy adult brains. Obtained
parametric maps as well as clustering results demonstrate the potential of the
technique regarding its ability to provide eloquent data with an acceleration
of roughly 20 compared to conventionally used approaches. The proposed
integrated acquisition, called ZEBRA, offers significant acceleration and
flexibility compared to existing diffusion-relaxometry studies and thus
facilitates wider use of these techniques both for research-driven and clinical
applications
Dual-encoded magnetization transfer and diffusion imaging and its application to tract-specific microstructure mapping
We present a novel dual-encoded magnetization transfer (MT) and
diffusion-weighted sequence and demonstrate its potential to resolve distinct
properties of white matter fiber tracts at the sub-voxel level. The sequence
was designed and optimized for maximal MT contrast efficiency. The resulting
whole brain 2.6 mm isotropic protocol to measure tract-specific MT ratio (MTR)
has a scan time under 7 minutes. Ten healthy subjects were scanned twice to
assess repeatability. Two different analysis methods were contrasted: a
technique to extract tract-specific MTR using Convex Optimization Modeling for
Microstructure Informed Tractography (COMMIT), a global optimization technique;
and conventional MTR tractometry. The results demonstrate that the
tract-specific method can reliably resolve the MT ratios of major white matter
fiber pathways and is less affected by partial volume effects than conventional
multi-modal tractometry. Dual-encoded MT and diffusion is expected to both
increase the sensitivity to microstructure alterations of specific tracts due
to disease, ageing or learning, as well as lead to weighted structural
connectomes with more anatomical specificity.Comment: 26 pages, 7 figure
Microstructural imaging of the human brain with a 'super-scanner': 10 key advantages of ultra-strong gradients for diffusion MRI
The key component of a microstructural diffusion MRI 'super-scanner' is a dedicated high-strength gradient system that enables stronger diffusion weightings per unit time compared to conventional gradient designs. This can, in turn, drastically shorten the time needed for diffusion encoding, increase the signal-to-noise ratio, and facilitate measurements at shorter diffusion times. This review, written from the perspective of the UK National Facility for In Vivo MR Imaging of Human Tissue Microstructure, an initiative to establish a shared 300 mT/m-gradient facility amongst the microstructural imaging community, describes ten advantages of ultra-strong gradients for microstructural imaging. Specifically, we will discuss how the increase of the accessible measurement space compared to a lower-gradient systems (in terms of Δ, b-value, and TE) can accelerate developments in the areas of 1) axon diameter distribution mapping; 2) microstructural parameter estimation; 3) mapping micro-vs macroscopic anisotropy features with gradient waveforms beyond a single pair of pulsed-gradients; 4) multi-contrast experiments, e.g. diffusion-relaxometry; 5) tractography and high-resolution imaging in vivo and 6) post mortem; 7) diffusion-weighted spectroscopy of metabolites other than water; 8) tumour characterisation; 9) functional diffusion MRI; and 10) quality enhancement of images acquired on lower-gradient systems. We finally discuss practical barriers in the use of ultra-strong gradients, and provide an outlook on the next generation of 'super-scanners'
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