Literature DB >> 22664569

Quantitative MR imaging of two-pool magnetization transfer model parameters in myelin mutant shaking pup.

Alexey Samsonov1, Andrew L Alexander, Pouria Mossahebi, Yu-Chien Wu, Ian D Duncan, Aaron S Field.   

Abstract

Magnetization transfer (MT) imaging quantitatively assesses cerebral white matter disease through its sensitivity to macromolecule-bound protons including those associated with myelin proteins and lipid bilayers. However, traditional MT contrast measured by the MT ratio (MTR) lacks pathologic specificity as demyelination, axon loss, inflammation and edema all impact MTR, directly and/or indirectly through multiple covariances among imaging parameters (particularly MTR with T(1)) and tissue features (e.g. axon loss with demyelination). In this study, more complex modeling of MT phenomena ("quantitative" MT or qMT) was applied to a less complex disease model (the myelin mutant shaking [sh] pup, featuring hypomyelination but neither inflammation nor axon loss) in order to eliminate the covariances on both sides of the MR-pathology "equation" and characterize these important relationships free from the usual confounds. qMT measurements were acquired longitudinally in 6 sh pups and 4 age-matched controls ranging from 3 to 21 months of age and compared with histology. The qMT parameter, bound pool fraction (f), was the most distinctive between diseased and control animals; both f and longitudinal relaxation rate R(1) tracked myelination with normal aging, whereas MTR did not--presumably owing to counterbalancing MT and R(1) effects. qMT imaging provides a more accurate and potentially more specific non-invasive tissue characterization.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22664569      PMCID: PMC3408843          DOI: 10.1016/j.neuroimage.2012.05.077

Source DB:  PubMed          Journal:  Neuroimage        ISSN: 1053-8119            Impact factor:   6.556


  52 in total

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  31 in total

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6.  Effects of magnetization transfer on T1 contrast in human brain white matter.

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7.  Rapid and quantitative chemical exchange saturation transfer (CEST) imaging with magnetic resonance fingerprinting (MRF).

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8.  Analysis and correction of biases in cross-relaxation MRI due to biexponential longitudinal relaxation.

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