Literature DB >> 16086363

Biexponential parameterization of diffusion and T2 relaxation decay curves in a rat muscle edema model: decay curve components and water compartments.

Zaid Ababneh1, Helene Beloeil, Charles B Berde, Giulio Gambarota, Stephan E Maier, Robert V Mulkern.   

Abstract

Quantitative T2 relaxation and diffusion imaging studies of a rat muscle edema model were performed in order to determine the effects of intra- and extracellular water compartmentation on the respective decay curves. The right hind paw of rats was injected with a carrageenan solution to generate edematous muscle. A Carr-Purcell-Meiboom-Gill (CPMG) imaging sequence was used to acquire T2 relaxation decay curves from both paws. A line scan diffusion imaging (LSDI) sequence was then used to acquire diffusion decay curves from the same paws over a wide b-factor range. Measurements were made from both edematous muscle (EM) and control muscle (CM). The EM and CM T2 relaxation decay curves were best fit with biexponential functions. The fraction of the fast T2 component dropped dramatically from approximately 0.95 in CM to 0.45 in EM, consistent with a water compartmentation model in which the fast and slow T2 components reflect intra- and extracellular water, respectively. Both CM and EM diffusion decay curves required biexponential fitting functions, and the diffusion coefficients of the fast and slow components were substantially larger in EM than CM. The fraction of the fast diffusion component, however, was not radically altered between CM and EM conditions (0.84 versus 0.89 for CM versus EM). Assuming a model in which intra- and extracellular water compartments are responsible for the fast and slow T2-decay components and for the slow and fast diffusion decay components, respectively, leads to fractional sizes of the diffusion components that are not supported by experiment. We conclude that intra- and extracellular water compartmentation is a reasonable interpretation for the two T2-decay components in both CM and EM but that other factors, such as restricted diffusion and/or alternate forms of water compartmentation like surface versus volume water, most probably have profound influences on the precise shapes of the diffusion decay curves, a complete understanding of which will require significant theoretical work. Copyright (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 16086363     DOI: 10.1002/mrm.20610

Source DB:  PubMed          Journal:  Magn Reson Med        ISSN: 0740-3194            Impact factor:   4.668


  36 in total

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Journal:  Tissue Eng Part C Methods       Date:  2012-02-21       Impact factor: 3.056

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Journal:  Magn Reson Imaging       Date:  2011-01-31       Impact factor: 2.546

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4.  Pilot Study of the Use of Hybrid Multidimensional T2-Weighted Imaging-DWI for the Diagnosis of Prostate Cancer and Evaluation of Gleason Score.

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Journal:  AJR Am J Roentgenol       Date:  2016-06-28       Impact factor: 3.959

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Journal:  Magn Reson Med       Date:  2018-04-06       Impact factor: 4.668

6.  Mapping proteoglycan-bound water in cartilage: Improved specificity of matrix assessment using multiexponential transverse relaxation analysis.

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Journal:  Magn Reson Med       Date:  2010-11-30       Impact factor: 4.668

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8.  Age-related differences in diffusion tensor indices and fiber architecture in the medial and lateral gastrocnemius.

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Journal:  J Magn Reson Imaging       Date:  2014-04-28       Impact factor: 4.813

9.  Multi-parametric MRI characterization of inflammation in murine skeletal muscle.

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Journal:  NMR Biomed       Date:  2014-04-29       Impact factor: 4.044

10.  Multicomponent T2 relaxation analysis in cartilage.

Authors:  David A Reiter; Ping-Chang Lin; Kenneth W Fishbein; Richard G Spencer
Journal:  Magn Reson Med       Date:  2009-04       Impact factor: 4.668

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