Literature DB >> 18228601

Quantitative magnetic resonance of postmortem multiple sclerosis brain before and after fixation.

Klaus Schmierer1, Claudia A M Wheeler-Kingshott, Daniel J Tozer, Phil A Boulby, Harold G Parkes, Tarek A Yousry, Francesco Scaravilli, Gareth J Barker, Paul S Tofts, David H Miller.   

Abstract

Unfixed and fixed postmortem multiple sclerosis (MS) brain is being used to probe pathology underlying quantitative MR (qMR) changes. Effects of fixation on qMR indices in MS brain are unknown. In 15 postmortem MS brain slices T(1), T(2), MT ratio (MTR), macromolecular proton fraction (f(B)), fractional anisotropy (FA), and mean, axial, and radial diffusivity (MD, D(ax), and D(rad)) were assessed in white matter (WM) lesions (WML) and normal appearing WM (NAWM) before and after fixation in formalin. Myelin content, axonal count, and gliosis were quantified histologically. Student's t-test and regression were used for analysis. T(1), T(2), MTR, and f(B) obtained in unfixed MS brain were similar to published values obtained in patients with MS in vivo. Following fixation T(1), T(2) (NAWM, WML) and MTR (NAWM) dropped, whereas f(B) (NAWM, WML) increased. Compared to published in vivo data all diffusivity measures were lower in unfixed MS brain, and dropped further following fixation (except for FA). MTR was the best predictor of T(myelin) (inversely related to myelin) in unfixed MS brain (r = -0.83; P < 0.01) whereas postfixation T(2) (r = 0.92; P < 0.01), T(1) (r = 0.89; P < 0.01), and f(B) (r = -0.86; P < 0.01) were superior. All diffusivity measures (except for D(ax) in unfixed tissue) were predictors of myelin content. (c) 2008 Wiley-Liss, Inc.

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Year:  2008        PMID: 18228601      PMCID: PMC2241759          DOI: 10.1002/mrm.21487

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


  58 in total

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9.  Axonal loss in multiple sclerosis lesions: magnetic resonance imaging insights into substrates of disability.

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  112 in total

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10.  In vivo diffusion tensor imaging and histopathology of the fimbria-fornix in temporal lobe epilepsy.

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