Quantitative assessment of demyelination in ischemic stroke in vivo using macromolecular proton fraction mapping; Journal of Cerebral Blood Flow and Metabolism; Vol. 38, iss. 5

Bibliografiske detaljer
Parent link:Journal of Cerebral Blood Flow and Metabolism
Vol. 38, iss. 5.— 2018.— [P. 919-931]
Institution som forfatter: Национальный исследовательский Томский политехнический университет Инженерная школа новых производственных технологий Научно-образовательный центр Н. М. Кижнера
Andre forfattere: Khodanovich M. Yu. Marina Yurjevna, Kisel A. A. Alena Andreevna, Akulov A. E. Andrey Evgenjevich, Atochin D. N. Dmitry Nikolaevich, Kudabaeva M. S. Marina Stanislavovna
Summary:Title screen
A recent MRI method, fast macromolecular proton fraction (MPF) mapping, was used to quantify demyelination in the transient middle cerebral artery occlusion (MCAO) rat stroke model. MPF and other quantitative MRI parameters (T1, T2, proton density, and apparent diffusion coefficient) were compared with histological and immunohistochemical markers of demyelination (Luxol Fast Blue stain, (LFB)), neuronal loss (NeuN immunofluorescence), axonal loss (Bielschowsky stain), and inflammation (Iba1 immunofluorescence) in three animal groups (n = 5 per group) on the 1st, 3rd, and 10th day after MCAO. MPF and LFB optical density (OD) were significantly reduced in the ischemic lesion on all days after MCAO relative to the symmetrical regions of the contralateral hemisphere. Percentage changes in MPF and LFB OD in the ischemic lesion relative to the contralateral hemisphere significantly differed on the first day only. Percentage changes in LFB OD and MPF were strongly correlated (R = 0.81, P < 0.001) and did not correlate with other MRI parameters. MPF also did not correlate with other histological variables. Addition of T2 into multivariate regression further improved agreement between MPF and LFB OD (R = 0.89, P < 0.001) due to correction of the edema effect. This study provides histological validation of MPF as an imaging biomarker of demyelination in ischemic stroke.
Sprog:engelsk
Udgivet: 2018
Fag:
Online adgang:https://doi.org/10.1177%2F0271678X18755203
Format: MixedMaterials Electronisk Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=659322

MARC

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200 1 |a Quantitative assessment of demyelination in ischemic stroke in vivo using macromolecular proton fraction mapping  |f M. Yu. Khodanovich [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: 47 tit.] 
330 |a A recent MRI method, fast macromolecular proton fraction (MPF) mapping, was used to quantify demyelination in the transient middle cerebral artery occlusion (MCAO) rat stroke model. MPF and other quantitative MRI parameters (T1, T2, proton density, and apparent diffusion coefficient) were compared with histological and immunohistochemical markers of demyelination (Luxol Fast Blue stain, (LFB)), neuronal loss (NeuN immunofluorescence), axonal loss (Bielschowsky stain), and inflammation (Iba1 immunofluorescence) in three animal groups (n = 5 per group) on the 1st, 3rd, and 10th day after MCAO. MPF and LFB optical density (OD) were significantly reduced in the ischemic lesion on all days after MCAO relative to the symmetrical regions of the contralateral hemisphere. Percentage changes in MPF and LFB OD in the ischemic lesion relative to the contralateral hemisphere significantly differed on the first day only. Percentage changes in LFB OD and MPF were strongly correlated (R = 0.81, P < 0.001) and did not correlate with other MRI parameters. MPF also did not correlate with other histological variables. Addition of T2 into multivariate regression further improved agreement between MPF and LFB OD (R = 0.89, P < 0.001) due to correction of the edema effect. This study provides histological validation of MPF as an imaging biomarker of demyelination in ischemic stroke. 
461 |t Journal of Cerebral Blood Flow and Metabolism 
463 |t Vol. 38, iss. 5  |v [P. 919-931]  |d 2018 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a macromolecular proton fraction 
610 1 |a middle cerebral artery occlusion 
610 1 |a myelin 
610 1 |a magnetic resonance imaging 
610 1 |a histology 
610 1 |a макромолекулярные реакции 
610 1 |a магнитно-резонансная томография 
610 1 |a гистология 
701 1 |a Khodanovich  |b M. Yu.  |g Marina Yurjevna 
701 1 |a Kisel  |b A. A.  |g Alena Andreevna 
701 1 |a Akulov  |b A. E.  |g Andrey Evgenjevich 
701 1 |a Atochin  |b D. N.  |c neuroscientist  |c The Head of the Laboratory of Tomsk Polytechnic University  |f 1960-  |g Dmitry Nikolaevich  |3 (RuTPU)RU\TPU\pers\37514 
701 1 |a Kudabaeva  |b M. S.  |g Marina Stanislavovna 
712 0 2 |a Национальный исследовательский Томский политехнический университет  |b Инженерная школа новых производственных технологий  |b Научно-образовательный центр Н. М. Кижнера  |3 (RuTPU)RU\TPU\col\23556 
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