MRI Assessment of Ischemic Lesion Evolution within White and Gray Matter

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MRI Assessment of Ischemic Lesion Evolution within White and Gray Matter. / Berner, Lise-Prune; Cho, Tae-Hee; Haesebaert, Julie; Bouvier, Julien; Wiart, Marlène; Hjort, Niels; Klærke Mikkelsen, Irene; Derex, Laurent; Thomalla, Götz; Pedraza, Salvador; Østergaard, Leif; Baron, Jean-Claude; Nighoghossian, Norbert; Berthezène, Yves.

in: CEREBROVASC DIS, Jahrgang 41, Nr. 5-6, 12.02.2016, S. 291-297.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Berner, L-P, Cho, T-H, Haesebaert, J, Bouvier, J, Wiart, M, Hjort, N, Klærke Mikkelsen, I, Derex, L, Thomalla, G, Pedraza, S, Østergaard, L, Baron, J-C, Nighoghossian, N & Berthezène, Y 2016, 'MRI Assessment of Ischemic Lesion Evolution within White and Gray Matter', CEREBROVASC DIS, Jg. 41, Nr. 5-6, S. 291-297. https://doi.org/10.1159/000444131

APA

Berner, L-P., Cho, T-H., Haesebaert, J., Bouvier, J., Wiart, M., Hjort, N., Klærke Mikkelsen, I., Derex, L., Thomalla, G., Pedraza, S., Østergaard, L., Baron, J-C., Nighoghossian, N., & Berthezène, Y. (2016). MRI Assessment of Ischemic Lesion Evolution within White and Gray Matter. CEREBROVASC DIS, 41(5-6), 291-297. https://doi.org/10.1159/000444131

Vancouver

Berner L-P, Cho T-H, Haesebaert J, Bouvier J, Wiart M, Hjort N et al. MRI Assessment of Ischemic Lesion Evolution within White and Gray Matter. CEREBROVASC DIS. 2016 Feb 12;41(5-6):291-297. https://doi.org/10.1159/000444131

Bibtex

@article{40d2074db6e3443b96be1c415fd3b153,
title = "MRI Assessment of Ischemic Lesion Evolution within White and Gray Matter",
abstract = "BACKGROUND: In acute ischemic stroke (AIS), gray matter (GM) and white matter (WM) have different vulnerabilities to ischemia. Thus, we compared the evolution of ischemic lesions within WM and GM using MRI.METHODS: From a European multicenter prospective database (I-KNOW), available T1-weighted images were identified for 50 patients presenting with an anterior AIS and a perfusion weighted imaging (PWI)/diffusion weighted imaging (DWI) mismatch ratio of 1.2 or more. Six lesion compartments were outlined: initial DWI (b = 1,000 s/mm2) lesion, initial PWI-DWI mismatch (Tmax >4 s and DWI-negative), final infarct mapped on 1-month fluid-attenuated inversion recovery (FLAIR) imaging, lesion growth between acute DWI and 1-month FLAIR, DWI lesion reversal at 1 month and salvaged mismatch. The WM and GM were segmented on T1-weighted images, and all images were co-registered within subjects to the baseline MRI. WM and GM proportions were calculated for each compartment.RESULTS: Fifty patients were eligible for the study. Median delay between symptom onset and baseline MRI was 140 min. The percentage of WM was significantly greater in the following compartments: initial mismatch (52.5 vs. 47.5%, p = 0.003), final infarct (56.7 vs. 43.3%, p < 0.001) and lesion growth (58.9 vs. 41.2%, p < 0.001). No significant difference was found between GM and WM percentages within the initial DWI lesion, DWI reversal and salvaged mismatch compartments.CONCLUSIONS: Ischemic lesions may extend preferentially within the WM. Specific therapeutic strategies targeting WM ischemic processes may deserve further investigation.",
author = "Lise-Prune Berner and Tae-Hee Cho and Julie Haesebaert and Julien Bouvier and Marl{\`e}ne Wiart and Niels Hjort and {Kl{\ae}rke Mikkelsen}, Irene and Laurent Derex and G{\"o}tz Thomalla and Salvador Pedraza and Leif {\O}stergaard and Jean-Claude Baron and Norbert Nighoghossian and Yves Berthez{\`e}ne",
note = "{\textcopyright} 2016 S. Karger AG, Basel.",
year = "2016",
month = feb,
day = "12",
doi = "10.1159/000444131",
language = "English",
volume = "41",
pages = "291--297",
journal = "CEREBROVASC DIS",
issn = "1015-9770",
publisher = "S. Karger AG",
number = "5-6",

}

RIS

TY - JOUR

T1 - MRI Assessment of Ischemic Lesion Evolution within White and Gray Matter

AU - Berner, Lise-Prune

AU - Cho, Tae-Hee

AU - Haesebaert, Julie

AU - Bouvier, Julien

AU - Wiart, Marlène

AU - Hjort, Niels

AU - Klærke Mikkelsen, Irene

AU - Derex, Laurent

AU - Thomalla, Götz

AU - Pedraza, Salvador

AU - Østergaard, Leif

AU - Baron, Jean-Claude

AU - Nighoghossian, Norbert

AU - Berthezène, Yves

N1 - © 2016 S. Karger AG, Basel.

PY - 2016/2/12

Y1 - 2016/2/12

N2 - BACKGROUND: In acute ischemic stroke (AIS), gray matter (GM) and white matter (WM) have different vulnerabilities to ischemia. Thus, we compared the evolution of ischemic lesions within WM and GM using MRI.METHODS: From a European multicenter prospective database (I-KNOW), available T1-weighted images were identified for 50 patients presenting with an anterior AIS and a perfusion weighted imaging (PWI)/diffusion weighted imaging (DWI) mismatch ratio of 1.2 or more. Six lesion compartments were outlined: initial DWI (b = 1,000 s/mm2) lesion, initial PWI-DWI mismatch (Tmax >4 s and DWI-negative), final infarct mapped on 1-month fluid-attenuated inversion recovery (FLAIR) imaging, lesion growth between acute DWI and 1-month FLAIR, DWI lesion reversal at 1 month and salvaged mismatch. The WM and GM were segmented on T1-weighted images, and all images were co-registered within subjects to the baseline MRI. WM and GM proportions were calculated for each compartment.RESULTS: Fifty patients were eligible for the study. Median delay between symptom onset and baseline MRI was 140 min. The percentage of WM was significantly greater in the following compartments: initial mismatch (52.5 vs. 47.5%, p = 0.003), final infarct (56.7 vs. 43.3%, p < 0.001) and lesion growth (58.9 vs. 41.2%, p < 0.001). No significant difference was found between GM and WM percentages within the initial DWI lesion, DWI reversal and salvaged mismatch compartments.CONCLUSIONS: Ischemic lesions may extend preferentially within the WM. Specific therapeutic strategies targeting WM ischemic processes may deserve further investigation.

AB - BACKGROUND: In acute ischemic stroke (AIS), gray matter (GM) and white matter (WM) have different vulnerabilities to ischemia. Thus, we compared the evolution of ischemic lesions within WM and GM using MRI.METHODS: From a European multicenter prospective database (I-KNOW), available T1-weighted images were identified for 50 patients presenting with an anterior AIS and a perfusion weighted imaging (PWI)/diffusion weighted imaging (DWI) mismatch ratio of 1.2 or more. Six lesion compartments were outlined: initial DWI (b = 1,000 s/mm2) lesion, initial PWI-DWI mismatch (Tmax >4 s and DWI-negative), final infarct mapped on 1-month fluid-attenuated inversion recovery (FLAIR) imaging, lesion growth between acute DWI and 1-month FLAIR, DWI lesion reversal at 1 month and salvaged mismatch. The WM and GM were segmented on T1-weighted images, and all images were co-registered within subjects to the baseline MRI. WM and GM proportions were calculated for each compartment.RESULTS: Fifty patients were eligible for the study. Median delay between symptom onset and baseline MRI was 140 min. The percentage of WM was significantly greater in the following compartments: initial mismatch (52.5 vs. 47.5%, p = 0.003), final infarct (56.7 vs. 43.3%, p < 0.001) and lesion growth (58.9 vs. 41.2%, p < 0.001). No significant difference was found between GM and WM percentages within the initial DWI lesion, DWI reversal and salvaged mismatch compartments.CONCLUSIONS: Ischemic lesions may extend preferentially within the WM. Specific therapeutic strategies targeting WM ischemic processes may deserve further investigation.

U2 - 10.1159/000444131

DO - 10.1159/000444131

M3 - SCORING: Journal article

C2 - 26867026

VL - 41

SP - 291

EP - 297

JO - CEREBROVASC DIS

JF - CEREBROVASC DIS

SN - 1015-9770

IS - 5-6

ER -