Elevated T2-values in MRI of stroke patients shortly after symptom onset do not predict irreversible tissue infarction.

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Elevated T2-values in MRI of stroke patients shortly after symptom onset do not predict irreversible tissue infarction. / Siemonsen, Susanne; Löbel, Ulrike; Sedlacik, Jan; Forkert, Nils; Mouridsen, Kim; Østergaard, Leif; Thomalla, Götz; Fiehler, Jens.

in: BRAIN, Jahrgang 135, Nr. Pt 6, Pt 6, 2012, S. 1981-1989.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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Siemonsen S, Löbel U, Sedlacik J, Forkert N, Mouridsen K, Østergaard L et al. Elevated T2-values in MRI of stroke patients shortly after symptom onset do not predict irreversible tissue infarction. BRAIN. 2012;135(Pt 6):1981-1989. Pt 6.

Bibtex

@article{df7e24d35b3f46ab94ecc17d6aa453aa,
title = "Elevated T2-values in MRI of stroke patients shortly after symptom onset do not predict irreversible tissue infarction.",
abstract = "Distinct from signal alterations in diffusion-weighted images, T(2)-values are also dependent on tissue water content and known to increase with time from symptom onset in acute ischaemic stroke. The purpose of this study was to evaluate whether there is a detectable increase of T(2)-values in different regions in acute ischaemic stroke in the acute and subacute situation and to study the effect of recanalization on the evaluation of T(2)-values in the subacute phase. In addition, we sought to evaluate whether this increase in T(2)-values is reversible. For this purpose, 22 patients with acute ischaemic stroke in the territory of the middle cerebral artery underwent magnetic resonance imaging including diffusion-weighted imaging, perfusion-weighted imaging, fluid-attenuated inversion recovery to determine final infarct size, time-of-flight-angiography (acute and on day 1 or 2) and a triple echo-T(2)-sequence (calculation of T(2) maps) within 6?h after symptom onset. Images were co-registered and regions of diffusion restriction and prolonged time-to-peak as well as surviving tissue (surviving tissue?=?time-to-peak - final infarct size) and lesion growth (lesion growth?=?final infarct size-diffusion restriction) were defined and superimposed onto the quantitative T(2) map. In addition, patients were dichotomized according to recanalization information. Mean quantitative T(2)-values were derived for each patient within each region of interest. Mean T(2)-values for patients with recanalization (n?=?15) in surviving tissue region of interest were 115.8?±?7.2?ms (mean?±?SD) and in the lesion growth region of interest 114.6?±?7.0?ms. T(2)-values for patients without recanalization (n?=?7) were 117.7?±?11.4?ms in surviving tissue region of interest and 117.3?±?12.1?ms in lesion growth region of interest. There was no significant difference between T(2)-values measured in lesion growth and surviving tissue region of interest for patients with or without recanalization. Even though it has been shown that T(2)-values increase with time from symptom onset within the infarct core, increased T(2)-values in areas of perfusion impairment do not identify irreversible damaged brain tissue and high T(2)-values are even found in tissue that is not part of the final infarct lesion and can therefore normalize. In conclusion, this study suggests that T(2)-values are not a valid imaging biomarker in acute stroke to predict tissue outcome.",
keywords = "Adult, Humans, Male, Aged, Female, Middle Aged, Aged, 80 and over, Reproducibility of Results, Predictive Value of Tests, Follow-Up Studies, Time Factors, Analysis of Variance, Functional Laterality, Brain/*pathology, *Brain Mapping, *Image Processing, Computer-Assisted, *Magnetic Resonance Imaging, Diffusion, Reading, Stroke/*pathology/physiopathology, Adult, Humans, Male, Aged, Female, Middle Aged, Aged, 80 and over, Reproducibility of Results, Predictive Value of Tests, Follow-Up Studies, Time Factors, Analysis of Variance, Functional Laterality, Brain/*pathology, *Brain Mapping, *Image Processing, Computer-Assisted, *Magnetic Resonance Imaging, Diffusion, Reading, Stroke/*pathology/physiopathology",
author = "Susanne Siemonsen and Ulrike L{\"o}bel and Jan Sedlacik and Nils Forkert and Kim Mouridsen and Leif {\O}stergaard and G{\"o}tz Thomalla and Jens Fiehler",
year = "2012",
language = "English",
volume = "135",
pages = "1981--1989",
journal = "BRAIN",
issn = "0006-8950",
publisher = "Oxford University Press",
number = "Pt 6",

}

RIS

TY - JOUR

T1 - Elevated T2-values in MRI of stroke patients shortly after symptom onset do not predict irreversible tissue infarction.

AU - Siemonsen, Susanne

AU - Löbel, Ulrike

AU - Sedlacik, Jan

AU - Forkert, Nils

AU - Mouridsen, Kim

AU - Østergaard, Leif

AU - Thomalla, Götz

AU - Fiehler, Jens

PY - 2012

Y1 - 2012

N2 - Distinct from signal alterations in diffusion-weighted images, T(2)-values are also dependent on tissue water content and known to increase with time from symptom onset in acute ischaemic stroke. The purpose of this study was to evaluate whether there is a detectable increase of T(2)-values in different regions in acute ischaemic stroke in the acute and subacute situation and to study the effect of recanalization on the evaluation of T(2)-values in the subacute phase. In addition, we sought to evaluate whether this increase in T(2)-values is reversible. For this purpose, 22 patients with acute ischaemic stroke in the territory of the middle cerebral artery underwent magnetic resonance imaging including diffusion-weighted imaging, perfusion-weighted imaging, fluid-attenuated inversion recovery to determine final infarct size, time-of-flight-angiography (acute and on day 1 or 2) and a triple echo-T(2)-sequence (calculation of T(2) maps) within 6?h after symptom onset. Images were co-registered and regions of diffusion restriction and prolonged time-to-peak as well as surviving tissue (surviving tissue?=?time-to-peak - final infarct size) and lesion growth (lesion growth?=?final infarct size-diffusion restriction) were defined and superimposed onto the quantitative T(2) map. In addition, patients were dichotomized according to recanalization information. Mean quantitative T(2)-values were derived for each patient within each region of interest. Mean T(2)-values for patients with recanalization (n?=?15) in surviving tissue region of interest were 115.8?±?7.2?ms (mean?±?SD) and in the lesion growth region of interest 114.6?±?7.0?ms. T(2)-values for patients without recanalization (n?=?7) were 117.7?±?11.4?ms in surviving tissue region of interest and 117.3?±?12.1?ms in lesion growth region of interest. There was no significant difference between T(2)-values measured in lesion growth and surviving tissue region of interest for patients with or without recanalization. Even though it has been shown that T(2)-values increase with time from symptom onset within the infarct core, increased T(2)-values in areas of perfusion impairment do not identify irreversible damaged brain tissue and high T(2)-values are even found in tissue that is not part of the final infarct lesion and can therefore normalize. In conclusion, this study suggests that T(2)-values are not a valid imaging biomarker in acute stroke to predict tissue outcome.

AB - Distinct from signal alterations in diffusion-weighted images, T(2)-values are also dependent on tissue water content and known to increase with time from symptom onset in acute ischaemic stroke. The purpose of this study was to evaluate whether there is a detectable increase of T(2)-values in different regions in acute ischaemic stroke in the acute and subacute situation and to study the effect of recanalization on the evaluation of T(2)-values in the subacute phase. In addition, we sought to evaluate whether this increase in T(2)-values is reversible. For this purpose, 22 patients with acute ischaemic stroke in the territory of the middle cerebral artery underwent magnetic resonance imaging including diffusion-weighted imaging, perfusion-weighted imaging, fluid-attenuated inversion recovery to determine final infarct size, time-of-flight-angiography (acute and on day 1 or 2) and a triple echo-T(2)-sequence (calculation of T(2) maps) within 6?h after symptom onset. Images were co-registered and regions of diffusion restriction and prolonged time-to-peak as well as surviving tissue (surviving tissue?=?time-to-peak - final infarct size) and lesion growth (lesion growth?=?final infarct size-diffusion restriction) were defined and superimposed onto the quantitative T(2) map. In addition, patients were dichotomized according to recanalization information. Mean quantitative T(2)-values were derived for each patient within each region of interest. Mean T(2)-values for patients with recanalization (n?=?15) in surviving tissue region of interest were 115.8?±?7.2?ms (mean?±?SD) and in the lesion growth region of interest 114.6?±?7.0?ms. T(2)-values for patients without recanalization (n?=?7) were 117.7?±?11.4?ms in surviving tissue region of interest and 117.3?±?12.1?ms in lesion growth region of interest. There was no significant difference between T(2)-values measured in lesion growth and surviving tissue region of interest for patients with or without recanalization. Even though it has been shown that T(2)-values increase with time from symptom onset within the infarct core, increased T(2)-values in areas of perfusion impairment do not identify irreversible damaged brain tissue and high T(2)-values are even found in tissue that is not part of the final infarct lesion and can therefore normalize. In conclusion, this study suggests that T(2)-values are not a valid imaging biomarker in acute stroke to predict tissue outcome.

KW - Adult

KW - Humans

KW - Male

KW - Aged

KW - Female

KW - Middle Aged

KW - Aged, 80 and over

KW - Reproducibility of Results

KW - Predictive Value of Tests

KW - Follow-Up Studies

KW - Time Factors

KW - Analysis of Variance

KW - Functional Laterality

KW - Brain/pathology

KW - Brain Mapping

KW - Image Processing, Computer-Assisted

KW - Magnetic Resonance Imaging

KW - Diffusion

KW - Reading

KW - Stroke/pathology/physiopathology

KW - Adult

KW - Humans

KW - Male

KW - Aged

KW - Female

KW - Middle Aged

KW - Aged, 80 and over

KW - Reproducibility of Results

KW - Predictive Value of Tests

KW - Follow-Up Studies

KW - Time Factors

KW - Analysis of Variance

KW - Functional Laterality

KW - Brain/pathology

KW - Brain Mapping

KW - Image Processing, Computer-Assisted

KW - Magnetic Resonance Imaging

KW - Diffusion

KW - Reading

KW - Stroke/pathology/physiopathology

M3 - SCORING: Journal article

VL - 135

SP - 1981

EP - 1989

JO - BRAIN

JF - BRAIN

SN - 0006-8950

IS - Pt 6

M1 - Pt 6

ER -