Literature DB >> 29221966

Lesion magnetic susceptibility response to hyperoxic challenge: A biomarker for malignant brain tumor microenvironment?

Pinar Senay Özbay1, Sonja Stieb2, Cristina Rossi3, Oliver Riesterer2, Andreas Boss3, Tobias Weiss4, Felix Pierre Kuhn5, Klaas Paul Pruessmann6, Daniel Nanz7.   

Abstract

BACKGROUND AND
PURPOSE: Quantitative susceptibility mapping has been previously used to differentiate lesions in patients with brain tumors. The aim of this work was to characterize the response of magnetic susceptibility differences in malignant brain tumors and surrounding edema to hyperoxic and hypercapnic respiratory challenges.
METHODS: Images of malignant brain tumor patients (2 glioblastoma multiforme, 2 anaplastic astrocytoma, 1 brain metastasis) with clinical MRI exams (contrast-enhanced T1w) were acquired at 3T. 3D multi-gradient-echo data sets were acquired while the patients inhaled medical-air (21% O2), oxygen (100% O2), and carbogen (95% O2, 5% CO2). Susceptibility maps were generated from real and imaginary data. Regions of interest were analyzed with respect to respiration-gas-induced susceptibility changes.
RESULTS: Contrast-enhancing tumor regions with high baseline magnetic susceptibility exhibited a marked susceptibility reduction under hyperoxic challenges, with a stronger effect (-0.040 to -0.100ppm) under hypercapnia compared to hyperoxia (-0.010 to -0.067ppm). In contrast, regions attributed to necrotic tissue and to edema showed smaller changes of opposite sign, i.e. paramagnetic shift. There was a correlation between malignant tumor tissue magnetic susceptibility at baseline under normoxia and the corresponding susceptibility reduction under hypercapnia and - to a lesser degree - under hyperoxia.
CONCLUSION: In this small cohort of analysis, quantification of susceptibility changes in response to respiratory challenges allowed a complementary, functional differentiation of tumorous sub-regions. Those changes, together with the correlations observed between baseline susceptibility under normoxia and susceptibility reduction with challenges, could prove helpful for a non-invasive characterization of local tumor microenvironment.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Glioblastoma; Hyperoxia; Magnetic susceptibility; Oxygenation; Quantitative susceptibility mapping

Mesh:

Substances:

Year:  2017        PMID: 29221966      PMCID: PMC5831359          DOI: 10.1016/j.mri.2017.12.004

Source DB:  PubMed          Journal:  Magn Reson Imaging        ISSN: 0730-725X            Impact factor:   2.546


  23 in total

1.  The concentration of oxygen dissolved in tissues at the time of irradiation as a factor in radiotherapy.

Authors:  L H GRAY; A D CONGER; M EBERT; S HORNSEY; O C SCOTT
Journal:  Br J Radiol       Date:  1953-12       Impact factor: 3.039

2.  Vascular component analysis of hyperoxic and hypercapnic BOLD contrast.

Authors:  Christian Schwarzbauer; Ralf Deichmann
Journal:  Neuroimage       Date:  2011-09-18       Impact factor: 6.556

3.  The effect of dissolved oxygen on the susceptibility of blood.

Authors:  Avery J L Berman; Yuhan Ma; Richard D Hoge; G Bruce Pike
Journal:  Magn Reson Med       Date:  2015-03-06       Impact factor: 4.668

4.  Reproducibility of quantitative susceptibility mapping in the brain at two field strengths from two vendors.

Authors:  Kofi Deh; Thanh D Nguyen; Sarah Eskreis-Winkler; Martin R Prince; Pascal Spincemaille; Susan Gauthier; Ilhami Kovanlikaya; Yan Zhang; Yi Wang
Journal:  J Magn Reson Imaging       Date:  2015-05-09       Impact factor: 4.813

5.  Determination of the maturity and functionality of tumor vasculature by MRI: correlation between BOLD-MRI and DCE-MRI using P792 in experimental fibrosarcoma tumors.

Authors:  Christine Baudelet; Gregory O Cron; Bernard Gallez
Journal:  Magn Reson Med       Date:  2006-11       Impact factor: 4.668

6.  Investigation of the influence of carbon dioxide concentrations on cerebral physiology by susceptibility-weighted magnetic resonance imaging (SWI).

Authors:  Jan Sedlacik; Christian Kutschbach; Alexander Rauscher; Andreas Deistung; Jürgen R Reichenbach
Journal:  Neuroimage       Date:  2008-07-18       Impact factor: 6.556

7.  Intratumoral oxygen pressure in malignant brain tumor.

Authors:  T Kayama; T Yoshimoto; S Fujimoto; Y Sakurai
Journal:  J Neurosurg       Date:  1991-01       Impact factor: 5.115

Review 8.  Radiotherapy after hyperbaric oxygenation in malignant gliomas.

Authors:  Jun-rui Chen; Hong-zhi Xu; Jian-bo Ding; Zhi-yong Qin
Journal:  Curr Med Res Opin       Date:  2015-09-28       Impact factor: 2.580

9.  Mapping of global R1 and R2* values versus lipids R1 values as potential markers of hypoxia in human glial tumors: A feasibility study.

Authors:  Marta M Safronova; Florence Colliez; Julie Magat; Nicolas Joudiou; Bénédicte F Jordan; Christian Raftopoulos; Bernard Gallez; Thierry Duprez
Journal:  Magn Reson Imaging       Date:  2015-10-30       Impact factor: 2.546

10.  Effects of radiotherapy after hyperbaric oxygenation on malignant gliomas.

Authors:  K Kohshi; Y Kinoshita; H Imada; N Kunugita; H Abe; H Terashima; N Tokui; S Uemura
Journal:  Br J Cancer       Date:  1999-04       Impact factor: 7.640

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  1 in total

1.  Feasibility of glioblastoma tissue response mapping with physiologic BOLD imaging using precise oxygen and carbon dioxide challenge.

Authors:  Vittorio Stumpo; Martina Sebök; Christiaan Hendrik Bas van Niftrik; Katharina Seystahl; Nicolin Hainc; Zsolt Kulcsar; Michael Weller; Luca Regli; Jorn Fierstra
Journal:  MAGMA       Date:  2021-12-07       Impact factor: 2.310

  1 in total

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