T2 mapping of molecular subtypes of WHO grade II/III gliomas

Abstract Background According to the new WHO classification from 2016, molecular profiles have shown to provide reliable information about prognosis and treatment response. The purpose of our study is to evaluate the diagnostic potential of non-invasive quantitative T2 mapping in the detection of ID...

Full description

Bibliographic Details
Main Authors: Maike Kern, Timo Alexander Auer, Thomas Picht, Martin Misch, Edzard Wiener
Format: Article
Language:English
Published: BMC 2020-01-01
Series:BMC Neurology
Subjects:
MRI
IDH
Online Access:https://doi.org/10.1186/s12883-019-1590-1
id doaj-26fa6c623a6c49c58f714536103c9f3a
record_format Article
spelling doaj-26fa6c623a6c49c58f714536103c9f3a2021-01-10T12:35:48ZengBMCBMC Neurology1471-23772020-01-012011910.1186/s12883-019-1590-1T2 mapping of molecular subtypes of WHO grade II/III gliomasMaike Kern0Timo Alexander Auer1Thomas Picht2Martin Misch3Edzard Wiener4Department of Neuroradiology, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of HealthDepartment of Radiology, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of HealthDepartment of Neurosurgery, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of HealthDepartment of Neurosurgery, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of HealthDepartment of Neuroradiology, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of HealthAbstract Background According to the new WHO classification from 2016, molecular profiles have shown to provide reliable information about prognosis and treatment response. The purpose of our study is to evaluate the diagnostic potential of non-invasive quantitative T2 mapping in the detection of IDH1/2 mutation status in grade II-III gliomas. Methods Retrospective evaluation of MR examinations in 30 patients with histopathological proven WHO-grade II (n = 9) and III (n = 21) astrocytomas (18 IDH-mutated, 12 IDH-wildtype). Consensus annotation by two observers by use of ROI’s in quantitative T2-mapping sequences were performed in all patients. T2 relaxation times were measured pixelwise. Results A significant difference (p = 0,0037) between the central region of IDH-mutated tumors (356,83 ± 114,97 ms) and the IDH-wildtype (199,92 ± 53,13 ms) was found. Furthermore, relaxation times between the central region (322,62 ± 127,41 ms) and the peripheral region (211,1 ± 74,16 ms) of WHO grade II and III astrocytomas differed significantly (p = 0,0021). The central regions relaxation time of WHO-grade II (227,44 ± 80,09 ms) and III gliomas (322,62 ± 127,41 ms) did not differ significantly (p = 0,2276). The difference between the smallest and the largest T2 value (so called “range”) is significantly larger (p = 0,0017) in IDH-mutated tumors (230,89 ± 121,11 ms) than in the IDH-wildtype (96,33 ± 101,46 ms). Interobserver variability showed no significant differences. Conclusions Quantitative evaluation of T2-mapping relaxation times shows significant differences regarding the IDH-status in WHO grade II and III gliomas adding important information regarding the new 2016 World Health Organization (WHO) Classification of tumors of the central nervous system. This to our knowledge is the first study regarding T2 mapping and the IDH1/2 status shows that the mutational status seems to be more important for the appearance on T2 images than the WHO grade.https://doi.org/10.1186/s12883-019-1590-1GliomasMRIIDHT2-mapping
collection DOAJ
language English
format Article
sources DOAJ
author Maike Kern
Timo Alexander Auer
Thomas Picht
Martin Misch
Edzard Wiener
spellingShingle Maike Kern
Timo Alexander Auer
Thomas Picht
Martin Misch
Edzard Wiener
T2 mapping of molecular subtypes of WHO grade II/III gliomas
BMC Neurology
Gliomas
MRI
IDH
T2-mapping
author_facet Maike Kern
Timo Alexander Auer
Thomas Picht
Martin Misch
Edzard Wiener
author_sort Maike Kern
title T2 mapping of molecular subtypes of WHO grade II/III gliomas
title_short T2 mapping of molecular subtypes of WHO grade II/III gliomas
title_full T2 mapping of molecular subtypes of WHO grade II/III gliomas
title_fullStr T2 mapping of molecular subtypes of WHO grade II/III gliomas
title_full_unstemmed T2 mapping of molecular subtypes of WHO grade II/III gliomas
title_sort t2 mapping of molecular subtypes of who grade ii/iii gliomas
publisher BMC
series BMC Neurology
issn 1471-2377
publishDate 2020-01-01
description Abstract Background According to the new WHO classification from 2016, molecular profiles have shown to provide reliable information about prognosis and treatment response. The purpose of our study is to evaluate the diagnostic potential of non-invasive quantitative T2 mapping in the detection of IDH1/2 mutation status in grade II-III gliomas. Methods Retrospective evaluation of MR examinations in 30 patients with histopathological proven WHO-grade II (n = 9) and III (n = 21) astrocytomas (18 IDH-mutated, 12 IDH-wildtype). Consensus annotation by two observers by use of ROI’s in quantitative T2-mapping sequences were performed in all patients. T2 relaxation times were measured pixelwise. Results A significant difference (p = 0,0037) between the central region of IDH-mutated tumors (356,83 ± 114,97 ms) and the IDH-wildtype (199,92 ± 53,13 ms) was found. Furthermore, relaxation times between the central region (322,62 ± 127,41 ms) and the peripheral region (211,1 ± 74,16 ms) of WHO grade II and III astrocytomas differed significantly (p = 0,0021). The central regions relaxation time of WHO-grade II (227,44 ± 80,09 ms) and III gliomas (322,62 ± 127,41 ms) did not differ significantly (p = 0,2276). The difference between the smallest and the largest T2 value (so called “range”) is significantly larger (p = 0,0017) in IDH-mutated tumors (230,89 ± 121,11 ms) than in the IDH-wildtype (96,33 ± 101,46 ms). Interobserver variability showed no significant differences. Conclusions Quantitative evaluation of T2-mapping relaxation times shows significant differences regarding the IDH-status in WHO grade II and III gliomas adding important information regarding the new 2016 World Health Organization (WHO) Classification of tumors of the central nervous system. This to our knowledge is the first study regarding T2 mapping and the IDH1/2 status shows that the mutational status seems to be more important for the appearance on T2 images than the WHO grade.
topic Gliomas
MRI
IDH
T2-mapping
url https://doi.org/10.1186/s12883-019-1590-1
work_keys_str_mv AT maikekern t2mappingofmolecularsubtypesofwhogradeiiiiigliomas
AT timoalexanderauer t2mappingofmolecularsubtypesofwhogradeiiiiigliomas
AT thomaspicht t2mappingofmolecularsubtypesofwhogradeiiiiigliomas
AT martinmisch t2mappingofmolecularsubtypesofwhogradeiiiiigliomas
AT edzardwiener t2mappingofmolecularsubtypesofwhogradeiiiiigliomas
_version_ 1724342520510414848