Multicomponent T

DTI MWI T2 diffusion tensor imaging multicomponent myelin water imaging proton therapy radiotherapy relaxation

Journal

Magnetic resonance in medicine
ISSN: 1522-2594
Titre abrégé: Magn Reson Med
Pays: United States
ID NLM: 8505245

Informations de publication

Date de publication:
12 2021
Historique:
revised: 21 05 2021
received: 20 04 2021
accepted: 14 06 2021
pubmed: 17 7 2021
medline: 1 2 2022
entrez: 16 7 2021
Statut: ppublish

Résumé

To investigate MRI myelin water imaging (MWI) by multicomponent T Sixteen patients underwent fractionated proton therapy (PT) receiving dose to the healthy tissue because of direct or indirect (base skull tumors) irradiation. MWI was performed by a multi-echo sequence with 32 equally spaced echoes (10-320 ms). Decay data were processed to identify 3 T Mw difference showed a positive correlation and IEw difference showed a negative correlation with BED considering end-pre changes (P < .01). The changes in CSFw were not significantly correlated with the delivered BED. The changes in DTI data, considering end-pre acquisitions, showed a positive correlation between fractional anisotropy and the delivered BED. MWI might detect early white matter radiation-induced alterations, providing additional information to DTI, which might improve the understanding of the pathogenesis of the radiation damage.

Identifiants

pubmed: 34268786
doi: 10.1002/mrm.28913
doi:

Substances chimiques

Protons 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3236-3245

Informations de copyright

© 2021 International Society for Magnetic Resonance in Medicine.

Références

Sheline GE, Wara WM, Smith V. Therapeutic irradiation and brain injury. Int J Radiat Oncol Biol Phys. 1980;6:1215-1228.
Wong CS, Van der Kogel AJ. Mechanisms of radiation injury to the central nervous system: implications for neuroprotection. Mol Interventions. 2004;4:273-284.
Soussain C, Ricard D, Fike JR, Mazeron JJ, Psimaras D, Delattre JY. CNS complications of radiotherapy and chemotherapy. Lancet. 2009;374:1639-1651.
Bentzen SM. Preventing or reducing late side effects of radiation therapy: radiobiology meets molecular pathology. Nat Rev Cancer. 2006;6:702-713.
Tofilon PJ, Fike JR. The radioresponse of the central nervous system: a dynamic process. Radiat Res. 2000;153:357-370.
Freeman JE, Johnston PG, Voke JM. Somnolence after prophylactic cranial irradiation in children with acute lymphoblastic leukaemia. Br Med J. 1973;4:523-525.
Chapman CH, Zhu T, Nazem-Zadeh M, et al. Diffusion tensor imaging predicts cognitive function change following partial brain radiotherapy for low-grade and benign tumors. Radiother Oncol. 2016;120:234-240.
Schultheiss TE, Stephens LC, Maor MH. Analysis of the histopathology of radiation myelopathy. Int J Radiat Oncol Biol Phys. 1988;27:27-32.
Lee J, Hyun J-W, Lee J, et al. So you want to image myelin using MRI: an overview and practical guide for myelin water imaging. J Magn Reson Imaging. 2021;53(2):360-373.
Heath F, Hurley SA, Johansen-Berg H, Sampaio-Baptista C. Advances in noninvasive myelin imaging. Dev Neurobiol. 2018;78:136-151.
Laule C, Vavasour IM, Kolind SH, et al. Magnetic resonance imaging of myelin. Neurotherapeutics. 2007;4:460-484. Review.
Alonso-Ortiz E, Levesque IR, Pike GB. MRI-based myelin water imaging: a technical review. Magn Reson Med. 2015;73:70-81.
MacKay AL, Laule C. Magnetic resonance of myelin water: an in vivo marker for myelin. Brain Plast. 2016;2:71-91.
Chapman CH, Nagesh V, Sundgren PC, et al. Diffusion tensor imaging of normal-appearing white matter as biomarker for radiation-induced late delayed cognitive decline. Int J Radiat Oncol Biol Phys. 2012;82:2033-2040.
Chapman CH, Nazem-Zadeh M, Lee OE, et al. Regional variation in brain white matter diffusion index changes following chemoradiotherapy: a prospective study using tract-based spatial statistics. PLoS One. 2013;8:e57768.
Connor M, Karunamuni R, McDonald C, et al. Dose-dependent white matter damage after brain radiotherapy. Radiother Oncol. 2016;121:209-216.
Karunamuni RA, White NS, McDonald CR, et al. Multi-component diffusion characterization of radiation-induced white matter damage. Med Phys. 2017;44:1747-1754.
Raschke F, Wesemann T, Wahl H, et al. Reduced diffusion in normal appearing white matter of glioma patients following radio(chemo)therapy. Radiother Oncol. 2019;140:110-115.
Zhu T, Chapman CH, Tsien C, et al. Effect of the maximum dose on white matter fiber bundles using longitudinal diffusion tensor imaging. Int J Radiat Oncol Biol Phys. 2016;96:696-705.
Connor M, Karunamuni R, McDonald C, et al. Regional susceptibility to dose-dependent white matter damage after brain radiotherapy. Radiother Oncol. 2017;123:209-217.
Uh J, Merchant TE, Li Y, et al. Differences in brainstem fiber tract response to radiation: a longitudinal diffusion tensor imaging study. Int J Radiat Oncol Biol Phys. 2013;86:292-297.
Hua C, Merchant TE, Gajjar A, et al. Brain tumor therapy-induced changes in normal-appearing brainstem measured with longitudinal diffusion tensor imaging. Int J Radiat Oncol Biol Phys. 2012;82:2047-2054.
Leung LH, Ooi GC, Kwong DL, Chan GC, Cao G, Khong PL. White-matter diffusion anisotropy after chemo-irradiation: a statistical parametric mapping study and histogram analysis. Neuroimage. 2004;21:261-268.
Qiu D, Leung LH, Kwong DL, Chan GC, Khong PL. Mapping radiation dose distribution on the fractional anisotropy map: applications in the assessment of treatment-induced white matter injury. Neuroimage. 2006;31:109-115.
Andersson JL, Skare S, Ashburner J. How to correct susceptibility distortions in spin-echo echo-planar images: application to diffusion tensor imaging. Neuroimage. 2003;20:870-888.
Smith SM, Jenkinson M, Woolrich MW, et al. Advances in functional and structural MR image analysis and implementation as FSL. Neuroimage. 2004;23:S208-S219.
MERA. Multi Exponential Relaxation Analysis toolbox for MATLAB. Free download available at https://github.com/markdoes/MERA.
Prasloski T, Mädler B, Xiang QS, MacKay A, Jones C. Applications of stimulated echo correction to multicomponent T2 analysis. Magn Reson Med. 2012;67:1803-1814.
Meyers SM, Laule C, Vavasour IM, et al. Reproducibility of myelin water fraction analysis: a comparison of region of interest and voxel-based analysis methods. Magn Reson Imaging. 2009;27:1096-1103.
Stewart WA, MacKay AL, Whittall KP, Moore GR, Paty DW. Spin-spin relaxation in experimental allergic encephalomyelitis. Analysis of CPMG data using a non-linear least squares method and linear inverse theory. Magn Reson Med. 1993;29:767-775.
Andersson JLR, Sotiropoulos SN. An integrated approach to correction for off-resonance effects and subject movement in diffusion MR imaging. Neuroimage. 2016;15:1063-1078.
Jenkinson M, Bannister P, Brady M, Smith S. Improved optimization for the robust and accurate linear registration and motion correction of brain images. Neuroimage. 2002;17:825-841.
Hope TR, Vardal J, Bjørnerud A, et al. Serial diffusion tensor imaging for early detection of radiation-induced injuries to normal-appearing white matter in high-grade glioma patients. J Magn Reson Imaging. 2015;41:414-423.
Ding Z, Zhang H, Lv X-F, et al. Radiation-induced brain structural and functional abnormalities in presymptomatic phase and outcome prediction. Hum Brain Mapp. 2018;39:407-427.
Cao Y, Tsien CI, Sundgren PC, et al. Dynamic contrast-enhanced magnetic resonance imaging as a biomarker for prediction of radiation-induced neurocognitive dysfunction. Clin Cancer Res. 2009;15:1747-1754.
Farjam R, Pramanik P, Aryal MP, et al. A radiation-induced hippocampal vascular injury surrogate marker predicts late neurocognitive dysfunction. Int J Radiat Oncol Biol Phys. 2015;93:908-915.
Petr J, Platzek I, Seidlitz A, et al. Early and late effects of radiochemotherapy on cerebral blood flow in glioblastoma patients measured with non-invasive perfusion MRI. Radiother Oncol. 2016;118:24-28.
Bontempi P, Rozzanigo U, Amelio D, Scartoni D, Amichetti M, Farace P. Quantitative multicomponent T2 relaxation showed greater sensitivity than flair imaging to detect subtle alterations at the periphery of lower grade gliomas. Front Oncol. 2021;22:651137.

Auteurs

Pietro Bontempi (P)

Proton Therapy Unit, Hospital of Trento, Azienda Provinciale per i Servizi Sanitari (APSS), Trento, Italy.

Daniele Scartoni (D)

Proton Therapy Unit, Hospital of Trento, Azienda Provinciale per i Servizi Sanitari (APSS), Trento, Italy.

Dante Amelio (D)

Proton Therapy Unit, Hospital of Trento, Azienda Provinciale per i Servizi Sanitari (APSS), Trento, Italy.

Marco Cianchetti (M)

Proton Therapy Unit, Hospital of Trento, Azienda Provinciale per i Servizi Sanitari (APSS), Trento, Italy.

Ana Turkaj (A)

Proton Therapy Unit, Hospital of Trento, Azienda Provinciale per i Servizi Sanitari (APSS), Trento, Italy.

Maurizio Amichetti (M)

Proton Therapy Unit, Hospital of Trento, Azienda Provinciale per i Servizi Sanitari (APSS), Trento, Italy.

Paolo Farace (P)

Proton Therapy Unit, Hospital of Trento, Azienda Provinciale per i Servizi Sanitari (APSS), Trento, Italy.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH