3D APT and NOE CEST-MRI of healthy volunteers and patients with non-enhancing glioma at 3 T
Magnetic Resonance Materials in Physics, Biology and Medicine, ISSN: 1352-8661, Vol: 35, Issue: 1, Page: 63-73
2022
- 13Citations
- 21Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations13
- Citation Indexes13
- 13
- Captures21
- Readers21
- 21
Article Description
Objective: Clinical application of chemical exchange saturation transfer (CEST) can be performed with investigation of amide proton transfer (APT) and nuclear Overhauser enhancement (NOE) effects. Here, we investigated APT- and NOE-weighted imaging based on advanced CEST metrics to map tumor heterogeneity of non-enhancing glioma at 3 T. Materials and methods: APT- and NOE-weighted maps based on Lorentzian difference (LD) and inverse magnetization transfer ratio (MTR) were acquired with a 3D snapshot CEST acquisition at 3 T. Saturation power was investigated first by varying B (0.5–2 µT) in 5 healthy volunteers then by applying B of 0.5 and 1.5 µT in 10 patients with non-enhancing glioma. Tissue contrast (TC) and contrast-to-noise ratios (CNR) were calculated between glioma and normal appearing white matter (NAWM) and grey matter, in APT- and NOE-weighted images. Volume percentages of the tumor showing hypo/hyperintensity (VP) in APT/NOE-weighted images were calculated for each patient. Results: LD APT resulting from using a B of 1.5 µT was found to provide significant positive TC and MTR NOE (B of 1.5 µT) provided significant negative TC in tissue differentiation. MTR-based NOE imaging under 1.5 µT provided significantly larger VP than MTR APT under 1.5 µT. Conclusion: This work showed that with a rapid CEST acquisition using a B saturation power of 1.5 µT and covering the whole tumor, analysis of both LD APT and MTR NOE allows for observing tumor heterogeneity, which will be beneficial in future studies using CEST-MRI to improve imaging diagnostics for non-enhancing glioma.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85122528029&origin=inward; http://dx.doi.org/10.1007/s10334-021-00996-z; http://www.ncbi.nlm.nih.gov/pubmed/34994858; https://link.springer.com/10.1007/s10334-021-00996-z; https://dx.doi.org/10.1007/s10334-021-00996-z; https://link.springer.com/article/10.1007/s10334-021-00996-z
Springer Science and Business Media LLC
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