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Article: Deep‐learning‐based super‐resolution for accelerating chemical exchange saturation transfer MRI

TitleDeep‐learning‐based super‐resolution for accelerating chemical exchange saturation transfer MRI
Authors
Keywordsacquisition time
amide CEST (amideCEST)
brain
chemical exchange saturation transfer (CEST)
deep-learning-based super-resolution (DLSR)
relayed nuclear Overhauser effect (rNOE)
Issue Date15-Mar-2024
PublisherWiley
Citation
NMR in Biomedicine, 2024, v. 37, n. 8 How to Cite?
Abstract

Chemical exchange saturation transfer (CEST) MRI is a molecular imaging tool that provides physiological information about tissues, making it an invaluable tool for disease diagnosis and guided treatment. Its clinical application requires the acquisition of high-resolution images capable of accurately identifying subtle regional changes in vivo, while simultaneously maintaining a high level of spectral resolution. However, the acquisition of such high-resolution images is time consuming, presenting a challenge for practical implementation in clinical settings. Among several techniques that have been explored to reduce the acquisition time in MRI, deep-learning-based super-resolution (DLSR) is a promising approach to address this problem due to its adaptability to any acquisition sequence and hardware. However, its translation to CEST MRI has been hindered by the lack of the large CEST datasets required for network development. Thus, we aim to develop a DLSR method, named DLSR-CEST, to reduce the acquisition time for CEST MRI by reconstructing high-resolution images from fast low-resolution acquisitions. This is achieved by first pretraining the DLSR-CEST on human brain T1w and T2w images to initialize the weights of the network and then training the network on very small human and mouse brain CEST datasets to fine-tune the weights. Using the trained DLSR-CEST network, the reconstructed CEST source images exhibited improved spatial resolution in both peak signal-to-noise ratio and structural similarity index measure metrics at all downsampling factors (2–8). Moreover, amide CEST and relayed nuclear Overhauser effect maps extrapolated from the DLSR-CEST source images exhibited high spatial resolution and low normalized root mean square error, indicating a negligible loss in Z-spectrum information. Therefore, our DLSR-CEST demonstrated a robust reconstruction of high-resolution CEST source images from fast low-resolution acquisitions, thereby improving the spatial resolution and preserving most Z-spectrum information.


Persistent Identifierhttp://hdl.handle.net/10722/344238
ISSN
2023 Impact Factor: 2.7
2023 SCImago Journal Rankings: 0.949

 

DC FieldValueLanguage
dc.contributor.authorPemmasani, Prabakaran Rohith Saai-
dc.contributor.authorPark, Se Weon-
dc.contributor.authorLai, Joseph H C-
dc.contributor.authorWang, Kexin-
dc.contributor.authorXu, Jiadi-
dc.contributor.authorChen, Zilin-
dc.contributor.authorIlyas, Abdul‐mojeed Olabisi-
dc.contributor.authorLiu, Huabing-
dc.contributor.authorHuang, Jianpan-
dc.contributor.authorChan, Kannie W Y-
dc.date.accessioned2024-07-16T03:41:53Z-
dc.date.available2024-07-16T03:41:53Z-
dc.date.issued2024-03-15-
dc.identifier.citationNMR in Biomedicine, 2024, v. 37, n. 8-
dc.identifier.issn0952-3480-
dc.identifier.urihttp://hdl.handle.net/10722/344238-
dc.description.abstract<p>Chemical exchange saturation transfer (CEST) MRI is a molecular imaging tool that provides physiological information about tissues, making it an invaluable tool for disease diagnosis and guided treatment. Its clinical application requires the acquisition of high-resolution images capable of accurately identifying subtle regional changes in vivo, while simultaneously maintaining a high level of spectral resolution. However, the acquisition of such high-resolution images is time consuming, presenting a challenge for practical implementation in clinical settings. Among several techniques that have been explored to reduce the acquisition time in MRI, deep-learning-based super-resolution (DLSR) is a promising approach to address this problem due to its adaptability to any acquisition sequence and hardware. However, its translation to CEST MRI has been hindered by the lack of the large CEST datasets required for network development. Thus, we aim to develop a DLSR method, named DLSR-CEST, to reduce the acquisition time for CEST MRI by reconstructing high-resolution images from fast low-resolution acquisitions. This is achieved by first pretraining the DLSR-CEST on human brain T1w and T2w images to initialize the weights of the network and then training the network on very small human and mouse brain CEST datasets to fine-tune the weights. Using the trained DLSR-CEST network, the reconstructed CEST source images exhibited improved spatial resolution in both peak signal-to-noise ratio and structural similarity index measure metrics at all downsampling factors (2–8). Moreover, amide CEST and relayed nuclear Overhauser effect maps extrapolated from the DLSR-CEST source images exhibited high spatial resolution and low normalized root mean square error, indicating a negligible loss in <em>Z</em>-spectrum information. Therefore, our DLSR-CEST demonstrated a robust reconstruction of high-resolution CEST source images from fast low-resolution acquisitions, thereby improving the spatial resolution and preserving most <em>Z</em>-spectrum information.</p>-
dc.languageeng-
dc.publisherWiley-
dc.relation.ispartofNMR in Biomedicine-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectacquisition time-
dc.subjectamide CEST (amideCEST)-
dc.subjectbrain-
dc.subjectchemical exchange saturation transfer (CEST)-
dc.subjectdeep-learning-based super-resolution (DLSR)-
dc.subjectrelayed nuclear Overhauser effect (rNOE)-
dc.titleDeep‐learning‐based super‐resolution for accelerating chemical exchange saturation transfer MRI-
dc.typeArticle-
dc.identifier.doi10.1002/nbm.5130-
dc.identifier.scopuseid_2-s2.0-85188431371-
dc.identifier.volume37-
dc.identifier.issue8-
dc.identifier.eissn1099-1492-
dc.identifier.issnl0952-3480-

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