File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Sensitivity schemes for dynamic glucose-enhanced magnetic resonance imaging to detect glucose uptake and clearance in mouse brain at 3 T

TitleSensitivity schemes for dynamic glucose-enhanced magnetic resonance imaging to detect glucose uptake and clearance in mouse brain at 3 T
Authors
KeywordsCarr–Purcell–Meiboom–Gill
cerebrospinal fluid
dynamic glucose-enhanced
multilinear singular value decomposition
on-resonance spin-lock
on-resonance variable delay multipulse
parenchyma
Issue Date2022
Citation
NMR in Biomedicine, 2022, v. 35, n. 3, article no. e4640 How to Cite?
AbstractWe investigated three dynamic glucose-enhanced (DGE) MRI methods for sensitively monitoring glucose uptake and clearance in both brain parenchyma and cerebrospinal fluid (CSF) at clinical field strength (3 T). By comparing three sequences, namely, Carr–Purcell–Meiboom–Gill (CPMG), on-resonance variable delay multipulse (onVDMP), and on-resonance spin-lock (onSL), a high-sensitivity DGE MRI scheme with truncated multilinear singular value decomposition (MLSVD) denoising was proposed. The CPMG method showed the highest sensitivity in detecting the parenchymal DGE signal among the three methods, while both onVDMP and onSL were more robust for CSF DGE imaging. Here, onVDMP was applied for CSF imaging, as it displayed the best stability of the DGE results in this study. The truncated MLSVD denoising method was incorporated to further improve the sensitivity. The proposed DGE MRI scheme was examined in mouse brain with 50%/25%/12.5% w/w D-glucose injections. The results showed that this combination could detect DGE signal changes from the brain parenchyma and CSF with as low as a 12.5% w/w D-glucose injection. The proposed DGE MRI schemes could sensitively detect the glucose signal change from brain parenchyma and CSF after D-glucose injection at a clinically relevant concentration, demonstrating high potential for clinical translation.
Persistent Identifierhttp://hdl.handle.net/10722/327913
ISSN
2023 Impact Factor: 2.7
2023 SCImago Journal Rankings: 0.949
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorHuang, Jianpan-
dc.contributor.authorLai, Joseph H.C.-
dc.contributor.authorHan, Xiongqi-
dc.contributor.authorChen, Zilin-
dc.contributor.authorXiao, Peng-
dc.contributor.authorLiu, Yang-
dc.contributor.authorChen, Lin-
dc.contributor.authorXu, Jiadi-
dc.contributor.authorChan, Kannie W.Y.-
dc.date.accessioned2023-06-05T06:52:37Z-
dc.date.available2023-06-05T06:52:37Z-
dc.date.issued2022-
dc.identifier.citationNMR in Biomedicine, 2022, v. 35, n. 3, article no. e4640-
dc.identifier.issn0952-3480-
dc.identifier.urihttp://hdl.handle.net/10722/327913-
dc.description.abstractWe investigated three dynamic glucose-enhanced (DGE) MRI methods for sensitively monitoring glucose uptake and clearance in both brain parenchyma and cerebrospinal fluid (CSF) at clinical field strength (3 T). By comparing three sequences, namely, Carr–Purcell–Meiboom–Gill (CPMG), on-resonance variable delay multipulse (onVDMP), and on-resonance spin-lock (onSL), a high-sensitivity DGE MRI scheme with truncated multilinear singular value decomposition (MLSVD) denoising was proposed. The CPMG method showed the highest sensitivity in detecting the parenchymal DGE signal among the three methods, while both onVDMP and onSL were more robust for CSF DGE imaging. Here, onVDMP was applied for CSF imaging, as it displayed the best stability of the DGE results in this study. The truncated MLSVD denoising method was incorporated to further improve the sensitivity. The proposed DGE MRI scheme was examined in mouse brain with 50%/25%/12.5% w/w D-glucose injections. The results showed that this combination could detect DGE signal changes from the brain parenchyma and CSF with as low as a 12.5% w/w D-glucose injection. The proposed DGE MRI schemes could sensitively detect the glucose signal change from brain parenchyma and CSF after D-glucose injection at a clinically relevant concentration, demonstrating high potential for clinical translation.-
dc.languageeng-
dc.relation.ispartofNMR in Biomedicine-
dc.subjectCarr–Purcell–Meiboom–Gill-
dc.subjectcerebrospinal fluid-
dc.subjectdynamic glucose-enhanced-
dc.subjectmultilinear singular value decomposition-
dc.subjecton-resonance spin-lock-
dc.subjecton-resonance variable delay multipulse-
dc.subjectparenchyma-
dc.titleSensitivity schemes for dynamic glucose-enhanced magnetic resonance imaging to detect glucose uptake and clearance in mouse brain at 3 T-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/nbm.4640-
dc.identifier.pmid34750891-
dc.identifier.scopuseid_2-s2.0-85118613878-
dc.identifier.volume35-
dc.identifier.issue3-
dc.identifier.spagearticle no. e4640-
dc.identifier.epagearticle no. e4640-
dc.identifier.eissn1099-1492-
dc.identifier.isiWOS:000715882200001-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats