Mitochondrial oxidative phosphorylation capacity in skeletal muscle measured by ultrafast Z‐spectroscopy (UFZ) MRI at 3T.
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| Title: | Mitochondrial oxidative phosphorylation capacity in skeletal muscle measured by ultrafast Z‐spectroscopy (UFZ) MRI at 3T. |
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| Authors: | Ju, Licheng1,2 (AUTHOR), Schär, Michael2 (AUTHOR), Wang, Kexin1,3 (AUTHOR), Li, Anna1 (AUTHOR), Wu, Yihan1,3 (AUTHOR), Samuel, T. Jake4 (AUTHOR), Ganji, Sandeep5,6 (AUTHOR), van Zijl, Peter C. M.1,2 (AUTHOR), Yadav, Nirbhay N.1,2 (AUTHOR), Weiss, Robert G.2,4 (AUTHOR), Xu, Jiadi1,2 (AUTHOR) jxu37@jh.edu |
| Source: | Magnetic Resonance in Medicine. Mar2025, Vol. 93 Issue 3, p1273-1284. 12p. |
| Subjects: | Magnetization transfer, Skeletal muscle, Oxidative phosphorylation, Creatine kinase, Calf muscles |
| Abstract: | Purpose: To investigate the feasibility of rapid CEST MRI acquisition for evaluating oxidative phosphorylation (OXPHOS) in human skeletal muscle at 3T, utilizing ultrafast Z‐spectroscopy (UFZ) combined with MRI and the Polynomial and Lorentzian line‐shape Fitting (PLOF) technique. Methods: UFZ MRI on muscle was evaluated with turbo spin echo (TSE) and 3D EPI readouts. Five healthy subjects performed in‐magnet plantar flexion exercise (PFE) and subsequent changes of amide, PCr, and partial PCr mixed Cr (Cr+) CEST dynamic signals post‐exercise were enabled by PLOF fitting. PCr/Cr CEST signal was further refined through pH correction by using the ratios between PCr/Cr and amide signals, named PCAR/CAR, respectively. Results: UFZ MRI with TSE readout significantly reduces acquisition time, achieving a temporal resolution of <50 s for collecting high‐resolution Z‐spectra. Following PFE, the recovery/decay times (τ) for both PCr and Cr in the gastrocnemius muscle of the calf were notably longer when determined using PCr/Cr CEST compared to those after pH correction with amideCEST, namely τCr+$$ {\tau}_{Cr^{+}} $$ = 87.1 ± 15.8 s and τPCr$$ {\tau}_{PCr} $$ = 98.1 ± 20.4 s versus τCAR$$ {\tau}_{CAR} $$ = 32.9 ± 19.7 s and τPCAR$$ {\tau}_{PCAR} $$ = 43.0 ± 13.0 s, respectively. τPCr$$ {\tau}_{PCr} $$ obtained via 31P MRS (τPCr$$ {\tau}_{PCr} $$ = 50.3 ± 6.2 s) closely resemble those obtained from pH‐corrected PCr/Cr CEST signals. Conclusion: The outcomes suggest potential of UFZ MRI as a robust tool for non‐invasive assessment of mitochondrial function in skeletal muscles. pH correction is critical for the reliable OXPHOS measurement by CEST. [ABSTRACT FROM AUTHOR] |
| Copyright of Magnetic Resonance in Medicine is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
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| Header | DbId: egs DbLabel: Engineering Source An: 181922295 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Mitochondrial oxidative phosphorylation capacity in skeletal muscle measured by ultrafast Z‐spectroscopy (UFZ) MRI at 3T. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Ju%2C+Licheng%22">Ju, Licheng</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Schär%2C+Michael%22">Schär, Michael</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wang%2C+Kexin%22">Wang, Kexin</searchLink><relatesTo>1,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Li%2C+Anna%22">Li, Anna</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wu%2C+Yihan%22">Wu, Yihan</searchLink><relatesTo>1,3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Samuel%2C+T%2E+Jake%22">Samuel, T. Jake</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ganji%2C+Sandeep%22">Ganji, Sandeep</searchLink><relatesTo>5,6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22van+Zijl%2C+Peter+C%2E+M%2E%22">van Zijl, Peter C. M.</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yadav%2C+Nirbhay+N%2E%22">Yadav, Nirbhay N.</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Weiss%2C+Robert+G%2E%22">Weiss, Robert G.</searchLink><relatesTo>2,4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Xu%2C+Jiadi%22">Xu, Jiadi</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> jxu37@jh.edu</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Magnetic+Resonance+in+Medicine%22">Magnetic Resonance in Medicine</searchLink>. Mar2025, Vol. 93 Issue 3, p1273-1284. 12p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Magnetization+transfer%22">Magnetization transfer</searchLink><br /><searchLink fieldCode="DE" term="%22Skeletal+muscle%22">Skeletal muscle</searchLink><br /><searchLink fieldCode="DE" term="%22Oxidative+phosphorylation%22">Oxidative phosphorylation</searchLink><br /><searchLink fieldCode="DE" term="%22Creatine+kinase%22">Creatine kinase</searchLink><br /><searchLink fieldCode="DE" term="%22Calf+muscles%22">Calf muscles</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Purpose: To investigate the feasibility of rapid CEST MRI acquisition for evaluating oxidative phosphorylation (OXPHOS) in human skeletal muscle at 3T, utilizing ultrafast Z‐spectroscopy (UFZ) combined with MRI and the Polynomial and Lorentzian line‐shape Fitting (PLOF) technique. Methods: UFZ MRI on muscle was evaluated with turbo spin echo (TSE) and 3D EPI readouts. Five healthy subjects performed in‐magnet plantar flexion exercise (PFE) and subsequent changes of amide, PCr, and partial PCr mixed Cr (Cr+) CEST dynamic signals post‐exercise were enabled by PLOF fitting. PCr/Cr CEST signal was further refined through pH correction by using the ratios between PCr/Cr and amide signals, named PCAR/CAR, respectively. Results: UFZ MRI with TSE readout significantly reduces acquisition time, achieving a temporal resolution of <50 s for collecting high‐resolution Z‐spectra. Following PFE, the recovery/decay times (τ) for both PCr and Cr in the gastrocnemius muscle of the calf were notably longer when determined using PCr/Cr CEST compared to those after pH correction with amideCEST, namely τCr+$$ {\tau}_{Cr^{+}} $$ = 87.1 ± 15.8 s and τPCr$$ {\tau}_{PCr} $$ = 98.1 ± 20.4 s versus τCAR$$ {\tau}_{CAR} $$ = 32.9 ± 19.7 s and τPCAR$$ {\tau}_{PCAR} $$ = 43.0 ± 13.0 s, respectively. τPCr$$ {\tau}_{PCr} $$ obtained via 31P MRS (τPCr$$ {\tau}_{PCr} $$ = 50.3 ± 6.2 s) closely resemble those obtained from pH‐corrected PCr/Cr CEST signals. Conclusion: The outcomes suggest potential of UFZ MRI as a robust tool for non‐invasive assessment of mitochondrial function in skeletal muscles. pH correction is critical for the reliable OXPHOS measurement by CEST. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Magnetic Resonance in Medicine is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/mrm.30354 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 12 StartPage: 1273 Subjects: – SubjectFull: Magnetization transfer Type: general – SubjectFull: Skeletal muscle Type: general – SubjectFull: Oxidative phosphorylation Type: general – SubjectFull: Creatine kinase Type: general – SubjectFull: Calf muscles Type: general Titles: – TitleFull: Mitochondrial oxidative phosphorylation capacity in skeletal muscle measured by ultrafast Z‐spectroscopy (UFZ) MRI at 3T. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Ju, Licheng – PersonEntity: Name: NameFull: Schär, Michael – PersonEntity: Name: NameFull: Wang, Kexin – PersonEntity: Name: NameFull: Li, Anna – PersonEntity: Name: NameFull: Wu, Yihan – PersonEntity: Name: NameFull: Samuel, T. Jake – PersonEntity: Name: NameFull: Ganji, Sandeep – PersonEntity: Name: NameFull: van Zijl, Peter C. M. – PersonEntity: Name: NameFull: Yadav, Nirbhay N. – PersonEntity: Name: NameFull: Weiss, Robert G. – PersonEntity: Name: NameFull: Xu, Jiadi IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 03 Text: Mar2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 07403194 Numbering: – Type: volume Value: 93 – Type: issue Value: 3 Titles: – TitleFull: Magnetic Resonance in Medicine Type: main |
| ResultId | 1 |