Interleaved 31P MRS/1H ASL for analysis of metabolic and functional heterogeneity along human lower leg muscles at 7T. Issue 6 (17th December 2019)

• Record Type: Journal Article
• Authors: Niess, Fabian; Schmid, Albrecht Ingo; Bogner, Wolfgang; Wolzt, Michael; Carlier, Pierre; Trattnig, Siegfried; Moser, Ewald; Meyerspeer, Martin
• Is Part Of: Magnetic resonance in medicine. Volume 83:Issue 6(2020)
• Page Start: 1909
• Page End: 1919
• Publication Date: 2019-12-17
• Subjects: 31P MRS -- energy metabolism -- interleaved acquisition -- muscle exercise -- perfusion -- pH; Nuclear magnetic resonance -- Periodicals; Electron paramagnetic resonance -- Periodicals; 616.07548
• DOI: 10.1002/mrm.28088
• Languages: English
• ISSNs: 0740-3194

Abstract

Abstract : Purpose: MR offers the unique possibility to noninvasively investigate cellular energy metabolism via 31P MRS, while blood perfusion, which provides oxygen and substrates to the tissue, is accessible by arterial spin labeling (ASL) 1H MRI. Because metabolic and hemodynamic parameters are linked, it would be desirable to study them simultaneously. A 3D‐resolved method is presented that allows such measurements with high spatiotemporal resolution and has the potential to discern differences along an exercising muscle. Methods: Multi‐voxel localized 31 P MRS was temporally interleaved with multi‐slice pASL 1H MRI. Phosphorus spectra were collected from two adjacent positions in gastrocnemius medialis (GM) during rest, submaximal plantar flexion exercise and recovery, while perfusion and T 2 * ‐weighted axial images were acquired at the same time. Seventeen healthy volunteers (9 f / 8 m) were studied at 7 T. Results: An increase of postexercise perfusion and T 2 * ‐weighted signal in GM positively correlated with end‐exercise PCr depletion and pH drop. At proximal positions functional and metabolic activity was higher than distally, that is, perfusion increase and peak T 2 * ‐weighted signal, end‐exercise PCr depletion, end‐exercise pH, and PCr recovery time constant were significantly different. An NOE‐induced SNR increase of approximately 20 % ( P < .001), at rest, was found in interleaved 31 P spectra, when comparing to 31 P‐only acquisitions. Conclusions: A technique for fast, simultaneous imaging of muscle functional heterogeneity in ASL, T 2 * and acquisition of time‐resolved 31 P MRS data is presented. These single exercise recovery experiments can be used to investigate local variations during disease progression in patients suffering from vascular or muscular diseases.