31 P magnetic resonance spectroscopy in skeletal muscle: Experts' consensus recommendations
Status Publisher Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
K99 HL125756
NHLBI NIH HHS - United States
MR/P020941/1
Medical Research Council - United Kingdom
PubMed
32037688
PubMed Central
PMC8243949
DOI
10.1002/nbm.4246
Knihovny.cz E-zdroje
- Klíčová slova
- 31P, MRI, exercise, metabolism, muscle, nuclear magnetic resonance spectroscopy, phosphorus MRS,
- Publikační typ
- časopisecké články MeSH
Skeletal muscle phosphorus-31 31 P MRS is the oldest MRS methodology to be applied to in vivo metabolic research. The technical requirements of 31 P MRS in skeletal muscle depend on the research question, and to assess those questions requires understanding both the relevant muscle physiology, and how 31 P MRS methods can probe it. Here we consider basic signal-acquisition parameters related to radio frequency excitation, TR, TE, spectral resolution, shim and localisation. We make specific recommendations for studies of resting and exercising muscle, including magnetisation transfer, and for data processing. We summarise the metabolic information that can be quantitatively assessed with 31 P MRS, either measured directly or derived by calculations that depend on particular metabolic models, and we give advice on potential problems of interpretation. We give expected values and tolerable ranges for some measured quantities, and minimum requirements for reporting acquisition parameters and experimental results in publications. Reliable examination depends on a reproducible setup, standardised preconditioning of the subject, and careful control of potential difficulties, and we summarise some important considerations and potential confounders. Our recommendations include the quantification and standardisation of contraction intensity, and how best to account for heterogeneous muscle recruitment. We highlight some pitfalls in the assessment of mitochondrial function by analysis of phosphocreatine (PCr) recovery kinetics. Finally, we outline how complementary techniques (near-infrared spectroscopy, arterial spin labelling, BOLD and various other MRI and 1 H MRS measurements) can help in the physiological/metabolic interpretation of 31 P MRS studies by providing information about blood flow and oxygen delivery/utilisation. Our recommendations will assist in achieving the fullest possible reliable picture of muscle physiology and pathophysiology.
Center for Medical Physics and Biomedical Engineering Medical University of Vienna Vienna Austria
Cognitive Neuroscience Center University Medical Center Groningen Groningen the Netherlands
DBMR and DIPR University and Inselspital Bern Switzerland
Department of Kinesiology University of Massachusetts Amherst MA USA
Department of Physical Therapy University of Florida Gainesville Florida USA
Department of Radiology Amsterdam University Medical Center|site AMC Amsterdam the Netherlands
Department of Radiology University Medical Center Utrecht the Netherlands
Duchenne Center The Netherlands
High Field MR Center Medical University of Vienna Vienna Austria
Institute for Applied Life Sciences University of Massachusetts Amherst MA USA
NMR Laboratory Neuromuscular Investigation Center Institute of Myology AIM CEA Paris France
Norwich Medical School University of East Anglia Norwich UK
Wellcome Trust MRC Institute of Metabolic Science University of Cambridge Cambridge UK
Wolfson Brain Imaging Centre University of Cambridge Cambridge UK
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