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Imaging & diagnostics

MR spectroscopy (MRS)

DEMR-Spektroskopie (MRS)

Magnetic resonance spectroscopy (MRS) uses the chemical-shift information in the MR signal to quantify tissue metabolites non-invasively, typically from a single voxel or a multi-voxel grid acquired on a standard MRI scanner. Brain 1H-MRS measures N-acetylaspartate (NAA, a marker of neuronal integrity), choline, creatine, lactate, myo-inositol, glutamate/glutamine and reduced glutathione; these are useful in tumour grading, mitochondrial disease, multiple sclerosis and neurodegenerative research. In the liver, MR proton density fat fraction (MR-PDFF), a chemical-shift-encoded MRI technique conceptually related to MRS, is the most accurate non-invasive measure of hepatic steatosis and has become the imaging endpoint of choice in MASLD/MASH trials, with good correlation to biopsy steatosis grades. MRS uses no ionising radiation; limitations include long acquisition times, susceptibility to motion and B0 inhomogeneity, modest spatial resolution and the need for specialised post-processing.

Sources

  1. Bottomley PA. (1988). Human in vivo phosphate metabolite imaging with 31P NMR. *Magnetic Resonance in Medicine*doi:10.1002/mrm.1910070309
  2. Caussy C, Reeder SB, Sirlin CB, Loomba R. (2018). Noninvasive, Quantitative Assessment of Liver Fat by MRI-PDFF as an Endpoint in NASH Trials. *Hepatology*doi:10.1002/hep.29797
  3. Öz G, Alger JR, Barker PB, et al.. (2014). Clinical Proton MR Spectroscopy in Central Nervous System Disorders. *Radiology*doi:10.1148/radiol.13130531