4.7 Article

Deuterium metabolic imaging and hyperpolarized 13C-MRI of the normal human brain at clinical field strength reveals differential cerebral metabolism

期刊

NEUROIMAGE
卷 257, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2022.119284

关键词

Metabolic imaging; Deuterium; Glucose; Pyruvate; Hyperpolarized C-13; MRI

资金

  1. Cancer Research UK (CRUK) [C19212/A27150, C19212/A16628]
  2. Lundbeck Foundation [2015-35]
  3. National Institute of Health Research (NIHR) Cambridge Biomedical Research center [BRC-1215-20014]
  4. Cambridge Experimental Cancer Medicine center
  5. Evelyn Trust
  6. Addenbrooke's Charitable Trust
  7. NIHR/Wellcome Trust Cambridge Clinical Research Facility
  8. Eu-ropean Union?s Horizon 2020 research and innovation program
  9. European Union [761214]

向作者/读者索取更多资源

Deuterium metabolic imaging (DMI) and hyperpolarized C-13-pyruvate MRI (C-13-HPMRI) are two emerging non-invasive imaging methods that can probe both oxidative and non-oxidative metabolism. This study directly compares these two methods in humans for the first time, showing that they provide different yet complementary readouts of metabolism.
Deuterium metabolic imaging (DMI) and hyperpolarized C-13-pyruvate MRI (C-13-HPMRI) are two emerging meth-ods for non-invasive and non-ionizing imaging of tissue metabolism. Imaging cerebral metabolism has potential applications in cancer, neurodegeneration, multiple sclerosis, traumatic brain injury, stroke, and inborn errors of metabolism. Here we directly compare these two non-invasive methods at 3 T for the first time in humans and show how they simultaneously probe both oxidative and non-oxidative metabolism. DMI was undertaken 1-2 h after oral administration of [6,6'-H-2(2)]glucose, and C-13-MRI was performed immediately following intravenous injection of hyperpolarized [1-C-13]pyruvate in ten and nine normal volunteers within each arm respectively. DMI was used to generate maps of deuterium-labelled water, glucose, lactate, and glutamate/glutamine (Glx) and the spectral separation demonstrated that DMI is feasible at 3 T. C-13-HPMRI generated maps of hyperpo-larized carbon-13 labelled pyruvate, lactate, and bicarbonate. The ratio of C-13-lactate/C-13-bicarbonate (mean 3.7 +/- 1.2) acquired with C-13-HPMRI was higher than the equivalent H-2-lactate/H-2-Glx ratio (mean 0.18 +/- 0.09) acquired using DMI. These differences can be explained by the route of administering each probe, the timing of imaging after ingestion or injection, as well as the biological differences in cerebral uptake and cellular physiol-ogy between the two molecules. The results demonstrate these two metabolic imaging methods provide different yet complementary readouts of oxidative and reductive metabolism within a clinically feasible timescale. Fur-thermore, as DMI was undertaken at a clinical field strength within a ten-minute scan time, it demonstrates its potential as a routine clinical tool in the future.

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