European Radiology Experimental (Dec 2021)

Quantification of H2 17O by 1H-MR imaging at 3 T: a feasibility study

  • Luis Martí-Bonmatí,
  • Alejandro Rodríguez-Ortega,
  • Amadeo Ten-Esteve,
  • Ángel Alberich-Bayarri,
  • Bernardo Celda,
  • Eduardo Ferrer

DOI
https://doi.org/10.1186/s41747-021-00246-w
Journal volume & issue
Vol. 5, no. 1
pp. 1 – 9

Abstract

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Abstract Background Indirect 1H-magnetic resonance (MR) imaging of 17O-labelled water allows imaging in vivo dynamic changes in water compartmentalisation. Our aim was to describe the feasibility of indirect 1H-MR methods to evaluate the effect of H2 17O on the MR relaxation rates by using conventional a 3-T equipment and voxel-wise relaxation rates. Methods MR images were used to calculate the R1, R2, and R2* relaxation rates in phantoms (19 vials with different H2 17O concentrations, ranging from 0.039 to 5.5%). Afterwards, an experimental animal pilot study (8 rats) was designed to evaluate the in vivo relative R2 brain dynamic changes related to the intravenous administration of 17O-labelled water in rats. Results There were no significant changes on the R1 and R2* values from phantoms. The R2 obtained with the turbo spin-echo T2-weighted sequence with 20-ms echo time interval had the higher statistical difference (0.67 s−1, interquartile range 0.34, p < 0.001) and Spearman correlation (rho 0.79). The R2 increase was adjusted to a linear fit between 0.25 and 5.5%, represented with equation R2 = 0.405 concentration + 0.3215. The highest significant differences were obtained for the higher concentrations (3.1–5.5%). The rat brain MR experiment showed a mean 10% change in the R2 value after the H2 17O injection with progressive normalisation. Conclusions Indirect 1H-MR imaging method is able to measure H2 17O concentration by using R2 values and conventional 3-T MR equipment. Normalised R2 relative dynamic changes after the intravenous injection of a H2 17O saline solution provide a unique opportunity to map water pathophysiology in vivo, opening the analysis of aquaporins status and modifications by disease at clinically available 3-T proton MR scanners.

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