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Reproducibility of 3D 1H MR spectroscopic imaging of the prostate at 1.5T. | LitMetric

AI Article Synopsis

  • The study assessed the reproducibility of 3D proton magnetic resonance spectroscopic imaging (1H-MRSI) for the prostate across multiple centers using 1.5T MRI.
  • Fourteen subjects underwent two measurements with a focus on the choline plus creatine to citrate ratio (CC/C) to evaluate consistency in results.
  • Findings indicated strong reproducibility, with over 90% of measurements showing no significant differences, suggesting that this technique can reliably assess prostate tumors.

Article Abstract

Purpose: To determine the reproducibility of 3D proton magnetic resonance spectroscopic imaging ((1)H-MRSI) of the human prostate in a multicenter setting at 1.5T.

Materials And Methods: Fourteen subjects were measured twice with 3D point-resolved spectroscopy (PRESS) (1)H-MRSI using an endorectal coil. MRSI voxels were selected in the peripheral zone and combined central gland at the same location in the prostate in both measurements. Voxels with approved spectral quality were included to calculate Bland-Altman parameters for reproducibility from the choline plus creatine to citrate ratio (CC/C). The repeated spectroscopic data were also evaluated with a standardized clinical scoring system.

Results: A total of 74 voxels were included for reproducibility analysis. The complete range of biologically interesting CC/C ratios was covered. The overall within-voxel standard deviation (SD) of the CC/C ratio of the repeated measurements was 0.13. This value is equal to the between-subject SD of noncancer prostate tissue. In >90% of the voxels the standardized clinical score did not differ relevantly between the measurements.

Conclusion: Repeated measurements of in vivo 3D (1)H-MRSI of the complete prostate at 1.5T produce equal and quantitative results. The reproducibility of the technique is high enough to provide it as a reliable tool in assessing tumor presence in the prostate.

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Source
http://dx.doi.org/10.1002/jmri.22827DOI Listing

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