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Denoising and Multiple Tissue Compartment Visualization of Multi-b-Valued Breast Diffusion MRI.
Tan, Ek T; Wilmes, Lisa J; Joe, Bonnie N; Onishi, Natsuko; Arasu, Vignesh A; Hylton, Nola M; Marinelli, Luca; Newitt, David C.
Afiliación
  • Tan ET; GE Global Research, Niskayuna, New York, USA.
  • Wilmes LJ; Department of Radiology and Imaging, Hospital for Special Surgery, New York, New York, USA.
  • Joe BN; Department of Radiology, University of California, San Francisco, California, USA.
  • Onishi N; Department of Radiology, University of California, San Francisco, California, USA.
  • Arasu VA; Department of Radiology, University of California, San Francisco, California, USA.
  • Hylton NM; Department of Radiology, University of California, San Francisco, California, USA.
  • Marinelli L; Department of Radiology, Kaiser Permanente Medical Center, Vallejo, California, USA.
  • Newitt DC; Division of Research, Kaiser Permanente Northern California, Oakland, California, USA.
J Magn Reson Imaging ; 53(1): 271-282, 2021 01.
Article en En | MEDLINE | ID: mdl-32614125
ABSTRACT

BACKGROUND:

Multi-b-valued/multi-shell diffusion provides potentially valuable metrics in breast MRI but suffers from low signal-to-noise ratio and has potentially long scan times.

PURPOSE:

To investigate the effects of model-based denoising with no loss of spatial resolution on multi-shell breast diffusion MRI; to determine the effects of downsampling on multi-shell diffusion; and to quantify these effects in multi-b-valued (three directions per b-value) acquisitions. STUDY TYPE Prospective ("fully-sampled" multi-shell) and retrospective longitudinal (multi-b).

SUBJECTS:

One normal subject (multi-shell) and 10 breast cancer subjects imaging at four timepoints (multi-b). FIELD STRENGTH/SEQUENCE 3T multi-shell acquisition and 1.5T multi-b acquisition. ASSESSMENT The "fully-sampled" multi-shell acquisition was retrospectively downsampled to determine the bias and error from downsampling. Mean, axial/parallel, radial diffusivity, and fractional anisotropy (FA) were analyzed. Denoising was applied retrospectively to the multi-b-valued breast cancer subject dataset and assessed subjectively for image noise level and tumor conspicuity. STATISTICAL TESTS Parametric paired t-test (P < 0.05 considered statistically significant) on mean and coefficient of variation of each metric-the apparent diffusion coefficient (ADC) from all b-values, fast ADC, slow ADC, and perfusion fraction. Paired and two-sample t-tests for each metric comparing normal and tumor tissue.

RESULTS:

In the multi-shell data, denoising effectively suppressed FA (-45% to -78%), with small biases in mean diffusivity (-5% in normal, +23% in tumor, and -4% in vascular compartments). In the multi-b data, denoising resulted in small biases to the ADC metrics in tumor and normal contralateral tissue (by -3% to +11%), but greatly reduced the coefficient of variation for every metric (by -1% to -24%). Denoising improved differentiation of tumor and normal tissue regions in most metrics and timepoints; subjectively, image noise level and tumor conspicuity were improved in the fast ADC maps. DATA

CONCLUSION:

Model-based denoising effectively suppressed erroneously high FA and improved the accuracy of diffusivity metrics. EVIDENCE LEVEL 3 TECHNICAL EFFICACY STAGE 1.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Mama / Imagen de Difusión por Resonancia Magnética Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans Idioma: En Revista: J Magn Reson Imaging Asunto de la revista: DIAGNOSTICO POR IMAGEM Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Mama / Imagen de Difusión por Resonancia Magnética Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans Idioma: En Revista: J Magn Reson Imaging Asunto de la revista: DIAGNOSTICO POR IMAGEM Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos