NeuroImage: Clinical | |
Non-parametric intravoxel incoherent motion analysis in patients with intracranial lesions: Test-retest reliability and correlation with arterial spin labeling | |
Tobias Weiss1  Matthias Guckenberger2  Oliver Riesterer2  Sonja Stieb2  Moritz C. Wurnig3  Cristina Rossi3  Andreas Boss3  Pinar S. Özbay3  | |
[1] Department of Neurology, University Hospital Zurich and University of Zurich, Switzerland;Department of Radiation Oncology, University Hospital Zurich and University of Zurich, Switzerland;Institute of Diagnostic and Interventional Radiology, University Hospital Zurich and University of Zurich, Switzerland; | |
关键词: Intravoxel incoherent motion; IVIM; Arterial spin labeling; ASL; Test-retest reliability; Glioblastoma multiforme; | |
DOI : 10.1016/j.nicl.2016.05.022 | |
来源: DOAJ |
【 摘 要 】
Intravoxel incoherent motion (IVIM) analysis of diffusion imaging data provides biomarkers of true passive water diffusion and perfusion properties. A new IVIM algorithm with variable adjustment of the b-value threshold separating diffusion and perfusion effects was applied for cerebral tissue characterization in healthy volunteers, computation of test-retest reliability, correlation with arterial spin labeling, and assessment of applicability in a small cohort of patients with malignant intracranial masses. The main results of this study are threefold: (i) accounting for regional differences in the separation of the perfusion and the diffusion components improves the reliability of the model parameters; (ii) if differences in the b-value threshold are not accounted for, a significant tissue-dependent systematic bias of the IVIM parameters occurs; (iii) accounting for voxel-wise differences in the b-value threshold improves the correlation with CBF measurements in healthy volunteers and patients. The proposed algorithm provides a robust characterization of regional micro-vascularization and cellularity without a priori assumptions on tissue diffusion properties. The glioblastoma multiforme with its inherently high variability of tumor vascularization and tumor cell density may benefit from a non-invasive clinical characterization of diffusion and perfusion properties.
【 授权许可】
Unknown