Purpose: The objective of this study was to demonstrate the feasibility of a cerebral metabolic rate of oxygen (CMRO 2 ) mapping method based on its minimum local variance (MLV) without vascular challenge using quantitative susceptibility mapping (QSM) and cerebral blood flow (CBF). Methods: Three-dimensional multi-echo gradient echo imaging and arterial spin labeling were performed in 11 healthy subjects to calculate QSM and CBF. Minimum local variance was used to compute whole-brain CMRO 2 map from QSM and CBF. The MLV method was compared with a reference method using the caffeine challenge. Their agreement within the cortical gray matter (CGM) was assessed on CMRO 2 and oxygen extraction fraction (OEF) maps at both baseline and challenge states. Results: Mean CMRO 2 (in mmol/100 g/min) obtained in CGM using the caffeine challenge and MLV were 142 6 16.5 and 139 6 14.8 mmol/100 g/min, respectively; the corresponding baseline OEF were 33.0 6 4.0% and 31.8 6 3.2%, respectively. The MLV and caffeine challenge methods showed no statistically significant differences across subjects with small ( < 4%) biases in CMRO 2 and OEF values. Conclusions: Minimum local variance-based CMRO 2 mapping without vascular challenge using QSM and arterial spin labeling is feasible in healthy subjects. Magn Reson Med 79:172-179,
Purpose: To improve the accuracy of QSM plus quantitative blood oxygen leveldependent magnitude (QSM + qBOLD or QQ)-based mapping of the oxygen extraction fraction (OEF) and cerebral metabolic rate of oxygen (CMRO 2 ) using cluster analysis of time evolution (CAT). Methods: 3D multi-echo gradient echo and arterial spin labeling images were acquired in 11 healthy subjects and 5 ischemic stroke patients. DWI was also carried out on patients. CAT was developed for analyzing signal evolution over TE.QQ-based OEF and CMRO 2 were reconstructed with and without CAT, and results were compared using region of interest analysis and a paired t-test. Results: Simulations demonstrated that CAT substantially reduced noise error in QQ-based OEF. In healthy subjects, QQ-based OEF appeared less noisy and more uniform with CAT than without CAT; average OEF with and without CAT in cortical gray matter was 32.7 ± 4.0% and 37.9 ± 4.5%, with corresponding CMRO 2 of 148.4 ± 23.8 and 171.4 ± 22.4 μmol/100 g/min, respectively. In patients, regions of low OEF were confined within the ischemic lesions defined on DWI when using CAT, which was not observed without CAT. Conclusion: The cluster analysis of time evolution (CAT) significantly improves the robustness of QQ-based OEF against noise.
K E Y W O R D Scerebral metabolic rate of oxygen, cluster analysis of time evolution, K-means, machine learning, oxygen extraction fraction, quantitative blood oxygenation level-dependent imaging, quantitative susceptibility mapping
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