4019

Oxygen extraction fraction (OEF) mapping by using multi-delay arterial spin labeling based on QSM+qBOLD
Xiaoyi Liu1, Yayan Yin1, Juan Wei2, and Jie Lu1
1Radiology and Nuclear Medicine, Xuanwu Hospital, Capital Medical University, Beijing 100053, China, Beijing, China, 2GE Healthcare, MR Research China, Beijing, Beijing, China

Synopsis

Keywords: Arterial spin labelling, Metabolism, oxygen extraction fraction

We aimed to improve the accuracy of OEF mapping by using multi-delay arterial spin labeling based on quantitative susceptibility mapping plus quantitative blood oxygen level-dependent magnitude (QSM+qBOLD, or QQ). 3D multi-echo gradient-echo and ASL sequence were performed in 7 healthy subjects. ROIs analysis and paired t-test compared QQ with single-delay ASL and QQ with multi-delay ASL. QQ with multi-delay ASL shows smaller OEFs than QQ with single-delay ASL method. Corresponding OEFs were 38.9±3.4% and 39.6±3.4% (P<0.01) in gray matter, 39.7±2.9% and 40.2±2.9% in whole brain(P<0.01), respectively. Our study suggests that QQ with multi-delay ASL provides more accurate OEF than QQ with single-delay ASL, which may have potential in the use of clinical diseases.

Introduction

Oxygen extraction fraction (OEF) is an essential biomarker for evaluating brain tissue vulnerability and function in various disorders such as stroke, lupus, and moyamoya [1-3]. A recent model combined quantitative susceptibility mapping plus quantitative blood oxygen level-dependent magnitude (QSM+qBOLD or QQ) has been used to evaluate OEF using both magnitude and phase of multi-echo gradient echo data [4]. This QQ method enables OEF mapping without vascular challenges, which has great potential in clinical applications. Nonetheless, some studies have pointed out that the accuracy of cerebral blood flow (CBF) quantification with arterial spin labeling (ASL) MRI perfusion is a challenge of OEF mapping [4-6]. Relatively cerebral blood volume (CBV) estimated from CBF by assuming an empirical relationship derived from normative PET data can also be a source of error [7]. Instead, multi-delay ASL can calibrate CBF by predicted arterial transit time (ATT) and calculated mean CBF measured from each post-labeling delay (PLD) [8]. In addition, multi-delay ASL can directly evaluate arterial cerebral blood volume (aCBV), which avoids errors caused by using empirical relationships. Accordingly, we propose to map OEF using multi-delay ASL based on QQ and investigate the differences between QQ with multi-delay ASL method and QQ with single-delay ASL method results.

Methods

Seven healthy volunteers underwent a brain MRI on a 3T scanner (Premier, GE Healthcare) using a 48-channel brain receiver coil. MRI was performed in a resting state using a 3D multi-echo spoiled gradient-echo (GRE) sequence, a 3D pseudo-continuous arterial spin labeling sequence (pcASL), and a 3D magnetization-prepared rapid gradient echo sequence (MPRAGE).
ASL protocols used pcASL and included both single and multiple PLD acquisitions. The multi-delay ASL data were acquired with 7 PLDs evenly spaced between 0.7 and 4s, and single-delay ASL data were acquired with a PLD of 2.15s. CBF maps (mL/100g/min) were generated from the ASL data using FuncTool (GE Healthcare, Waukesha, WI). QSM reconstruction was performed using STISuite Toolbox. All images were co-registered to the T1 image implemented in SPM12.
ROI analyses and paired t-test were performed to compare OEF values between QQ with single-delay ASL and QQ with multi-delay ASL methods in gray matter (GM), white matter (WM), and whole brain.

Results

The OEFs in GM were 39.6±3.4% and 38.9±3.4% (P<0.01) for QQ with single-delay ASL and QQ with multi-delay ASL methods. Figure 1 shows OEF maps generated by QQ with single-delay ASL and QQ with multi-delay ASL methods of an exemplar subject. QQ with multi-delay ASL showed lower OEF than QQ with single-delay ASL; the OEF values for the whole brain and WM were 40.2±2.9% and 39.7±2.9% (P<0.01), 40.3±2.1% and 40.2±2.2% (P<0.05) for QQ with single-delay ASL and QQ with multi-delay ASL, respectively. (Figure 2)

Discussion

Our results demonstrate the feasibility of OEF mapping by QQ with multi-delay ASL method. The result ties well with previous studies wherein other independent OEF estimation methods, such as PET and vascular challenges QSM methods [6,9-12]. The OEFs in GM were 39.6±3.4% and 38.9±3.4% (P<0.01) for QQ with single-delay ASL and QQ with multi-delay ASL methods. This discrepancy could be attributed to using a directly measured CBV, which in QQ with single-delay ASL method is estimated using empirical relationship derived from normative PET data.
There are several limitations in this study that warrant further investigation. First, although QQ with multi-delay ASL removed the linear CBF/CBV assumption in QQ with single-delay ASL, it retains a constant ratio between venous and total blood volume (0.77), which may vary among subjects and diseases. Another limitation is that the contribution of macroscopic field inhomogeneities to the GRE signal has been neglected. This may be addressed by using high-order MR shimming in further study.

Conclusion

Our study demonstrates the feasibility of OEF mapping by QQ with multi-delay ASL method. In healthy subjects, the OEF mapping by QQ with multi-delay ASL shows an accurate value compared to QQ with single-delay ASL method, which may have the potential for the application of OEF to clinical diseases.

Acknowledgements

This study was supported by The National Natural Science Foundation of China (81901722).

References

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Figures

Figure 1 Comparison of the OEF map from a subject (22 years, female) using QQ with single-delay ASL and QQ with multi-delay ASL. T1-weight anatomical images are shown for reference. QQ with multi-delay ASL showed lower OEF than QQ with single-delay ASL methods.

Figure 2 Average and SD of OEF maps in GM, WM, and whole brain among QQ with single-delay ASL (black) and QQ with multi-delay ASL (white). QQ with multi-delay ASL shows smaller OEF values than QQ with single-delay ASL method (P<0.05). *P<0.05 (paired t-test).

Proc. Intl. Soc. Mag. Reson. Med. 31 (2023)
4019
DOI: https://doi.org/10.58530/2023/4019