Evaluation of single-delay arterial spin labeling-based spatial coefficient of variation and histogram-based parameters in relation to cerebrovascular reserve in patients with Moyamoya disease

评估基于单延迟动脉自旋标记的空间变异系数和直方图参数与烟雾病患者脑血管储备的关系

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Abstract

INTRODUCTION: Single-delay Arterial Spin Labeling (ASL)-based spatial coefficient of variation (CoV(CBF)) has been suggested as a measure of hemodynamic disturbance in patients with cerebrovascular diseases. However, spatial CoV(CBF) and other histogram-based parameters such as skewness and kurtosis and the volume of the arterial transit time artefact (ATA(vol)), has not been evaluated in patients with MMD nor against cerebrovascular reserve (CVR). The aim of this study was to assess whether any associations between spatial CoV(CBF), skewness, kurtosis, and ATA(vol) are present and to analyze any potential associations with CVR, derived from single-delay ASL in patients with MMD. METHODS: Fifteen MMD patients were included before or after revascularization surgery. Cerebral blood flow (CBF) maps were acquired using pseudo-continuous ASL before, and 5, 15, and 25 min after an intravenous acetazolamide injection. CVR(max) was defined as the highest percentual increase in CBF at any of the three post-injection time points. A vascular territory template was spatially normalized to each patient, including the bilateral anterior, middle, and posterior cerebral arteries. All affected anterior and middle cerebral artery regions and all unaffected posterior cerebral artery regions were included, based on Suzuki grading by digital subtraction angiography. RESULTS: Significant differences between affected and unaffected regions were found for CBF, CVR(max), and ATA(vol). No association was found between CVR(max) and any other parameter. High correlations were found between spatial CoV(CBF), skewness and ATA(vol). CONCLUSION: Spatial CoV(CBF) derived from single-delay ASL does not correlate with CVR in patients with MMD. Moreover, skewness and kurtosis did not provide additional information of clinical value.

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