Medical Physics Group, Department of Diagnostic and Interventional Radiology, Jena University Hospital, Philosophenweg 3, D-07743 Jena, Germany.
Neuroimage. 2010 Jun;51(2):765-74. doi: 10.1016/j.neuroimage.2010.02.037. Epub 2010 Feb 24.
Measuring the morphology of the cerebral microvasculature by vessel-size imaging (VSI) is a promising approach for clinical applications, such as the characterization of tumor angiogenesis and stroke. Despite the great potential of VSI, this method has not yet found widespread use in practice due to the lack of experience in testing it on healthy humans. Since this limitation derives mainly from the need for an invasive injection of a contrast agent, this work explores the possibility to employ instead the easily accessible blood oxygenation level dependent (BOLD) effect for VSI of the venous microstructure. It is demonstrated that BOLD-VSI in humans can be realized by a hypercapnic challenge using a fast gradient-echo (GE) and spin-echo (SE) sequence at 7T. Reproducible maps of the mean venous vessel radius, based on the BOLD-induced changes in GE and SE relaxation rates, could be obtained within a scan time of 10min. Moreover, the method yields maps of venous blood volume and vessel density. Owing to its non-invasive character, BOLD-VSI provides a low-risk method to analyze the venous microstructure, which will not only be useful in clinical applications, but also provide a better understanding of BOLD effect.
通过血管大小成像(VSI)测量脑微血管形态是一种很有前途的临床应用方法,例如肿瘤血管生成和中风的特征描述。尽管 VSI 具有巨大的潜力,但由于缺乏在健康人群中测试它的经验,该方法尚未在实践中得到广泛应用。由于这种限制主要源于需要对对比剂进行侵入性注射,因此这项工作探索了使用更容易获得的血氧水平依赖(BOLD)效应来代替静脉微结构的 VSI 的可能性。研究表明,在 7T 下使用快速梯度回波(GE)和自旋回波(SE)序列进行高碳酸血症挑战,可以在 10 分钟的扫描时间内实现 BOLD-VSI。此外,该方法还可以得到静脉血管半径、静脉血容量和血管密度的图。由于其非侵入性,BOLD-VSI 提供了一种低风险的方法来分析静脉微结构,这不仅将在临床应用中有用,而且还将提供对 BOLD 效应的更好理解。