Thomas Binu P, Liu Peiying, Aslan Sina, King Kevin S, van Osch Matthias J P, Lu Hanzhang
Advanced Imaging Research Center, UT Southwestern Medical Center, Dallas, TX 75390, USA; Biomedical Engineering Graduate Program, UT Southwestern Medical Center, Dallas, TX 75390, USA; Department of Bioengineering, UT Arlington, Arlington, TX 76019, USA.
Neuroimage. 2013 Dec;83:505-12. doi: 10.1016/j.neuroimage.2013.07.005. Epub 2013 Jul 10.
With a growing need for specific biomarkers in vascular diseases, there has been a surging interest in mapping cerebrovascular reactivity (CVR) of the brain. This index can be measured by conducting a hypercapnia challenge while acquiring blood-oxygenation-level-dependent (BOLD) signals. A BOLD signal increase with hypercapnia is the expected outcome and represents the majority of literature reports; in this work we report an intriguing observation of an apparently negative BOLD CVR response at 3T, during inhalation of 5% CO2 with balance medical air. These "negative-CVR" clusters were specifically located in the ventricular regions of the brain, where CSF is abundant and results in an intense baseline signal. The amplitude of the CVR response was -0.51±0.44% (N=14, age 26±4 years). We hypothesized that this observation might not be due to a decrease in oxygenation but rather a volume effect in which bright CSF signal is replaced by a less intensive blood signal as a result of vasodilation. To test this, we performed an inversion-recovery (IR) experiment to suppress the CSF signal (N=10, age 27±5 years). This maneuver in imaging sequence reversed the sign of the signal response (to 0.66±0.25%), suggesting that the volume change was the predominant reason for the apparently negative CVR in the BOLD experiment. Further support of this hypothesis was provided by a BOLD hyperoxia experiment, in which no voxels showed a negative response, presumably because vasodilation is not usually associated with this challenge. Absolute CBF response to hypercapnia was measured in a new group of subjects (N=8, age 29±7 years) and it was found that CBF in ventricular regions increased by 48% upon CO2 inhalation, suggesting that blood oxygenation most likely increased rather than decreased. The findings from this study suggest that CO2 inhalation results in the dilation of ventricular vessels accompanied by shrinkage in CSF space, which is responsible for the apparently negative CVR in brain ventricles.
随着血管疾病中对特定生物标志物的需求不断增加,人们对绘制大脑脑血管反应性(CVR)的兴趣激增。该指标可通过在获取血氧水平依赖(BOLD)信号时进行高碳酸血症激发试验来测量。高碳酸血症时BOLD信号增加是预期结果,并且代表了大多数文献报道;在本研究中,我们报告了一个有趣的观察结果,即在3T时,吸入5%二氧化碳与平衡医用空气时,BOLD CVR反应明显为负。这些“负CVR”簇特别位于脑室区域,此处脑脊液丰富,导致强烈的基线信号。CVR反应的幅度为-0.51±0.44%(N = 14,年龄26±4岁)。我们推测,这一观察结果可能不是由于氧合作用降低,而是一种容积效应,即由于血管舒张,明亮的脑脊液信号被强度较低的血液信号所取代。为了验证这一点,我们进行了反转恢复(IR)实验以抑制脑脊液信号(N = 10,年龄27±5岁)。成像序列中的这一操作使信号反应的符号反转(变为0.66±0.25%),表明容积变化是BOLD实验中明显负CVR的主要原因。BOLD高氧实验进一步支持了这一假设,在该实验中没有体素显示负反应,推测是因为血管舒张通常与这种激发试验无关。在一组新的受试者(N = 8,年龄29±7岁)中测量了对高碳酸血症的绝对脑血流量(CBF)反应,发现吸入二氧化碳后脑室区域的CBF增加了48%,这表明血液氧合很可能增加而非减少。本研究结果表明,吸入二氧化碳导致脑室血管扩张,同时脑脊液空间缩小,这是脑室中明显负CVR的原因。