He Mu, Driehuys Bastiaan, Que Loretta G, Huang Yuh-Chin T
Center for In Vivo Microscopy, Duke University Medical Center, Durham, North Carolina; Department of Electrical and Computer Engineering, Duke University, Durham, North Carolina.
Center for In Vivo Microscopy, Duke University Medical Center, Durham, North Carolina; Department of Electrical and Computer Engineering, Duke University, Durham, North Carolina; Department of Biomedical Engineering, Duke University, Durham, North Carolina; Department of Radiology, Duke University Medical Center, Durham, North Carolina.
Acad Radiol. 2016 Dec;23(12):1521-1531. doi: 10.1016/j.acra.2016.07.014. Epub 2016 Sep 9.
Ventilation heterogeneity is impossible to detect with spirometry. Alternatively, pulmonary ventilation can be imaged three-dimensionally using inhaled Xe magnetic resonance imaging (MRI). To date, such images have been quantified primarily based on ventilation defects. Here, we introduce a robust means to transform Xe MRI scans such that the underlying ventilation distribution and its heterogeneity can be quantified.
Quantitative Xe ventilation MRI was conducted in 12 younger (24.7 ± 5.2 years) and 10 older (62.2 ± 7.2 years) healthy individuals, as well as in 9 younger (25.9 ± 6.4 yrs) and 10 older (63.2 ± 6.1 years) asthmatics. The younger healthy population was used to establish a reference ventilation distribution and thresholds for six intensity bins. These bins were used to display and quantify the ventilation defect region (VDR), the low ventilation region (LVR), and the high ventilation region (HVR).
The ventilation distribution in young subjects was roughly Gaussian with a mean and standard deviation of 0.52 ± 0.18, resulting in VDR = 2.1 ± 1.3%, LVR = 15.6 ± 5.4%, and HVR = 17.4 ± 3.1%. Older healthy volunteers exhibited a significantly right-skewed distribution (0.46 ± 0.20, P = 0.034), resulting in significantly increased VDR (7.0 ± 4.8%, P = 0.008) and LVR (24.5 ± 11.5%, P = 0.025). In the asthmatics, VDR and LVR increased in the older population, and HVR was significantly reduced (13.5 ± 4.6% vs 18.9 ± 4.5%, P = 0.009). Quantitative Xe MRI also revealed altered ventilation heterogeneity in response to albuterol in two asthmatics with normal spirometry.
Quantitative Xe MRI provides a robust and objective means to display and quantify the pulmonary ventilation distribution, even in subjects who have airway function impairment not appreciated by spirometry.
肺活量测定法无法检测通气异质性。另外,可以使用吸入式氙磁共振成像(MRI)对肺通气进行三维成像。迄今为止,此类图像主要是基于通气缺陷进行量化的。在此,我们引入一种可靠的方法来转换氙MRI扫描图像,以便能够量化潜在的通气分布及其异质性。
对12名年轻(24.7±5.2岁)和10名年长(62.2±7.2岁)的健康个体,以及9名年轻(25.9±6.4岁)和10名年长(63.2±6.1岁)的哮喘患者进行了定量氙通气MRI检查。以年轻健康人群为参照,建立了六个强度区间的通气分布及阈值。这些区间用于显示和量化通气缺陷区域(VDR)、低通气区域(LVR)和高通气区域(HVR)。
年轻受试者的通气分布大致呈高斯分布,均值和标准差为0.52±0.18,VDR = 2.1±1.3%,LVR = 15.6±5.4%,HVR = 17.4±3.1%。年长健康志愿者的通气分布明显右偏(0.46±0.20,P = 0.034),导致VDR(7.0±4.8%,P = 0.008)和LVR(24.5±11.5%,P = 0.025)显著增加。在哮喘患者中,年长人群的VDR和LVR增加,HVR显著降低(13.5±4.6%对18.9±4.5%,P = 0.009)。定量氙MRI还显示,两名肺活量测定正常的哮喘患者在使用沙丁胺醇后通气异质性发生改变。
定量氙MRI提供了一种可靠且客观的方法来显示和量化肺通气分布,即使是在那些肺活量测定未发现气道功能受损的受试者中。