中重度哮喘患者的肺部 129Xe 磁共振气体交换异常

Grace Parraga, Sam Tcherner, Ali Mozaffaripour, Alexander M Matheson, Alexander Biancaniello, Cory Yamashita
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引用次数: 0

摘要

背景:哮喘被认为是一种气道炎症性疾病,但炎症也可能影响肺实质和肺血管。超极化 129Xe MRI 和 MR 光谱(MRS)为量化气体从气道通过肺泡膜的转移及其与肺微血管红细胞(RBC)中血红蛋白的结合提供了一种方法。绝大多数 129Xe MRS 研究都是针对间质性肺病以及 129Xe 与红细胞结合的比率和存在于肺泡膜中的 129Xe 的比率(RBC:膜)(RBC:膜是氧气体转移到血液中的替代物)进行的。我们想知道哮喘患者与健康志愿者相比,129Xe RBC:membrane 是否会有所不同,因为最近的研究表明,重度哮喘患者的肺血管小血管结构异常减弱。研究问题:129Xe MRI 气体转移测量结果在中度-重度哮喘患者中是否有显著差异?研究设计和方法:在这项回顾性研究中,对提供书面知情同意书的健康(NCT02484885)和哮喘(NCT04651777;NCT02351141)参与者进行了评估。结果:对31名哮喘参与者(平均年龄=55岁±18岁;22名女性)和32名健康志愿者(平均年龄=31岁±14岁;12名女性)进行了129Xe MRS评估。与健康参与者相比,哮喘患者的 FEV1、VDP 和 DLCO/KCO 有显著差异。与健康参与者(0.47±0.12,P=.01)相比,中重度哮喘患者的年龄校正 1RBC:membrane 显著不同(0.32±0.09)。RBC:membrane 与脉搏氧饱和度血红蛋白估计值(ρ=.29;P=.04)和 DLCO(ρ=.71;P<.001)明显相关。经性别调整后,健康参与者(ρ=-.55;P=.002)和哮喘参与者(ρ=-0.49;P=.006)的 129Xe RBC:membrane 与年龄之间存在显著关系。一个有意义的方差分析模型还显示了年龄(P=.002)、性别(P<.001)、血红蛋白(P=.003)和哮喘状态(P=.02)对 RBC:membrane 的影响。阐释:与健康志愿者相比,中重度哮喘患者的 129Xe RBC:membrane 值有显著差异,年龄、性别、血红蛋白和哮喘状态可解释这种差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pulmonary 129Xe Magnetic Resonance Gas-exchange Abnormalities in Moderate-Severe Asthma
BACKGROUND: Asthma is recognized as an inflammatory disease of the airways, but inflammation may also affect the parenchyma and pulmonary vasculature. Hyperpolarized 129Xe MRI and MR spectroscopy (MRS) provide a way to quantify the transfer of gas from the airways through the alveolar membrane and its binding to hemoglobin in the red blood cells (RBC) of the pulmonary microvasculature. The vast majority of 129Xe MRS studies have investigated interstitial lung disease and the ratio of 129Xe binding to the RBC and 129Xe present in the alveolar membrane, (RBC:membrane) which is a surrogate of oxygen gas-transfer to the blood. We wondered if 129Xe RBC:membrane would differ in asthma patients as compared to healthy volunteers because of recent work showing abnormally diminished pulmonary vascular small-vessel structure in severe- asthma. RESEARCH QUESTION: Do 129Xe MRI gas-transfer measurements differ significantly in patients with moderate-severe asthma? STUDY DESIGN AND METHODS: In this retrospective study, healthy (NCT02484885) and asthma (NCT04651777; NCT02351141) participants were evaluated who provided written informed consent. RESULTS: Thirty-one participants with asthma (mean age=55 years ± 18; 22 females) and 32 healthy volunteers (mean age=31 years ± 14; 12 females) with 129Xe MRS were evaluated. FEV1, VDP and DLCO/KCO were significantly different in asthma compared to healthy participants. Age-corrected 1RBC:membrane was significantly different in moderate-severe asthma (0.32±0.09) as compared to healthy participants (0.47±0.12, P=.01). RBC:membrane was significantly related to pulse-oximetry hemoglobin estimates (ρ=.29; P=.04) and DLCO (ρ=.71; P<.001). Significant relationships between 129Xe RBC:membrane and age were observed in healthy (ρ=-.55; P=.002) and asthma participants (ρ=-0.49; P=.006), adjusted for sex. A significant ANCOVA model also revealed the influence of age (P=.002), sex (P<.001), hemoglobin (P=.003) and asthma status (P=.02) on RBC:membrane. INTERPRETATION: 129Xe RBC:membrane values were significantly different in moderate-severe asthma compared to healthy volunteers and were explained by age, sex, hemoglobin, and asthma status.
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