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使用涡轮反转恢复-幅度磁共振成像定量评估节段性变应原挑战后的肺部炎症。

Quantification of pulmonary inflammation after segmental allergen challenge using turbo-inversion recovery-magnitude magnetic resonance imaging.

机构信息

1 Institute of Diagnostic and Interventional Radiology and.

出版信息

Am J Respir Crit Care Med. 2014 Mar 15;189(6):650-7. doi: 10.1164/rccm.201310-1825OC.

Abstract

RATIONALE

There is a need to develop novel noninvasive imaging biomarkers that help to evaluate antiinflammatory asthma treatments.

OBJECTIVES

To investigate whether the extent of the segmental lung edema measured noninvasively using turbo-inversion recovery-magnitude magnetic resonance imaging (TIRM MRI) corresponds to the severity of the regional allergic reaction determined by the percentage of eosinophils in bronchoalveolar lavage fluid (BAL) 24 hours after segmental allergen challenge in patients with asthma compared with normal control subjects.

METHODS

Eleven volunteers with allergic asthma and five healthy volunteers underwent segmental challenges with different allergen doses by two bronchoscopies 24 hours apart. They had lung MRI at baseline and 6 and 24 hours after segmental challenge. MRI TIRM scores were correlated with the eosinophilic response at 24 hours.

MEASUREMENTS AND MAIN RESULTS

In patients with asthma, there were significant differences of eosinophil percentages in BAL at 24 hours from segments given standard-dose, low-dose, or no allergen (saline) (P < 0.001). Correspondingly significant differences between the TIRM score in allergen standard-dose, low-dose, and saline-treated segments were observed at 24 hours post-challenge (P < 0.001). With increasing TIRM score at 24 hours the percent eosinophils per segment 24 hours post-challenge also increased accordingly (P < 0.001). There was interobserver agreement for TIRM score grading (kappa = 0.72 for 24-h time point).

CONCLUSIONS

The MRI-based noninvasive TIRM score is a promising biomarker for the noninvasive detection of the inflammatory response after segmental allergen challenge in patients with asthma and may serve to monitor the therapeutic effectiveness of novel antiinflammatory drugs in future human trials.

摘要

背景

需要开发新的非侵入性成像生物标志物,以帮助评估抗炎性哮喘治疗方法。

目的

通过 turbo-inversion recovery-magnitude 磁共振成像(TIRM MRI)无创性测量节段性肺水肿的程度,来研究其与哮喘患者 24 小时后支气管肺泡灌洗液(BAL)中嗜酸性粒细胞百分比确定的区域性过敏反应严重程度的相关性,与正常对照组进行比较。

方法

11 名过敏性哮喘志愿者和 5 名健康志愿者通过两次支气管镜检查,在 24 小时内接受不同过敏原剂量的节段性挑战。他们在基线、节段性挑战后 6 小时和 24 小时进行了肺部 MRI。MRI TIRM 评分与 24 小时时的嗜酸性粒细胞反应相关。

测量和主要结果

哮喘患者 BAL 中嗜酸性粒细胞百分比在 24 小时时,标准剂量、低剂量或无过敏原(盐水)的节段之间存在显著差异(P < 0.001)。在挑战后 24 小时,TIRM 评分在标准剂量、低剂量和盐水处理的节段之间也存在显著差异(P < 0.001)。随着 24 小时 TIRM 评分的增加,挑战后 24 小时每个节段的嗜酸性粒细胞百分比也相应增加(P < 0.001)。TIRM 评分分级的观察者间一致性良好(24 小时时间点的kappa = 0.72)。

结论

基于 MRI 的无创性 TIRM 评分是一种很有前途的生物标志物,可用于无创性检测哮喘患者节段性过敏原挑战后的炎症反应,并可能在未来的人类试验中用于监测新型抗炎药物的治疗效果。

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