Suppr超能文献

多容积质子 MRI 和 CT 评估婴幼儿囊性纤维化的肺结构-功能关系。

Assessment of pulmonary structure-function relationships in young children and adolescents with cystic fibrosis by multivolume proton-MRI and CT.

机构信息

Dipartimento di Elettronica, Informazione e Bioingegneria, Politecnico di Milano, Milano, Italy.

Center for Pulmonary Imaging Research, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.

出版信息

J Magn Reson Imaging. 2018 Aug;48(2):531-542. doi: 10.1002/jmri.25978. Epub 2018 Feb 19.

Abstract

BACKGROUND

Lung disease is the most frequent cause of morbidity and mortality in patients with cystic fibrosis (CF), and there is a shortage of sensitive biomarkers able to regionally monitor disease progression and to assess early responses to therapy.

PURPOSE

To determine the feasibility of noncontrast-enhanced multivolume MRI, which assesses intensity changes between expiratory and inspiratory breath-hold images, to detect and quantify regional ventilation abnormalities in CF lung disease, with a focus on the structure-function relationship.

STUDY TYPE

Retrospective.

POPULATION

Twenty-nine subjects, including healthy young children (n = 9, 7-37 months), healthy adolescents (n = 4, 14-22 years), young children with CF lung disease (n = 10, 7-47 months), and adolescents with CF lung disease (n = 6, 8-18 years) were studied.

FIELD STRENGTH/SEQUENCE: 3D spoiled gradient-recalled sequence at 1.5T.

ASSESSMENT

Subjects were scanned during breath-hold at functional residual capacity (FRC) and total lung capacity (TLC) through noncontrast-enhanced MRI and CT. Expiratory-inspiratory differences in MR signal-intensity (Δ H-MRI) and CT-density (ΔHU) were computed to estimate regional ventilation. MR and CT images were also evaluated using a CF-specific scoring system.

STATISTICAL TESTS

Quadratic regression, Spearman's correlation, one-way analysis of variance (ANOVA).

RESULTS

Δ H-MRI maps were sensitive to ventilation heterogeneity related to gravity dependence in healthy lung and to ventilation impairment in CF lung disease. A high correlation was found between MRI and CT ventilation maps (R  = 0.79, P < 0.001). Globally, Δ H-MRI and ΔHU decrease with increasing morphological score (respectively, R  = 0.56, P < 0.001 and R  = 0.31, P < 0.001). Locally, Δ H-MRI was higher in healthy regions (median 15%) compared to regions with bronchiectasis, air trapping, consolidation, and to segments fed by airways with bronchial wall thickening (P < 0.001).

DATA CONCLUSION

Multivolume noncontrast-enhanced MRI, as a nonionizing imaging modality that can be used on nearly any MRI scanner without specialized equipment or gaseous tracers, may be particularly valuable in CF care, providing a new imaging biomarker to detect early alterations in regional lung structure-function.

LEVEL OF EVIDENCE

3 Technical Efficacy: Stage 3 J. MAGN. RESON. IMAGING 2018;48:531-542.

摘要

背景

肺部疾病是囊性纤维化(CF)患者发病率和死亡率的最常见原因,并且缺乏能够局部监测疾病进展和评估早期治疗反应的敏感生物标志物。

目的

确定非增强多容积 MRI 的可行性,该方法通过评估呼气和吸气屏气图像之间的强度变化,来检测和量化 CF 肺部疾病中的区域性通气异常,并重点关注结构-功能关系。

研究类型

回顾性。

人群

共 29 名受试者,包括健康的幼儿(n=9,7-37 个月)、健康的青少年(n=4,14-22 岁)、患有 CF 肺部疾病的幼儿(n=10,7-47 个月)和患有 CF 肺部疾病的青少年(n=6,8-18 岁)。

磁场强度/序列:1.5T 下的 3D 扰相梯度回波序列。

评估

受试者在功能残气(FRC)和肺总量(TLC)时通过非增强 MRI 和 CT 进行屏气扫描。计算 MR 信号强度(Δ H-MRI)和 CT 密度(ΔHU)的呼气相-吸气相差异,以估计区域性通气。还使用 CF 特异性评分系统对 MR 和 CT 图像进行了评估。

统计学检验

二次回归、Spearman 相关分析、单因素方差分析(ANOVA)。

结果

Δ H-MRI 图对与重力依赖相关的健康肺部通气异质性和 CF 肺部疾病中的通气损害敏感。MRI 和 CT 通气图之间存在高度相关性(R=0.79,P<0.001)。总体而言,Δ H-MRI 和 ΔHU 随形态学评分的增加而降低(分别为 R=0.56,P<0.001 和 R=0.31,P<0.001)。局部来看,与支气管扩张、空气潴留、实变以及由气道壁增厚的气道供应的节段相比,健康区域的 Δ H-MRI 更高(中位数为 15%)(P<0.001)。

数据结论

多容积非增强 MRI 作为一种非电离成像方式,几乎可以在任何 MRI 扫描仪上使用,无需特殊设备或气态示踪剂,可能在 CF 护理中特别有价值,为检测区域性肺结构-功能的早期改变提供了新的成像生物标志物。

证据水平

3 级技术功效:3 级 JMRI 2018;48:531-542。

相似文献

2
Longitudinal Assessment of Patients With Cystic Fibrosis Lung Disease With Multivolume Noncontrast MRI and Spirometry.
J Magn Reson Imaging. 2021 May;53(5):1570-1580. doi: 10.1002/jmri.27461. Epub 2020 Dec 10.
4
Pulmonary ventilation imaging in asthma and cystic fibrosis using oxygen-enhanced 3D radial ultrashort echo time MRI.
J Magn Reson Imaging. 2018 May;47(5):1287-1297. doi: 10.1002/jmri.25877. Epub 2017 Oct 31.
5
Volumetric dynamic oxygen-enhanced MRI (OE-MRI): comparison with CT Brody score and lung function in cystic fibrosis patients.
Eur Radiol. 2018 Oct;28(10):4037-4047. doi: 10.1007/s00330-018-5383-5. Epub 2018 Apr 13.
7
Current state of the art MRI for the longitudinal assessment of cystic fibrosis.
J Magn Reson Imaging. 2020 Nov;52(5):1306-1320. doi: 10.1002/jmri.27030. Epub 2019 Dec 17.
8
Air trapping in early cystic fibrosis lung disease-Does CT tell the full story?
Pediatr Pulmonol. 2017 Sep;52(9):1150-1156. doi: 10.1002/ppul.23754. Epub 2017 Jul 6.
9
Intra- and Inter-visit Repeatability of Xenon Multiple-Breath Washout MRI in Children With Stable Cystic Fibrosis Lung Disease.
J Magn Reson Imaging. 2023 Sep;58(3):936-948. doi: 10.1002/jmri.28638. Epub 2023 Feb 14.

引用本文的文献

1
Lung functional imaging.
Breathe (Sheff). 2023 Sep;19(3):220272. doi: 10.1183/20734735.0272-2022. Epub 2023 Nov 14.
4
Global research status and trends of bronchiectasis in children from 2003 to 2022: A 20-year bibliometric analysis.
Front Pediatr. 2023 Feb 3;11:1095452. doi: 10.3389/fped.2023.1095452. eCollection 2023.
5
Lung and chest wall volume during vital capacity manoeuvre in Osteogenesis Imperfecta.
Orphanet J Rare Dis. 2022 Oct 28;17(1):397. doi: 10.1186/s13023-022-02535-y.
7
Lung MRI in Children: The Road Less Travelled.
Indian J Radiol Imaging. 2021 Jan;31(1):237-241. doi: 10.1055/s-0041-1729126. Epub 2021 Apr 17.
8
Postinfectious Bronchiolitis Obliterans in Children: Diagnostic Workup and Therapeutic Options: A Workshop Report.
Can Respir J. 2020 Jan 30;2020:5852827. doi: 10.1155/2020/5852827. eCollection 2020.
9
A multi-scale model of gas transport in the lung to study heterogeneous lung ventilation during the multiple-breath washout test.
PLoS Comput Biol. 2019 Jun 17;15(6):e1007079. doi: 10.1371/journal.pcbi.1007079. eCollection 2019 Jun.

本文引用的文献

1
Advances in Imaging Cystic Fibrosis Lung Disease.
Pediatr Allergy Immunol Pulmonol. 2015 Dec;28(4):220-229. doi: 10.1089/ped.2015.0588.
2
Correlation of Lung Clearance Index with Hyperpolarized Xe Magnetic Resonance Imaging in Pediatric Subjects with Cystic Fibrosis.
Am J Respir Crit Care Med. 2017 Oct 15;196(8):1073-1075. doi: 10.1164/rccm.201611-2228LE.
3
Quantification of neonatal lung parenchymal density via ultrashort echo time MRI with comparison to CT.
J Magn Reson Imaging. 2017 Oct;46(4):992-1000. doi: 10.1002/jmri.25643. Epub 2017 Feb 3.
4
Quantitative CT characterization of pediatric lung development using routine clinical imaging.
Pediatr Radiol. 2016 Dec;46(13):1804-1812. doi: 10.1007/s00247-016-3686-8. Epub 2016 Aug 30.
5
Hyperpolarized Xe for investigation of mild cystic fibrosis lung disease in pediatric patients.
J Cyst Fibros. 2017 Mar;16(2):275-282. doi: 10.1016/j.jcf.2016.07.008. Epub 2016 Jul 29.
6
Retrospective respiratory self-gating and removal of bulk motion in pulmonary UTE MRI of neonates and adults.
Magn Reson Med. 2017 Mar;77(3):1284-1295. doi: 10.1002/mrm.26212. Epub 2016 Mar 12.
9
Ivacaftor for patients with cystic fibrosis.
Expert Rev Respir Med. 2014 Oct;8(5):533-8. doi: 10.1586/17476348.2014.951333. Epub 2014 Aug 22.
10
Comparison between multivolume CT-based surrogates of regional ventilation in healthy subjects.
Acad Radiol. 2014 Oct;21(10):1268-75. doi: 10.1016/j.acra.2014.05.022. Epub 2014 Aug 7.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验