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Hyperpolarized Xenon-129: A New Tool to Assess Pulmonary Physiology in Patients with Pulmonary Fibrosis

Purpose: The existing tools to quantify lung function in interstitial lung diseases have significant limitations. Lung MRI imaging using inhaled hyperpolarized xenon-129 gas ((129)Xe) as a contrast agent is a new technology for measuring regional lung physiology. We sought to assess the utility of t...

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Detalles Bibliográficos
Autores principales: Qing, Kun, Altes, Talissa A., Mugler, John P., Mata, Jaime F., Tustison, Nicholas J., Ruppert, Kai, Bueno, Juliana, Flors, Lucia, Shim, Yun M., Zhao, Li, Cassani, Joanne, Teague, William G., Kim, John S., Wang, Zhixing, Ruset, Iulian C., Hersman, F. William, Mehrad, Borna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10294784/
https://www.ncbi.nlm.nih.gov/pubmed/37371626
http://dx.doi.org/10.3390/biomedicines11061533
Descripción
Sumario:Purpose: The existing tools to quantify lung function in interstitial lung diseases have significant limitations. Lung MRI imaging using inhaled hyperpolarized xenon-129 gas ((129)Xe) as a contrast agent is a new technology for measuring regional lung physiology. We sought to assess the utility of the (129)Xe MRI in detecting impaired lung physiology in usual interstitial pneumonia (UIP). Materials and methods: After institutional review board approval and informed consent and in compliance with HIPAA regulations, we performed chest CT, pulmonary function tests (PFTs), and (129)Xe MRI in 10 UIP subjects and 10 healthy controls. Results: The (129)Xe MRI detected highly heterogeneous abnormalities within individual UIP subjects as compared to controls. Subjects with UIP had markedly impaired ventilation (ventilation defect fraction: UIP: 30 ± 9%; healthy: 21 ± 9%; p = 0.026), a greater amount of (129)Xe dissolved in the lung interstitium (tissue-to-gas ratio: UIP: 1.45 ± 0.35%; healthy: 1.10 ± 0.17%; p = 0.014), and impaired (129)Xe diffusion into the blood (RBC-to-tissue ratio: UIP: 0.20 ± 0.06; healthy: 0.28 ± 0.05; p = 0.004). Most MRI variables had no correlation with the CT and PFT measurements. The elevated level of (129)Xe dissolved in the lung interstitium, in particular, was detectable even in subjects with normal or mildly impaired PFTs, suggesting that this measurement may represent a new method for detecting early fibrosis. Conclusion: The hyperpolarized (129)Xe MRI was highly sensitive to regional functional changes in subjects with UIP and may represent a new tool for understanding the pathophysiology, monitoring the progression, and assessing the effectiveness of treatment in UIP.