Dynamic evaluation of acute lung injury using hyperpolarized 129 Xe magnetic resonance

NMR Biomed. 2024 Apr;37(4):e5078. doi: 10.1002/nbm.5078. Epub 2023 Dec 12.

Abstract

Prognosticating acute lung injury (ALI) is challenging, in part because of a lack of sensitive biomarkers. Hyperpolarized gas magnetic resonance (MR) has unique advantages in pulmonary function measurement and can provide promising biomarkers for the assessment of lung injuries. Herein, we employ hyperpolarized 129 Xe MRI and generate a number of imaging biomarkers to detect the pulmonary physiological and morphological changes during the progression of ALI in an animal model. We find the measured ratio of 129 Xe in red blood cells to interstitial tissue/plasma (RBC/TP) is significantly lower in the ALI group on the second (0.32 ± 0.03, p = 0.004), seventh (0.23 ± 0.03, p < 0.001), and 14th (0.29 ± 0.04, p = 0.001) day after lipopolysaccharide treatment compared with that in the control group (0.41 ± 0.04). In addition, significant differences are also observed for RBC/TP measurements between the second and seventh day (p = 0.001) and between the seventh and 14th day (p = 0.018) in the ALI group after treatment. Besides RBC/TP, significant differences are also observed in the measured exchange time constant (T) on the second (p = 0.038) and seventh day (p = 0.009) and in the measured apparent diffusion coefficient (ADC) and alveolar surface-to-volume ratio (SVR) on the 14th day (ADC: p = 0.009 and SVR: p = 0.019) after treatment in the ALI group compared with that in the control group. These findings indicate that the parameters measured with 129 Xe MR can detect the dynamic changes in pulmonary structure and function in an ALI animal model.

Keywords: acute lung injury; alveolar structure; gas exchange; hyperpolarized 129Xe; pulmonary function.

MeSH terms

  • Acute Lung Injury* / diagnostic imaging
  • Acute Lung Injury* / pathology
  • Animals
  • Biomarkers
  • Lung / diagnostic imaging
  • Lung / pathology
  • Magnetic Resonance Imaging* / methods
  • Magnetic Resonance Spectroscopy / methods
  • Xenon Isotopes / chemistry

Substances

  • Xenon Isotopes
  • Biomarkers