In vivo assessment of pulmonary fibrosis and edema in rodents using the backscatter coefficient and envelope statistics

Quantitative ultrasound methods based on the backscatter coefficient (BSC) and envelope statistics have been used to quantify disease in a wide variety of tissues, such as prostate, lymph nodes, breast, and thyroid. However, to date, these methods have not been investigated in the lung. In this stud...

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Veröffentlicht in:The Journal of the Acoustical Society of America 2021-07, Vol.150 (1), p.183-192
Hauptverfasser: Lye, Theresa H, Roshankhah, Roshan, Karbalaeisadegh, Yasamin, Montgomery, Stephanie A, Egan, Thomas M, Muller, Marie, Mamou, Jonathan
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Sprache:eng
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Zusammenfassung:Quantitative ultrasound methods based on the backscatter coefficient (BSC) and envelope statistics have been used to quantify disease in a wide variety of tissues, such as prostate, lymph nodes, breast, and thyroid. However, to date, these methods have not been investigated in the lung. In this study, lung properties were quantified by BSC and envelope statistical parameters in normal, fibrotic, and edematous rat lungs in vivo. The average and standard deviation of each parameter were calculated for each lung as well as the evolution of each parameter with acoustic propagation time within the lung. The transport mean free path and backscattered frequency shift, two parameters that have been successfully used to assess pulmonary fibrosis and edema in prior work, were evaluated in combination with the BSC and envelope statistical parameters. Multiple BSC and envelope statistical parameters were found to provide contrast between control and diseased lungs. BSC and envelope statistical parameters were also significantly correlated with fibrosis severity using the modified Ashcroft fibrosis score as the histological gold standard. These results demonstrate the potential for BSC and envelope statistical parameters to improve the diagnosis of pulmonary fibrosis and edema as well as monitor pulmonary fibrosis.
ISSN:0001-4966
1520-8524
DOI:10.1121/10.0005481