Quantification of lung damage in an elastase-induced mouse model of emphysema

Int J Biomed Imaging. 2012;2012:734734. doi: 10.1155/2012/734734. Epub 2012 Nov 8.


Objective. To define the sensitivity of microcomputed tomography- (micro-CT-) derived descriptors for the quantification of lung damage caused by elastase instillation. Materials and Methods. The lungs of 30 elastase treated and 30 control A/J mice were analyzed 1, 6, 12, and 24 hours and 7 and 17 days after elastase instillation using (i) breath-hold-gated micro-CT, (ii) pulmonary function tests (PFTs), (iii) RT-PCR for RNA cytokine expression, and (iv) histomorphometry. For the latter, an automatic, parallel software toolset was implemented that computes the airspace enlargement descriptors: mean linear intercept (L(m)) and weighted means of airspace diameters (D(0), D(1), and D(2)). A Support Vector Classifier was trained and tested based on three nonhistological descriptors using D(2) as ground truth. Results. D(2) detected statistically significant differences (P < 0.01) between the groups at all time points. Furthermore, D(2) at 1 hour (24 hours) was significantly lower (P < 0.01) than D(2) at 24 hours (7 days). The classifier trained on the micro-CT-derived descriptors achieves an area under the curve (AUC) of 0.95 well above the others (PFTS AUC = 0.71; cytokine AUC = 0.88). Conclusion. Micro-CT-derived descriptors are more sensitive than the other methods compared, to detect in vivo early signs of the disease.