Classification of collagen remodeling in asthma using second-harmonic generation imaging, supervised machine learning and texture-based analysis.

IF 2.8 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Frontiers in bioinformatics Pub Date : 2025-04-17 eCollection Date: 2025-01-01 DOI:10.3389/fbinf.2025.1539936
Natasha N Kunchur, Joshua J A Poole, Jesse Levine, Tillie-Louise Hackett, Rebecca Thornhill, Leila B Mostaço-Guidolin
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Abstract

Airway remodeling is present in all stages of asthma severity and has been linked to reduced lung function, airway hyperresponsiveness and increased deposition of fibrillar collagens. Traditional histological staining methods used to visualize the fibrotic response are poorly suited to capture the morphological traits of extracellular matrix (ECM) proteins in their native state, hindering our understanding of disease pathology. Conversely, second harmonic generation (SHG), provides label-free, high-resolution visualization of fibrillar collagen; a primary ECM protein contributing to the loss of asthmatic lung elasticity. From a cohort of 13 human lung donors, SHG-imaged collagen belonging to non-asthmatic (control) and asthmatic donors was evaluated through a custom textural classification pipeline. Integrated with supervised machine learning, the pipeline enables the precise quantification and characterization of collagen, delineating amongst control and remodeled airways. Collagen distribution is quantified and characterized using 80 textural features belonging to the Gray Level Cooccurrence Matrix (GLCM), Gray Level Size Zone Matrix (GLSZM), Gray Level Run Length Matrix (GLRLM), Gray Level Dependence Matrix (GLDM) and Neighboring Gray Tone Difference Matrix (NGTDM). To denote an accurate subset of features reflective of fibrillar collagen formation; filter, wrapper, embedded and novel statistical methods were applied as feature refinement. Textural feature subsets of high predictor importance trained a support vector machine model, achieving an AUC-ROC of 94% ± 0.0001 in the classification of remodeled airway collagen vs. control lung tissue. Combined with detailed texture analysis and supervised ML, we demonstrate that morphological variation amongst remodeled SHG-imaged collagen in lung tissue can be successfully characterized.

利用二次谐波成像、监督机器学习和基于纹理的分析对哮喘中的胶原重构进行分类。
气道重塑存在于哮喘严重程度的所有阶段,并与肺功能降低、气道高反应性和纤维性胶原沉积增加有关。用于可视化纤维化反应的传统组织学染色方法不适合捕捉细胞外基质(ECM)蛋白在其天然状态下的形态特征,阻碍了我们对疾病病理学的理解。相反,二次谐波生成(SHG)提供无标记、高分辨率的纤维胶原可视化;一种导致哮喘肺弹性丧失的初级ECM蛋白。从13名人类肺供体队列中,通过自定义纹理分类管道评估非哮喘(对照)和哮喘供体的shg成像胶原。与监督机器学习相结合,该管道能够精确量化和表征胶原蛋白,描绘控制和重塑的气道。利用灰度共生矩阵(GLCM)、灰度大小区域矩阵(GLSZM)、灰度运行长度矩阵(GLRLM)、灰度依赖矩阵(GLDM)和相邻灰度色差矩阵(NGTDM)等80个纹理特征对胶原蛋白的分布进行量化和表征。表示反映纤维性胶原形成的准确特征子集;采用滤波、包装、嵌入和新颖的统计方法进行特征细化。高预测重要性的纹理特征子集训练了一个支持向量机模型,在重建气道胶原与对照肺组织的分类中实现了94%±0.0001的AUC-ROC。结合详细的纹理分析和监督ML,我们证明在肺组织中重建的shg成像胶原之间的形态学变化可以成功地表征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
2.60
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