Leibniz Institute of Photonic Technology, Member of Leibniz Health Technology, 07745 Jena, Germany.
Department of Internal Medicine IV (Gastroenterology, Hepatology, Infectious Disease), Jena University Hospital, 07747 Jena, Germany.
Anal Chem. 2020 Oct 20;92(20):13776-13784. doi: 10.1021/acs.analchem.0c02163. Epub 2020 Oct 7.
Ulcerative colitis (UC) is one of the main types of chronic inflammatory diseases that affect the bowel, but its pathogenesis is yet to be completely defined. Assessing the disease activity of UC is vital for developing a personalized treatment. Conventionally, the assessment of UC is performed by colonoscopy and histopathology. However, conventional methods fail to retain biomolecular information associated to the severity of UC and are solely based on morphological characteristics of the inflamed colon. Furthermore, assessing endoscopic disease severity is limited by the requirement for experienced human reviewers. Therefore, this work presents a nondestructive biospectroscopic technique, for example, Raman spectroscopy, for assessing endoscopic disease severity according to the four-level Mayo subscore. This contribution utilizes multidimensional Raman spectroscopic data to generate a predictive model for identifying colonic inflammation. The predictive modeling of the Raman spectroscopic data is performed using a one-dimensional deep convolutional neural network (1D-CNN). The classification results of 1D-CNN achieved a mean sensitivity of 78% and a mean specificity of 93% for the four Mayo endoscopic scores. Furthermore, the results of the 1D-CNN are interpreted by a first-order Taylor expansion, which extracts the Raman bands important for classification. Additionally, a regression model of the 1D-CNN model is constructed to study the extent of misclassification and border-line patients. The overall results of Raman spectroscopy with 1D-CNN as a classification and regression model show a good performance, and such a method can serve as a complementary method for UC analysis.
溃疡性结肠炎(UC)是一种主要的肠道慢性炎症性疾病,但它的发病机制尚未完全确定。评估 UC 的疾病活动对于制定个性化治疗方案至关重要。传统上,UC 的评估是通过结肠镜检查和组织病理学进行的。然而,传统方法无法保留与 UC 严重程度相关的生物分子信息,并且仅基于发炎结肠的形态特征。此外,评估内镜疾病严重程度受到需要有经验的人类审查员的限制。因此,这项工作提出了一种非破坏性的生物光谱技术,例如拉曼光谱,用于根据四级 Mayo 亚评分评估内镜疾病严重程度。本研究利用多维拉曼光谱数据来生成用于识别结肠炎症的预测模型。使用一维深度卷积神经网络(1D-CNN)对拉曼光谱数据进行预测建模。1D-CNN 的分类结果对于四个 Mayo 内镜评分的平均敏感性为 78%,平均特异性为 93%。此外,通过一阶泰勒展开对 1D-CNN 的结果进行解释,从而提取出用于分类的拉曼波段。此外,还构建了 1D-CNN 模型的回归模型,以研究误分类和边界患者的程度。基于 1D-CNN 的拉曼光谱整体结果显示出良好的性能,该方法可以作为 UC 分析的辅助方法。