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使用共聚焦拉曼显微光谱法开发非酒精性脂肪性肝炎(NASH)的分类模型。

Development of a classification model for non-alcoholic steatohepatitis (NASH) using confocal Raman micro-spectroscopy.

作者信息

Yan Jie, Yu Yang, Kang Jeon Woong, Tam Zhi Yang, Xu Shuoyu, Fong Eliza Li Shan, Singh Surya Pratap, Song Ziwei, Tucker-Kellogg Lisa, So Peter T C, Yu Hanry

机构信息

Institute of Bioengineering and Nanotechnology, Agency for Science, Technology and Research (A*STAR), Singapore, 138669.

Department of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, 2 Medical Drive, Singapore, 117597.

出版信息

J Biophotonics. 2017 Dec;10(12):1703-1713. doi: 10.1002/jbio.201600303. Epub 2017 Jun 21.

Abstract

Non-alcoholic fatty liver disease (NAFLD) is the most common liver disorder in developed countries [1]. A subset of individuals with NAFLD progress to non-alcoholic steatohepatitis (NASH), an advanced form of NAFLD which predisposes individuals to cirrhosis, liver failure and hepatocellular carcinoma. The current gold standard for NASH diagnosis and staging is based on histological evaluation, which is largely semi-quantitative and subjective. To address the need for an automated and objective approach to NASH detection, we combined Raman micro-spectroscopy and machine learning techniques to develop a classification model based on a well-established NASH mouse model, using spectrum pre-processing, biochemical component analysis (BCA) and logistic regression. By employing a selected pool of biochemical components, we identified biochemical changes specific to NASH and show that the classification model is capable of accurately detecting NASH (AUC=0.85-0.87) in mice. The unique biochemical fingerprint generated in this study may serve as a useful criterion to be leveraged for further validation in clinical samples.

摘要

非酒精性脂肪性肝病(NAFLD)是发达国家最常见的肝脏疾病[1]。一部分NAFLD患者会进展为非酒精性脂肪性肝炎(NASH),这是NAFLD的一种晚期形式,会使个体易患肝硬化、肝衰竭和肝细胞癌。目前NASH诊断和分期的金标准基于组织学评估,该评估在很大程度上是半定量和主观的。为了满足对NASH检测采用自动化和客观方法的需求,我们将拉曼显微光谱和机器学习技术相结合,基于一个成熟的NASH小鼠模型,利用光谱预处理、生化成分分析(BCA)和逻辑回归开发了一个分类模型。通过采用一组选定的生化成分,我们确定了NASH特有的生化变化,并表明该分类模型能够准确检测小鼠中的NASH(AUC = 0.85 - 0.87)。本研究中生成的独特生化指纹可能作为一个有用的标准,用于在临床样本中进行进一步验证。

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