Please use this identifier to cite or link to this item: https://doi.org/10.1002/jbio.201600303
Title: Development of a classification model for non-alcoholic steatohepatitis (NASH) using confocal Raman micro-spectroscopy
Authors: Yan, Jie
Yu, Yang
Kang, Jeon Woong
Tam, Zhi Yang
Xu, Shuoyu
Fong Li Shan Eliza 
Singh, Surya Pratap
Song, Ziwei
Lisa Tucker-Kellogg 
So, Peter T. C.
Yu,Hanry 
Keywords: Raman micro-spectroscopic imaging
biochemical component analysis
model fitting
non-alcoholic fatty liver disease
non-alcoholic steatohepatitis
Issue Date: 1-Dec-2017
Publisher: Wiley-VCH Verlag
Citation: Yan, Jie, Yu, Yang, Kang, Jeon Woong, Tam, Zhi Yang, Xu, Shuoyu, Fong Li Shan Eliza, Singh, Surya Pratap, Song, Ziwei, Lisa Tucker-Kellogg, So, Peter T. C., Yu,Hanry (2017-12-01). Development of a classification model for non-alcoholic steatohepatitis (NASH) using confocal Raman micro-spectroscopy. Journal of biophotonics 10 (12) : 1703-1713. ScholarBank@NUS Repository. https://doi.org/10.1002/jbio.201600303
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.
Source Title: Journal of biophotonics
URI: http://scholarbank.nus.edu.sg/handle/10635/137961
ISSN: 1864063X
DOI: 10.1002/jbio.201600303
Appears in Collections:Staff Publications

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