Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41598-018-35096-x
Title: Tear Proteins Calcium binding protein A4 (S100A4) and Prolactin Induced Protein (PIP) are Potential Biomarkers for Thyroid Eye Disease
Authors: Chng, C.-L 
Seah, L.L 
Yang, M 
Shen, S.Y 
Koh, S.K
Gao, Y
Deng, L
Tong, L
Beuerman, R.W 
Zhou, L 
Keywords: biological marker
calvasculin
carrier protein
eye protein
glycoprotein
PIP protein, human
S100A4 protein, human
tear proteins
endocrine ophthalmopathy
human
metabolism
metabolome
metabolomics
procedures
Biomarkers
Carrier Proteins
Eye Proteins
Glycoproteins
Graves Ophthalmopathy
Humans
Metabolome
Metabolomics
S100 Calcium-Binding Protein A4
Issue Date: 2018
Publisher: Nature Publishing Group
Citation: Chng, C.-L, Seah, L.L, Yang, M, Shen, S.Y, Koh, S.K, Gao, Y, Deng, L, Tong, L, Beuerman, R.W, Zhou, L (2018). Tear Proteins Calcium binding protein A4 (S100A4) and Prolactin Induced Protein (PIP) are Potential Biomarkers for Thyroid Eye Disease. Scientific Reports 8 (1) : 16936. ScholarBank@NUS Repository. https://doi.org/10.1038/s41598-018-35096-x
Rights: Attribution 4.0 International
Abstract: There are no reliable biomarkers to predict thyroid eye disease (TED) in patients with autoimmune thyroid disease (AITD) currently. Several evidences support the involvement of the lacrimal gland in TED. The aim of our study was to quantitatively correlate the changes in tear protein profile with increasing severity of TED. Tear samples were collected from four groups of patients; AITD without TED (AITD), AITD with mild TED (mild TED), AITD with severe TED (severe TED) and normal controls. A total of 72 patients were recruited for the study. In discovery phase, isobaric tags for relative and absolute quantification (iTRAQ) 4-plex was used for quantitative proteomics analysis. For verification of results from discovery phase, sequential window acquisition of all theoretical fragment ion spectra (SWATH) was used to analyze an independent cohort from normal controls, AITD, mild TED and severe TED. Two proteins, S100A4 and PIP showed consistent dysregulation trends in the discovery and validation phase experiments. Our study demonstrated the differences in tear proteome across the spectrum of different severity and activity of TED in patients with AITD. Two tear proteins, S100A4 and PIP may serve as potential biomarkers to predict progression to severe TED in patients with AITD. © 2018, The Author(s).
Source Title: Scientific Reports
URI: https://scholarbank.nus.edu.sg/handle/10635/178382
ISSN: 2045-2322
DOI: 10.1038/s41598-018-35096-x
Rights: Attribution 4.0 International
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