Tear Proteins Calcium binding protein A4 (S100A4) and Prolactin Induced Protein (PIP) are Potential Biomarkers for Thyroid Eye Disease

被引:28
作者
Chng, Chiaw-Ling [1 ]
Seah, Lay Leng [2 ]
Yang, Morgan [2 ]
Shen, Sunny Yu [2 ]
Koh, Siew Kwan [3 ]
Gao, Yan [3 ]
Deng, Lu [3 ]
Tong, Louis [4 ]
Beuerman, Roger Wilmer [3 ]
Zhou, Lei [3 ]
机构
[1] Singapore Gen Hosp, Dept Endocrinol, Level 3,20 Coll Rd, Singapore 169856, Singapore
[2] Singapore Natl Eye Ctr, Oculoplast Dept, 11 Third Hosp Ave, Singapore 168751, Singapore
[3] Singapore Eye Res Inst, Discovery Tower,Level 6 Acad,20 Coll Rd, Singapore 169856, Singapore
[4] Singapore Natl Eye Ctr, Corneal & External Eye Dis Dept, 11 Third Hosp Ave, Singapore 168751, Singapore
基金
英国医学研究理事会;
关键词
SUPERIOR LIMBIC KERATOCONJUNCTIVITIS; OCULAR SURFACE; DRY EYE; GRAVES OPHTHALMOPATHY; PROTEOMICS; EXPRESSION; FLUID; VERIFICATION; ORBITOPATHY; CYTOKINES;
D O I
10.1038/s41598-018-35096-x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页数:10
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