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Tear Proteins Calcium binding protein A4 (S100A4) and Prolactin Induced Protein (PIP) are Potential Biomarkers for Thyroid Eye Disease.
Chng, Chiaw-Ling; Seah, Lay Leng; Yang, Morgan; Shen, Sunny Yu; Koh, Siew Kwan; Gao, Yan; Deng, Lu; Tong, Louis; Beuerman, Roger Wilmer; Zhou, Lei.
Affiliation
  • Chng CL; Department of Endocrinology, Singapore General Hospital Level 3, The Academia, 20 College Road, Singapore, 169856, Singapore.
  • Seah LL; Oculoplastic Department, Singapore National Eye Centre 11 Third Hospital Avenue, Singapore, 168751, Singapore.
  • Yang M; Oculoplastic Department, Singapore National Eye Centre 11 Third Hospital Avenue, Singapore, 168751, Singapore.
  • Shen SY; Oculoplastic Department, Singapore National Eye Centre 11 Third Hospital Avenue, Singapore, 168751, Singapore.
  • Koh SK; Singapore Eye Research Institute, Discovery Tower Level 6 The Academia, 20 College Road, Singapore, 169856, Singapore.
  • Gao Y; Singapore Eye Research Institute, Discovery Tower Level 6 The Academia, 20 College Road, Singapore, 169856, Singapore.
  • Deng L; Singapore Eye Research Institute, Discovery Tower Level 6 The Academia, 20 College Road, Singapore, 169856, Singapore.
  • Tong L; Corneal and External Eye Disease Department, Singapore National Eye Centre 11 Third Hospital Avenue, Singapore, 168751, Singapore.
  • Beuerman RW; Singapore Eye Research Institute, Discovery Tower Level 6 The Academia, 20 College Road, Singapore, 169856, Singapore.
  • Zhou L; Singapore Eye Research Institute, Discovery Tower Level 6 The Academia, 20 College Road, Singapore, 169856, Singapore. zhou.lei@seri.com.sg.
Sci Rep ; 8(1): 16936, 2018 11 16.
Article de En | MEDLINE | ID: mdl-30446693
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.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Glycoprotéines / Marqueurs biologiques / Protéines de transport / Ophtalmopathie basedowienne / Protéines de l'oeil / Protéine S100A4 liant le calcium Type d'étude: Diagnostic_studies / Prognostic_studies Limites: Humans Langue: En Journal: Sci Rep Année: 2018 Type de document: Article Pays d'affiliation: Singapour Pays de publication: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Glycoprotéines / Marqueurs biologiques / Protéines de transport / Ophtalmopathie basedowienne / Protéines de l'oeil / Protéine S100A4 liant le calcium Type d'étude: Diagnostic_studies / Prognostic_studies Limites: Humans Langue: En Journal: Sci Rep Année: 2018 Type de document: Article Pays d'affiliation: Singapour Pays de publication: Royaume-Uni