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泪蛋白钙结合蛋白 A4(S100A4)和催乳素诱导蛋白(PIP)是甲状腺眼病的潜在生物标志物。

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

机构信息

Department of Endocrinology, Singapore General Hospital Level 3, The Academia, 20 College Road, Singapore, 169856, Singapore.

Oculoplastic Department, Singapore National Eye Centre 11 Third Hospital Avenue, Singapore, 168751, Singapore.

出版信息

Sci Rep. 2018 Nov 16;8(1):16936. doi: 10.1038/s41598-018-35096-x.

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.

摘要

目前,尚无可靠的生物标志物可用于预测自身免疫性甲状腺疾病(AITD)患者的甲状腺眼病(TED)。有几项证据表明泪腺参与了 TED 的发生。本研究旨在定量分析泪蛋白谱的变化与 TED 严重程度增加之间的相关性。我们收集了四组患者的泪液样本:无 TED 的 AITD(AITD)、轻度 TED(mild TED)、重度 TED(severe TED)和正常对照组。共有 72 名患者入组。在发现阶段,采用同位素相对标记与绝对定量(iTRAQ)4 plex 进行定量蛋白质组学分析。为了验证发现阶段的结果,我们使用连续窗口采集所有理论片段离子谱(SWATH)来分析来自正常对照组、AITD、轻度 TED 和重度 TED 的独立队列。两种蛋白,S100A4 和 PIP 在发现和验证阶段的实验中表现出一致的失调趋势。我们的研究表明,在 AITD 患者中,不同严重程度和活动度 TED 的泪液蛋白质组存在差异。两种泪液蛋白,S100A4 和 PIP 可能可作为预测 AITD 患者进展为重度 TED 的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d980/6240106/b9fc2a56b5cb/41598_2018_35096_Fig1_HTML.jpg

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