Novel Biomarkers for Screening Retinal Detachment Associated with Choroidal Detachment Using DIA-MS-Based Proteomics.

IF 1.7 4区 医学 Q3 OPHTHALMOLOGY
Pingping Li, Mengyao Han, Rui Zhang, Fangyu Chen, Yanzi Li, Jing Yuan, Ning Ma, Lu Li, Jianhua Wu
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Abstract

Purpose: Rhegmatogenous retinal detachment associated with choroidal detachment (RRDCD) is known for its rapid progression and poor prognosis, making it a subject of significant clinical interest due to its complex pathogenesis. This study aims to utilize mass spectrometry for proteomic analysis of vitreous humor to identify proteins and biomarkers critical to the pathophysiology of RRDCD.

Methods: Data-independent acquisition (DIA) mass spectrometry was employed to analyze vitreous humor samples from RRDCD and Rhegmatogenous retinal detachment (RRD) patients. The analysis focused on identifying differentially expressed proteins (DEPs) and determining their functional roles. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses were performed to explore the biological processes and pathways associated with these DEPs. DEPs were validated using ELISA to confirm the reliability of the mass spectrometry results.

Results: A total of 237 DEPs were identified, including 63 upregulated and 174 downregulated proteins. GO functional analysis showed enrichment in terms related to molecular function regulators, biological adhesion, and the extracellular region. KEGG pathway analysis revealed significant associations with the Extracellular environment (ECM)-receptor interaction, complement and coagulation cascades, and lysosome pathways. Receiver operating characteristic (ROC) analysis further confirmed that Serum amyloid A-4 protein (SAA4), Inter-alpha-trypsin inhibitor heavy chain H1 (ITIH1), and Vitronectin (VTN) exhibit excellent performance in the diagnosis of RRDCD. Both VTN and SAA4 showed positive correlations with BCVA at 6 months post-surgery.

Conclusion: RRDCD activates a variety of cellular pathways, not only complement and inflammation, but also the remodeling of the extracellular matrix and the activation of lysosome-related pathways disrupt normal retinal cell function. SAA4, ITIH1, and VTN in vitreous fluid can serve as effective biomarkers for diagnosing patients with RRDCD. Additionally, both VTN and SAA4 are correlated with post-operative visual outcomes.

使用基于dia - ms的蛋白质组学筛选视网膜脱离与脉络膜脱离相关的新生物标志物。
目的:孔源性视网膜脱离合并脉络膜脱离(RRDCD)以其进展迅速、预后差而闻名,因其复杂的发病机制而成为临床研究的重要课题。本研究旨在利用质谱法对玻璃体进行蛋白质组学分析,以鉴定对RRDCD病理生理至关重要的蛋白质和生物标志物。方法:采用数据独立采集(DIA)质谱法对RRDCD和孔源性视网膜脱离(RRD)患者的玻璃体样本进行分析。分析的重点是鉴定差异表达蛋白(DEPs)并确定其功能作用。通过基因本体(GO)和京都基因与基因组百科全书(KEGG)分析,探索与这些dep相关的生物学过程和途径。采用ELISA法对DEPs进行验证,以确认质谱分析结果的可靠性。结果:共鉴定出237个DEPs,其中上调63个,下调174个。氧化石墨烯功能分析显示,在分子功能调节剂、生物粘附和细胞外区域等方面富集。KEGG通路分析显示与细胞外环境(ECM)-受体相互作用、补体和凝血级联以及溶酶体通路有显著关联。受试者工作特征(ROC)分析进一步证实血清淀粉样蛋白A-4蛋白(SAA4)、α -胰蛋白酶抑制剂重链H1 (ITIH1)、Vitronectin (VTN)在RRDCD的诊断中表现优异。术后6个月VTN、SAA4与BCVA均呈正相关。结论:RRDCD激活多种细胞通路,不仅是补体和炎症,而且细胞外基质的重塑和溶酶体相关通路的激活破坏了正常的视网膜细胞功能。玻璃体液中SAA4、ITIH1和VTN可作为诊断RRDCD患者的有效生物标志物。此外,VTN和SAA4均与术后视力结果相关。
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来源期刊
Current Eye Research
Current Eye Research 医学-眼科学
CiteScore
4.60
自引率
0.00%
发文量
163
审稿时长
12 months
期刊介绍: The principal aim of Current Eye Research is to provide rapid publication of full papers, short communications and mini-reviews, all high quality. Current Eye Research publishes articles encompassing all the areas of eye research. Subject areas include the following: clinical research, anatomy, physiology, biophysics, biochemistry, pharmacology, developmental biology, microbiology and immunology.
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