蛋白质组学
小桶
医学
类风湿性关节炎
基因本体论
疾病
定量蛋白质组学
血液蛋白质类
生物信息学
计算生物学
自身免疫性疾病
生物标志物
免疫学
病态的
基因
血沉
鉴别诊断
下调和上调
类风湿因子
基因表达
基因表达谱
关节炎
DNA微阵列
蛋白质-蛋白质相互作用
内科学
蛋白质组
蛋白质表达
作者
Yang Zhao,Yuan Li,Meng Qi,Junhua Xu,Fengwei Ji,Yan Kan,Chunyu Kong
标识
DOI:10.1111/1756-185x.70766
摘要
BACKGROUND: Rheumatoid Arthritis (RA) is a Prevalent Autoimmune Disorder Affecting Millions of People Worldwide. A Thorough Understanding of Its Clinical and Pathological Features Is Essential to Improve Patient Outcomes. METHODS: This Study Combined Data-Independent Acquisition Proteomics and Enzyme-Linked Immunosorbent Assay (ELISA) to Identify and Validate Potential Plasma Protein Biomarkers for the Early Diagnosis of RA. RESULTS: Differential Proteomic Analysis Identified Differentially Expressed Proteins Between Patients With RA and Healthy Controls and Characterized Their Functions. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes Enrichment Analyses Were Performed to Explore Protein Functions and Associated Biological Pathways. The STRING Database and the Metascape Platform Were Used to Conduct an in-Depth Analysis of the Protein-Protein Interaction Network, Highlighting the Functional Attributes and Interconnections of Upregulated Proteins and Identifying Key Protein Complexes Involved in RA. ELISA Analysis of Plasma Samples Revealed Significantly Elevated SERPINA3 Levels in Patients With RA, Which Were Positively Correlated With Disease Activity Indicators-Including Erythrocyte Sedimentation Rate, C-Reactive Protein, and Disease Activity Score 28-But Were Not Correlated With Rheumatoid Factor or Its Subtypes. CONCLUSIONS: This Study Provides New Insights and Identifies Potential Biomarkers for the Early Diagnosis of RA.
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