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基于难治性高血压患者蛋白质组学特征的血浆生物标志物筛查

Plasma Biomarker Screening Based on Proteomic Signature of Patients with Resistant Hypertension.

作者信息

Du Jianmin, Yu Xiaoqian, Zhang Wenyu, Zhang Xinghai, Zhao Hengli, Xu Rui, Wen Qing

机构信息

Department of Clinical Research Center, Central Hospital Affiliated to Shandong First Medical University, Jinan, 250013, China.

Department of Cardiology, Jinan Central Hospital, Shandong University, Jinan, 250013, China.

出版信息

J Cardiovasc Transl Res. 2024 Dec;17(6):1286-1294. doi: 10.1007/s12265-024-10541-7. Epub 2024 Jul 6.

Abstract

Resistant hypertension (RH) poses a significant health challenge, yet its underlying pathogenesis remains unclear. This study employs untargeted proteomic techniques to analyze the plasma of patients with RH and controlled hypertension (CH), identifying 157 differentially expressed proteins, with TGFB1 emerging as a key candidate. Through gene ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment, Protein-Protein Interaction Networks (PPI) topological analysis, TGFB1's differential regulation in RH is established. ELISA verification solidifies TGFB1's role, marking it as a potential biological target for early RH diagnosis and treatment. The study underscores the importance of proteomic approaches in enhancing our understanding of RH and improving therapeutic strategies. These findings carry implications for advancing RH diagnostics and treatment modalities, addressing a critical gap in current knowledge.

摘要

难治性高血压(RH)对健康构成重大挑战,但其潜在发病机制仍不清楚。本研究采用非靶向蛋白质组学技术分析RH患者和血压控制良好的高血压(CH)患者的血浆,鉴定出157种差异表达蛋白,其中转化生长因子β1(TGFB1)成为关键候选蛋白。通过基因本体论(GO)、京都基因与基因组百科全书(KEGG)富集分析、蛋白质-蛋白质相互作用网络(PPI)拓扑分析,确定了TGFB1在RH中的差异调节。酶联免疫吸附测定(ELISA)验证巩固了TGFB1的作用,将其标记为早期RH诊断和治疗的潜在生物学靶点。该研究强调了蛋白质组学方法在增强我们对RH的理解和改进治疗策略方面的重要性。这些发现对推进RH诊断和治疗模式具有重要意义,填补了当前知识的关键空白。

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