Novel Proteomic Insights into Hip Fractures in the Elderly: Unraveling Immunologic Biomarkers, Temporal Expression Patterns, and Clinical Correlations.

IF 4.2 2区 医学 Q2 IMMUNOLOGY
Journal of Inflammation Research Pub Date : 2025-06-12 eCollection Date: 2025-01-01 DOI:10.2147/JIR.S513035
Yining Lu, Jiaoran Liu, Wei Chen, Pan Hu, Yan Pei, Yiming Gao, Hairong Lu, Ling Wang, Yingze Zhang
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引用次数: 0

Abstract

Background: Hip fractures in the elderly triggers a severe inflammatory immune response.

Methods: Peripheral blood samples from 16 elderly hip fracture patients and 16 healthy controls were analysed for 92 inflammatory biomarkers using proximity extension assay (PEA) at different stages after trauma.

Results: Dynamic trends in inflammatory proteins after surgery were assessed. Correlation analyses showed significant associations between inflammation-related proteins and clinical parameters. A prognostic risk score model was developed: on day 1, CCL19, FGF-19 and MCP-2 were significant; on day 3, TGF-α, FGF-5, CCL19, IL-22RA1 and IL-12B were included; and on day 7, IL-2RB, CCL19 and 4E-BP1 were significant. High-risk patients had a significantly lower rate of recovery compared with low-risk patients.

Conclusion: In this study, we have highlighted the complex inflammatory response during fracture healing and emphasised the importance of long-term monitoring of protein dynamics.

老年髋部骨折的蛋白质组学新见解:揭示免疫生物标志物、时间表达模式和临床相关性。
背景:老年人髋部骨折引发严重的炎症免疫反应。方法:对16例老年髋部骨折患者和16例健康对照者外伤后不同阶段外周血92种炎症标志物进行近距离延伸试验(PEA)分析。结果:评估术后炎症蛋白的动态变化趋势。相关分析显示炎症相关蛋白与临床参数之间存在显著相关性。建立预后风险评分模型:第1天,CCL19、FGF-19和MCP-2显著;第3天加入TGF-α、FGF-5、CCL19、IL-22RA1、IL-12B;第7天,IL-2RB、CCL19、4E-BP1均有显著性变化。高危患者的康复率明显低于低危患者。结论:在这项研究中,我们强调了骨折愈合过程中的复杂炎症反应,并强调了长期监测蛋白质动力学的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Inflammation Research
Journal of Inflammation Research Immunology and Microbiology-Immunology
CiteScore
6.10
自引率
2.20%
发文量
658
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed, open access, online journal that welcomes laboratory and clinical findings on the molecular basis, cell biology and pharmacology of inflammation.
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