中华创伤杂志(英文版)2024,Vol.27Issue(2) :97-106.DOI:10.1016/j.cjtee.2024.01.002

Exploration of potential biomarkers and therapeutic targets for trauma-related acute kidney injury

Peng Qi Meng-Jie Huang Wei Wu Xue-Wen Ren Yong-Zhi Zhai Chen Qiu Hai-Yan Zhu
中华创伤杂志(英文版)2024,Vol.27Issue(2) :97-106.DOI:10.1016/j.cjtee.2024.01.002

Exploration of potential biomarkers and therapeutic targets for trauma-related acute kidney injury

Peng Qi 1Meng-Jie Huang 2Wei Wu 3Xue-Wen Ren 1Yong-Zhi Zhai 1Chen Qiu 4Hai-Yan Zhu1
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作者信息

  • 1. Department of Emergency,First Medical Center of Chinese PLA General Hospital,Beijing,100853,China
  • 2. Department of Nephrology,First Medical Center of Chinese PLA General Hospital,Beijing,100853,China
  • 3. Department of Anesthesiology,First Medical Center of Chinese PLA General Hospital,Beijing,100853,China
  • 4. Department of Orthopedics,Fourth Medical Center of Chinese PLA General Hospital,Beijing,100853,China
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Abstract

Purpose:Acute kidney injury(AKI)is one of the most common functional injuries observed in trauma patients.However,certain trauma medications may exacerbate renal injury.Therefore,the early detection of trauma-related AKI holds paramount importance in improving trauma prognosis.Methods:Qualified datasets were selected from public databases,and common differentially expressed genes related to trauma-induced AKI and hub genes were identified through enrichment analysis and the establishment of protein-protein interaction(PPI)networks.Additionally,the specificity of these hub genes was investigated using the sepsis dataset and conducted a comprehensive literature review to assess their plausibility.The raw data from both datasets were downloaded using R software(version 4.2.1)and processed with the"affy"package19 for correction and normalization.Results:Our analysis revealed 585 upregulated and 629 downregulated differentially expressed genes in the AKI dataset,along with 586 upregulated and 948 downregulated differentially expressed genes in the trauma dataset.Concurrently,the establishment of the PPI network and subsequent topological analysis highlighted key hub genes,including CD44,CD163,TIMP metallopeptidase inhibitor 1,cytochrome b-245 beta chain,versican,membrane spanning 4-domains A4A,mitogen-activated protein kinase 14,and early growth response 1.Notably,their receiver operating characteristic curves displayed areas exceeding 75%,indicating good diagnostic performance.Moreover,our findings postulated a unique molecular mecha-nism underlying trauma-related AKI.Conclusion:This study presents an alternative strategy for the early diagnosis and treatment of trauma-related AKI,based on the identification of potential biomarkers and therapeutic targets.Additionally,this study provides theoretical references for elucidating the mechanisms of trauma-related AKI.

Key words

Trauma/Acute kidney injury/Bioinformatic analysis/Differentially expressed genes/Biomarker

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基金项目

National Key Research and Development Program of the Ministry of Science and Technology(2019YFC0119601)

Special Program for Military Nursing Innovation and cultivation Project(2021HL091)

Special Program for Military Nursing Innovation and cultivation Project(2021HL075)

Young Elite Scientist Sponsorship Program by CAST(2020QNRC001)

出版年

2024
中华创伤杂志(英文版)
中华医学会

中华创伤杂志(英文版)

CSTPCDCSCD
影响因子:0.608
ISSN:1008-1275
参考文献量50
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