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铁代谢紊乱及炎症性铁生物标志物在肝移植预后中的作用

Role of Iron Metabolic Disturbances and Inflammatory Iron Biomarkers in Liver Transplant Prognosis.

作者信息

Yu Lu, Xu Jun, Que Ting, Miao Zhezhi, Zhou Yifeng, Que Shuping, Zheng Shusen, Liu Zhengtao

机构信息

Key Laboratory of Artificial Organs and Computational Medicine in Zhejiang Province, Shulan International Medical College, Zhejiang Shuren University, Hangzhou, China.

Shulan (Hangzhou) Hospital, Shulan International Medical College, Zhejiang Shuren University, Hangzhou, China.

出版信息

Int J Med Sci. 2025 Jul 1;22(13):3202-3219. doi: 10.7150/ijms.113479. eCollection 2025.

DOI:10.7150/ijms.113479
PMID:40765572
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12320645/
Abstract

Iron metabolism plays a pivotal role in liver transplantation, significantly impacting outcomes for both donors and recipients. The liver, central to iron homeostasis, is often impaired in chronic liver diseases leading to metabolic disorders that exacerbate liver damage. Liver transplantation (LT) is a critical treatment for end-stage liver diseases, with iron status in both donors and recipients influencing post-transplant outcomes. Studies indicate that pre-transplant iron overload in recipients is associated with poor liver function recovery, increased graft rejection risk, and reduced patient survival. The iron metabolic state of donors also affects the functionality of the transplanted liver, impacting transplant success and patient prognosis. Biomarkers such as hepcidin, serum ferritin, and total iron-binding capacity are significant predictors of LT prognosis, yet their specific roles and impacts remain inconclusive. This review systematically assesses how variations in iron metabolic levels of donors and recipients affect patient outcomes following LT, aiming to optimize iron metabolism regulation in clinical management to enhance transplant success, reduce postoperative complications, and improve long-term patient quality of life. Future research should focus on developing personalized iron metabolism management protocols to refine these approaches and enhance transplant care.

摘要

铁代谢在肝移植中起着关键作用,对供体和受体的结局均有重大影响。肝脏是铁稳态的核心器官,在慢性肝病中常受到损害,导致代谢紊乱,进而加剧肝损伤。肝移植(LT)是终末期肝病的关键治疗方法,供体和受体的铁状态都会影响移植后的结局。研究表明,受体移植前的铁过载与肝功能恢复不良、移植排斥风险增加以及患者生存率降低有关。供体的铁代谢状态也会影响移植肝脏的功能,从而影响移植成功率和患者预后。铁调素、血清铁蛋白和总铁结合力等生物标志物是肝移植预后的重要预测指标,但其具体作用和影响仍尚无定论。本综述系统评估了供体和受体铁代谢水平的变化如何影响肝移植术后患者的结局,旨在优化临床管理中的铁代谢调节,以提高移植成功率、减少术后并发症并改善患者的长期生活质量。未来的研究应专注于制定个性化的铁代谢管理方案,以完善这些方法并加强移植护理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0532/12320645/7e004ceb688f/ijmsv22p3202g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0532/12320645/7e004ceb688f/ijmsv22p3202g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0532/12320645/7e004ceb688f/ijmsv22p3202g001.jpg

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本文引用的文献

1
Molecular Mechanisms of Ischemia/Reperfusion Injury and Graft Dysfunction in Liver Transplantation: Insights from Multi-Omics Studies in Rodent Animal Models.肝移植中缺血/再灌注损伤及移植物功能障碍的分子机制:来自啮齿动物模型多组学研究的见解
Int J Biol Sci. 2025 Feb 24;21(5):2135-2154. doi: 10.7150/ijbs.109449. eCollection 2025.
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The role of mitochondria in iron overload-induced damage.线粒体在铁过载诱导损伤中的作用。
J Transl Med. 2024 Nov 25;22(1):1057. doi: 10.1186/s12967-024-05740-4.
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Dose-response relationship of serum ferritin and dietary iron intake with metabolic syndrome and non-alcoholic fatty liver disease incidence: a systematic review and meta-analysis.
血清铁蛋白和膳食铁摄入量与代谢综合征及非酒精性脂肪性肝病发病率的剂量反应关系:一项系统评价和荟萃分析
Front Nutr. 2024 Oct 1;11:1437681. doi: 10.3389/fnut.2024.1437681. eCollection 2024.
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Novel Models for Assessing and Pathophysiology of Hepatic Ischemia-Reperfusion Injury Mechanisms.评估和肝脏缺血再灌注损伤机制病理生理学的新型模型。
Medicina (Kaunas). 2024 Sep 15;60(9):1507. doi: 10.3390/medicina60091507.
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Ferroptosis Inhibition: A Key Opportunity for the Treatment of Ischemia/Reperfusion Injury in Liver Transplantation.铁死亡抑制:肝移植中缺血/再灌注损伤治疗的关键契机。
Transplantation. 2025 May 1;109(5):e228-e236. doi: 10.1097/TP.0000000000005199. Epub 2024 Sep 19.
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Ferroptosis: a new target for hepatic ischemia-reperfusion injury?铁死亡:肝脏缺血再灌注损伤的新靶点?
Free Radic Res. 2024 May-Jun;58(6-7):396-416. doi: 10.1080/10715762.2024.2386075. Epub 2024 Jul 31.
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Advance in Iron Metabolism, Oxidative Stress and Cellular Dysfunction in Experimental and Human Kidney Diseases.实验性和人类肾脏疾病中铁代谢、氧化应激与细胞功能障碍的研究进展
Antioxidants (Basel). 2024 May 27;13(6):659. doi: 10.3390/antiox13060659.
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Antioxidants (Basel). 2024 Apr 27;13(5):537. doi: 10.3390/antiox13050537.
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