Calcineurin Inhibitor Associated Nephrotoxicity in Kidney Transplantation—A Transplant Nephrologist's Perspective

IF 5.6 2区 医学 Q1 PHYSIOLOGY
Carla M. Hansen, Sebastian Bachmann, Mingzhen Su, Klemens Budde, Mira Choi
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引用次数: 0

Abstract

Aim

Calcineurin inhibitors (CNIs) have revolutionized transplant medicine, improving allograft survival but posing challenges like calcineurin inhibitor-induced nephrotoxicity (CNT). Acute CNT, often dose-dependent, leads to vasoconstriction and acute kidney injury, with treatment focusing on CNI exposure reduction. Chronic CNT manifests as progressive allograft function decline, with challenges in distinguishing it from nonspecific allograft nephropathy.

Methods

This narrative review provides a concise overview of the clinical management of CNT, covering acute and chronic CNT. We reviewed original articles, landmark papers, and meta-analyses on CNT mitigation strategies, including CNI-sparing approaches.

Results

Preventive measures include co-medications, CNI exposure monitoring, and CNI sparing strategies, such as reducing target trough levels and converting to mTOR inhibitors (mTORi) or belatacept. Despite improvements in graft function, challenges persist in demonstrating significant differences in allograft survival with CNI-sparing regimens. The paradigm shift from chronic CNT as the main cause of chronic allograft nephropathy toward rather immunologic triggered injuries and/or comorbidities as relevant contributors to allograft deterioration over time must be kept in mind.

Conclusion

CNIs have significantly improved kidney transplant outcomes, but their associated nephrotoxicity necessitates mitigation strategies. The decision to implement such regimens is always an individual choice balancing against the risk of immunologic injuries. Further long-term studies are needed to optimize immunosuppressive approaches and refine CNT management.

Abstract Image

肾移植中钙调磷酸酶抑制剂相关的肾毒性——移植肾病专家的观点
钙调磷酸酶抑制剂(CNIs)已经彻底改变了移植医学,提高了同种异体移植物的存活率,但也带来了钙调磷酸酶抑制剂引起的肾毒性(CNT)等挑战。急性CNT,通常是剂量依赖性的,可导致血管收缩和急性肾损伤,治疗的重点是减少CNI暴露。慢性CNT表现为进行性同种异体移植功能下降,与非特异性同种异体移植肾病的区别具有挑战性。方法本文简要综述了急性和慢性CNT的临床治疗。我们回顾了原始文章、里程碑式的论文和碳纳米管缓解策略的荟萃分析,包括cni节约方法。结果预防措施包括联合用药、CNI暴露监测和CNI保护策略,如降低靶谷水平和转换为mTOR抑制剂(mTORi)或belatacept。尽管移植物功能有所改善,但证明保留cni方案在同种异体移植物存活方面存在显着差异的挑战仍然存在。从慢性碳纳米管作为慢性同种异体移植肾病的主要原因,到免疫引发的损伤和/或合并症作为同种异体移植恶化的相关因素,这种范式的转变必须牢记在心。结论CNIs可显著改善肾移植预后,但其相关的肾毒性需要缓解策略。实施这种方案的决定总是一个个人的选择,以平衡免疫损伤的风险。需要进一步的长期研究来优化免疫抑制方法和完善碳纳米管管理。
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
Acta Physiologica
Acta Physiologica 医学-生理学
CiteScore
11.80
自引率
15.90%
发文量
182
审稿时长
4-8 weeks
期刊介绍: Acta Physiologica is an important forum for the publication of high quality original research in physiology and related areas by authors from all over the world. Acta Physiologica is a leading journal in human/translational physiology while promoting all aspects of the science of physiology. The journal publishes full length original articles on important new observations as well as reviews and commentaries.
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