他克莫司和霉酚酸介导的毒性:移植后患者管理的临床考虑和选择。

IF 4.1 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Current Issues in Molecular Biology Pub Date : 2024-12-24 DOI:10.3390/cimb47010002
Alan D Kaye, Shivam S Shah, Coplen D Johnson, Adalyn S De Witt, Austin S Thomassen, Charles P Daniel, Shahab Ahmadzadeh, Sridhar Tirumala, Kristin Nicole Bembenick, Adam M Kaye, Sahar Shekoohi
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引用次数: 0

摘要

他克莫司和麦考酚酸酯是重要的免疫抑制剂,用于预防器官移植后患者的排斥反应。虽然非常有效,但它们的使用与严重的毒性有关,需要仔细管理。他克莫司是一种钙调磷酸酶抑制剂,与肾毒性、神经毒性、代谢紊乱(如糖尿病和血脂异常)以及心血管并发症(如高血压和心律失常)有关。霉酚酸酯是一种可逆的肌苷单磷酸脱氢酶抑制剂,经常引起胃肠道紊乱,包括腹泻和结肠炎,以及贫血和白细胞减少等血液学副作用,增加感染风险。治疗性药物监测(TDM)和药物基因组学已成为减轻这些毒性的基本策略。TDM确保他克莫司谷底水平维持在治疗范围内,最大限度地减少肾毒性和排斥反应的风险。药物基因组学的见解,如CYP3A5多态性,允许基于个人代谢谱的个性化他克莫司剂量。对于霉酚酸,监测肌苷单磷酸脱氢酶活性提供了一种药效学方法来优化剂量,减少胃肠道和血液毒性。新兴工具,包括干血点采样和药代动力学建模,提供了创新的方法来简化监测和提高门诊环境的精度。尽管这些药物具有实用性,但它们的毒性,包括早期免疫抑制剂如环孢素和硫唑嘌呤的毒性,需要进一步考虑替代免疫抑制剂如西罗莫司、依维莫司和贝拉他普。尽管前景看好,但这些新药物需要仔细选择患者并进一步研究。免疫抑制治疗的未来方向包括整合个体药理学数据,以完善剂量,减少副作用,并改善长期移植结果。这篇叙述性综述强调了个性化医疗和先进监测在优化移植后护理中的重要性。
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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Tacrolimus- and Mycophenolate-Mediated Toxicity: Clinical Considerations and Options in Management of Post-Transplant Patients.

Tacrolimus and mycophenolate are important immunosuppressive agents used to prevent organ rejection in post-transplant patients. While highly effective, their use is associated with significant toxicity, requiring careful management. Tacrolimus, a calcineurin inhibitor, is linked to nephrotoxicity, neurotoxicity, metabolic disturbances such as diabetes mellitus and dyslipidemia, and cardiovascular complications such as hypertension and arrhythmias. Mycophenolate, a reversible inhibitor of inosine monophosphate dehydrogenase, frequently causes gastrointestinal disturbances, including diarrhea and colitis, as well as hematologic side effects like anemia and leukopenia, which increase infection risk. Therapeutic drug monitoring (TDM) and pharmacogenomics have emerged as essential strategies for mitigating these toxicities. TDM ensures tacrolimus trough levels are maintained within a therapeutic range, minimizing the risks of nephrotoxicity and rejection. Pharmacogenomic insights, such as CYP3A5 polymorphisms, allow for personalized tacrolimus dosing based on individual metabolic profiles. For mycophenolate, monitoring inosine monophosphate dehydrogenase activity provides a pharmacodynamic approach to dose optimization, reducing gastrointestinal and hematologic toxicities. Emerging tools, including dried blood spot sampling and pharmacokinetic modeling, offer innovative methods to simplify monitoring and enhance precision in outpatient settings. Despite their utility, the toxicity profiles of these drugs, including those of early immunosuppressants such as cyclosporine and azathioprine, necessitate further consideration of alternative immunosuppressants like sirolimus, everolimus, and belatacept. Although promising, these newer agents require careful patient selection and further research. Future directions in immunosuppressive therapy include integrating individual pharmacogenetic data to refine dosing, minimize side effects, and improve long-term graft outcomes. This narrative review underscores the importance of personalized medicine and advanced monitoring in optimizing post-transplant care.

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来源期刊
Current Issues in Molecular Biology
Current Issues in Molecular Biology 生物-生化研究方法
CiteScore
2.90
自引率
3.20%
发文量
380
审稿时长
>12 weeks
期刊介绍: Current Issues in Molecular Biology (CIMB) is a peer-reviewed journal publishing review articles and minireviews in all areas of molecular biology and microbiology. Submitted articles are subject to an Article Processing Charge (APC) and are open access immediately upon publication. All manuscripts undergo a peer-review process.
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