Tremor Induced by Cyclosporine, Tacrolimus, Sirolimus, or Everolimus: A Review of the Literature.

IF 2.2 4区 医学 Q3 PHARMACOLOGY & PHARMACY Drugs in Research & Development Pub Date : 2023-12-01 Epub Date: 2023-08-22 DOI:10.1007/s40268-023-00428-4
Aparna Wagle Shukla, Caroline Lunny, Omar Mahboob, Uzair Khalid, Malea Joyce, Nivedita Jha, Nandakumar Nagaraja, Ashutosh M Shukla
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引用次数: 2

Abstract

Calcineurin inhibitors such as cyclosporine and tacrolimus are immunosuppressant drugs that are known to induce tremors. Non-calcineurin inhibitors such as sirolimus and everolimus have also reportedly been accompanied by tremors, albeit less likely. However, the prevalence rates reported in the literature are notably wide, and the risk profiles for these drug-induced tremors are less understood. We searched PubMed to extract data on the risk of tremors with these drugs when prescribed for various transplant and non-transplant indications. We ascertained whether the risk of drug-induced tremor is influenced by the underlying diagnosis, dosing formulations, drug concentrations, and blood monitoring. We extracted data on treatment strategies and outcomes for tremors. Articles were primarily screened based on English language publications, abstracts, and studies with n ≥ 5, which included case series, retrospective studies, case-controlled studies, and prospective studies. We found 81 eligible studies comprising 33 cyclosporine, 43 tacrolimus, 6 sirolimus, and 1 everolimus that discussed tremor as an adverse event. In the pooled analysis of studies with n > 100, the incidence of tremor was 17% with cyclosporine, 21.5% with tacrolimus, and 7.8% with sirolimus and everolimus together. Regarding the underlying diagnosis, tremor was more frequently reported in kidney transplant (cyclosporine 28%, tacrolimus 30.1%) and bone marrow transplant (cyclosporine 40%, tacrolimus 41.9%) patients compared with liver transplant (cyclosporine 9%, tacrolimus 11.5%) and nontransplant indications (cyclosporine 21.5%, tacrolimus 11.3%). Most studies did not report whether the risk of tremors correlated with drug concentrations in the blood. The prevalence of tremors when using the twice-daily formulation of tacrolimus was nearly the same as the once-daily formulation (17% vs 18%). Data on individual-level risk factors for tremors were lacking. Except for three studies that found some benefit to maintaining magnesium levels, there were minimal data on treatments and outcomes. A large body of data supports a substantive and wide prevalence of tremor resulting from tacrolimus use followed by cyclosporine, especially in patients receiving a kidney transplant. However, there is little reporting on the patient-related risk factors for tremor, risk relationship with drug concentrations, treatment strategies, and outcomes.

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环孢素、他克莫司、西罗莫司或依维莫司引起的震颤:文献综述。
钙调磷酸酶抑制剂如环孢素和他克莫司是免疫抑制药物,已知会引起震颤。据报道,非钙调磷酸酶抑制剂如西罗莫司和依维莫司也伴有震颤,尽管可能性较小。然而,文献中报道的患病率非常广泛,并且对这些药物引起的震颤的风险概况了解较少。我们检索了PubMed,提取了这些药物用于各种移植和非移植适应症时震颤风险的数据。我们确定药物性震颤的风险是否受到潜在诊断、剂量配方、药物浓度和血液监测的影响。我们提取了有关震颤的治疗策略和结果的数据。文章筛选主要基于英文出版物、摘要和n≥5的研究,包括病例系列、回顾性研究、病例对照研究和前瞻性研究。我们发现81项符合条件的研究,包括33项环孢素、43项他克莫司、6项西罗莫司和1项依维莫司,都将震颤作为不良事件进行了讨论。在n > 100的研究汇总分析中,环孢素组震颤发生率为17%,他克莫司组为21.5%,西罗莫司和依维莫司联合组为7.8%。关于潜在的诊断,与肝移植(环孢素9%,他克莫司11.5%)和非移植适应症(环孢素21.5%,他克莫司11.3%)患者相比,肾移植(环孢素28%,他克莫司30.1%)和骨髓移植(环孢素40%,他克莫司41.9%)患者报道震颤的频率更高。大多数研究没有报告震颤的风险是否与血液中的药物浓度相关。他克莫司每日两次的震颤发生率与每日一次的几乎相同(17% vs 18%)。个人层面的地震危险因素数据缺乏。除了三项研究发现维持镁水平有一些好处外,关于治疗和结果的数据很少。大量数据支持他克莫司后使用环孢素引起的大量和广泛的震颤,特别是在接受肾移植的患者中。然而,关于震颤的患者相关危险因素、与药物浓度的风险关系、治疗策略和结果的报道很少。
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
Drugs in Research & Development
Drugs in Research & Development Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
5.10
自引率
0.00%
发文量
31
审稿时长
8 weeks
期刊介绍: Drugs in R&D is an international, peer reviewed, open access, online only journal, and provides timely information from all phases of drug research and development that will inform clinical practice. Healthcare decision makers are thus provided with knowledge about the developing place of a drug in therapy. The Journal includes: Clinical research on new and established drugs; Preclinical research of direct relevance to clinical drug development; Short communications and case study reports that meet the above criteria will also be considered; Reviews may also be considered.
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