Clinical Pharmacokinetic and Pharmacodynamic Considerations in the Treatment of Moderate-to-Severe Psoriasis.

IF 4.6 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Clinical Pharmacokinetics Pub Date : 2024-02-01 Epub Date: 2024-01-27 DOI:10.1007/s40262-023-01341-4
Jonathan Greenzaid, Steven Feldman
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引用次数: 0

Abstract

Psoriasis is a common inflammatory immune disorder due to chronic activation of the adaptive and innate immune responses. Therapies for psoriasis target reducing inflammatory cytokines such as tumor necrosis factor-alpha, interleukin-17, and interleukin-22. Patients with inflammatory disorders have reduced metabolism by cytochrome P450 enzymes in the liver. The pharmacokinetic and pharmacodynamic changes due to psoriasis also have an impact on reaching therapeutic concentrations of the drug. Pharmacokinetic and pharmacodynamic data help determine the safety and clinical considerations necessary when utilizing drugs for plaque psoriasis. A literature search was performed on PubMed and Ovid MEDLINE for the pharmacokinetic and pharmacodynamic data of oral therapies and biologics utilized for moderate-to-severe plaque psoriasis. The findings from the literature search were organized into two sections: oral therapies and biologics. The pharmacokinetic and pharmacodynamic parameters in healthy patients, patients with psoriasis, and special populations are discussed in each section. The oral therapies described in this review include methotrexate, cyclosporine, apremilast, tofacitinib, and deucravacitinib. Biologics include tumor necrosis factor-alpha inhibitors, interleukin-17 inhibitors, ustekinumab, and interleukin-23 inhibitors. Clinical considerations for these therapies include drug toxicities, dosing frequency, and anti-drug antibodies. Methotrexate and cyclosporine have a risk for hepatoxicity and renal impairment, respectively. Moreover, drugs metabolized via cytochrome P450, including tofacitinib and apremilast have decreased clearance in patients with psoriasis, requiring dose adjustments. Patients treated with therapies such as adalimumab can develop anti-drug antibodies that reduce the long-term efficacy of the drug. Additionally, overweight patients benefit from more frequent dosing to achieve better psoriasis clearance.

Abstract Image

治疗中度至重度银屑病的临床药代动力学和药效学考虑因素。
银屑病是一种常见的炎症性免疫疾病,是由适应性免疫反应和先天性免疫反应长期激活引起的。银屑病疗法的目标是减少炎症细胞因子,如肿瘤坏死因子-α、白细胞介素-17 和白细胞介素-22。炎症性疾病患者肝脏中细胞色素 P450 酶的代谢减少。银屑病引起的药代动力学和药效学变化也会影响药物达到治疗浓度。药代动力学和药效学数据有助于确定使用药物治疗斑块状银屑病时的安全性和临床注意事项。我们在 PubMed 和 Ovid MEDLINE 上对治疗中重度斑块状银屑病的口服疗法和生物制剂的药代动力学和药效学数据进行了文献检索。文献检索结果分为两部分:口服疗法和生物制剂。每一部分都讨论了健康患者、银屑病患者和特殊人群的药代动力学和药效学参数。本综述中介绍的口服疗法包括甲氨蝶呤、环孢素、阿普瑞司特、托法替尼和去氯法替尼。生物制剂包括肿瘤坏死因子-α抑制剂、白细胞介素-17抑制剂、乌斯特库单抗和白细胞介素-23抑制剂。这些疗法的临床注意事项包括药物毒性、给药频率和抗药性抗体。甲氨蝶呤和环孢素分别有肝毒性和肾功能损害的风险。此外,通过细胞色素 P450 代谢的药物,包括托法替尼(tofacitinib)和阿普仑司特(apremilast),在银屑病患者体内的清除率降低,需要调整剂量。接受阿达木单抗等疗法的患者会产生抗药性抗体,从而降低药物的长期疗效。此外,体重超重的患者可通过增加用药次数来提高银屑病清除率。
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
CiteScore
8.80
自引率
4.40%
发文量
86
审稿时长
6-12 weeks
期刊介绍: Clinical Pharmacokinetics promotes the continuing development of clinical pharmacokinetics and pharmacodynamics for the improvement of drug therapy, and for furthering postgraduate education in clinical pharmacology and therapeutics. Pharmacokinetics, the study of drug disposition in the body, is an integral part of drug development and rational use. Knowledge and application of pharmacokinetic principles leads to accelerated drug development, cost effective drug use and a reduced frequency of adverse effects and drug interactions.
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