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系统性红斑狼疮患者的治疗药物监测:效用与差距

Therapeutic Drug Monitoring in Patients with Systemic Lupus Erythematosus: Utility and Gaps.

作者信息

Chong Kar Mun, Jiang He, Lo Elaine Ah Gi, Hong Wei-Zhen, Wong Emmett Tsz-Yeung, Chan Gek Cher, Cho Jiacai

机构信息

Division of Rheumatology, Department of Medicine, National University Hospital, Singapore 119074, Singapore.

Department of Pharmacy, National University Hospital, Singapore 119074, Singapore.

出版信息

J Clin Med. 2024 Jan 13;13(2):451. doi: 10.3390/jcm13020451.

Abstract

Despite advances in the treatment of patients with systemic lupus erythematous (SLE), outcomes have remained suboptimal. Persistent disease activity, patient comorbidities and drug toxicities contribute to the accrual of progressive irreversible damage and high rates of morbidity and mortality. Currently, similar drug doses and regimens are promulgated in the treatment guidelines for all SLE patients, despite the vast differences in patient and environmental factors that affect the drugs' metabolism and blood concentrations. This causes a disconnect between drug dosing and drug blood concentrations, which can then result in unpredictability in drug toxicities and therapeutic effects. In this review, we discuss commonly used oral immunosuppressive medications in SLE, their pharmacogenomics, and factors affecting their metabolism and blood concentrations. Further, we highlight the role of therapeutic drug monitoring in SLE, which is the first accessible step to individualising therapy.

摘要

尽管系统性红斑狼疮(SLE)患者的治疗取得了进展,但其治疗效果仍不尽人意。持续性疾病活动、患者合并症和药物毒性导致了进行性不可逆损伤的累积以及高发病率和死亡率。目前,尽管影响药物代谢和血药浓度的患者及环境因素存在巨大差异,但所有SLE患者的治疗指南中仍采用相似的药物剂量和治疗方案。这导致药物剂量与血药浓度之间脱节,进而可能导致药物毒性和治疗效果的不可预测性。在本综述中,我们讨论了SLE中常用的口服免疫抑制药物、它们的药物基因组学以及影响其代谢和血药浓度的因素。此外,我们强调了治疗药物监测在SLE中的作用,这是实现个体化治疗的首个可及步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/98a5/10816431/7bfd98968fec/jcm-13-00451-g001.jpg

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