Please use this identifier to cite or link to this item: https://doi.org/10.3390/jcm13020451
Title: Therapeutic Drug Monitoring in Patients with Systemic Lupus Erythematosus: Utility and Gaps
Authors: Chong, Kar Mun
Jiang, He
Lo, Elaine Ah Gi 
Hong, Wei-Zhen 
Wong, Emmett Tsz-Yeung 
Chan, Gek Cher 
Cho, Jiacai 
Keywords: Science & Technology
Life Sciences & Biomedicine
Medicine, General & Internal
General & Internal Medicine
systemic lupus erythematosus
therapeutic drug monitoring
pharmacogenomics
hydroxychloroquine
mycophenolate
cyclosporine
tacrolimus
azathioprine
RENAL-TRANSPLANT PATIENTS
MYCOPHENOLIC-ACID
LONG-TERM
BLOOD HYDROXYCHLOROQUINE
MULTITARGET THERAPY
INDUCTION TREATMENT
PHARMACOKINETICS
NEPHRITIS
MOFETIL
AZATHIOPRINE
Issue Date: Jan-2024
Publisher: MDPI
Citation: Chong, Kar Mun, Jiang, He, Lo, Elaine Ah Gi, Hong, Wei-Zhen, Wong, Emmett Tsz-Yeung, Chan, Gek Cher, Cho, Jiacai (2024-01). Therapeutic Drug Monitoring in Patients with Systemic Lupus Erythematosus: Utility and Gaps. JOURNAL OF CLINICAL MEDICINE 13 (2). ScholarBank@NUS Repository. https://doi.org/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.
Source Title: JOURNAL OF CLINICAL MEDICINE
URI: https://scholarbank.nus.edu.sg/handle/10635/248779
ISSN: 2077-0383
DOI: 10.3390/jcm13020451
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