Please use this identifier to cite or link to this item: https://doi.org/10.3390/jcm13020451
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dc.titleTherapeutic Drug Monitoring in Patients with Systemic Lupus Erythematosus: Utility and Gaps
dc.contributor.authorChong, Kar Mun
dc.contributor.authorJiang, He
dc.contributor.authorLo, Elaine Ah Gi
dc.contributor.authorHong, Wei-Zhen
dc.contributor.authorWong, Emmett Tsz-Yeung
dc.contributor.authorChan, Gek Cher
dc.contributor.authorCho, Jiacai
dc.date.accessioned2024-06-11T06:28:48Z
dc.date.available2024-06-11T06:28:48Z
dc.date.issued2024-01
dc.identifier.citationChong, 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
dc.identifier.issn2077-0383
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/248779
dc.description.abstractDespite 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.
dc.language.isoen
dc.publisherMDPI
dc.sourceElements
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectMedicine, General & Internal
dc.subjectGeneral & Internal Medicine
dc.subjectsystemic lupus erythematosus
dc.subjecttherapeutic drug monitoring
dc.subjectpharmacogenomics
dc.subjecthydroxychloroquine
dc.subjectmycophenolate
dc.subjectcyclosporine
dc.subjecttacrolimus
dc.subjectazathioprine
dc.subjectRENAL-TRANSPLANT PATIENTS
dc.subjectMYCOPHENOLIC-ACID
dc.subjectLONG-TERM
dc.subjectBLOOD HYDROXYCHLOROQUINE
dc.subjectMULTITARGET THERAPY
dc.subjectINDUCTION TREATMENT
dc.subjectPHARMACOKINETICS
dc.subjectNEPHRITIS
dc.subjectMOFETIL
dc.subjectAZATHIOPRINE
dc.typeReview
dc.date.updated2024-06-11T01:44:15Z
dc.contributor.departmentPHARMACY
dc.contributor.departmentMEDICINE
dc.description.doi10.3390/jcm13020451
dc.description.sourcetitleJOURNAL OF CLINICAL MEDICINE
dc.description.volume13
dc.description.issue2
dc.published.statePublished
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