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Association between the cumulative dose of cyclosporine and liver enzyme abnormalities in dermatology patients managed with a low‐dose regimen

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Cyclosporine (CsA) is an immunosuppressive agent that specifically inhibits T cell‐related immune responses. There is little evidence regarding the association between low‐dose CsA administration and abnormal hepatic function in dermatology… Click to show full abstract

Cyclosporine (CsA) is an immunosuppressive agent that specifically inhibits T cell‐related immune responses. There is little evidence regarding the association between low‐dose CsA administration and abnormal hepatic function in dermatology patients. This study aimed to examine the association between the cumulative dose of CsA and liver enzyme abnormalities obtained from peripheral blood tests in patients with skin diseases. A retrospective single‐center study of 697 patients who were prescribed CsA for skin disease in the outpatient dermatology clinic between 2015 and 2019 were performed. Multiple logistic regression with confounder adjustment was performed to assess the association between the cumulative dose of CsA and liver enzyme abnormalities. Compared to patients with the lowest cumulative dose of CsA (˂7.0 g), patients with the highest cumulative dose of CsA (≥30.6 g) were significantly associated with an increased likelihood of developing liver enzyme abnormalities (odds ratio [OR] = 1.96; 95% confidence interval [CI] = 1.02–3.79). In the stratified analysis, patients with the highest cumulative dose of CsA (≥30.6 g) were significantly associated with a 1.5‐or higher alanine aminotransferase elevation from baseline (OR = 2.26, CI = 1.08–4.73). Patients prescribed long‐term, low‐dose CsA up to a high cumulative dose (≥30.6 g) may be associated with an increased risk of developing liver enzyme abnormalities. However, these liver enzyme elevations were not severe in magnitude and were reversible.

Keywords: liver enzyme; dose csa; dose; dermatology; enzyme abnormalities; cumulative dose

Journal Title: Dermatologic Therapy
Year Published: 2022

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