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Risk of Dyslipidemia Associated With Oral Janus Kinase Inhibitors: A Systematic Review and Meta‐Analysis of Randomized Placebo‐Controlled Trials

医学 血脂异常 内科学 不利影响 安慰剂 随机对照试验 入射(几何) 置信区间 临床试验 血脂谱 家族性高胆固醇血症 贾纳斯激酶 胆固醇 胃肠病学 脂蛋白 荟萃分析 系统回顾 低密度脂蛋白胆固醇 内分泌学
作者
Daniel Isufi,Niloufar Javanmardi,Mikkel Bak Jensen,Nikolai Loft,Lone Skov,Jesper Elberling,Simon Francis Thomsen,Farzad Alinaghi
出处
期刊:International Journal of Dermatology [Wiley]
卷期号:65 (4): 737-745 被引量:2
标识
DOI:10.1111/ijd.70122
摘要

Janus kinase inhibitors (JAKi) have sparked a new era in the treatment of immune-mediated diseases. While some studies have reported an increased incidence of dyslipidemia in JAKi-treated patients, the full extent of this adverse event is not established. The study aimed to assess the association between treatment with oral JAKi and dyslipidemia in phases 2 and 3 placebo-controlled randomized clinical trials (RCTs). A systematic review and meta-analysis were conducted, encompassing phase 2 and 3 RCTs. The Embase, PubMed, and Web of Science databases were searched up to March 9, 2025. Only RCTs reporting lipid levels before and after treatment with JAKi were included. Data were extracted for changes in high-density lipoprotein (HDL), low-density lipoprotein (LDL), total cholesterol (TC), and triglycerides (TG) with values reported in mg/dL. A total of 13 studies were included in the analysis, comprising nine studies on rheumatoid arthritis, two on atopic dermatitis, one on Crohn's disease, and one on psoriasis. The studies encompassed a total of 3978 patients treated with JAKi and 1680 controls. Across all indications, the mean difference between JAKi and placebo for individual drug, was increased by 6.07 mg/dL (95% confidence interval [CI], 5.01-7.14) for HDL and 9.05 mg/dL (95% CI, 7.78-10.32) for LDL for baricitinib; HDL 5.4 mg/dL (95% CI, 3.2-7.7) and LDL 12.4 mg/dL (95% CI, 8.9-15.9) for upadacitinib; HDL 7.0 mg/dL (95% CI, 5.7-8.3) and LDL 15.7 mg/dL (95% CI, 12.9-18.6) for tofacitinib; and lastly HDL 3.0 mg/dL (95% CI, 0.2-5.8) and LDL 14.9 mg/dL (95% CI, 3.6-26.3) for decernotinib. This systematic review and meta-analysis highlight the risk of dyslipidemia during treatment with JAKi, which could pose cardiovascular risks. Thus, regular assessments of cardiovascular risk factors and routine lipid monitoring in patients undergoing JAKi therapy may be essential for managing dyslipidemia and evaluating long-term cardiovascular safety.
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