Department of Dermatology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Department of Clinical Epidemiology and Biostatistics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
J Dermatolog Treat. 2024 Dec;35(1):2321194. doi: 10.1080/09546634.2024.2321194. Epub 2024 Feb 25.
Few studies have investigated the impact of biologics on the risk of major adverse cardiovascular events (MACEs) among Korean patients with psoriatic diseases. We compared the risk of MACEs and all-cause mortality among patients with psoriatic disease treated with tumor necrosis factor (TNF)-α and interleukin (IL)-12/23 inhibitors in Korea.
Patients with psoriatic disease prescribed with TNF-α and IL-12/23 inhibitors since 2016 were selected from the Korean National Health Insurance Service (NHIS) Database. Follow-up data for MACEs and all-cause mortality between 2016 and 2020 were collected. A total of 2886 individuals were included, including 1987 IL-12/23 inhibitor users and 899 TNF-α inhibitor users.
Compared with IL-12/23 inhibitor users, TNF-α inhibitor users had a higher prevalence of dyslipidemia and a significantly higher risk of all-cause mortality but not MACE. After controlling for age, female TNF-α inhibitor users had a significantly increased risk of all-cause mortality. Meanwhile, after controlling for sex, TNF-α inhibitor users aged 60 years or older demonstrated a significantly elevated risk of all-cause mortality. In conclusion, No statistically significant difference in MACE risk was observed between patients who used TNF-α and IL-12/23 inhibitors. Nevertheless, the use of IL-12/23 inhibitors, especially among older and female patients, resulted in a lower overall mortality.
鲜有研究调查生物制剂对韩国银屑病患者发生主要不良心血管事件(MACEs)风险的影响。我们比较了韩国接受肿瘤坏死因子(TNF)-α和白细胞介素(IL)-12/23 抑制剂治疗的银屑病患者发生 MACEs 和全因死亡率的风险。
从韩国国家健康保险服务(NHIS)数据库中选取了 2016 年以来接受 TNF-α 和 IL-12/23 抑制剂治疗的银屑病患者。收集了 2016 年至 2020 年期间 MACEs 和全因死亡率的随访数据。共纳入 2886 人,包括 1987 名 IL-12/23 抑制剂使用者和 899 名 TNF-α 抑制剂使用者。
与 IL-12/23 抑制剂使用者相比,TNF-α 抑制剂使用者的血脂异常患病率更高,全因死亡率风险显著更高,但 MACE 风险并无显著差异。在校正年龄后,女性 TNF-α 抑制剂使用者的全因死亡率风险显著增加。同时,在校正性别后,年龄在 60 岁及以上的 TNF-α 抑制剂使用者的全因死亡率风险显著升高。总之,TNF-α 和 IL-12/23 抑制剂使用者的 MACE 风险无统计学显著差异。然而,IL-12/23 抑制剂的使用,特别是在老年和女性患者中,导致了更低的总死亡率。