接受肿瘤坏死因子-α和白细胞介素-12/23抑制剂治疗的银屑病患者发生主要不良心血管事件和全因死亡率的风险:一项基于韩国全国人口的队列研究。

Hyesoo Cho, Ye-Jee Kim, Ik Jun Moon, Woo Jin Lee, Chong Hyun Won, Mi Woo Lee, Sung Eun Chang, Joon Min Jung
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引用次数: 0

摘要

研究目的很少有研究调查了生物制剂对韩国银屑病患者主要不良心血管事件(MACE)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的MACEs风险和全因死亡率:从韩国国民健康保险服务(NHIS)数据库中选取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年间MACE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:结果: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发生率更高,全因死亡风险显著增加,但MACE风险没有增加。在控制年龄后,女性TNF-α抑制剂使用者的全因死亡风险明显增加。同时,在控制了性别因素后,60 岁或以上 TNF-α 抑制剂使用者的全因死亡风险明显升高。总之,使用TNF-α和IL-12/23抑制剂的患者之间的MACE风险无统计学差异。不过,使用IL-12/23抑制剂(尤其是老年患者和女性患者)可降低总死亡率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk of major adverse cardiovascular events and all-cause mortality among patients with psoriatic disease treated with tumor necrosis factor-α and interleukin-12/23 inhibitors: a nationwide population-based cohort study in Korea.

Purpose: 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.

Methods: 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.

Results: 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.

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