Assessment of Major Adverse Cardiovascular Event Across Diverse Racial Groups of Psoriasis Patients on Biologic Therapy: A Retrospective Cohort Study

IF 2.3 3区 医学 Q2 DERMATOLOGY
Journal of Dermatology Pub Date : 2026-10-08 Epub Date: 2026-07-26 DOI:10.1111/1346-8138.70396
Chunghwan Ro, Ana Ormaza Vera, Waleed Adawi, Clinton W. Enos
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引用次数: 0

Abstract

Psoriasis is associated with an increased risk of major adverse cardiovascular events (MACE), and biologic therapy may reduce this risk by targeting systemic inflammation. However, limited data exist on whether long term MACE risk differs by biologic class or across racial groups. We conducted a retrospective cohort study to assess the risk of primary MACE in psoriasis patients receiving biological therapies, stratified by biological class, compared with biologic-naïve psoriasis patients. Whether MACE risk among biologic-treated patients varied by race was further examined. After 1:1 propensity score matching, 36 330 biologic-treated patients were compared with 36 330 non-biologic-treated patients. Incident MACE was assessed over 10 years. Class-specific analyses evaluated mutually exclusive biologic exposure groups, including TNF inhibitors (TNFi), IL-17 inhibitors (IL-17i), IL-12/23 inhibitors (IL-12/23i), and IL-23 inhibitors (IL-23i), each compared with an independently matched nonbiologic psoriasis comparator cohort. Race stratified analyses were restricted to biologic-treated patients, with White patients serving as the reference group. Psoriasis patients treated with biologics exhibited a 37% lower hazard of MACE compared with non-biologic users over the 10-year follow-up period [2160 vs. 3294; HR 0.63 (0.60–0.67)]. Class-specific analyses revealed reductions in MACE risk for TNFi [1403 vs. 1844; HR: 0.74 (0.69–0.80)], IL-17i [285 vs. 450; HR: 0.61 (0.53–0.72)], IL-12/23i [280 vs. 374; HR: 0.73 (0.62–0.86)], and IL-23i [238 vs. 363; HR: 0.64 (0.54–0.76)]. Race stratified analyses showed broadly similar MACE risk across racial groups; although, patients identifying as Non-White treated with TNFi did experience a reduced MACE risk compared to White patients [127 vs. 162; HR: 0.79 (0.62–0.99)]. This isolated finding should be interpreted cautiously given multiple race stratified comparisons. Overall, biologic therapy is associated with lower 10-year MACE risk among patients with psoriasis, with findings observed across biologic classes and largely consistent across racial strata.

不同种族银屑病患者生物治疗中主要心血管不良事件的评估:一项回顾性队列研究。
银屑病与主要不良心血管事件(MACE)的风险增加有关,生物治疗可以通过靶向全身性炎症来降低这种风险。然而,关于长期MACE风险是否因生物类别或种族群体而异的数据有限。我们进行了一项回顾性队列研究,以评估接受生物治疗的银屑病患者原发性MACE的风险,按生物类别分层,与biologic-naïve银屑病患者进行比较。进一步研究了生物治疗患者的MACE风险是否因种族而异。经1:1倾向评分匹配后,36 330例接受生物制剂治疗的患者与36 330例未接受生物制剂治疗的患者进行比较。事件MACE是在10年内评估的。类别特异性分析评估了相互排斥的生物暴露组,包括TNF抑制剂(TNFi), IL-17抑制剂(IL-17i), IL-12/23抑制剂(IL-12/23i)和IL-23抑制剂(IL-23i),每个组与独立匹配的非生物银屑病比较物队列进行比较。种族分层分析仅限于接受生物治疗的患者,白人患者作为参照组。在10年的随访期间,接受生物制剂治疗的银屑病患者的MACE风险比未使用生物制剂的患者低37% [2160 vs. 3294];Hr 0.63(0.60-0.67)]。分类分析显示TNFi的MACE风险降低[1403 vs. 1844;HR: 0.74 (0.69-0.80)], IL-17i[285比450;HR: 0.61 (0.53-0.72)], IL-12/23i[280比374;HR: 0.73 (0.62-0.86)], IL-23i [238 vs. 363;Hr: 0.64(0.54-0.76)]。种族分层分析显示,不同种族的MACE风险大致相似;虽然,与白人患者相比,接受TNFi治疗的非白人患者确实经历了较低的MACE风险[127对162;Hr: 0.79(0.62-0.99)]。考虑到多种族分层比较,这一孤立的发现应谨慎解释。总体而言,生物疗法与银屑病患者的10年MACE风险降低相关,这一发现在不同的生物类别和不同的种族阶层中基本一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Dermatology
Journal of Dermatology 医学-皮肤病学
CiteScore
4.60
自引率
9.70%
发文量
368
审稿时长
4-8 weeks
期刊介绍: The Journal of Dermatology is the official peer-reviewed publication of the Japanese Dermatological Association and the Asian Dermatological Association. The journal aims to provide a forum for the exchange of information about new and significant research in dermatology and to promote the discipline of dermatology in Japan and throughout the world. Research articles are supplemented by reviews, theoretical articles, special features, commentaries, book reviews and proceedings of workshops and conferences. Preliminary or short reports and letters to the editor of two printed pages or less will be published as soon as possible. Papers in all fields of dermatology will be considered.
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