坏疽性脓皮病与主要不良心血管事件相关。

IF 0.5
Nana Ama Adjei-Frimpong, Francesco Delacqua, Ben A Croker, Reid Oldenburg
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引用次数: 0

摘要

背景:坏疽性脓皮病(Pyoderma gangrenosum, PG)是一种中性粒细胞性皮肤病,其特点是迅速发作疼痛性溃疡。先前基于人群的回顾性研究已经确定PG与主要不良心血管事件(MACE)之间的关系。然而,这些研究缺乏适当的对照组,并且没有在美国进行。目的:本研究使用我们所有人(AoU)数据库检查PG和MACE之间的关系,AoU是一个全国性的倡议,旨在增加对代表性不足人群的研究。方法:我们于2018年5月6日至2025年3月2日在AoU项目的美国成年人中进行了一项巢式病例对照研究。SNOMED代码用于识别所有条件。根据年龄、性别、种族和吸烟状况,PG病例与对照组的比例为4:1。采用logistic回归对高血压、糖尿病、高脂血症、系统性红斑狼疮和类风湿关节炎进行校正。结果:我们发现579例PG。与对照组相比,MACE与PG显著相关,显示(OR, 2.19;95% ci, 1.47-3.27;结论:在这个具有全国代表性的美国队列中,PG与MACE的发生率增加独立相关。这些发现强调了对PG患者进行全面心血管筛查的重要性,并支持了主动风险管理的必要性。进一步研究探索这种关联背后的病理生理机制可能有助于指导更有针对性和有效的护理策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pyoderma gangrenosum associated with major adverse cardiovascular events.

Background: Pyoderma gangrenosum (PG) is a neutrophilic dermatosis characterized by the rapid onset of painful ulcers. Previous retrospective population-based studies have identified a relationship between PG and major adverse cardiovascular events (MACE). However, these studies lacked appropriate control groups and were not conducted in the United States (US).

Objectives: This study examines the association between PG and MACE using the All of Us (AoU) database, a nationwide initiative created to increase research in underrepresented populations.

Methods: We performed a nested case-control study among US adults in the AoU program from May 6, 2018 to March 2, 2025. SNOMED codes were used to identify all conditions. PG cases were then matched 4:1 to controls by age, sex, ethnicity, and smoking status. MACE was assessed using logistic regression adjusting for hypertension, diabetes mellitus, hyperlipidemia, systemic lupus erythematosus, and rheumatoid arthritis.

Results: We identified 579 PG cases. MACE was significantly associated with PG compared to controls, showing (OR, 2.19; 95% CI, 1.47-3.27; p<.001) in our multivariable model.

Conclusions: In this nationally representative US cohort, PG was independently associated with increased odds of MACE. These findings highlight the importance of comprehensive cardiovascular screening in patients with PG and support the need for proactive risk management. Further studies exploring the pathophysiological mechanisms underlying this association may help guide more targeted and effective care strategies.

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