与匹配的对照队列相比,真菌样霉菌病和ssamzary综合征患者心血管疾病的相关性

Courtney M. Johnson , Sai M. Talluru , Bianka Bubic , Michelle Colbert , Priyanka Kumar , Hua-ling Tsai , Ravi Varadhan , Sima Rozati
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引用次数: 0

摘要

蕈样真菌病/ ssamzary综合征(MF/SS)产生低度慢性炎症状态,可能与心血管(CV)事件风险增加有关,这在其他慢性全身性皮肤病中也可见到。为了评估这种关联,设计了一项回顾性横断面研究,其中421名活检证实诊断为MF/SS的患者与从国家健康和营养评估调查数据库中随机选择的4210名年龄、性别和种族匹配的对照队列患者进行比较。MF/SS组CV事件发生率为14%,与对照组13%的发生率无统计学差异。在MF/SS队列中,多变量logistic回归模型显示,年龄较大的患者(OR = 1.05, 95%可信区间= 1.02-1.07)和诊断为高血压的患者(OR = 3.40, 95%可信区间= 1.71-6.75)发生CV事件的风险较高(P <0.001)。性别、种族、吸烟、糖尿病和肥胖等危险因素与心血管事件无显著相关性。研究结果表明,在MF/SS人群中,年龄增长和高血压是CV事件的危险因素,需要临床识别和管理。此外,还需要进一步的研究来了解MF/SS慢性炎症如何影响CV疾病的免疫发展的复杂相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of Cardiovascular Disease in Patients with Mycosis Fungoides and Sézary Syndrome Compared to a Matched Control Cohort

Mycosis fungoides/Sézary syndrome (MF/SS) produces a low-grade chronic inflammatory state that may be associated with an increased risk of cardiovascular (CV) events, as seen in other chronic, systemic dermatologic diseases. To assess this association, a retrospective, cross-sectional study was designed in which 421 patients with a biopsy-proven diagnosis of MF/SS were compared with a control cohort of 4,210 age-, gender-, and race-matched patients randomly selected from the National Health and Nutritional Evaluation Survey database. The MF/SS cohort had a 14% prevalence of CV events, which was not statistically different from the control population’s prevalence of 13%. In the MF/SS cohort, a multivariable logistic regression model showed that older patients (OR = 1.05 for each year of age, 95% confidence interval = 1.02–1.07) and those diagnosed with hypertension (OR = 3.40, 95% confidence interval = 1.71–6.75) had a higher risk of a CV event (P < 0.001). Risk factors such as gender, race, smoking, diabetes, and obesity were not significantly associated with CV events. Findings suggest that in the MF/SS population, advancing age and hypertension are risk factors for CV events, requiring clinical recognition and management. In addition, further research is needed to understand the complex interplay of how chronic inflammation in MF/SS impacts the immune development of CV disease.

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