Pulmonary Arterial Hypertension Incidence in Scleroderma Patients Treated with Bosentan for Digital Ulcers: Evidence from the Italian SPRING Registry.

Fabio Cacciapaglia,Rossella De Angelis,Clodoveo Ferri,Gianluigi Bajocchi,Silvia Bellando-Randone,Cosimo Bruni,Martina Orlandi,Marco Fornaro,Edoardo Cipolletta,Giovanni Zanframundo,Roberta Foti,Giovanna Cuomo,Alarico Ariani,Edoardo Rosato,Gemma Lepri,Francesco Girelli,Elisabetta Zanatta,Silvia Laura Bosello,Ilaria Cavazzana,Francesca Ingegnoli,Maria De Santis,Giuseppe Murdaca,Giuseppina Abignano,Pettiti Giorgio,Alessandra Della Rossa,Maurizio Caminiti,Annamaria Iuliano,Giovanni Ciano,Lorenzo Beretta,Gianluca Bagnato,Ennio Lubrano,Ilenia De Andres,Alessandro Giollo,Marta Saracco,Cecilia Agnes,Corrado Campochiaro,Federica Lumetti,Amelia Spinella,Luca Magnani,Giacomo De Luca,Veronica Codullo,Elisa Visalli,Carlo Iandoli,Antonietta Gigante,Greta Pellegrino,Franco Cozzi,Maria Grazia Lazzaroni,Elena Generali,Gianna Mennillo,Simone Barsotti,Giuseppa Pagano-Mariano,Federica Furini,Licia Vultaggio,Simone Parisi,Clara Lisa Peroni,Gerolamo Bianchi,Enrico Fusaro,Gian Domenico Sebastiani,Marcello Govoni,Salvatore D'Angelo,Erika Pigatto,Franco Franceschini,Serena Guiducci,Lorenzo Dagna,Andrea Doria,Dilia Giuggioli,Valeria Riccieri,Carlo Salvarani,Marco Matucci-Cerinic,Florenzo Iannone,
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Abstract

OBJECTIVE Bosentan (BOS) is approved for treating pulmonary arterial hypertension (PAH) and preventing digital ulcers (DU) in systemic sclerosis (SSc). Our study aimed to evaluate whether BOS prescribed for DU could reduce the incidence of PAH in a large SSc cohort from the SPRING registry. METHODS Patients with SSc from the SPRING registry, meeting ACR/EULAR 2013 classification criteria with data on PAH onset, DU status, BOS exposure, and at least a one-year follow-up between 2015 and 2020, and no known PAH at baseline were included. PAH was diagnosed with right heart catheterization during the follow-up, and its incidence rate (IR) was calculated. Kaplan-Meier curves were determined, and multivariate regression identified PAH risk factors. RESULTS Among 727 eligible patients with SSc, followed for a median of 2.0 years, 54 (7.4%) developed PAH [IR 3.71 per 100 patients/years]. Patients with DU who were never exposed to BOS had a higher incidence of PAH [IR 4.90 per 100 patients/years] compared to those exposed to BOS, whose rates matched those without DU and who were never exposed to BOS. Risk factors independently associated with PAH development included DU (HR 1.85), age (HR 1.05), modified Rodnan Skin Score (mRSS) >4 (HR 2.07), ILD (HR 2.29), and acetylsalicylic acid treatment (HR 1.78). CONCLUSION In our cohort, DU were confirmed as a leading risk factor for PAH development, and BOS use for DU prevention may reduce this risk. Only patients with DU who were not on BOS had an increased PAH incidence.
用波生坦治疗数字溃疡的硬皮病患者肺动脉高压发生率:来自意大利SPRING注册的证据。
目的 玻生坦(BOS)被批准用于治疗系统性硬化症(SSc)患者的肺动脉高压(PAH)和预防数字溃疡(DU)。方法纳入符合 ACR/EULAR 2013 年分类标准的 SPRING 登记的 SSc 患者,这些患者均有 PAH 发病、DU 状态、BOS 暴露数据,并在 2015 年至 2020 年期间至少随访一年,且基线时未发现 PAH。随访期间通过右心导管检查确诊 PAH,并计算其发病率(IR)。结果在随访中位数为 2.0 年的 727 名符合条件的 SSc 患者中,有 54 人(7.4%)发展为 PAH [IR:3.71/100 患者/年]。与暴露于 BOS 的患者相比,从未暴露于 BOS 的 DU 患者的 PAH 发病率更高[IR 为 4.90/100例患者/年],而从未暴露于 BOS 的 DU 患者的 PAH 发病率与无 DU 患者相当。与 PAH 发病独立相关的风险因素包括:DU(HR 1.85)、年龄(HR 1.05)、改良罗德南皮肤评分(mRSS)>4(HR 2.07)、ILD(HR 2.29)和乙酰水杨酸治疗(HR 1.78)。只有未服用 BOS 的 DU 患者 PAH 发生率才会升高。
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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