A cohort study in HigAshi-nippon of Pulmonary hyPertensIoN in systEmic SclerosiS (HAPPINESS study): protocol and baseline data for an observational study.

IF 2.1 Q3 RHEUMATOLOGY
Shuhei Takeyama, Hironari Hanaoka, Akiyoshi Hashimoto, Yusho Ishii, Yuka Shimizu, Toshiharu Takeuchi, Shuhei Shimoyama, Masataka Kuwana, Tomoaki Higuchi, Masaru Yoshimura, Hiroshi Kataoka, Yuko Shirota, Kazufumi Okada, Yoichi M Ito, Ryo Hisada, Kazuro Kamada, Sho Ishigaki, Tetsuya Horita, Tatsuya Atsumi, Masaru Kato
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引用次数: 0

Abstract

Background: Pulmonary hypertension (PH) is the leading cause of death among patients with systemic sclerosis (SSc). Recently, early therapeutic intervention to improve the prognosis was suggested, and the definition of PH was recently revised by lowering the cut-off value of mean pulmonary arterial pressure (mPAP) from ≥ 25 to > 20 mmHg. However, the optimal threshold for therapeutic intervention remains unclear. We aim to evaluate the prognosis of patients with SSc and its relationship with mPAP.

Methods: For this non-interventional retrospective and prospective cohort study, we enrolled patients with SSc or scleroderma spectrum disorders accompanied by other connective tissue diseases who underwent right heart catheterization (RHC) for suspected PH from 2010 to 2023. The date of the first RHC was defined as the baseline. Enrolled patients were classified into three groups based on their mPAP at the first RHC (≤ 20, 21-24, and ≥ 25 mmHg) and are being observed from baseline up to three years. The primary endpoint is the time between the first RHC and the first hospitalisation or death due to worsening PH.

Results: This study was approved by the Ethics Committee of Hokkaido University Hospital. A total of 229 patients were enrolled from 12 participating centres, with 41 prospectively followed up and 188 retrospectively followed up. The number of patients in each group (an mPAP of ≤ 20, 21-24, and ≥ 25 mmHg) is 79, 26, and 124, respectively. The observation is expected to be completed by December 2026. Findings will be disseminated at scientific conferences, peer-reviewed journals.

Conclusions: The findings of this study that we will obtain are expected to provide important information that will lead to improvements in the diagnosis of PH and the prognosis of patients.

Trial registration: This study was approved by the Ethics Committee of Hokkaido University Hospital (approval number 022-0109). It has been registered in the Japan Registry of Clinical Trials as jRCT1010220025 since November 7, 2022.

一项在日本进行的系统性硬化症肺动脉高压队列研究(HAPPINESS研究):一项观察性研究的方案和基线数据。
背景:肺动脉高压(PH)是系统性硬化症(SSc)患者死亡的主要原因。最近,早期治疗干预被建议改善预后,并且PH的定义最近被修改,将平均肺动脉压(mPAP)的临界值从≥25降低到bb0 20 mmHg。然而,治疗干预的最佳阈值仍不清楚。我们的目的是评估SSc患者的预后及其与mPAP的关系。方法:在这项非介入性回顾性和前瞻性队列研究中,我们招募了2010年至2023年因疑似PH接受右心导管(RHC)治疗的SSc或硬皮病谱系障碍伴其他结缔组织疾病患者。第一次RHC的日期被定义为基线。根据首次RHC时的mPAP(≤20mmhg、21-24 mmHg和≥25mmhg)将入组患者分为三组,从基线开始观察至3年。主要终点为首次RHC与首次因ph恶化而住院或死亡之间的时间。结果:本研究获得北海道大学医院伦理委员会批准。共有来自12个参与中心的229例患者入组,其中41例进行前瞻性随访,188例进行回顾性随访。两组(mPAP≤20、21-24、≥25 mmHg)患者分别为79、26、124例。这项观测预计将于2026年12月完成。研究结果将在科学会议和同行评议的期刊上传播。结论:我们将获得的研究结果有望提供重要信息,从而改善PH的诊断和患者的预后。试验注册:本研究经北海道大学附属医院伦理委员会批准(批准号022-0109)。它已于2022年11月7日在日本临床试验注册中心注册为jRCT1010220025。
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
BMC Rheumatology
BMC Rheumatology Medicine-Rheumatology
CiteScore
3.80
自引率
0.00%
发文量
73
审稿时长
15 weeks
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