Improvements and challenges of long-term survival in patients with systemic lupus erythematosus-associated pulmonary arterial hypertension: A 10-year multi-center cohort study

Xingbei Dong, Jiuliang Zhao, Junyan Qian, Wei Wei, Miaojia Zhang, Xiao Zhang, Xiaofei Shi, Yisha Li, Xiaoping Hong, Qiang Shu, Shuhong Chi, Xin Dong, Ping Zhu, Rong Zhang, Zhuoli Zhang, Hongfeng feng Zhang, Xinwang Duan, Jing Xue, Shuhong Zhou, Hongbin Li, Dan Chen, Junwei Zhang, Yanhong WANG, Zhuang Tian, Yong-Tai Liu, Mengtao Li, Xiaofeng ZENG, Qian Wang
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Abstract

Background: Prior studies indicated improved survival in systemic sclerosis-associated pulmonary arterial hypertension (PAH) patients, but trends in systemic lupus erythematosus-associated PAH (SLE-PAH) survival remained unclear. Methods: Analyzing SLE-PAH patients from the nationwide CSTAR-PAH cohort, we divided them into two cohorts: A (2011-2016) and B (2016-2021), based on baseline right heart catheterization dates. We compared clinical characteristics, mortality, and treatment outcomes between these cohorts and with idiopathic PAH (IPAH) patients. Results: We enrolled 610 and 104 patients with SLE-PAH and IPAH, respectively. Patients with SLE-PAH were younger, had a higher proportion of low-risk patients, and had a significantly higher 10-year survival rate than those with IPAH (66.6% vs. 44.1%, p < 0.001). Cohort B had a longer 6-min walk distance, lower mean pulmonary arterial pressure and pulmonary vascular resistance, a better-preserved cardiac index, and less right ventricular dilation than cohort A. More patients in cohort B received intensive immunosuppressant- and PAH-targeted therapies. The 5-year survival rate was significantly higher in cohort B (88.1% vs. 77.5%, p = 0.006). Reaching low-risk profile of PAH (hazard ratio [HR] 0.34, 95% confidence interval [CI] 0.15-0.79, p = 0.012) and reaching lupus low-disease-activity state (HR 0.33, 95% CI 0.14-0.82, p = 0.016) were independent predictors of survival. The rate of achieving low-risk profile for PAH was considerably higher in patients initially treated with intensive immunosuppressive and dual-PAH-targeted therapies. Conclusions: Over the last decade in China, the clinical characteristics of patients with SLE-PAH have evolved and survival has improved. Early PAH detection and dual treatment-to-target strategies for both PAH and SLE have contributed to this improvement in survival.
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系统性红斑狼疮相关肺动脉高压患者长期生存的改善与挑战:一项为期10年的多中心队列研究
背景:先前的研究表明,系统性硬化症相关性肺动脉高压(PAH)患者的生存率有所提高,但系统性红斑狼疮相关性肺动脉高压(SLE-PAH)患者的生存率趋势仍不明确:分析全国范围内的 CSTAR-PAH 队列中的系统性红斑狼疮相关 PAH 患者,我们将其分为两个队列:根据基线右心导管检查日期,我们将其分为 A 组(2011-2016 年)和 B 组(2016-2021 年)。我们比较了这些队列与特发性 PAH(IPAH)患者的临床特征、死亡率和治疗效果:我们分别招募了 610 名和 104 名 SLE-PAH 和 IPAH 患者。SLE-PAH患者更年轻,低风险患者比例更高,10年生存率明显高于IPAH患者(66.6% vs. 44.1%,p <0.001)。与 A 组相比,B 组患者的 6 分钟步行距离更长,平均肺动脉压和肺血管阻力更低,心脏指数保存得更好,右心室扩张更少。B 组患者的 5 年生存率明显更高(88.1% 对 77.5%,P = 0.006)。达到PAH低风险状态(危险比[HR] 0.34,95% 置信区间[CI] 0.15-0.79,p = 0.012)和达到狼疮低疾病活动状态(HR 0.33,95% CI 0.14-0.82,p = 0.016)是生存率的独立预测因素。在最初接受强化免疫抑制和双PAH靶向治疗的患者中,达到PAH低危状态的比例要高得多:结论:近十年来,中国系统性红斑狼疮-PAH患者的临床特征发生了变化,生存率也有所提高。PAH的早期发现以及针对PAH和系统性红斑狼疮的双重治疗策略为生存率的提高做出了贡献。
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