Pulmonary arterial hypertension with cardiopulmonary comorbidities: is it a unique phenotype?

IF 2.6 3区 医学 Q2 RESPIRATORY SYSTEM
Meng Zhang, Xueran Guo, Wei Guo, Yan Wang, Yao Xiao, Jiancheng Han, Ye Li, Tingting Man, Jie Li, Yong Chen, Shengchen Duan, Wenmei Zhang, Hui Li, Ao Yin, Jiafei Peng, Chunrong An, Wanmu Xie, Qian Gao, Shuai Zhang, Yunxia Zhang, Zhenguo Zhai, Jun Wan
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引用次数: 0

Abstract

Background: Pulmonary arterial hypertension (PAH) patients with cardiopulmonary comorbidities have been prevalent nowadays. However, there was limited data on clinical characteristics and therapeutic responses in these populations.

Methods: Patients diagnosed with right heart catheterization (RHC)-confirmed PAH between October 2021 to March 2023 were included in our study. According to whether they had cardiopulmonary diseases or not, they were classified into two groups: comorbidities group and non-comorbidities group. We aimed to compare the clinical data, PAH-targeted strategies, and therapeutic responses between these two PAH groups. We further analyzed the impact of the numbers and categories of comorbidities on therapeutic responses.

Results: Almost half of the patients co-existed with cardiopulmonary diseases. Compared with non-comorbidities group (n = 40), comorbidities group (n = 36) were senior (p = 0.000) and male predominantly (p = 0.005). Comorbidities group also associated inconsistencies between hemodynamics and 6-min walking distance (6MWD), with a shorter 6MWD (p = 0.000), but a lower mean pulmonary artery pressure (mPAP) (p = 0.008). Non-comorbidities group showed an upturn in the WHO-FC (p = 0.010) and risk assessment (p = 0.033), while the improvement of hemodynamics [decreased mPAP (p = 0.009) and pulmonary vascular resistance (PVR) (p = 0.001), increased cardiac index (p = 0.001)] in comorbidities group did not match the change in clinical severity (no significant improvements in WHO-FC, risk stratification and 6MWD). When categorized by the comorbidities counts, it demonstrated that the more comorbidities, the more severe the clinical conditions, and the worse the therapeutic responses.

Conclusion: PAH patients with cardiopulmonary comorbidities represent a unique phenotype, with different clinical manifestation and treatment responses from typical PAH and inconsistencies between hemodynamics and functional status from baseline to follow-up.

肺动脉高压合并心肺合并症:是一种独特的表型吗?
背景:肺动脉高压(PAH)患者合并心肺合并症已成为当今社会的普遍现象。然而,关于这些人群的临床特征和治疗反应的数据有限。方法:纳入2021年10月至2023年3月期间诊断为右心导管(RHC)确诊的PAH患者。根据是否患有心肺疾病分为两组:合并症组和非合并症组。我们的目的是比较这两个PAH组的临床数据、PAH靶向策略和治疗反应。我们进一步分析了合并症的数量和类别对治疗反应的影响。结果:近半数患者合并心肺疾病。与无合并症组(n = 40)相比,合并症组(n = 36)以老年人(p = 0.000)和男性为主(p = 0.005)。合共病组血液动力学与6分钟步行距离(6MWD)之间也存在不一致,6MWD较短(p = 0.000),但平均肺动脉压(mPAP)较低(p = 0.008)。非合并症组在WHO-FC (p = 0.010)和风险评估(p = 0.033)方面有所改善,而合并症组血流动力学的改善[mPAP降低(p = 0.009)、肺血管阻力(PVR) (p = 0.001)、心脏指数升高(p = 0.001)]与临床严重程度的变化不匹配(WHO-FC、风险分层和6MWD无显著改善)。当按合并症计数分类时,它表明合并症越多,临床状况越严重,治疗反应越差。结论:PAH合并心肺合并症患者具有独特的表型,其临床表现和治疗反应与典型PAH不同,且从基线到随访的血流动力学和功能状态不一致。
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 Pulmonary Medicine
BMC Pulmonary Medicine RESPIRATORY SYSTEM-
CiteScore
4.40
自引率
3.20%
发文量
423
审稿时长
6-12 weeks
期刊介绍: BMC Pulmonary Medicine is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of pulmonary and associated disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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