Tello Khodr, Yogeswaran Athiththan, Majeed Raphael W, Kiely David G, Lawrie Allan, Brittain Evan, Annis Jeffrey S, Olschewski Horst, Kovacs Gabor, Hassoun Paul M, Balasubramanian Aparna, Konswa Ziad, Sweatt Andrew J, Zamanian Roham T, Wilkins Martin R, Howard Luke, Arvanitaki Alexandra, Giannakoulas George, Cajigas Hector R, Frantz Robert, Williams Paul G, Frauendorf Marlize, Marquardt Kurt, Antoine Tobiah, Fuenderich Meike, Richter Manuel, Grimminger Friedrich, Ghofrani Hossein-Ardeschir, Wilhelm Jochen, Seeger Werner
Department of Internal Medicine, Universities of Giessen and Marburg Lung Center (UGMLC), Member of the German Center for Lung Research (DZL), Giessen, Germany; Institute for Lung Health, Cardio-Pulmonary Institute (CPI), Giessen, Germany.
Department of Internal Medicine, Universities of Giessen and Marburg Lung Center (UGMLC), Member of the German Center for Lung Research (DZL), Giessen, Germany; Institute of Medical Informatics, RWTH Aachen University, Aachen, Germany.
Chest. 2025 Jan;167(1):224-240. doi: 10.1016/j.chest.2024.08.016. Epub 2024 Sep 7.
Patients with COPD frequently demonstrate pulmonary hypertension (PH). Severe PH in patients with COPD, identified by pulmonary vascular resistance (PVR) of > 5 Wood units (WU), is closely linked to impaired transplant-free survival. The impact of PH-targeting pharmacotherapy in this context remains unclear.
Is PH-targeted therapy associated with improved transplant-free survival in patients with COPD and PH?
This study included Pulmonary Vascular Research Institute GoDeep meta-registry patients with COPD and PH and available right heart catheterization at diagnosis. We investigated PH-targeted therapy prevalence and its association with transplant-free survival using diverse statistical methods, including Cox regression and subgroup analyses based on PH severity, comorbidities, and pulmonary function test results. Immortal time bias was addressed through a landmark approach.
As of December 2023, the GoDeep meta-registry included 26,981 patients (28% in PH group 1, 13% in PH group 2, 12% in PH group 3, 10% in PH group 4, 2% in PH group 5, 26% undefined, and 9% control participants). Of these, 836 patients had a diagnosis of COPD with PH and were included in this analysis, with median age of 66 years (interquartile range [IQR], 59-73 years), FEV of 51% predicted (IQR, 34%-69% predicted), mPAP of 35 mm Hg (IQR, 28-44 mm Hg), PVR of 5 WU (IQR, 4-8 WU), cardiac index of 2.5 L/min/m (IQR, 2.0-2.9 L/min/m), and mostly World Health Organization functional class III were included. Five-year transplant-free survival was 42%, significantly worse than in group 1 PH. A multivariable Cox proportional hazards model identified PVR, but not FEV, as a major predictor of outcome. Four hundred eighteen patients (50%) received phosphodiesterase-5 inhibitor (PDE5i) therapy, which was associated with significantly reduced mortality: hazard ratio of 0.65 (IQR, 0.57-0.75) for the entire cohort of patients with COPD and PH and of 0.83 (IQR, 0.74-0.94) when performing landmark analysis. This PDE5i effect was reproduced robustly when performing subgroup analyses for patients with moderate to severe PH, various comorbidities, and supplemental oxygen requirement and when assessing the impact of unobserved confounders.
Patients with COPD and PH exhibit poor transplant-free survival, with PVR being a predictor of mortality. In this meta-registry, PDE5i therapy was associated with a significant reduction in mortality across all tested models.
慢性阻塞性肺疾病(COPD)患者常表现出肺动脉高压(PH)。COPD患者中,肺血管阻力(PVR)>5伍德单位(WU)所确定的重度PH与无移植生存期受损密切相关。在这种情况下,针对PH的药物治疗的影响仍不清楚。
针对PH的治疗是否与COPD合并PH患者的无移植生存期改善相关?
本研究纳入了肺血管研究所GoDeep荟萃登记中诊断为COPD合并PH且诊断时可进行右心导管检查的患者。我们使用多种统计方法,包括Cox回归以及基于PH严重程度、合并症和肺功能测试结果的亚组分析,调查了针对PH的治疗的患病率及其与无移植生存期的关联。通过标志性方法解决了不朽时间偏倚问题。
截至2023年12月,GoDeep荟萃登记包括26981名患者(PH 1组占28%,PH 2组占13%,PH 3组占12%,PH 4组占10%,PH 5组占2%,26%未定义,9%为对照参与者)。其中,836例患者被诊断为COPD合并PH并纳入本分析,中位年龄为66岁(四分位间距[IQR],59 - 73岁),预测FEV为51%(IQR,预测值的34% - 69%),平均肺动脉压(mPAP)为35 mmHg(IQR,28 - 44 mmHg),PVR为5 WU(IQR,4 - 8 WU),心脏指数为2.5 L/min/m²(IQR,2.0 - 2.9 L/min/m²),且大多为世界卫生组织功能分级III级。五年无移植生存率为42%,显著低于PH 1组。多变量Cox比例风险模型确定PVR而非FEV是结果的主要预测因素。四百一十八名患者(50%)接受了磷酸二酯酶-5抑制剂(PDE5i)治疗,这与死亡率显著降低相关:整个COPD合并PH患者队列的风险比为0.65(IQR,0.57 - 0.75),进行标志性分析时为0.83(IQR,0.74 - 0.94)。在对中重度PH、各种合并症和需要补充氧气的患者进行亚组分析以及评估未观察到的混杂因素的影响时,这种PDE5i效应得到了有力重现。
COPD合并PH患者的无移植生存期较差,PVR是死亡率的预测因素。在这个荟萃登记中,PDE5i治疗在所有测试模型中均与死亡率显著降低相关。