Boucly Athénaïs, Montani David, Bauer Fabrice, Artaud-Macari Elise, Bergot Emmanuel, Boissin Clément, Chaouat Ari, Cottin Vincent, Dauphin Claire, Degano Bruno, De Groote Pascal, du Roure Camille, Favrolt Nicolas, Horeau-Langlard Delphine, Jaïs Xavier, Jevnikar Mitja, Lacoste-Palasset Thomas, Picard François, Prévôt Grégoire, Reynaud-Gaubert Martine, Roche Anne, Turquier Ségolène, Humbert Marc, Sitbon Olivier, Savale Laurent
INSERM UMR_S 999 "Pulmonary Hypertension: Pathophysiology and Novel Therapies", Hôpital Marie Lannelongue, Le Plessis-Robinson, France.
Université Paris-Saclay, Faculté de Médecine, HPPIT, Pulmonary Hypertension: Pathophysiology and Novel Therapies, Le Kremlin-Bicêtre, France.
Eur Respir J. 2025 May 6;65(5). doi: 10.1183/13993003.00895-2024. Print 2025 May.
European guidelines recommend initial monotherapy in pulmonary arterial hypertension patients with cardiovascular comorbidities based on the limited evidence for combination therapy in this growing population.
A retrospective analysis was conducted on incident pulmonary arterial hypertension patients enrolled in the French Pulmonary Hypertension Registry between 2009 and 2020. Propensity score matching was used to investigate initial dual oral combination therapy oral monotherapy in patients with at least one cardiovascular comorbidity ( hypertension, obesity, diabetes and coronary artery disease).
Of the 1784 patients identified, 1088 had at least one cardiovascular comorbidity, including 20% with three or comorbidities. In the propensity score-matched population (n=708), the majority of patients were female, with idiopathic/heritable/drug-induced pulmonary arterial hypertension at intermediate 1-year mortality risk. At first follow-up, initial dual therapy led to larger improvements in symptoms, exercise capacity, haemodynamic parameters and risk status than initial monotherapy, with no differences in long‑term survival. Treatment discontinuation was observed in 23% of patients initiated on dual therapy and 24% of those initiated on monotherapy.
Initial dual oral combination therapy may be beneficial and well-tolerated in most pulmonary arterial hypertension patients with cardiovascular comorbidities.
欧洲指南建议,鉴于在这一不断增长的患者群体中联合治疗的证据有限,肺动脉高压合并心血管疾病的患者应初始采用单药治疗。
对2009年至2020年纳入法国肺动脉高压登记处的初发肺动脉高压患者进行回顾性分析。倾向评分匹配法用于研究至少合并一种心血管疾病(高血压、肥胖、糖尿病和冠状动脉疾病)的患者初始口服联合双药治疗与口服单药治疗的情况。
在1784例确诊患者中,1088例至少合并一种心血管疾病,其中20%合并三种或更多疾病。在倾向评分匹配人群(n = 708)中,大多数患者为女性,患有特发性/遗传性/药物性肺动脉高压,1年死亡风险为中度。在首次随访时,与初始单药治疗相比,初始联合双药治疗在症状、运动能力、血流动力学参数和风险状态方面有更大改善,长期生存率无差异。接受联合双药治疗的患者中有23%、接受单药治疗的患者中有24%出现治疗中断。
对于大多数合并心血管疾病的肺动脉高压患者,初始口服联合双药治疗可能有益且耐受性良好。