Gendron Nicolas, Planquette Benjamin, Roche Anne, Chocron Richard, Helley Dominique, Philippe Aurélien, Morange Pierre-Emmanuel, Gaussem Pascale, Sanchez Olivier, Smadja David M
Hematology Department, Assistance Publique - Hôpitaux de Paris-Centre Université Paris Cité (APHP-CUP), Hôpital européen Georges Pompidou, Paris, 75015, France.
Paris Cité University, INSERM UMR-S 970, Paris Cardiovascular Research Centre, Paris, France.
Stem Cell Rev Rep. 2025 Mar 14. doi: 10.1007/s12015-025-10865-0.
Pulmonary embolism (PE) is a life-threatening condition with long-term complications, including residual pulmonary vascular obstruction (RPVO). RPVO is associated with an increased risk of venous thromboembolism recurrence, chronic symptoms, and reduced quality of life. We hypothesize that an endothelial activation and vascular injury play a central role in the pathophysiology of RPVO. This prospective monocentric study investigates the potential of circulating biomarkers, including CD34⁺ cells, circulating endothelial cells (CECs), and platelet-derived growth factor BB (PDGF-BB), as indicators of vascular sequelae and predictors of RPVO. We included 56 patients with a first episode of PE. Biomarker levels were measured at PE diagnosis and six months later, coinciding with RPVO assessment using ventilation-perfusion lung scans. This defined groups of patients with (RPVO ≥ 10%) and without (RPVO < 10%) perfusion defects. Associations between biomarker levels, presence of perfusion defects, and clinical parameters were analyzed. At PE diagnosis, CEC and PDGF-BB levels were significantly elevated in patients compared to healthy controls, while CD34⁺ levels showed no difference. At the six-month follow-up, patients with perfusion defects exhibited significantly lower CD34⁺ cell levels compared to those without (median 1440 cells/mL vs. 2960 cells/mL). No significant differences in CEC or PDGF-BB levels were observed at follow-up. In conclusion, low CD34⁺ cell levels at RPVO assessment suggest a decreased regenerative potential contributing to thrombus persistence. CD34⁺ cells may serve as biomarkers for perfusion defects and warrant further study for their potential role in guiding clinical management of PE complications.
肺栓塞(PE)是一种危及生命的疾病,伴有长期并发症,包括残余肺血管阻塞(RPVO)。RPVO与静脉血栓栓塞复发风险增加、慢性症状及生活质量下降相关。我们假设内皮激活和血管损伤在RPVO的病理生理过程中起核心作用。这项前瞻性单中心研究调查了循环生物标志物的潜力,包括CD34⁺细胞、循环内皮细胞(CEC)和血小板衍生生长因子BB(PDGF-BB),作为血管后遗症的指标和RPVO的预测因子。我们纳入了56例首次发生PE的患者。在PE诊断时及六个月后测量生物标志物水平,同时使用通气灌注肺扫描进行RPVO评估。这确定了有(RPVO≥10%)和无(RPVO<10%)灌注缺损的患者组。分析了生物标志物水平、灌注缺损的存在与临床参数之间的关联。在PE诊断时,与健康对照相比,患者的CEC和PDGF-BB水平显著升高,而CD34⁺水平无差异。在六个月的随访中,有灌注缺损的患者与无灌注缺损的患者相比,CD34⁺细胞水平显著降低(中位数分别为1440个细胞/mL和2960个细胞/mL)。随访时CEC或PDGF-BB水平未观察到显著差异。总之,RPVO评估时低CD34⁺细胞水平提示再生潜力降低,导致血栓持续存在。CD34⁺细胞可能作为灌注缺损的生物标志物,其在指导PE并发症临床管理中的潜在作用值得进一步研究。