Department of Cardiac and Vascular Diseases, John Paul II Hospital in Krakow, 31-202 Krakow, Poland.
Pulmonary Circulation Centre, Department of Cardiac and Vascular Diseases, Faculty of Medicine, Jagiellonian University Medical College, 31-008 Krakow, Poland.
Cells. 2022 Apr 29;11(9):1491. doi: 10.3390/cells11091491.
Background: Inflammatory response and endothelial dysfunction contribute to the progression of chronic thromboembolic pulmonary hypertension (CTEPH). We aimed to assess changes in biomarkers involved in those processes in inoperable CTEPH patients treated with balloon pulmonary angioplasty (BPA). Methods: We enrolled 20 patients with inoperable CTEPH qualified for BPA and a control group. Interleukin 6, 8, 10 (IL-6, IL-8, IL-10), monocyte chemoattractant protein-1 (MCP-1), and C-reactive protein (hsCRP) constituted the markers of systemic inflammation. Endothelin 1 (ET-1) served as a marker of endothelial dysfunction. Selected markers were assessed before the BPA treatment, 24 h after the first BPA, and six months after completion of the BPA treatment. Results: At baseline, the CTEPH patients had increased serum concentrations of IL-6, IL-8 and ET-1. Twenty-four hours after a BPA session, we observed an increase in concentrations of IL-6 (∆ = 3.67 (1.41; 7.16); p < 0.001), of IL-10 (∆ = 0.25 (0; 0.47); p = 0.003), of MCP-1 (∆ = 111 (60.1; 202.8); p = 0.002), and of hsCRP (∆ = 4.81 (3.46; 8.47); p < 0.001). Six months after completion of the BPA treatment, there was a decrease in concentrations of IL-6 (∆ = −1.61 (−3.11; −0.20); p = 0.03), of IL8 (∆ = −3.24 (−7.72; 0.82); p = 0.01), and of ET-1 (∆ = −0.47 (−0.96; 0.05); p = 0.005). Conclusions: Patients with inoperable CTEPH exhibit increased systemic inflammation and endothelial dysfunction, which improves after completion of the BPA treatment. A single BPA session evokes an acute inflammatory response.
炎症反应和内皮功能障碍导致慢性血栓栓塞性肺动脉高压(CTEPH)的进展。我们旨在评估接受球囊肺动脉成形术(BPA)治疗的不可手术 CTEPH 患者中参与这些过程的生物标志物的变化。
我们纳入了 20 名符合 BPA 条件的不可手术 CTEPH 患者和对照组患者。白细胞介素 6、8、10(IL-6、IL-8、IL-10)、单核细胞趋化蛋白 1(MCP-1)和 C 反应蛋白(hsCRP)构成全身炎症的标志物。内皮素 1(ET-1)作为内皮功能障碍的标志物。在 BPA 治疗前、第一次 BPA 后 24 小时和 BPA 治疗完成后 6 个月评估选定的标志物。
在基线时,CTEPH 患者的血清 IL-6、IL-8 和 ET-1 浓度升高。BPA 治疗后 24 小时,我们观察到 IL-6 浓度升高(Δ=3.67(1.41;7.16);p<0.001),IL-10 浓度升高(Δ=0.25(0;0.47);p=0.003),MCP-1 浓度升高(Δ=111(60.1;202.8);p=0.002)和 hsCRP 浓度升高(Δ=4.81(3.46;8.47);p<0.001)。BPA 治疗完成后 6 个月,IL-6 浓度降低(Δ=-1.61(-3.11;-0.20);p=0.03),IL8 浓度降低(Δ=-3.24(-7.72;0.82);p=0.01),和 ET-1 浓度降低(Δ=-0.47(-0.96;0.05);p=0.005)。
不可手术的 CTEPH 患者表现出全身炎症和内皮功能障碍增加,这些在 BPA 治疗完成后得到改善。单次 BPA 治疗会引发急性炎症反应。