Changes in Inflammatory Markers in Patients with Chronic Thromboembolic Pulmonary Hypertension Treated with Balloon Pulmonary Angioplasty

Cells. 2022 Apr 29;11(9):1491. doi: 10.3390/cells11091491.

Abstract

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.

Keywords: biomarker; chronic thromboembolic pulmonary hypertension; endothelial function; endothelin 1; interleukin 6; interleukin 8.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angioplasty, Balloon* / adverse effects
  • Biomarkers
  • C-Reactive Protein
  • Humans
  • Hypertension, Pulmonary* / therapy
  • Inflammation
  • Interleukin-10
  • Interleukin-6
  • Interleukin-8
  • Pulmonary Artery
  • Pulmonary Embolism* / complications
  • Pulmonary Embolism* / therapy

Substances

  • Biomarkers
  • Interleukin-6
  • Interleukin-8
  • Interleukin-10
  • C-Reactive Protein

Grants and funding

This article was supported by the science fund of the John Paul II Hospital, Cracow, Poland (no. FN/03/2022 to G.K.). This article was supported by the science fund of Jagiellonian University Medical College, Krakow, Poland. This article was supported by the science fund of Wroclaw Medical University, Wroclaw, Poland.