Neopterin in patients with COPD, asthma, and ACO: association with endothelial and lung functions

Respir Res. 2024 Apr 18;25(1):171. doi: 10.1186/s12931-024-02784-4.

Abstract

Background and objective: Endothelial dysfunction has been widely recognized in chronic airway diseases, including chronic obstructive pulmonary disease (COPD) and asthma; however, it remains unclear in asthma-COPD overlap (ACO). Neopterin (NP), a metabolite of guanosine triphosphate, is a novel biomarker for identifying the increased risk of adverse cardiovascular events. This study aims to investigate the association of NP with endothelial dysfunction and impaired lung function in COPD, asthma, and ACO patients.

Methods: A total of 77 subjects were prospectively recruited. All the participants underwent lung function test, endothelial function evaluation, including pulse wave velocity (PWV) and flow-mediated dilation (FMD), and blood sample detection. Moreover, the effect of NP on endothelial cells (ECs) in anoxic environments was assessed in vitro.

Results: Endothelial function was significantly decreased in the COPD and ACO patients compared with that in the healthy controls (P < 0.05). Forced expiratory volume in 1 s (FEV1) was negatively correlated with PWV and positively correlated with FMD (P < 0.05). NP was significantly increased in patients with chronic respiratory diseases compared with that in the control group, with COPD being the highest, followed by asthma, and ACO as the last (P < 0.05). The plasma level of NP exhibited negative correlations with FEV1 and positive correlations with PWV (P < 0.05). In vitro, a high level of NP increased the reactive oxygen species (ROS) and decreased the mitochondrial membrane potential (ΔΨm) of ECs dose-dependently in a hypoxic environment (P < 0.05).

Conclusion: NP was related to disease severity of chronic airway diseases and involved in the pathogenesis of endothelial dysfunction. A high NP level may contribute to endothelial dysfunction by increasing the oxidative stress of ECs dose-dependently in a hypoxic environment. Our findings may provide a novel evaluation and therapeutic target for endothelial dysfunction related to chronic airway diseases.

Keywords: Asthma; Asthma-COPD overlap (ACO); Chronic obstructive pulmonary disease (COPD); Endothelial dysfunction; Neopterin.

MeSH terms

  • Asthma*
  • Endothelial Cells / metabolism
  • Forced Expiratory Volume
  • Humans
  • Lung / metabolism
  • Neopterin
  • Pulmonary Disease, Chronic Obstructive*
  • Pulse Wave Analysis

Substances

  • Neopterin

Supplementary concepts

  • Pulmonary Disease, Chronic Obstructive, Severe Early-Onset