The Diagnostic and Assessment Value of Plasma Pentraxin 3 in Acute Exacerbation of Chronic Obstructive Pulmonary Disease

Int J Chron Obstruct Pulmon Dis. 2023 Jul 10:18:1391-1400. doi: 10.2147/COPD.S402463. eCollection 2023.

Abstract

Background: Pentraxin 3 (PTX3) is an acute-phase protein and an important inflammatory mediator. We hypothesized plasma PTX3 could be a valuable diagnostic biomarker in acute exacerbation of chronic obstructive pulmonary disease (AECOPD).

Methods: In this prospective controlled study, 458 COPD patients and 71 healthy controls from May 2019 to December 2020 in two hospitals were enrolled. COPD patients were divided into AECOPD group (n = 173) and stable COPD group (n = 285). AECOPD patients were subdivided into mild or moderate group (n = 43) and severe group (n = 130) based on severity. Plasma PTX3 levels were detected by ELISA.

Results: Plasma PTX3 levels were significantly higher in AECOPD (2.8 ng/mL) compared to stable COPD (0.87 ng/mL) and healthy controls (0.83 ng/mL). In the analysis of AECOPD subgroups, plasma PTX3 level of severe group (4.51 ng/mL) was significantly higher than that of mild or moderate group (1.25 ng/mL). Patients with respiratory failure had higher PTX3 than those without respiratory failure. No difference was observed between stable COPD patients and healthy controls. ROC analysis showed that plasma PTX3 had a considerable ability to distinguish AECOPD from stable COPD [AUC: 0.85, 95% CI (0.81-0.88), P < 0.0001; cut-off 1.25 ng/mL, sensitivity 77.5%, specificity 74%]. AUC of PTX3 was better than CRP regarding diagnosis of AECOPD. Combination of PTX3 and CRP was superior to either of them in diagnosing AECOPD.

Conclusion: Plasma PTX3 levels were significantly higher in AECOPD than stable COPD. The level was associated with the severity of exacerbation. Plasma PTX3 has potential value as a biomarker to diagnose and evaluate AECOPD.

Keywords: AECOPD; C-reactive protein; diagnosis; pentraxin 3; severity.

MeSH terms

  • Biomarkers
  • C-Reactive Protein / analysis
  • Disease Progression
  • Humans
  • Prospective Studies
  • Pulmonary Disease, Chronic Obstructive*
  • Respiratory Insufficiency*

Substances

  • PTX3 protein
  • C-Reactive Protein
  • Biomarkers

Grants and funding

This work was supported by the Project of Natural Science Foundation of China (82270019, 82070011), the Key Project of Jiangsu Commission of Health (K2019004), and Beijing Bethune Charitable Foundation (Grant Number BJ-RW2020004J).