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. 2021 Mar 29:8:633442.
doi: 10.3389/fmed.2021.633442. eCollection 2021.

Serum 8-iso-PGF2α Predicts the Severity and Prognosis in Patients With Community-Acquired Pneumonia: A Retrospective Cohort Study

Affiliations

Serum 8-iso-PGF2α Predicts the Severity and Prognosis in Patients With Community-Acquired Pneumonia: A Retrospective Cohort Study

Ling Zheng et al. Front Med (Lausanne). .

Abstract

Background: Many studies have identified the important role of 8-isoprostane (8-iso-PGF2α) in pulmonary diseases. However, the role of 8-iso-PGF2α in community-acquired pneumonia (CAP) remains unclear. Therefore, the main goal was to investigate the correlations of serum 8-iso-PGF2α with the severity and prognosis in CAP patients through a hospital-based retrospective cohort study. Methods: All 220 patients with CAP were enrolled. Demographic information and clinical data were collected. Levels of 8-iso-PGF2α and inflammatory cytokines were detected in serum using ELISA. Results: The levels of 8-iso-PGF2α were gradually increased in parallel with the CAP severity scores. Univariate and multivariate logistic regression analyses revealed a positive association between serum 8-iso-PGF2α and the CAP severity scores. Additionally, serum 8-iso-PGF2α levels were positively correlated with circulating inflammatory cytokines (CRP and TNFα). Serum 8-iso-PGF2α levels were increased in the patients with a longer hospital stay than those with a shorter hospital stay. Additionally, 20 patients died after hospitalization. Dead patients presented a higher serum 8-iso-PGF2α than surviving patients. A subsequent survival analysis revealed that higher serum 8-iso-PGF2α levels positively correlated with the risk of death in patients with CAP. Conclusions: Serum 8-iso-PGF2α levels on admission are positively associated with the severity of CAP patients. Elevated serum 8-iso-PGF2α on admission prolongs hospital stay and increases the risk of death in patients with CAP, indicating that 8-iso-PGF2α may be involved in the progression of CAP and serve as an early serum prognostic biomarker for CAP.

Keywords: 8-iso-PGF2α; CAP; CAP severity scores; biomarker; inflammatory cytokines.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Flow diagram of recruitment and follow-up research in this cohort study.
Figure 2
Figure 2
The levels of serum 8-iso-PGF2α in patients with CAP and Control subjects. (A–F) Serum 8-iso-PGF2α was measured using ELISA in CAP patients and Control subjects. (A) The levels of serum 8-iso-PGF2α were compared in patients with CAP and Control subjects. (B) The levels of serum 8-iso-PGF2α according to different grades of the CURB-65 score in patients with CAP. (C) The levels of serum 8-iso-PGF2α in different grades of CRB-65 score in patients with CAP. (D) The levels of serum 8-iso-PGF2α in different grades of the CURXO score in patients with CAP. (E) The levels of serum 8-iso-PGF2α in different grades of PSI score in patients with CAP. (F) The levels of serum 8-iso-PGF2α in different grades of SMART-COP score in patients with CAP. All data were expressed as mean ± SEM. *P < 0.05, **P < 0.01.
Figure 3
Figure 3
The levels of serum 8-iso-PGF2α in alive and dead CAP patients. (A,B) Serum 8-iso-PGF2α was measured using ELISA. (A) The levels of serum 8-iso-PGF2α in CAP patients with different lengths of hospital stay. (B) The levels of serum 8-iso-PGF2α in alive and dead patients. (C) Kaplan Meier plot of the probability survival of CAP patients during hospitalization. All data were expressed as mean ± SEM. *P < 0.05, **P < 0.01.

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