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. 2018 Mar;12(3):1228-1239.
doi: 10.1111/crj.12656. Epub 2017 Jun 15.

Analysis of viral infection and biomarkers in patients with acute exacerbation of chronic obstructive pulmonary disease

Affiliations

Analysis of viral infection and biomarkers in patients with acute exacerbation of chronic obstructive pulmonary disease

Tiping Yin et al. Clin Respir J. 2018 Mar.

Abstract

Objective: To investigate viral infection in patients with acute exacerbation of chronic obstructive pulmonary disease (AECOPD) in Shanghai, and to analyze the clinical characteristics and biomarkers in viral infection.

Methods: This study included all consecutive patients who were admitted for a diagnosis of AECOPD during June 2013 to May 2015. Thirty-one stable COPD patients and 31 healthy controls were also recruited. Oropharyngeal samples were assessed, PCR for respiratory viruses were performed. Patients were divided into AECOPD virus-positive (+) group and AECOPD virus-negative (-) group according to viral detection. Luminex was used to detect the concentrations of inflammatory cytokines in the serum.

Results: A total of 264 patients were included with a mean age of 75 ± 0.5 years. There were 72 patients (27.3%) identified with viral positive, of whom two patients were detected with double viral infections (FluA + FluB and RSVA + HRV, respectively). The rate of viral detection was associated with season, highest in winter. Comparisons of clinical characteristics showed no significant differences between AECOPD virus+ group and AECOPD virus- group. However, serum concentrations of interferon-inducible protein-10 (IP-10) and interferon-gamma (IFN-γ) in virus+ AECOPD patients were significantly higher than those in the virus- AECOPD, stable COPD and healthy control groups (P < .05).

Conclusion: Viral infection was an important pathogen in AECOPD patients; the most common viruses included FluA, HRV and FluB. It was very difficult to diagnose the viral infection according to clinical characteristics. The increased of serum IP-10 and IFN-γ levels might be value to indicate viral infection in AECOPD.

Keywords: IP-10; acute exacerbation of chronic obstructive pulmonary disease; chronic obstructive pulmonary disease; cytokine; viral infection.

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Conflict of interest statement

The authors have stated explicitly that there are no conflicts of interest in connection with this article.

Figures

Figure 1
Figure 1
The proportions of patients with a negative viral infection, dual viral infection and single viral infection from the 264 AECOPD patients. Abbreviation: AECOPD, acute exacerbation of chronic obstructive pulmonary disease
Figure 2
Figure 2
Identified viruses in 264 AECOPD patients. Abbreviations: FluA, influenza virus type A; HRV, rhinovirus; FluB, influenza virus type B; HADV, human adenovirus; RSVA, respiratory syncytial virus type A; HCoV, human coronavirus; HBoV, human Bocavirus; HMPV, human metapneumovirus; AECOPD, acute exacerbation of chronic obstructive pulmonary disease
Figure 3
Figure 3
Seasonal variability of viruses detected in 264 AECOPD patients. Abbreviations: FluA, influenza virus type A; FluB, influenza virus type B; HADV, human adenovirus; RSVA, respiratory syncytial virus type A; HRV, rhinovirus; AECOPD, acute exacerbation of chronic obstructive pulmonary disease
Figure 4
Figure 4
Correlations between IP‐10 concentrations and FEV1% predicted values in the AECOPD virus+ group (A) and AECOPD virus− group (B). Abbreviations: IP‐10, interferon‐γ inducible protein 10; FEV1, forced expiratory volume in one second; AECOPD, acute exacerbation of chronic obstructive pulmonary disease Note: P < .05 indicates statistical significance in the Spearman correlation test

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