Publication

Pneumococcal colonisation density: a new marker for disease severity in HIV-infected adults with pneumonia

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Last modified
  • 02/20/2025
Type of Material
Authors
    Werner C Albrich, Kantonsspital St GallenShabir A Madhi, University of WitwatersrandPeter V Adrian, University of WitwatersrandNadia van Niekerk, University of WitwatersrandJean-Noel Telles, Fondation MérieuxN Ebrahim, University of WitwatersrandMelina Messaoudi, Fondation MérieuxGlaucia Paranhos-Baccala, Fondation MérieuxSven Giersdorf, Thermo Sci BiomarkersGuy Vernet, Fondation MérieuxBeat Mueller, Kantonsspital AarauKeith Klugman, Emory University
Language
  • English
Date
  • 2014-08-09
Publisher
  • BMJ Publishing Group: Open Access
Publication Version
Copyright Statement
  • Published by the BMJ Publishing Group Limited.
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 2044-6055
Volume
  • 4
Issue
  • 8
Start Page
  • e005953
End Page
  • e005953
Grant/Funding Information
  • This work was funded by the Center for AIDS Research/NIH Grant P30 A1050409 to KPK; C-polysaccharide Antigen was provided free of charge by Binax; PCT sensitive LIA, MR-proADM KRYPTOR, MR-proANP KRYPTOR, Copeptin KRYPTOR were provided free of charge by Thermo Scientific Biomarkers, Hennigsdorf, Germany.
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Abstract
  • Objective A high genomic load of Pneumococcus from blood or cerebrospinal fluid has been associated with increased mortality. We aimed to analyse whether nasopharyngeal colonisation density in HIV-infected patients with community-acquired pneumonia (CAP) is associated with markers of disease severity or poor outcome. Methods Quantitative lytA real-time PCR was performed on nasopharyngeal swabs in HIV-infected South African adults hospitalised for acute CAP at Chris Hani Baragwanath Hospital, Soweto, South Africa. Pneumonia aetiology was considered pneumococcal if any sputum culture or Gram stain, urinary pneumococcal C-polysaccharide-based antigen, blood culture or whole blood lytA real-time PCR revealed pneumococci. Results There was a moderate correlation between the mean nasopharyngeal colonisation densities and increasing CURB65 scores among all-cause patients with pneumonia (Spearman correlation coefficient r=0.15, p=0.06) or with the Pitt bacteraemia score among patients with pneumococcal bacteraemia (p=0.63). In patients with pneumococcal pneumonia, nasopharyngeal pneumococcal colonisation density was higher among non-survivors than survivors (7.7 vs 6.1 log10 copies/mL, respectively, p=0.02) and among those who had pneumococci identified from blood cultures and/or by whole blood lytA real-time PCR than those with non-bacteraemic pneumococcal pneumonia (6.6 vs 5.6 log10 copies/mL, p=0.03). Nasopharyngeal colonisation density correlated positively with the biomarkers procalcitonin (Spearman correlation coefficient r=0.37, p<0.0001), proadrenomedullin (r=0.39, p=0.008) and copeptin (r=0.30, p=0.01). Conclusions In addition to its previously reported role as a diagnostic tool for pneumococcal pneumonia, quantitative nasopharyngeal colonisation density also correlates with mortality and prognostic biomarkers. It may also be useful as a severity marker for pneumococcal pneumonia in HIV-infected adults.
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Research Categories
  • Health Sciences, Epidemiology
  • Health Sciences, Medicine and Surgery
  • Health Sciences, Pathology

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