Biomarkers in atypical pneumonia: a systematic review of diagnostic and prognostic utility

Atypical pneumonia, driven by pathogens like Mycoplasma pneumoniae, Chlamydia pneumoniae, and Legionella pneumophila, is challenging to diagnose due to non-specific symptoms. This systematic review assessed the diagnostic accuracy and prognostic value of biomarkers in atypical pneumonia. A comprehe...

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Main Authors: Debashis Priyadarshan Sahoo, Bikash Ranjan Rout
Format: Article
Language:English
Published: PAGEPress Publications 2025-06-01
Series:Monaldi Archives for Chest Disease
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Online Access:https://www.monaldi-archives.org/macd/article/view/3564
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author Debashis Priyadarshan Sahoo
Bikash Ranjan Rout
author_facet Debashis Priyadarshan Sahoo
Bikash Ranjan Rout
author_sort Debashis Priyadarshan Sahoo
collection DOAJ
description Atypical pneumonia, driven by pathogens like Mycoplasma pneumoniae, Chlamydia pneumoniae, and Legionella pneumophila, is challenging to diagnose due to non-specific symptoms. This systematic review assessed the diagnostic accuracy and prognostic value of biomarkers in atypical pneumonia. A comprehensive search of PubMed, Scopus, Web of Science, and Google Scholar (2000-2024) identified 27 studies, including observational, cohort, case-control, and review designs. Studies focused on biomarkers such as C-reactive protein (CRP), procalcitonin (PCT), ferritin, D-dimer, and pathogen-specific antibodies, with quality evaluated using the Newcastle-Ottawa Scale and AMSTAR 2. CRP was elevated in 85% of cases, with a pooled sensitivity of 82.3% [95% confidence interval (CI) 76.5-88.1, I²=78%] but moderate specificity (65.2%, 95% CI 58.0-72.4). PCT exhibited high specificity (88.7%, 95% CI 83.2-94.2, I²=65%) for bacterial etiologies, making it valuable for distinguishing bacterial from viral infections. Anti-Mycoplasma pneumoniae immunoglobulin M (IgM) showed excellent diagnostic accuracy (sensitivity 90.1%, 95% CI 85.0-95.2). Ferritin levels >400 ng/mL were strongly associated with severe outcomes [odds ratio (OR) 3.15, 95% CI 2.10-4.72, I²=70%]. Elevated biomarkers correlated with increased hospitalization (OR 2.78, 95% CI 1.95-3.96) and mortality (OR 3.42, 95% CI 2.30-5.08). Heterogeneity was significant (I²=65-78%), reflecting variability in study populations and methods. PCT and anti-Mycoplasma pneumoniae IgM enhance diagnostic precision, while ferritin and CRP are robust prognostic markers. Standardized biomarker thresholds are essential to optimize their clinical utility and improve patient outcomes in atypical pneumonia management.
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spelling doaj-art-e771d3b5ef9f433fa4340859bd0e35d12025-08-20T03:28:22ZengPAGEPress PublicationsMonaldi Archives for Chest Disease1122-06432532-52642025-06-0110.4081/monaldi.2025.3564Biomarkers in atypical pneumonia: a systematic review of diagnostic and prognostic utilityDebashis Priyadarshan Sahoo0https://orcid.org/0000-0002-6198-0626Bikash Ranjan Rout1https://orcid.org/0009-0001-3609-2037All India Institute of Medical Sciences, GuwahatiBarasat Government Medical College, Banamalipur, Kolkata Atypical pneumonia, driven by pathogens like Mycoplasma pneumoniae, Chlamydia pneumoniae, and Legionella pneumophila, is challenging to diagnose due to non-specific symptoms. This systematic review assessed the diagnostic accuracy and prognostic value of biomarkers in atypical pneumonia. A comprehensive search of PubMed, Scopus, Web of Science, and Google Scholar (2000-2024) identified 27 studies, including observational, cohort, case-control, and review designs. Studies focused on biomarkers such as C-reactive protein (CRP), procalcitonin (PCT), ferritin, D-dimer, and pathogen-specific antibodies, with quality evaluated using the Newcastle-Ottawa Scale and AMSTAR 2. CRP was elevated in 85% of cases, with a pooled sensitivity of 82.3% [95% confidence interval (CI) 76.5-88.1, I²=78%] but moderate specificity (65.2%, 95% CI 58.0-72.4). PCT exhibited high specificity (88.7%, 95% CI 83.2-94.2, I²=65%) for bacterial etiologies, making it valuable for distinguishing bacterial from viral infections. Anti-Mycoplasma pneumoniae immunoglobulin M (IgM) showed excellent diagnostic accuracy (sensitivity 90.1%, 95% CI 85.0-95.2). Ferritin levels >400 ng/mL were strongly associated with severe outcomes [odds ratio (OR) 3.15, 95% CI 2.10-4.72, I²=70%]. Elevated biomarkers correlated with increased hospitalization (OR 2.78, 95% CI 1.95-3.96) and mortality (OR 3.42, 95% CI 2.30-5.08). Heterogeneity was significant (I²=65-78%), reflecting variability in study populations and methods. PCT and anti-Mycoplasma pneumoniae IgM enhance diagnostic precision, while ferritin and CRP are robust prognostic markers. Standardized biomarker thresholds are essential to optimize their clinical utility and improve patient outcomes in atypical pneumonia management. https://www.monaldi-archives.org/macd/article/view/3564Atypical pneumoniabiomarkersC-reactive proteinprocalcitoninferritinmycoplasma pneumoniae
spellingShingle Debashis Priyadarshan Sahoo
Bikash Ranjan Rout
Biomarkers in atypical pneumonia: a systematic review of diagnostic and prognostic utility
Monaldi Archives for Chest Disease
Atypical pneumonia
biomarkers
C-reactive protein
procalcitonin
ferritin
mycoplasma pneumoniae
title Biomarkers in atypical pneumonia: a systematic review of diagnostic and prognostic utility
title_full Biomarkers in atypical pneumonia: a systematic review of diagnostic and prognostic utility
title_fullStr Biomarkers in atypical pneumonia: a systematic review of diagnostic and prognostic utility
title_full_unstemmed Biomarkers in atypical pneumonia: a systematic review of diagnostic and prognostic utility
title_short Biomarkers in atypical pneumonia: a systematic review of diagnostic and prognostic utility
title_sort biomarkers in atypical pneumonia a systematic review of diagnostic and prognostic utility
topic Atypical pneumonia
biomarkers
C-reactive protein
procalcitonin
ferritin
mycoplasma pneumoniae
url https://www.monaldi-archives.org/macd/article/view/3564
work_keys_str_mv AT debashispriyadarshansahoo biomarkersinatypicalpneumoniaasystematicreviewofdiagnosticandprognosticutility
AT bikashranjanrout biomarkersinatypicalpneumoniaasystematicreviewofdiagnosticandprognosticutility