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Advanced oxidation protein products and ischemia-modified albumin as prognostic biomarkers of long-term mortality in community-acquired pneumonia: a prospective observational study
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  • Published: 09 February 2026

Advanced oxidation protein products and ischemia-modified albumin as prognostic biomarkers of long-term mortality in community-acquired pneumonia: a prospective observational study

  • Marta Napiórkowska-Mastalerz1,
  • Tomasz Wybranowski1,
  • Joanna Sikora2,
  • Patrycja Wszelaki2,
  • Jerzy Pyskir1,
  • Wiktoria Michalska1,
  • Marta Pilaczyńska-Cemel3,
  • Stefan Kruszewski1 &
  • …
  • Barbara Ciastek4 

Scientific Reports , Article number:  (2026) Cite this article

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We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Biomarkers
  • Cardiology
  • Diseases
  • Medical research
  • Risk factors

Abstract

Oxidative stress is increasingly recognized as a contributor to the pathophysiology and outcomes of community-acquired pneumonia (CAP). This study examined whether plasma levels of advanced oxidation protein products (AOPPs) and ischemia-modified albumin (IMA) measured at hospital admission are associated with 100-day mortality. A cohort of 71 hospitalized CAP patients was analyzed. Plasma AOPPs and IMA were measured within 24 h of admission and evaluated in relation to clinical data, the Charlson Comorbidity Index (CCI), and routine laboratory parameters. Statistical analyses included receiver operating characteristic (ROC) curve evaluation, Kaplan–Meier survival estimates, and Spearman correlations. AOPPs correlated positively with D-dimer, while IMA showed positive associations with N-terminal pro–B-type natriuretic peptide and high-sensitivity cardiac troponin I, and inversely with serum albumin, indicating links between oxidative stress, inflammation, and cardiovascular dysfunction. Higher admission levels of AOPPs and IMA were independently associated with increased 100-day mortality. In ROC analysis, AOPPs demonstrated good discriminatory ability for 100-day mortality (area under the curve [AUC] = 0.75, p < 0.0001), and a combined multivariable model including AOPPs, IMA, and CCI further improved performance (AUC = 0.851, p < 0.0001). These findings suggest that oxidative stress biomarkers measured at admission may serve as accessible indicators of long-term mortality risk in CAP.

Data availability

The datasets generated and analyzed during the current study are available from the corresponding author upon reasonable request.

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Author information

Authors and Affiliations

  1. Department of Biophysics, Faculty of Pharmacy, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, Bydgoszcz, 85-067, Poland

    Marta Napiórkowska-Mastalerz, Tomasz Wybranowski, Jerzy Pyskir, Wiktoria Michalska & Stefan Kruszewski

  2. Research and Education Unit for Experimental Biotechnology, Department of Transplantology and General Surgery, Faculty of Medicine, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, Bydgoszcz, 85-094, Poland

    Joanna Sikora & Patrycja Wszelaki

  3. Department of Lung Diseases, Neoplasms and Tuberculosis, Faculty of Medicine, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Toruń, Bydgoszcz, 85-326, Poland

    Marta Pilaczyńska-Cemel

  4. Institute of Health Sciences, University of Opole, Katowicka 68, Opole, 45-060, Poland

    Barbara Ciastek

Authors
  1. Marta Napiórkowska-Mastalerz
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  2. Tomasz Wybranowski
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  9. Barbara Ciastek
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Contributions

M.N.-M. and T.W.: Conceptualization; T.W., M.N.-M., P.W., J.S., W.M.: methodology, M.N.-M.: data analysis; M.N.-M. and T.W.: investigation; M.P.-C. and J.P.: resources; M.N.-M., T.W., and B.C.: writing—original draft; M.N.-M., B.C., and T.W.: writing—review and editing; M.N.-M.: visualization; B.C. and S.K.: supervision; M.N.-M. and T.W.: project administration. All authors have read and agreed to the published version of the manuscript.

Corresponding author

Correspondence to Marta Napiórkowska-Mastalerz.

Ethics declarations

Competing interests

The authors declare no competing interests.

Ethical statement

This study was conducted in accordance with the guidelines of the Declaration of Helsinki and was approved by the Ethics Committee of Nicolaus Copernicus University in Toruń, Collegium Medicum in Bydgoszcz, Poland (KB 343/2021).

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Napiórkowska-Mastalerz, M., Wybranowski, T., Sikora, J. et al. Advanced oxidation protein products and ischemia-modified albumin as prognostic biomarkers of long-term mortality in community-acquired pneumonia: a prospective observational study. Sci Rep (2026). https://doi.org/10.1038/s41598-026-36643-7

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  • Received: 21 November 2025

  • Accepted: 14 January 2026

  • Published: 09 February 2026

  • DOI: https://doi.org/10.1038/s41598-026-36643-7

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Keywords

  • Community-acquired pneumonia
  • Oxidative stress
  • Advanced oxidation protein products
  • Ischemia-modified albumin
  • Long-term mortality
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