Assessing the diagnostic utility of serum surfactant protein D concentration in childhood community-acquired pneumonia
ORIGINAL STUDIES
Abstract
Background.Currently, there is a need to identify new biomarkers for assessing the severity of community-acquired pneumonia in children. Traditional diagnostic methods, which rely on the analysis of leukocyte counts, C-reactive protein levels, and procalcitonin levels, have limited predictive value due to the low specificity of these indicators. Surfactant protein D is produced by alveolar type II cells and reflects the degree of lung tissue damage.
The aim of the studywas to evaluate the diagnostic significance of serum surfactant protein D levels in children with community-acquired pneumonia of varying severity.
Materials and methods.The concentration of surfactant protein D in serum was measured using enzyme-linked immunosorbent assay in 65 children with community-acquired pneumonia and 31 healthy children. The participants were divided into three groups: 1st— patients with severe community-acquired pneumonia(n=20); 2nd— patients with non-severe community-acquired pneumonia (n=45); 3rd— control group (n=31).
Results.Serum surfactant protein D concentrations in children with community-acquired pneumonia significantly differed from those in the control group (p <0,0001). Statistically significant differences in serum surfactant protein D concentrations were recorded among children with community-acquired pneumonia depending on disease severity (p <0,0001). A set of significant correlations was identified between the serum surfactant protein D concentration and clinical indicators of disease severity, as well as the levels of other markers of systemic inflammation. It was found that serum surfactant protein D concentration has a higher discriminatory ability compared to standard laboratory markers (AUC=0,95, p <0,0001).
Conclusions.The findings indicate that surfactant protein D is involved in the development of the systemic inflammatory response in community-acquired pneumonia and demonstrate the advantages of measuring this marker for differentiating disease severity.
References
1. Белых Н.А., Жулева А.Ю., Аникеева Н.А. Диагностические и прогностические возможности современных биомаркеров при внебольничных пневмониях у детей. Профилактическая медицина. 2025;28(4):130–135. https://doi.org/10.17116/profmed202528041130.
2. Ильенкова Н.А., Конуркина Н.С., Перетятько О.В., Кобаненко В.О. Сурфактантные белки A и D в диагностике внебольничной пневмонии у детей. Вопросы практической педиатрии. 2025;20(2):63–69. https://doi.org/10.20953/1817-7646-2025-2-63-69.
3. Пахнова Л.Р., Воронина Л.П., Пахнов Д.В. Роль белков сурфактанта в развитии отека легких. Российский медико-биологический вестник имени академика И.П. Павлова. 2025;33(1):145–156. https://doi.org/10.17816/PAVLOVJ568729.
4. Пневмония (внебольничная). Клинические рекомендации — 2025–2026–2027 (08.09.2025). Утверждены Минздравом РФ. М.; 2025.
5. Шустова С.А., Мирошкина Т.А. Защитные механизмы легких. Российский медико-биологический вестник имени академика И.П. Павлова. 2020;28(4):567–577. https://doi.org/10.23888/PAVLOVJ2020284567-577.
6. Dahmer M.K., Flori H., Sapru A., Kohne J., Weeks H.M., et al.; BALI and RESTORE Study Investigators and Pediatric Acute Lung Injury and Sepsis Investigators (PALISI) Network. surfactant protein d is associated with severe pediatric ARDS, prolonged ventilation, and death in children with acute respiratory failure. Chest. 2020;158(3):1027–1035. https://doi.org/10.1016/j.chest.2020.03.041.
7. de Souza Xavier Costa N., da Costa Sigrist G., Schalch A.S., Belotti L., Dolhnikoff M., da Silva L.F.F. Lung tissue expression of epithelial injury markers is associated with acute lung injury severity but does not discriminate sepsis from ARDS. Respir Res. 2024;25(1):129. https://doi.org/10.1186/s12931-024-02761-x.
8. Florin T.A., Ambroggio L., Brokamp C., Zhang Y., Rattan M., Crotty E. et al. Biomarkers and disease severity in children with community-acquired pneumonia. Pediatrics. 2020;145(6):e20193728. https://doi.org/10.1542/peds.2019-3728. Erratum in: Pediatrics. 2020;146(3):e2020011452. https://doi.org/10.1542/peds.2020-011452.
9. Meyer Sauteur P.M. Childhood community-acquired pneumonia. Eur J Pediatr. 2024;183(3):1129–1136. https://doi.org/10.1007/s00431-023-05366-6.
10. Peukert K., Sauer A., Seeliger B., Feuerborn C., Fox M., Schulz S. et al. Increased alveolar epithelial damage markers and inflammasome-regulated cytokines are associated with pulmonary superinfection in ARDS. J Clin Med. 2023;12(11):3649. https://doi.org/10.3390/jcm12113649.
11. Saleh N.Y., Ibrahem R.A.L., Saleh A.A.H., Soliman S.E.S., Mahmoud A.A.S. Surfactant protein D: a predictor for severity of community-acquired pneumonia in children. Pediatr Res. 2022;91(3):665–671. https://doi.org/10.1038/s41390-021-01492-9.
12. Shamim A., Abdul Aziz M., Saeed F., Kumari R., Joseph A.M., Ponnachan P., Kishore U., Masmoudi K. Revisiting surfactant protein D: an immune surveillance molecule bridging innate and adaptive immunity. Front Immunol. 2024;15:1491175. https://doi.org/10.3389/fimmu.2024.1491175.
13. Tsao Y.T., Tsai Y.H., Liao W.T., Shen C.J., Shen C.F., Cheng C.M. Differential markers of bacterial and viral infections in children for point of care testing. Trends Mol Med. 2020;26(12):1118–1132. https://doi.org/10.1016/j.molmed.2020.09.004.



