Surfactant Protein A (SP-A) is a Prognostic Molecular Biomarker in Acute Respiratory Distress Syndrome

The problem of predicting the development and outcomes of acute respiratory distress syndrome (ARDS) remains to be solved. Objective: to estimate the informative value of the plasma levels of surfactant protein A (SP2A) as a prognostic biomarker for the development and outcome of ARDS in patients wi...

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Bibliographic Details
Published in:Obshchai͡a︡ reanimatologii͡a Vol. 9; no. 3; p. 5
Main Authors: Moroz, V. V., Golubev, A. M., Kuzovlev, A. N., Pisarev, V. M, Polovnikov, S. G, Shabanov, A. K, Golubev, M. A.
Format: Journal Article
Language:English
Published: Federal Research and Clinical Center of Intensive Care Medicine and Rehabilitology, Moscow, Russia 20-06-2013
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Summary:The problem of predicting the development and outcomes of acute respiratory distress syndrome (ARDS) remains to be solved. Objective: to estimate the informative value of the plasma levels of surfactant protein A (SP2A) as a prognostic biomarker for the development and outcome of ARDS in patients with severe pyoseptic complications in critical conditions. Subjects and methods. This investigation was conducted at the Research Institute of General Reanimatology (RIGR), Russian Academy of Medical Sciences, in 2010—2012. It enrolled 80 patients (including 25 analyzed ones) in accordance with the inclusion and exclusion criteria, as well as 30 apparently healthy donors. ARDS and its stages were diagnosed using the RIGR criteria. Plasma SP2A levels were determined by enzyme immunoassay using a Human Surfactant Protein A ELISA, RD191139200R kit (BioVendor, USA). The findings were statistically analyzed using a Statistica 7.0 package.Sensitivity and specificity of SP2A testing were determined by ROC analysis. The difference between groups at pResults. In patients with ARDS plasma SP2A level was higher than in those without ARDS within the whole study independing on a day of testing. There were no significant dif2 ferences between plasma SP2A levels in the patients with Stages 1 and 2 ARDS. On day 1, the plasma SP2A content of 24.5 ng/ml had a sensitivity of 60.0% and a specificity of 85.7% in predicting the development of ARDS on days 4—5 of intensive care unit admission (the area under the curve 0.74; 95% confidence interval, 0.527—0.872; p=0.0031). On study day 1, the SP2A level of 38.8 ng/ml had a sensitivity of 65.0% and a specificity of 80.0% in predicting a fatal outcome in patients with ARDS (the area under curve 0.74; 95% confidence interval, 0.577—0.866; p=0.0026). Conclusion. On a day when a severe pyoseptic complication was diagnosed, the SP2A level of 24.5 ng/ml served as a sensitive and specific prognostic biomarker for the development of ARDS on days 4—5 of an intensive care unit stay. Within the first 24 hours (on the day when ARDS was diagnosed), the plasma SP2A content of 38.8 ng/ml was a sensitive and specific prognostic biomarker for death prediction in ARDS. Key words: acute respiratory distress syndrome, surfactant protein A, biomarker, prediction, outcomes.
ISSN:1813-9779
2411-7110
DOI:10.15360/1813-9779-2013-3-5