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Evaluation of a potential prognostic parameter for the inflammatory status in COVID-19 patients: The inflammatory
Francescopaolo Antonucci1, Domenico Di Carlo2, Michele Falcone3
1University Hospital "Ospedali Riuniti", Foggia; PhD course in Microbiology, Immunology, Infectious Diseases, and Transplants (MIMIT), University of Rome Tor Vergata, Rome, Italy.
Insights
A new Inflammatory Protein Ratio (IPR) effectively monitors inflammation in COVID-19 patients. This novel marker, derived from serum protein electrophoresis, correlates with established inflammatory markers like C-reactive protein (CRP).
Area of Science:
- Clinical Chemistry
- Immunology
- Infectious Diseases
Background:
- Hospitalized patients with and without COVID-19 (n=2745) were analyzed for inflammatory markers.
- Established markers include C-reactive protein (CRP), fibrinogen, and d-dimer, assessed via immunoassay and turbidimetric methods.
- SARS-CoV-2 positivity was confirmed using real-time polymerase chain reaction (RT-PCR).
Purpose of the Study:
- To introduce and validate a new parameter from serum protein electrophoresis (SPE) for assessing inflammatory status.
- To evaluate the correlation of the novel Inflammatory Protein Ratio (IPR) with established inflammatory markers.
- To determine the specificity of IPR in differentiating inflammatory states, particularly in COVID-19 patients.
Main Methods:
- Serum protein electrophoresis (SPE) was performed on all patients to quantify serum proteins.
- A novel Inflammatory Protein Ratio (IPR) was calculated using albumin, α1-globulin, and α2-globulin concentrations.
- Statistical analyses including ANOVA and correlation tests (Pearson's, Kruskal-Wallis, Spearman's) were employed.
Main Results:
- The Inflammatory Protein Ratio (IPR) showed a significant direct correlation with d-dimer, CRP, and fibrinogen.
- IPR, along with d-dimer, CRP, and fibrinogen, was significantly elevated (p < 0.001) in COVID-19 patients.
- IPR demonstrated high specificity for monitoring inflammatory status due to its reliance on key inflammatory proteins.
Conclusions:
- The novel Inflammatory Protein Ratio (IPR) is a valuable and specific marker for assessing inflammatory status.
- IPR correlates strongly with established inflammatory markers and is significantly elevated in COVID-19 patients.
- IPR offers a simplified interpretation of SPE results for clinical evaluation of inflammation.
Abstract:
C-reactive protein (CRP), fibrinogen, and d-dimer are determined in the human plasma of 2745 hospitalized patients with and without coronavirus disease 2019 (COVID-19) by automated-latex enhanced immunoassay and immuno-turbidimetric assay. SARS-COV-2 RNA qualitative test, real time polymerase chain reaction (RT-PCR) based, is performed in nasopharyngeal swabs to confirm those with SARS-COV-2 positivity. Furthermore, serum proteins are separated and quantified in all the patients by serum protein electrophoresis (SPE). A new SPE parameter, inflammatory protein ratio (IPR), is elaborated for the first time by a mathematical equation that considers the albumin, α1-globulin, and α2-globulin. IPR normal reference range (10.7%-28.3%) is calculated considering the normal reference range of albumin, α1-globulin, and α2-globulin obtained for controls. Analysis of variance (ANOVA), Pearson's, Kruskal-Wallis, and Spearman's tests application show that IPR significantly correlates with direct proportionality with d-dimer, CRP, and fibrinogen. Significant (p < 0.001) increase of these parameters, IPR included, is detected in COVID-19 patients only. Our results show that IPR is more specific for monitoring inflammatory status thanks to its correlation with the only three serum proteins involved in inflammation: albumin, α1-globulin, and α2-globulin. Furthermore, IPR can simplify the interpretation of SPE results about inflammatory status, being of unique value compared to the six-serum protein classes separately presented in the typical SPE clinical reports.
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