Correlation analysis of FABP3, MCP-4, and CXCL9 levels and myocardial damage in patients with severe pneumonia: FABP3, MCP-4, and CXCL9 levels in myocardial damage of severe pneumonia
Scindeks Assistant Scindeks Assistant — A system for serious journals and those aspiring to become one
PDF

Abstract

[Objective] To explore the correlations between the levels of serum monocyte chemoattractant protein-4 (MCP-4), heart-type fatty acid binding protein (FABP3), and chemokine ligand 9 (CXCL9) and myocardial damage in severe Mycoplasma pneumoniae (SMPP) patients. [Methods] A total of 158 patients with severe Mycoplasma pneumoniae complicated with myocardial damage were included in the SMPP group. They were divided into a myocardial damage group (n=42) and a nonmyocardial damage group (n=116) according to whether myocardial damage occurred. The control group consisted of an additional 102 healthy people who were examined throughout the same time period. The levels of serum MCP-4, FABP3 and CXCL9 in the two groups were compared. The general clinical data of the patients were recorded. Multivariate logistic analysis was conducted to analyze the risk factors for myocardial damage in patients with severe mycoplasma complicated with pneumonia.

[Results] The levels of serum MCP-4, FABP3 and CXCL9 in the SMPP group were significantly greater (all P<0.05). Compared with those in the nonmyocardial damage group, Serum MCP-4, FABP3, and CXCL9 levels were considerably higher (all P<0.05) in the group with myocardial injury.  Age, sex, diabetes, smoking history, hypoxemia, jaundice, and chronic obstructive pulmonary disease (COPD) did not differ statistically significantly between the two groups (all P>0.05). Compared with those in the nonmyocardial damage group, the proportions of patients with hypertension, coronary heart disease and anemia, as well as the levels of serum MCP-4, FABP3 and CXCL9, in the myocardial damage group were significantly greater (all P<0.05). Combined hypertension, coronary heart disease, anemia, and high levels of serum MCP-4, FABP3, and CXCL9 are risk factors for myocardial damage in patients with severe mycoplasma infection. The levels of serum MCP-4, FABP3 and CXCL9 in patients were positively correlated with the incidence of myocardial damage in patients with severe mycoplasma infection (all P<0.05). [Conclusion] The levels of serum MCP-4, FABP3 and CXCL9 are positively correlated with myocardial damage in patients with severe Mycoplasma pneumoniae. Moreover, combined hypertension, coronary heart disease, anemia and high levels of serum MCP-4, FABP3 and CXCL9 are risk factors for myocardial damage in patients with severe mycoplasma infection. These three factors can be used as biological indicators of myocardial damage in patients with severe mycoplasma infection in clinical practice and are highly important for the assessment of patients' conditions and the formulation of treatment plans.

Keywords

Array
Array
Array
Array
Array
Array
DOI: 10.5937/jomb0-61605

References

The published articles will be distributed under the Creative Commons Attribution 4.0 International License (CC BY). It is allowed to copy and redistribute the material in any medium or format, and remix, transform, and build upon it for any purpose, even commercially, as long as appropriate credit is given to the original author(s), a link to the license is provided and it is indicated if changes were made. Users are required to provide full bibliographic description of the original publication (authors, article title, journal title, volume, issue, pages), as well as its DOI code. In electronic publishing, users are also required to link the content with both the original article published in Journal of Medical Biochemistry and the licence used.

Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.

Downloads

Download data is not yet available.