# Markers of inflammation and immunological competence: Assessment in the early postoperative phase of cardiac surgery involving extracorporeal circulation

**Authors:** Selma Mutevelić, Lejla Bajramović-Omeragić, Merima Šehić, Sumejja Baljević-Spahić, Kelle Belma Pehlivanović, Ermin Begović, Berina Hasanefendić, Ermina Mujičić, Marina Delić-Mašović, Drago Batinić

PMC · DOI: 10.5937/jomb0-56889 · Journal of Medical Biochemistry · 2025-11-05

## TL;DR

This study examines how inflammation and immune markers change after heart surgery using a heart-lung machine, showing significant postoperative changes that could help guide patient care.

## Contribution

The study provides new insights into the dynamics of specific immune markers in the early postoperative phase of cardiac surgery involving extracorporeal circulation.

## Key findings

- CRP and SAA levels, along with CD14 and pro-inflammatory monocyte proportions, significantly increased postoperatively.
- HLA-DR CD14 monocyte proportions significantly decreased after surgery.
- No significant age-related differences were observed in the studied immune markers.

## Abstract

To gain insight into the role and relevance of inflammatory and immunological markers in the comprehensive assessment of a patient's immune response to surgical procedures. This study focused on investigating preoperative and postoperative serum levels dynamics of SAA, CRP and proportion of HLA-DR CD14 monocytes, CD14 monocytes, and pro-inflammatory monocytes CD16 T CD14 T in patients who underwent heart surgery using extracorporeal circulation (on-pump).

An observational, prospective study was conducted at the Heart Center of the Clinical Center of the University of Sarajevo on 53 patients divided into 3 age groups: 50-59, 60-69, and 70-80. The serum levels of CRP and SAA were quantitatively determined by immunonephelometry. At the same time, flow cytometry technology was applied to measure the proportion of CD14 monocytes, HLA-DR CD14 monocytes, and pro-inflammatory CD16 CD14 monocytes.

Measured values of CRP; SAA, proportion of monocytes CD14, and proportion of pro-inflammatory monocytes CD16 CD14 are significantly increased postoperatively compared to the preoperative values (p &lt; 0.05). The proportion of HLA-DR CD14 monocytes is lower postoperatively compared to preoperative values (p &lt; 0.001). Furthermore, there are no significant gender differences in the preoperative or postoperative parameters (p &gt; 0.05), with the notable exception of the preoperative proportion of CD14 monocytes (p &lt; 0.05). The analysis of age-related differences indicates no significant changes in the observed preoperative and postoperative parameters among the defined age groups (p &gt;0.05).

Early monitoring of inflammatory and immunological markers in the postoperative phase could be valuable for healthcare professionals to implement prompt interventions to mitigate negative outcomes.

## Linked entities

- **Proteins:** CRP (C-reactive protein), SAA1 (serum amyloid A1), CD14 (CD14 molecule), FCGR3B (Fc gamma receptor IIIb)

## Full-text entities

- **Genes:** FCGR3A (Fc gamma receptor IIIa) [NCBI Gene 2214] {aka CD16-II, CD16A, FCG3, FCGR3, FCRIIIA, FcGRIIIA}, CD14 (CD14 molecule) [NCBI Gene 929], IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, PTPRC (protein tyrosine phosphatase receptor type C) [NCBI Gene 5788] {aka B220, CD45, CD45R, GP180, IMD105, L-CA}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, UROD (uroporphyrinogen decarboxylase) [NCBI Gene 7389] {aka PCT, UPD}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CD86 (CD86 molecule) [NCBI Gene 942] {aka B7-2, B7.2, B70, BU63, CD28LG2, CD86 v6}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, SAA [NCBI Gene 6287]
- **Diseases:** CD (MESH:D003027), hepatitis B and C (MESH:D006509), cardiovascular diseases (MESH:D002318), SIRS (MESH:D018746), infection (MESH:D007239), EC (MESH:D005955), immunological deficiencies (MESH:D007153), metabolic syndromes (MESH:D024821), inflammation (MESH:D007249), hypothermia (MESH:D007035), disease (MESH:D004194), cardiac sepsis (MESH:D018805), tissue damage (MESH:D017695), HIV infection (MESH:D015658), microbial infections (MESH:D015163), organ dysfunction (MESH:D009102), autoimmune disorders (MESH:D001327)
- **Chemicals:** EDTA (MESH:D004492)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090], Human immunodeficiency virus (species) [taxon 12721], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Full text

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## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC12966988/full.md

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Source: https://tomesphere.com/paper/PMC12966988