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. 2022 Oct 27;11(21):6350.
doi: 10.3390/jcm11216350.

Evaluation of IL-33R and Galectin-3 as New Biomarkers of Cardiac Damage after Polytrauma-Association with Cardiac Comorbidities and Risk Factors

Affiliations

Evaluation of IL-33R and Galectin-3 as New Biomarkers of Cardiac Damage after Polytrauma-Association with Cardiac Comorbidities and Risk Factors

Birte Weber et al. J Clin Med. .

Abstract

Polytrauma is one of the disorders with the greatest economic impact on healthcare in society and one predictor for poor outcome is cardiac damage. Interleukin 33 receptors (IL-33R) and galectin-3 are two new potential cardiac trauma biomarkers that are the subjects of this investigation. Additionally, this study assesses pre-existing cardiac damage or risk factors as predictors of cardiac damage after polytrauma. This retrospective study includes 107 polytraumatized patients with an ISS ≥16 admitted in a Level 1 Trauma Centre. Plasma samples were taken at admission. IL-33R and galectin-3 concentrations were detected in plasma samples by ELISA. Both did not correlate with the cardiac damage measured by troponin. Next to troponin, IL-33R was increased in patients with pre-existing cardiac comorbidities. In the subgroup of patients with cardiac comorbidities, the BMI and the initial blood sugar level were significantly increased compared to patients without cardiac comorbidities. Galectin-3 and IL-33R were shown to not correlate with cardiac damage. However, our data suggests that IL-33R protein should be revised in future studies as a marker of cardiac comorbidities. Further, our data indicate that patients with cardiac comorbidities represent a separate group of polytrauma patients characterized by higher concentrations of troponin, IL-33R, BMI and initial sugar level.

Keywords: IL-33 receptor; biomarker; cardiac damage; cardiac risk factors; comorbidities; galectin-3; polytrauma.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Relationship among ISS, IL-6, need in catecholamines and patient outcome with plasma troponin T. (A) Injury severity score (ISS) in the troponin subgroups of patients. (B) IL-6 concentration in the troponin subgroups. (C) Time on intensive care unit/intermediate care in days in the troponin subgroups. (D) Ventilation time in days in the troponin subgroups. (E) Troponin T concentrations in patients with (yes) and without (no) need in catecholamines. (F) Table 2 Troponin concentrations in survivors and in non-survivors. (G) Correlation analysis between troponin T and IL-6 measurements. (H) Correlation analysis between troponin T level and the ISS. n = 107 patients, * p ≤ 0.05, ** p ≤ 0.01; *** p ≤ 0.001; **** p ≤ 0.0001.
Figure 2
Figure 2
Interleukin 33 receptor (IL-33R) level in different groups of polytrauma patients. (A) IL-33R concentration in different troponin T patient subgroups. (B) IL-33R concentration in survivors and non-survivors. (C) IL-33R concentration in patients with (yes) and without (no) need in catecholamines. (D) IL-33R concentrations in patients with and without cardiac comorbidities. (E) Correlation analysis between IL-33R and IL-6 plasma concentrations. (F) Correlation analysis between IL-33R plasma concentrations and the injury severity score (ISS). n = 107 patients, ** p ≤ 0.01; *** p ≤ 0.001.
Figure 3
Figure 3
Galectin-3 concentration in different groups of polytrauma patients. (A) Galectin 3 concentration in the troponin T patients’ subgroups (≤12 pg/mL; between 13–49 pg/mL and ≥50 pg/mL). (B) Galectin-3 concentration in survivors and non-survivors. (C) Galectin-3 concentration in patients with (yes) and without (no) need in catecholamines. (D) Galectin-3 concentrations in patients with and without cardiac comorbidities. (E) Correlation analysis between galectin-3 and IL-6 plasma concentrations. (F) Correlation analysis between galectin-3 plasma concentration and the injury severity score (ISS). n = 107 patients, * p ≤ 0.05; *** p ≤ 0.001.
Figure 4
Figure 4
Cardiac risk factors and comorbidities in different groups of polytrauma patients. (A) Initial blood glucose concentration in the troponin subgroups (≤12 pg/mL; between 13–49 pg/mL and ≥50 pg/mL). (B) Initial triglyceride (TAG) blood concentrations in the troponin patients’ subgroups. (C) Body mass index (BMI) in the troponin subgroups. (D) Troponin T concentrations in patients with and without cardiac comorbidities. n = 107 patients, *** p ≤ 0.001 and **** p ≤ 0.0001.
Figure 5
Figure 5
Patients with cardiac comorbidities–subgroup analysis. Body Mass Index (BMI) (A) and initial blood glucose concentration (B) in patients with (yes) and without (no) cardiac comorbidities. (C) Troponin T concentration in the subgroup of patients with cardiac comorbidities depending on the need of catecholamines. (D) Patients with cardiac comorbidities: Troponin T concentration in survivors and non-survivors. (E) Correlation analysis between galectin-3 and the Injury Severity Score (ISS). Correlation analysis between galectin-3 and IL-6 (F) or the ventilation time (G). (H) Correlation analysis between troponin T concentration and the ventilation time. n = 24 patients, * p ≤ 0.05; ** p ≤ 0.01; *** p ≤ 0.001.

References

    1. Vos T., Lim S.S., Abbafati C., Abbas K.M., Abbasi M., Abbasifard M., Abbasi-Kangevari M., Abbastabar H., Abd-Allah F., Abdelalim A., et al. GBD 2019 Diseases and Injuries Collaborators. Global burden of 369 diseases and injuries in 204 countries and territories, 1990–2019: A systematic analysis for the Global Burden of Disease Study 2019. Lancet. 2020;396:1204–1222. doi: 10.1016/S0140-6736(20)30925-9. - DOI - PMC - PubMed
    1. Hardy B.M., Enninghorst N., King K.L., Balogh Z.J. The most critically injured polytrauma patient mortality: Should it be a measurement of trauma system performance? Eur. J. Trauma Emerg. Surg. 2022:1–5. doi: 10.1007/s00068-022-02073-z. - DOI - PMC - PubMed
    1. Hanschen M., Kanz K.-G., Kirchhoff C., Khalil P.N., Wierer M., van Griensven M., Laugwitz K.-L., Biberthaler P., Lefering R., Huber-Wagner S. Blunt Cardiac Injury in the Severely Injured—A Retrospective Multicentre Study. PLoS ONE. 2015;10:e0131362. doi: 10.1371/journal.pone.0131362. - DOI - PMC - PubMed
    1. Crown L.A., Hawkins W. Commotio cordis: Clinical implications of blunt cardiac trauma. Am. Fam. Physician. 1997;55:2467–2470. - PubMed
    1. Huber S., Biberthaler P., Delhey P., Trentzsch H., Winter H., van Griensven M., Lefering R., Huber-Wagner S. Predictors of poor outcomes after significant chest trauma in multiply injured patients: A retrospective analysis from the German Trauma Registry (Trauma Register DGU®) Scand. J. Trauma Resusc. Emerg. Med. 2014;22:52. doi: 10.1186/s13049-014-0052-4. - DOI - PMC - PubMed

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