Cytokine markers of clinical variants of infective endocarditis
- Authors: Samoylenko E.S.1,2, Kolesnikova N.V.1, Podsadnyaya A.A.3, Bratova A.V.2
-
Affiliations:
- Kuban State Medical University
- Scientific Research Institute – Ochapovsky Regional Clinical Hospital №1
- Specialized Clinical Infectious Diseases Hospital
- Issue: Vol 12, No 2 (2022)
- Pages: 271-278
- Section: ORIGINAL ARTICLES
- URL: https://journals.rcsi.science/2220-7619/article/view/119050
- DOI: https://doi.org/10.15789/2220-7619-CMO-1851
- ID: 119050
Cite item
Full Text
Abstract
Introduction. Infective endocarditis is a bacterial disease. Pathogen is localized mainly on heart valves and endocardium. This condition is accompanied by immunopathological manifestations and potential generation of septic process being unfavorable prognosis for disease outcome. Currently, the causes of death of patients with endocarditis have been increasingly presented as thromboembolic complications, which severity depends on variant of the disease course. An important role in imbalanced immune system in the infectious process is assigned to altered intercellular interaction mediated via cytokine network. Activated immune cells produce cytokines, which investigating is important in terms of interpreting changes in immune system functionality, assessing the severity of diseases and controlling therapeutic effectiveness. Infective endocarditis remains a severe disease associated with high mortality despite current advances in diagnostics and treatment. A timely diagnostic process and early initiation of treatment are major factors for successful patient management necessitating to improve diagnostics of various clinical variants of endocarditis course, taking into account pathogenetically relevant cytokines. Objective was to comparatively evaluate the importance of serum cytokine concentrations in patients with uncomplicated course of infective endocarditis and its thromboembolic complications and determine cytokine markers of various variants of endocarditis course. Materials and methods. An immunological examination of 119 blood serum samples from patients with confirmed diagnosis of infectious endocarditis and 20 samples from apparently healthy persons was carried out. Depending on the clinical disease form, the patients were divided into 4 groups: group 1 — primary infective endocarditis (PIE) with thromboembolic complications (n = 24), 2 — PIE without thromboembolic complications (n = 34), 3 — secondary IE with thromboembolic complications (n = 27), 4 — secondary IE without thromboembolic complications (n = 34). The control group consisted of 20 apparently healthy subjects. Immunological studies of serum cytokine concentrations were conducted in all groups. Results. Statistically significant increase in serum concentration of IL-10, IL-6, VEGF-A, IL-18, IL-1Ra and IL-8 was revealed in all clinical groups of patients compared to those in control group (p < 0,05). By correlation analysis, we found a significant positive relationship between IL-10 and IL-18 or IL-6. An increase in the concentration of IL-10 leads to increased level of pro-inflammatory IL-18 and IL-6. The marker of secondary endocarditis was observed as increased level of serum concentrations of IFNγ. A characteristic feature of primary infective endocarditis with thromboembolic complications was revealed as significantly increased serum concentration of IL-8, IL-1Ra and IL-6. Markers of secondary complicated endocarditis were identified as increased level of IL-6, VEGF-A and IL-18.
Full Text
##article.viewOnOriginalSite##About the authors
Ekaterina S. Samoylenko
Kuban State Medical University; Scientific Research Institute – Ochapovsky Regional Clinical Hospital №1
Email: kondrenko.ekaterina@yandex.ru
ORCID iD: 0000-0003-3147-0286
PhD student, Department of Clinical Immunology, Allergology and Laboratory Diagnostics of FPS and PPS, Pathologist
Russian Federation, 350063, Krasnodar, Mitrofana Sedina str., 4; KrasnodarN. V. Kolesnikova
Kuban State Medical University
Email: nvk24071954@mail.com
ORCID iD: 0000-0002-9773-3408
PhD, MD (Biology), Professor, Professor of the Department of Clinical Immunology, Allergology and Laboratory Diagnostics of FPS and PPS
Russian Federation, 350063, Krasnodar, Mitrofana Sedina str., 4A. A. Podsadnyaya
Specialized Clinical Infectious Diseases Hospital
Email: Podsadnyaya.lina@mail.ru
Infectiologist
Russian Federation, 350063, Krasnodar, Mitrofana Sedina str., 4A. V. Bratova
Scientific Research Institute – Ochapovsky Regional Clinical Hospital №1
Author for correspondence.
Email: brat_alla@mail.ru
ORCID iD: 0000-0002-0711-7653
Head of Clinical Diagnostic Laboratory
Russian Federation, 350063, Krasnodar, Mitrofana Sedina str., 4References
- Виноградова Т.Л. Инфекционный эндокардит: современное течение // Клиницист. 2011. Т. 5, № 3. С. 4–9. [Vinogradova T.L. Infective endocarditis: modern course. Klinitsist = The Clinician, 2011, vol. 5, no. 3, pp. 4–9. (In Russ.)] doi: 10.17650/1818-8338-2011-3-4-9
- Железникова Г.Ф. Цитокины как предикторы течения и исхода инфекций // Цитокины и воспаление. 2009. Т. 8, № 1. С. 10–17. [Zheleznikova G.F. Cytokines as predictors of infection course and outcome. Tsitokiny i vospalenie = Cytokines and Inflammation, 2009, vol. 8, no. 1, pp. 10–17. (In Russ.)]
- Лутфарахманов И.И., Миронов П.И., Тихонов А.С. Взаимосвязь полиморфизма гена фактора некроза опухоли альфа с развитием гнойно-септических осложнений тяжелого острого панкреатита // Медицинский вестник Северного Кавказа. 2017. Т. 12, № 2. С. 145–148. [Lutfarakhmanov I.I., Mironov P.I., Tikhonov A.S. Relationship between tumor necrosis factor alpha gene polymorphism and development of purulent septic complications of severe acute pancreatitis. Medicinskij vestnik Severnogo Kavkaza = Medical News of North Caucasus, 2017, vol. 12, no. 2, pp. 145–148. (In Russ.)] doi: 10.14300/mnnc.2017.12041
- Орадова А.Ш., Канжигалина З.К., Касенова Р.К. Лабораторная диагностика цитокинов (обзорная статья) // Вестник КазНМУ. 2015. № 1. С. 357–360. [Oradova A.S., Kangigalina Z.K., Kasenova R.K. Laboratory diagnosis of cytokines. Vestnik KazNMU = Bulletin of the Kazakh National Medical University, 2015, no. 1, pp. 357–360. (In Russ.)]
- Araújo I.R., Ferrari T.C., Teixeira-Carvalho A., Campi-Azevedo A.C., Rodrigues L.V., Guimarães Júnior M.H., Barros T.L., Gelape C.L., Sousa G.R., Nunes M.C. Cytokine signature in infective endocarditis. PLoS One, 2015, vol. 10, no. 7: e0133631. doi: 10.1371/journal.pone.0133631
- Carmeliet P., Jain R.K. Molecular mechanisms and clinical applications of angiogenesis. Nature, 2011, vol. 473, no. 7347, pp. 298–307. doi: 10.1038/nature10144
- Cresti A., Chiavarelli M., Scalese M., Nencioni C., Valentini S., Guerrini F., D’Aiello I., Picchi A., De Sensi F., Habib G. Epidemiological and mortality trends in infective endocarditis, a 17-year population-based prospective study. Cardiovasc. Diagn. and Ther., 2017, vol. 7, no. 1, pp. 27–35. doi: 10.21037/cdt.2016.08.09
- Ekdahl C., Broqvist M., Franzen S., Ljunghusen O., Mailer R., Sander B. IL-8 and tumor necrosis factor alpha in heart valves from patients with infective endocarditis. Scand. J. Infect. Dis., 2002, vol. 34, no. 10, pp. 759–762. doi: 10.1080/00365540210147912
- Ferrara N. Vascular endothelial growth factor. Arterioscler. Thromb. Vasc. Biol., 2009, vol. 29, no. 6, pp. 789–791. doi: 10.1161/ATVBAHA.108.179663
- Ferrara N. VEGF-A: a critical regulator of blood vessel growth. Eur. Cytokine Netw., 2009, vol. 20, no. 4, pp. 158–163. doi: 10.1684/ecn.2009.0170
- Guerrero M.L.F., Alvarez B., Manzarbeitia F., Manzarbeitia F., Renedo G. Infective endocarditis at autopsy: a review of pathologic manifestations and clinical correlates. Medicine (Baltimore), 2012, vol. 91, no. 3, pp. 152–164. doi: 101097/MD.0b013e31825631ea
- Habib G., Erba P.A., Iung B., Donal E., Cosyns B., Laroche C., Popescu B.A., Prendergast B., Tornos P., Sadeghpour A., Oliver A., Vaskelyte J.J., Sow R., Axler O., Maggioni A.P., Lancellotti P. Clinical presentation, aetiology and outcome of infective endocarditis. Results of the ESC-EORP EURO-ENDO (European infective endocarditis) registry: a prospective cohort study. Eur. Heart J., 2019, vol. 40, no. 39, pp. 3222–3232. doi: 10.1093/ eurheartj/ehz620
- Habib G., Lancellotti P., Antunes M.J., Bongiorni M.G., Casalta J.P., Del Zotti F., Dulgheru R., El Khoury G., Erba P.A., Iung B., Miro J.M., Mulder B.J., Plonska-Gosciniak E., Price S., Roos-Hesselink J., Snygg-Martin U., Thuny F., Mas P.T., Vilacosta I., Zamorano J.L. 2015 ESC guidelines for the management of infective endocarditis: the task force for the management of Infective Endocarditis of the European Society of Cardiology (ESC). Endorsed by: European Association for Cardio-Thoracic Surgery (EACTS), the European Association of Nuclear Medicine (EANM). Eur. Heart J., 2015, vol. 36, no. 44, pp. 3075–3128. doi: 10.1093/eu-rheartj/ehv319
- Hubers S.A., DeSimone D.C., Gersh B.J., Anavekar N.S. Infective endocarditis: a contemporary review. Mayo Clin. Proc., 2020, vol. 95, no. 5, pp. 982–997. doi: 101016/j.mayocp.2019.12.008
- Marques A., Cruz I., Caldeira D., Alegria S., Gomes A., Broa A., João I., Pereira H. Risk factors for inhospital mortality in infective endocarditis. Arq. Bras. Cardiol., 2020, vol. 114, no. 1, pp. 1–8. doi: 10.36660/abc.20180194
- Martínez R., Menéndez R., Reyes S., Polverino E., Cillóniz C., Martínez A., Esquinas C., Filella X., Ramírez P., Torres A. Factors associated with inflammatory cytokine patterns in community-acquired pneumonia. Eur. Resp. J., 2011, vol. 37, no. 2, pp. 393–399. doi: 10.1183/09031936.00040710
- Nunes M.C.P., Araujo I.R., Carvalho A.T., Andrade L.A., Resende M.H.L., Silva J.L.P., Ferrari T.C.A. Do cytokines play a role in predicting some features and outcome in infective endocarditis? Adv. Infect. Dis., 2013, vol. 3, pp. 115–119. doi: 10.4236/aid.2013.32018
- Rajani R., Klein J.L. Infective endocarditis: a contemporary update. Clin. Med. (Lond.), 2020, vol. 20, no. 1, pp. 31–35. doi: 10.7861/clinmed.cme.20.1.1.
- Shibuya M. Vascular endothelial growth factor and its receptor system: physiological functions in angiogenesis and pathological roles in various diseases. J. Biochem., 2013, vol. 153, no. 1, pp. 13–19. doi: 10.1093/jb/mvs136
- Sun B.J., Choi S.W., Park K.H., Jang J.Y., Kim D.H., Song J.M., Kang D.H., Kim Y.S., Song J.K. Infective endocarditis involving apparently structurally normal valves in patients without previously recognized predisposing heart disease. J. Am. Coll. Cardiol., 2015, vol. 65, no. 3, pp. 307–309. doi: 10.1016/j.jacc.201410.046
- Toyoda N., Chikwe J., Itagaki S., Gelijns A.C., Adams D.H., Egorova N.N. Trends in infective endocarditis in California and New York State, 1998–2013. JAMA, 2017, vol. 317, no. 16, pp. 1652–1660. doi: 101001/jama.2017.4287
- Yang E., Frazee B.W. Infective Endocarditis. Emerg. Med. Clin. N. Am., 2018, vol. 36, no. 4, pp. 645–663. doi: 10.1016/ j.emc.2018.06.002