ISSN 2415-3060 (print), ISSN 2522-4972 (online)
  • 55 of 67
Up
JMBS 2020, 5(3): 410–416
https://doi.org/10.26693/jmbs05.03.410
Biology

Study of Platelet Aggregation Capacity in Patients with Chronic Tonsillitis

Burlaka Yu. B., Klys Yu. G., Shuklina Yu. V., Verevka S. V.
Abstract

Chronic tonsillitis possesses a peculiar place in otolaryngology. Somatic diseases associated with tonsillitis are characterized by a prolonged, intermittent course and lead to partial disability and disability of persons of working age. Finding perfect methods for laboratory evaluation of the degree of the pathological process in patients with chronic tonsillitis is an urgent question in otolaryngological practice. The purpose of our study was to investigate the functional activity of platelet and indices of the coagulative link of hemostasis system in patients with decompensated form of chronic tonsillitis. Material and methods. We examined 30 patients who were hospitalized in the department of inflammatory diseases of ENT organs of the State Institution «O. S. Kolomiychenko Institute of Otolaryngology of National Academy of Medical Sciences of Ukraine». The control group consisted of 20 healthy persons. Platelet aggregation was studied using аdenosine diphosphate as inductor at final concentrations of 1.25, 2.5 and 10 μmol/l. Results and discussion. To evaluate the aggregation process, the degree, the rate and the reaching time of the maximum aggregation were determined. Thrombin-like activity, fibrinogen concentration and von Willebrand factor level were studied. Patients with chronic tonsillitis have pronounced changes in the degree and rate of platelet aggregation toward increasing their levels relative to the indices of a control group. The increase in the time of platelet aggregation at the lowest and medium concentrations of аdenosine diphosphate and its reduction at the highest one can indicate the decrease function of the platelet. The increase of amidolytic thrombin-like activity, fibrinogen levels and von Willebrand factor were shown, which is a manifestation of the inflammatory process and may be the one of the reasons for increase of the platelet aggregation. Conclusion. Our results indicate the necessity for laboratory studies of platelet activity and indicators of the coagulation link of the hemostasis system in patients with chronic tonsillitis to detect changes in the hemostasis system associated with an increased risk of operative bleeding and take measures to prevent them. Moreover, the studies of platelet activity can be used for the development of objective criterions for evaluation of the severity of the inflammatory process at the chronic tonsillitis.

Keywords: tonsillitis, platelet aggregation, thrombin-like activity, fibrinogen, von Willebrand factor

Full text: PDF (Ukr) 357K

References
  1. Dyudina OY. The dependence of the use of platelet aggregation on the form of chronic tonsillitis in children. Russian otorhinolaryngology. 2003; 1: 54-6. [Russian]
  2. Kirichuk VF, Mareev OV, Dyudina OY. Changes in the functional activity of platelets in chronic tonsillitis and tonsillitis in children. Vestn otorhinolar. 2004; 5: 13-6. [Russian]
  3. Turnova EV, Maltsev GS. Clinical biochemistry methods in the diagnosis of chronic tonsillitis. Russian otorinolarin. 2005; 4(17): 108-11. [Russian]
  4. Palchun VT. Therapeutic and diagnostic approaches to the problem of chronic tonsillitis. Vestn otolarin. 2001; 1: 4-7. [Russian]
  5. Zabolotny DI, Melnikov OF. Theoretical aspects of the genesis and treatment of chronic tonsillitis. Health's: Kiev; 1999. 145 p. [Russian]
  6. Portenko EG. Development of a comprehensive diagnosis and control of the treatment of chronic tonsillitis based on the method of infrared spectrometry. Abstr. PhDr. (Med.). SPb; 2007. 28 p. [Russian]
  7. Bykova VP. Modern aspects of the problem of tonsillar pathology. Russian rhinology. 1996; 2(3): 13-5. [Russian]
  8. Antoniv VF, Perekrest AI, Korobkova TV. Some aspects of the tonsillar problem are currently underway. Vestn otolarin. 1995; 6: 43-5. [Russian]
  9. Soldatov IB. Guide of otolaryngology. M: Medicine; 1997. 472 p. [Russian]
  10. Menshikov VV. Laboratory research methods in the clinic. Directory. M: Medicine; 1987. 368 p. [Russian]
  11. Cheshevik MA. Instructions for determining platelet aggregation activity on an AP 2110 analyzer. Minsk; 1995. 30 p. [Russian]
  12. Abilgaard U, Lie M, Odegard OR. Antitrombin assay with new chromogenic substrates (S-2238 and chromozym TH). Tromb Res. 1977; 11(4): 549-53. https://www.ncbi.nlm.nih.gov/pubmed/72424. https://doi.org/10.1016/0049-3848(77)90208-0
  13. Belitser VO, Varetskaya TV, Veremeenko KM. Quantitative determination of fibrinogen in human blood plasma. Lab diagnostics. 1997; 2: 53-5. [Russian]
  14. Harlow E, Lane D. Antibodies. Cold Spring Harbor Laboratory Press. NY; 1988. р. 345-405.
  15. Gubler EV. Computational methods of analysis and recognition of pathological processes. Lviv: Medicine; 1978. 296 p. [Russian]
  16. Maltsev EV. Methodology of scientific creativity in medicine: Practical aspects. Odessa: Astroprint; 2006. 120 p. [Russian]
  17. Shevchuk SV. Characteristic of the state of platelet aggregation capacity in patients with systemic lupus erythematosus. Ukr rheumatol. 2007; 2(28): 32-6. [Ukraine]
  18. Yee DL. Aggregometry detects platelet hyperreactivity in healthy individuals. Blood. 2005; 106(8): 2723-9. https://www.ncbi.nlm.nih.gov/pubmed/15972447. https://www.ncbi.nlm.nih.gov/pmc/articles/1634759. https://doi.org/10.1182/blood-2005-03-1290
  19. Prinkova TYu, Prokhorova VI, Cyrus TP. et al. Significance of the study of indicators for assessing the hemostatic potential of blood (fibrinogen, von Willebrand factor, and D-dimers) as potential laboratory criteria for the prevalence and differentiation of a tumor in uterine body cancer. Lab diagnostics. Eastern Europe. 2012; 3: 112-20. [Russian]
  20. Volkov GL, Platonova TN, Savchuk AN. Current ideas about the hemostatic system. Kiev: Naukova Dumka; 2005. 296 p. [Russian]
  21. Serebryanaya NB, Shanin SN, Fomicheva EE. et al. Platelets as activators and regulators of inflammatory and immune reactions. Part 2. Platelets as participants in immune responses. Medical immunology. 2019; 21(1): 9-20. [Russian] https://doi.org/10.15789/1563-0625-2019-1-9-20
  22. Ma L, Dorling A. The roles of thrombin and protease-activated receptors in inflammation. Semin Immunopathol. 2012; 34(1): 63-72. https://www.ncbi.nlm.nih.gov/pubmed/21809138. https://doi.org/10.1007/s00281-011-0281-9
  23. Chen D, Dorling A. Critical roles for thrombin in acute and chronic inflammation. J Thromb Haemost. 2009; 7: 122-6. https://www.ncbi.nlm.nih.gov/pubmed/19630783. https://doi.org/10.1111/j.1538-7836.2009.03413.x
  24. Jennewein C, Tran N, Paulus P, Ellinghaus P, Eble JA, Zacharowski K. Novel aspects of fibrin(ogen) fragments during inflammation. Mol Med. 2011; 17(5-6): 568-73. https://www.ncbi.nlm.nih.gov/pubmed/21210072. https://www.ncbi.nlm.nih.gov/pmc/articles/3105136. https://doi.org/10.2119/molmed.2010.00146
  25. Davalos D, Akassoglou K. Fibrinogen as a key regulator of inflammation in disease. Semin Immunopathol. 2012; 34: 43-62. https://www.ncbi.nlm.nih.gov/pubmed/2203794. https://doi.org/10.1007/s00281-011-0290-8
  26. Ruggeri ZM. von Willebrand factor. J Clin Invest. 1997; 99: 559-64. https://www.ncbi.nlm.nih.gov/pubmed/9045854. https://www.ncbi.nlm.nih.gov/pmc/articles/507834.
  27. https://doi.org/10.1172/JCI119195
  28. Meucci G, Pareti F, Vecchi M, Saibeni S, Bressi C, Franchis R. Serum von Willebrand factor levels in patients with inflammatory bowel disease are related to systemic inflammation. Scand J Gastroenterol. 1999; 34: 287-90. https://www.ncbi.nlm.nih.gov/pubmed/10232874. https://doi.org/10.1080/00365529950173708