Influences of IL-1 and VEGF-A cytokines in acute sensoneural hearing loss

Influences of IL-1 and VEGF-A cytokines in acute sensoneural hearing loss

Authors

  • U.S. Khasanov Tashkent Medical Academy
  • U.P. Abdullaev Tashkent Medical Academy

Keywords:

cytokine, sensorineural hearing loss, steroid therapy

Abstract

The study of cytokine regulation is of great importance in predicting the development of irreversible changes in the auditory analyzer as a result of OSNEZ and in assessing the effectiveness of the therapeutic interventions. The level of VEGF-A in the blood of practically healthy people was 0.89 (0.6; 2.7) ng/ml, with a minimum value of 0.30 ng/ml and a maximum of 32.8 ng/ml. During our study, it was observed that the level of the studied indicator in patients with OSNEZ was almost 100 times higher than in healthy people. In group 1 of patients with OSNEZ who received complex therapy and GBO, the VEGF-A level during hospitalization was 310.1 (127.4; 320.5) ng/ml, with a minimum and maximum value of 120.5 and 335.8 ng/ml, respectively. In group 2 of patients with OSNEZ who received complex therapy and intratympanic steroid therapy, the VEGF-A level was 193.2 (152.2; 169.4) ng/ml, with individual variations from 50.8 to 188.2 ng/ml.

References

Cadoni G. et al. A case‐control study on proinflammatory genetic Polymorphisms on sudden sensorineural hearing loss //The Laryngoscope. – 2015. – Т. 125. – №. 1. – С. E28-E32.

Cao Z. et al. Genetic polymorphisms and susceptibility to sudden sensorineural hearing loss: a systematic review //Audiology and Neurotology. – 2019. – Т. 24. – №. 1. – С. 8-19.

Chien C. Y. et al. Heat shock protein 70 gene polymorphisms in sudden sensorineural hearing loss //Audiology and Neurotology. – 2012. – Т. 17. – №. 6. – С. 381-385.

Corazzi V. et al. Genetic polymorphisms in sudden sensorineural hearing loss: an update //Ear, Nose & Throat Journal. – 2021. – Т. 100. – №. 3_suppl. – С. 337S-342S.

Hiramatsu M. et al. Polymorphisms in genes involved in inflammatory pathways in patients with sudden sensorineural hearing loss //Journal of Neurogenetics. – 2012. – Т. 26. – №. 3-4. – С. 387-396.

Kasztelewicz B. et al. Cytokine gene polymorphism associations with congenital cytomegalovirus infection and sensorineural hearing loss //European Journal of Clinical Microbiology & Infectious Diseases. – 2017. – Т. 36. – №. 10. – С. 1811-1818.

Kitoh R. et al. SOD1 gene polymorphisms in sudden sensorineural hearing loss //Acta Oto-Laryngologica. – 2016. – Т. 136. – №. 5. – С. 465-469.

Teranishi M. et al. Polymorphisms in genes involved in oxidative stress response in patients with sudden sensorineural hearing loss and Meniere's disease in a Japanese population //DNA and cell biology. – 2012. – Т. 31. – №. 10. – С. 1555-1562.

Teranishi M. et al. Polymorphisms in genes involved in the free-radical process in patients with sudden sensorineural hearing loss and Meniere's disease //Free radical research. – 2013. – Т. 47. – №. 6-7. – С. 498-506.

Uchida Y. et al. Endothelin‐1 gene polymorphism in sudden sensorineural hearing loss //The Laryngoscope. – 2013. – Т. 123. – №. 11. – С. E59-E65.

Published

2024-09-30

Issue

Section

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