The role of interleukin-10 gene polymorphism (rs 1800872) in the course of herpes zoster in adults

Authors

  • N. V. Onishchenko Zaporizhzhia State Medical University, Ukraine,
  • Yu. Yu. Riabokon Zaporizhzhia State Medical University, Ukraine,
  • O. V. Riabokon Zaporizhzhia State Medical University, Ukraine,

DOI:

https://doi.org/10.14739/2310-1237.2018.3.151810

Keywords:

herpes zoster, interleukin-10, gene polymorphism

Abstract

Aim. The aim of the work was to determine the role of polymorphism of the interleukin-10 gene (rs 1800872) in the course
of herpes zoster in adults.
Materials and methods. 50 adult patients with herpes zoster were included into the study. The clinical course of the disease and development of the certain nature of complications were analyzed depending on the genetic polymorphism of the interleukin-10 gene. Statistical data processing was performed with using the formed patient database in the program STATISTICA
for Windows 13 (StatSoft Inc., № JPZ804I382130ARCN10-J).
Results. It was established that genotype TT of the IL-10 gene (rs 1800872) was recorded in 30 (60.0 %) patients with herpes zoster versus 14 (35.0 %) healthy people from the control group (P = 0.02), which confirmed the significance of the gene polymorphism IL-10 in reactivation of the varicella zoster virus and the manifestation of shingles. Analysis of the polymorphism
of the IL-10 gene depending on the clinical form and the severity of shingle showed that genotype TT was significantly more frequently recorded in patients with severe course disease (86.7 % vs. 48.6 %, P = 0.01), however, did not influenced on the formation of certain clinical forms of the disease (P > 0.05). In patients with herpes zoster polymorphism of the IL-10 gene
(rs 1800872) influenced the severity of the course of the disease, namely, the TT genotype was associated with a severe course
of the disease (P = 0.01) and the development of neurological complications (P = 0.03), which were represented by meningitis
(6), Ramsey-Hunt syndrome (3) and the subsequent formation of postherpetic neuralgia (3), as well as of ophthalmic nature
(P = 0.0001), which were represented by herpetic blepharoconjunctivitis (16), keratouveitis (3), iridocyclitis (1), subconjunctival
hemorrhages (1). Unlike the TT genotype, genotype TG of the IL-10 gene (rs 1800872) was associated with the development of complications with the addition of secondary bacterial microflora (χ2 = 4.5, P = 0.03), the incidence of which did not depend n the severity of herpes zoster (P > 0.05).
Conclusions. In patients with herpes zoster, the TT-genotype of the IL-10 gene (rs 1800872) was associated with reactivation
of the varicella zoster virus and development of a severe disease course, with formation of neurological (χ2 = 4.75, P = 0.03) and ophthalmic (χ2 = 14.75, P = 0.0001) complications. The TG genotype of the IL-10 gene (rs 1800872) is
associated with the development of complications associated with the addition of secondary bacterial microflora (χ2 = 4.5, P = 0.03).

References

Koshy, E., Mengting, L., Kumar, H., & Jianbo, W. (2018). Epidemiology, treatment and prevention of herpes zoster: A comprehensive review. Indian J Dermatol Venereol Leprol, 84(3), 251–262. doi: 10.4103/ijdvl.IJDVL_1021_16.

Kawai, K., Gebremeskel, B. G., & Acosta, C. (2014). Systematic review of incidence and complications of herpes zoster: towards a global perspective. BMJ Open, 2014, 4(6), e004833. doi: 10.1136/bmjopen-2014.

Johnson, R. W., Alvarez-Pasquin, M.-J., Bijl, M., Franco, E., Gaillat, J., Clara, J. G., et al. (2015). Herpes zoster epidemiology, management, and disease and economic burden in Europe: a multidisciplinary perspective. Therapeutic Advances in Vaccines, 3(4), 109–120. doi: 10.1177/2051013615599151.

Kawai, K., & Yawn, B. (2017). Risk Factors for Herpes Zoster: a Systematic Review and Meta-Analysis. Open Forum Infectious Diseases, 4(1), 313–314. doi: 10.1093/ofid/ofx163.733.

Tseng, H. F., Chia, M., Hung, P., Harpaz, R., Schmid, D. S., LaRussa, P., et al. (2018). Family history of zoster and risk of developing herpes zoster. International Journal of Infectious Diseases, 66, 99–106. doi: 10.1016/j.ijid.2017.11.016.

Borbinha, C., Marto, J. P., Calado, S., & Viana-Baptista, M. (2016). A Young Woman with Ischemic Stroke: Should We Pay More Attention to Varicella Zoster Infection. Case Rep Neurol, 8(2), 145–150. doi: 10.1159/000447296.

Zheleznikova, G. F., Skripchenko, N. V., & Skripchenko, E. Y. (2013). Virus vetryanoj ospy-opoyasyvayuschego gerpesa i immunnyj otvet [Varicella-zoster virus and immune response]. Rossijskij immunologicheskij zhurnal, 7(16), 1, 35–48. [in Russian].

Hao, M., Wang, X., Du, J., Liu, L., Jiao, Y., Wu, H., et al. (2015). Cytokine levels are associated with the severity of varicella infections. Infect Dev Ctries, 9(2), 190–196. doi: 10.3855/jidc.5255.

Rojas, J. M., Avia, M., Martín, V., & Sevilla, N. (2017). IL-10: A Multifunctional Cytokine in Viral Infections. Journal of Immunology Research, 2017, 6104054. doi: 10.1155/2017/6104054.

Puzyryova, L., & Safonov, A. D. (2016). Geneticheskij polimorfizm citokinov: proshloe i buduschee [Cytokines genetic polymorphism: the past and the future]. Infekciya i immunitet, 6(2), 103–108. [in Russian].

Trifunovic, J., Miller, L., Debeljak, Z., & Horvat, V. (2015). Pathologic patterns of interleukin 10 expression-a review. Biochem Med (Zagreb), 25(1), 36–48. doi: 10.11613/BM.2015.004.

Hurme, M., Haanpää, M., Nurmikko, T., Wang, X. Y., Virta, M., Pessi, T., et al. (2003). IL-10 gene polymorphism and herpesvirus infections. J Med Virol, 70(1), 48–50. doi: 10.1002/jmv.10320.

Moraru, M., Cisneros, E., Gomez-Lozano, N., de Pablo, R., Portero, F., Cañizares, M., et al. (2012). Host genetic factors in susceptibility to herpes simplex type 1 virus infection: contribution of polymorphic genes at the interface of innate and adaptive immunity. J Immunol, 188(9), 4412–4420. doi: 10.4049/jimmunol.1103434.

Werner, R. N., Nikkels, A. F., Marinovoc, B., Schäfer, M., Czarnecka-Operacz, M., Agius, A. M., et al. (2016). European consensus-based (S2k) Guideline on the Management of Herpes Zoster – guided by the European Dermatology Forum (EDF) in cooporation with the European Academy of Dermatology and Venereology (EADV), Part 2: Treatment. J Eur Acad Dermatol Venereol, 31(1). 20–29. doi: 10.1111/jdv.13957.

Hoppe, F. M., Hoppe, D. J., & Walter, S. D. (2018). Explaining odds ratios as conditional risk ratios. Journal of Clinical Epidemiology, 97, 123–124. doi: 10.1016/j.jclinepi.2017.10.009.

Jones, D., Neff, C. P., Palmer, B. E., Stenmark, K., & Nagel, M. A. (2017). Varicella zoster virus–infected cerebrovascular cells produce a proinflammatory environment. Neurology. Neuroimmunology & Neuroinflammation, 4(5), e382. doi: 10.1212/NXI.0000000000000382.

Marin, M., Harpaz, R., Zhang, J., Wollan, P. C., Bialek, S. R., & Yawn, B. P. (2016). Risk Factors for Herpes Zoster Among Adults. Open forum infectious diseases, 3(3), ofw119. doi: 10.1093/ofid/ofw119.

Serebrennikova, S., Seminsky, I., Semenov, N., & Guzovskaya, E. (2012). Interlejkin-1, interlejkin-10 v regulyacii vospalitel'nogo processa [Interleukin-1, interleukin-10 in regulation of inflammatory process]. Sibirskij medicinskij zhurnal (Irkuck), 115(8), 5–7. [in Russian].

Karpova, M. I. (2011). Izuchenie urovnya citokinov u bol'nyhk migren'yu i golovnoj bol'yu napryazheniya [The study of cytokine levels in patients with migraine and tension-type headache]. Citokiny i vospalenie, 10(1), 32–36. [in Russian].

Zheleznikova, G. F., Lobzin, Y. V., Skripchenko, N. V., Ivanova, G. P., Skripchenko, E. Y., & Monakhova, N. E. (2015). Klinicheskoe znachenie syvorotochnykh urovnej citokinov pri vetryanoj ospe u detej [Clinical significance of cytokines serum levels in children with chicken pox]. Infekciya i immunitet, 5(1), 79–84. [in Russian].

Hai-Jun, Shi, & Zhi-Qiang, Cui. (2017). Correlation of serum inflammatory cytokine and immunoglobulin content with post-herpetic neuralgia in patients with acute herpes zoster. Journal of Hainan Medical University, 23(1), 97–100.

Cho, J. W., Shin, D. H., & Lee, K. S. (2007). Polymorphism of the IL-10 gene is associated with susceptibility to herpes zoster in Korea. J Dermatol Sci., 45(3), 213–215. doi: 10.1016/j.jdermsci.2006.11.004.

Haanpaa, M., Nurmikko, T., & Hurme, M. (2002). Polymorphism of the IL-10 gene is associated with susceptibility to herpes zoster. Scand J Infect Dis., 34(2), 112–114. doi: 10.1080/00365540110077218.

Crosslin, D. R., Carrell, D. S., Burt, A., Kim, D. S., Underwood, J. G., Hanna, D. S., et al. (2015). Genetic variation in the HLA region is associated with susceptibility to herpes zoster. Genes and Immunity, 16(1), 1–7. doi: 10.1038/gene.2014.51.

Grahn, A., Bergstrom, T., Runesson, J., & Studahl, M. (2016). Varicella-zoster virus (VZV) DNA in serum of patients with VZV central nervous system infections. J Infect, 73(3), 254–60. doi: 10.1016/j.jinf.2016.04.035.

Tran, K. D., Falcone, M. M., Choi, D. S., Goldhardt, R., Karp, C. L., Davis, J. L., & Galor, A. (2016). Epidemiology of Herpes Zoster Ophthalmicus: Recurrence and Chronicity. J Ophthalmology, 123(7), 1469–1475. doi: 10.1016/j.ophtha.2016.03.005.

Serinken, M., Eken, C., Dal, O., & Kutlu, M. (2016). Man with facial nerve palsy and ear pain. Ramsay Hunt syndrome. Ann Emerg Med, 67(1), 141–148. doi: 10.1016/j.annemergmed.2015.04.010.

Lee, C-Y., Tsai, H-C., Lee, SS-J., & Chen, Y-S. (2015). Orbital apex syndrome: an unusual complication of herpes zoster ophthalmicus. BMC Infectious Diseases, 15, 33. doi: 10.1186/s12879-015-0760-z.

Forbes, H. J., Thomas, S. L., Smeeth, L., Clayton, T., Farmer, R., Bhaskaran, K., & Langan, S. M. (2016). A systematic review and meta-analysis of risk factors for postherpetic neuralgia. J Pain, 157(1), 30–54. doi: 10.1097/j.pain.0000000000000307.

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Onishchenko NV, Riabokon YY, Riabokon OV. The role of interleukin-10 gene polymorphism (rs 1800872) in the course of herpes zoster in adults. Pathologia [Internet]. 2018Dec.19 [cited 2024Dec.24];(3). Available from: http://pat.zsmu.edu.ua/article/view/151810

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