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Down-regulation of the auto-aggressive processes in patients with hypothyroid Hashimoto’s thyroiditis following substitutive treatment with L-thyroxine

Feyzullah Guclu1, Bilgin Ozmen1, Cengiz Kirmaz2, Sabriye Ozkaya Kafesciler1, Papatya Bayrak Degirmenci2, Fatma Taneli3, Zeliha Hekimsoy1

1 Celal Bayar University, Medical Faculty, Department of Internal Medicine, Division of Endocrinology, Manisa, Turkiye
2 Celal Bayar University, Medical Faculty, Department of Internal Medicine, Division of Immunology, Manisa, Turkiye
3 Celal Bayar University, Medical Faculty, Department of Clinical Biochemsitry, Manisa, Turkiye

* Corresponding Author: C. Kirmaz, email

European Cytokine Network 2009, 20(1), 27-32. https://doi.org/10.1684/ecn.2009.0147

Abstract

Background. Hashimoto’s thyroiditis is a chronic, organ-specific autoimmune disease. It is the most common cause of primary hypothyroidism during the adolescent period, via autoimmune thyroid tissue destruction, affecting 2% of the population. The pathogenesis of Hashimoto’s thyroiditis involves a complex interaction between predisposing genetic and environmental factors. Objective. In this study, we wanted to inves-tigate the role of cytokines such as IL-2, IL-4, IL-12 and IFN-γ in the pathogenesis of the disease, and the changes to cytokine levels brought about by treatment with L-thyroxine. Methods. Sixty five female patients, aged 18-73 years with Hashimoto’s thyroiditis, referred to the Celal Bayar University Medical Faculty Endocri-nology out-patients clinic, were included in this study. After a 10-12 week period of L-thyroxine treatment, all patients were restored to the euthyroid state. At the beginning and end of the treatment period, serum-free tri-iodothyronine (FT3), free thyroxine (FT4), thyroid-stimulating hormone (TSH), autoantibodies against thyroid peroxidase (anti-TPO), autoantibodies against thyroglobulin (anti-Tg) levels were measured using a chemilumi-necent, immunometric method, and cytokine levels were measured using ELISA. Results. There was a statisti-cally significant decrease in the serum levels of TSH (p < 0.0001) and a concomitant increase in FT4 serum levels (p < 0.0001). Also, during the post-treatment period, serum levels of anti-Tg (p < 0.01) and anti-TPO (p < 0.001) were significantly lower than during the pre-treatment period. A statistically significant decrease was shown for interleukin (IL)-12 serum levels during the post-treatment period (p < 0.001). However, the decrease in interferon (IFN)-γ serum levels was not statistically significant (p = 0.276). On the other hand, no change was demonstrated in serum IL-2 and IL-4 levels (p = 0.953 and p = 0.313, respectively) after treatment with L-thyroxine. Conclusion. Considering that our study involved a 10-12 week period of treatment, the statis-tically significant decrease in serum IL-12 levels, and the statistically non-significant decrease in IFN-γ levels, might indicate that a T helper type 1 inflammatory process had been halted or slowed down.

Keywords

hashimoto’s thyroiditis, L-thyroxine, cytokine, serum, Th1, Th2

Cite This Article

APA Style
Guclu, F., Ozmen, B., Kirmaz, C., Kafesciler, S.O., Degirmenci, P.B. et al. (2009). Down-regulation of the auto-aggressive processes in patients with hypothyroid Hashimoto’s thyroiditis following substitutive treatment with L-thyroxine. European Cytokine Network, 20(1), 27–32. https://doi.org/10.1684/ecn.2009.0147
Vancouver Style
Guclu F, Ozmen B, Kirmaz C, Kafesciler SO, Degirmenci PB, Taneli F, et al. Down-regulation of the auto-aggressive processes in patients with hypothyroid Hashimoto’s thyroiditis following substitutive treatment with L-thyroxine. Eur Cytokine Network. 2009;20(1):27–32. https://doi.org/10.1684/ecn.2009.0147
IEEE Style
F. Guclu et al., “Down-regulation of the auto-aggressive processes in patients with hypothyroid Hashimoto’s thyroiditis following substitutive treatment with L-thyroxine,” Eur. Cytokine Network, vol. 20, no. 1, pp. 27–32, 2009. https://doi.org/10.1684/ecn.2009.0147



cc Copyright © 2009 The Author(s). Published by Tech Science Press.
This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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