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Novel Research in Sciences

Nutrient Factors for Risk of Nodular Goiter

Victor Kravchenko*

Department of Epidemiology Endocrine Diseases, Institute of Endocrinology and Metabolism, Ukraine

*Corresponding author:Victor Kravchenko, Department of Epidemiology Endocrine Diseases, Institute of Endocrinology and Metabolism, VP Komissarenko National Academy of Medical Sciences of Ukraine, Ukraine

Submission: December 06, 2022;Published: December 16, 2022

DOI: 10.31031/NRS.2022.13.000802

Volume13 Issue1
December , 2022

Abstract

A brief review of the literature presents current data on micro- and macronutrients in euthyroid nodular goiter. Among them are iodine (I), selenium (Se), iron (Ir), zinc (Zn), copper (Cu), magnesium (Mg), calcium (Ca). The role of iodine deficiency in the development of pathology was determined. The possible fate of other specified elements in the occurrence of the disease was considered. Presented data of the author’s research.

Keywords: Iodine deficiency; Magnesium; Nodular goiter; Thyroid gland; Tomography

Introduction

Nodular Goiter (NG) is an extremely common endocrine pathology, which leads to an increase in the thyroid gland (thyroid gland) in the form of diffuse and nodular neoplasms. NG is an overgrowth of thyroid tissue caused by structural and functional changes in several parts of the gland [1]. It was reported that 10% of the population has this pathology [2]. The use of modern diagnostic methods, ultrasound and computed tomography significantly increased the prevalence of this disease to 19-68% in randomly selected individuals, with a higher frequency in women and the elderly [3,4].

Micro and Macro Elements in Nodular Goiter

The main risk factor for NG is insufficient intake of iodine. Iodine deficiency causes an increase in TSH and accumulation of peroxide in the thyroid gland, which leads to an increase in insulin-like growth factor, fibroblast growth factor and mutation of follicular cells [5-7]. The follicular cells will continue to change by forming single nodules in the thyroid tissue. There is a large number of studies showing a significant decrease in goiter cases after iodine prophylaxis [8-11]. The presence of nodular pathology even after the introduction of iodine prophylaxis indicates the importance of other factors in their occurrence. An important role in the normal metabolism of thyroid hormones is played by selenium, which is part of glutathione peroxidase and acts as an antioxidant, a protector of thyrocytes from peroxide damage [12,13]. Se can affect the progression of autoimmune thyroid diseases, affecting the immune response [14,15]. There are reports that it also affects the size of the thyroid gland [16]. The joint action of iodine and selenium is presented in many publications [17-21]. The effect of other elements on thyroid function and nodule formation is under study. A number of studies in animals and humans have shown that iron deficiency can alter the synthesis of thyroid hormones, which is explained by a decrease in the activity of Thyroxine Peroxidase (TPO), which is a heme-dependent protein [22,23]. Zinc is necessary for the proper functioning of the enzyme iodothyronine deiodinase, which is responsible for the conversion of thyroxine (T4) into the active form of triiodothyronine (T3) [24-26]. The role of copper in thyroid tissue is not yet clear. Magnesium is required for the thyroid to use iodine and convert inactive T4 to active T3 [27] and its serum level, due to its effect on DNA mutations, correlates with thyroid cancer [28-30]. Regarding calcium, there is evidence that. an increased concentration of TSH can increase the concentration of Ca2+ in human thyrocytes and serum of experimental rats [31]. Our studies in Ukraine in a region with mild iodine deficiency found that the median serum concentrations of selenium, zinc, calcium, magnesium and other elements were lower in the NG group compared to the control group. Risk analysis of nodular goiter odds ratio (OR) after adjusting the results for sex, age and ioduria showed the highest values with a simultaneous deficiency of macro- and microelements [32]. The OR was found to be 5.83 (95%, CI 1.87-18.9, p<0.01) at low concentrations. Ca, Mg and Zn in serum, whereas with a simultaneous decrease in the concentration of zinc, calcium and magnesium in serum, together with low values of ioduria, the OR increased to 12.5 (95%, CI 2.15- 79.42, p<0.05).

Conclusion

The combined deficiency of essential micro and macro elements in the body against the background of iodine deficiency suggests the highest risk for the occurrence of nodular goiter. Further study of the content of nutrients in the body of patients with nodular goiter will be an important premise for the development of methods for preventing NG and thyroid cancer in iodine prophylaxis and food fortification.

References

  1. Rocha HS, Lopesa RT, Valiante PM, Tirao G, Mazzarod I, et al. (2005) Diagnosis of thyroid nodular goiter using diffraction-enhanced imaging. Nucl Instrum 548(1-2): 175-180.
  2. Zimmermann MB (2009) Iodine deficiency. Endocr Rev 30(4): 376-408.
  3. Tan GH, Gharib H (1997) Thyroid incidentalomas: management approaches to nonpalpable nodules discovered incidentally on thyroid imaging. Ann Intern Med 126(3): 226-231.
  4. Guth S, Theune U, Aberle J, Galach A, Bamberger CM (2009) Very high prevalence of thyroid nodules detected by high frequency (13 MHz) ultrasound examination. Eur J Clin Invest 39(8): 699-706.          
  5. Corvillian B, Van Sande J, Laurent E, Dumont JE (1991) The H2O2-generating system modulates protein iodination and the activity of the pentose phosphate pathway in dog thyroid. Endocrinology 128(2): 779-785.
  6. Gydee H, O’Neill JT, Patel A, Bauer AJ, Tuttle RM, et al. (2004) Differentiated thyroid carcinomas from children and adolescents express IGF-I and the IGF-I-receptor (IGF-I-R). Pediatr Res 55(4): 709-715.
  7. Yeh MW, Rougier JP, Park JW, Duh QY, Wong M, et al. (2006) Differentiated thyroid cancer cells invasion is regulated through epidermal growth factor receptor-dependent activation of matrix metalloproteinase (MMP)-2 gelatinase. Endocr Relat Cancer 13(4): 1173-1183.
  8. Chen Z, Xu W, Huang Y, Jin X, Deng J, et al. (2013) Associations of noniodized salt and thyroid nodule among the Chinese population: a large cross sectional study. Am J Clin Nutr 98(3): 684-692.
  9. Vejbjerg P, Knudsen N, Perrild H, Carlé A, Laurberg P, et al. (2007) Effect of a mandatory iodization program on thyroid gland volume based on individuals ’age, gender, and preceding severity of dietary iodine deficiency: A prospective, population-based study. J Clin Endocrinol Metab 92(4): 1397-1401.
  10. Krejbjerg A, Bjergved L, Pedersen IB, Carlé A, Jørgensen T, et al. (2014) Iodine fortification may influence the age-related change in thyroid volume: A longitudinal population-based study (danthyr). Eur J Endocrinol 170(4): 507-517.
  11. Aghini Lombardi F, Fiore E, Tonacchera M, Rago T, Antonangeli L, et al. (2013) The effect of voluntary iodine prophylaxis in a small rural community: the pescopagano survey 15 years later. J Clin Endocrinol Metab 98(3): 1031-1039.
  12. Köhrle J, Jakob F, Contempre B, Dumont JE (2005) Selenium, the thyroid, and the endocrine system. Endocr Rev 26(7): 944-984.
  13. Beckett GJ, Arthur JR (2005) Selenium and endocrine systems. J Endocrinol 184(3): 455-465.
  14. Wang Y, Zhao F, Rijntjes E, Wu L, Wu Q, et al. (2019) Role of selenium intake for risk and development of hyperthyroidism. J Clin Endocrinol Metab 104(2): 568-580.
  15. Winther KH, Rayman MP, Bonnema SJ, Hegedus L (2020) Selenium in thyroid disorders-essential knowledge for clinicians. Nat Rev Endocrinol 16(3): 165-176.
  16. Liu Y, Huang H, Zeng J, Sun C (2013) Thyroid volume, goiter prevalence, and selenium levels in an iodine-sufficient area: A cross-sectional study. BMC Public Health 13: 1153.
  17. Stuss M, Michalska-Kasiczak M, Sewerynek E (2017) The role of selenium in thyroid gland pathophysiology. Endokrynol Pol.68(4): 440-465. 
  18. Rasmussen LB, Schomburg L, Köhrle J, Pedersen IB, Hollenbach B, et al. (2011) Selenium status, thyroid volume, and multiple nodule formation in an area with mild iodine deficiency. Eur J Endocrinol 164(4): 585-590. 
  19. Çelik T, Savaş N, Kurtoğlu S, Sangün Ö Aydñn Z, et al. (2014) Iodine, copper, zinc, selenium and molybdenum levels in children aged between 6 and 12 years in the rural area with iodine deficiency and in the city center without iodine deficiency in hatay. Turk Pediatri Ars 49(2):111-116.
  20. Zimmermann MB (2006) The influence of iron status on iodine utilization and thyroid function. Annu Rev Nutr 26: 367-389.
  21. Yucel R, Ozdemir S, Dariyerli N, Toplan S, Akyolcu MC, et al. (2009) Erythrocyte osmotic fragility and lipid peroxidation in experimental hyperthyroidism. Endocrine 36(3): 498-502.
  22. Beard JL, Brigham DE, Kelley SK, Green MH (1998) Plasma thyroid hormone kinetics are altered in iron-deficient rats. J Nutr 128(8) :1401-1408.
  23. Wada L, King JC (1986) Effect of low zinc intakes on basal metabolic rate, thyroid hormones and protein utilization in adult men. J Nutr 116(6): 1045-1053.
  24. Danforth E, Burger AG (1989) The impact of nutrition on thyroid hormone physiology and action. Annu Rev Nutr 9: 201-227.
  25. Freake HC, Govoni KE, Guda K, Huang C, Zinn SA (2001) Actions and interactions of thyroid hormone and zinc status in growing rats. J Nutr 131(4): 1135-1141.
  26. Digiesi V, Bandinelli R, Bisceglie P, Santoro E (1983) Magnesium in tumoral tissues, in the muscle and serum of subjects suffering from neoplasia. Biochem Med 29(3): 360-363.
  27. Assem FL, Holmes P, Levy LS (2011) The mutagenicity and carcinogenicity of inorganic manganese compounds: A synthesis of the evidence. J Toxicol Environ Health B Crit Rev 14(8): 537-570.
  28. Anastassopoulou J, Theophanides T (2002) Magnesium-DNA interactions and the possible relation of magnesium to carcinogenesis. irradiation and free radicals. Crit Rev Oncol Hematol 42(1): 79-91.
  29. Leung PL, Li XL (1996) Multielement analysis in serum of thyroid cancer patients before and after a surgical operation. Biol Trace Elem Res 5(3): 259-266.
  30. MacNeil S, Munro DS, Metcalfe R, Cotterell S, Ruban L (1994) An investigation of the ability of TSH and Graves’ immunoglobulin G to increase intracellular calcium in human thyroid cells, rat FRTL-5 thyroid cells and eukaryotic cells transfected with the human TSH receptor. J Endocrinol 143(3): 527-540.
  31. Kravchenko V, Andrusyshyna I, Luzanchuk I, Polumbryk M, Tarashchenko Y (2020) Association between thyroid hormone status and trace elements in serum of patients with nodular goiter. Biol Trace Elem Res 196(2): 393-399.
  32. Turan E, Turksoy VA (2021) Selenium, zinc, and copper status in euthyroid nodular goiter: A Cross-Sectional Study. Int J Prev Med 12: 46.

© 2022 Victor Kravchenko. This is an open access article distributed under the terms of the Creative Commons Attribution License , which permits unrestricted use, distribution, and build upon your work non-commercially.