Effect of Thyroid Hormones and Trace Elements (Zn, Mg) on Obesity
Main Article Content
Abstract
Background: Obesity is characterized by abnormal or excessive fat accumulation that is the result of a chronic imbalance between energy intake and energy expenditure. Thyroid hormones have profound effect on many physiological processes, such as development, growth in children and metabolism. Thyroid hormones stimulate diverse metabolic activates in most tissues, leading to an increase in basal metabolic rate. Trace elements are essential nutrients with regulatory, immunologic, and antioxidant functions resulting from their action as essential components or cofactors of enzymes throughout metabolism.
Methods: In this study conducted on 176 individuals in the age group from (20-55) years, from Tikrit and Kirkuk Governorates. Blood samples were divided into three groups according to BMI: Group One: Control group (Normal Weight): 66 individual BMI (18.5 - 24.9 kg/m2). Group Two: Overweight group: 50 individual BMI (25.0 – 29.9 kg/m2).Group Three: Obese group: 60 individual BMI (≥ 30 kg/m2).
Results: The results showed a high significant increase (p<0.0001) in the BMI level in obese and overweight groups comparison with normal weight group. The results showed a significant decrease (p<0.001) in (T3 and T4) hormones levels in obese and overweight groups comparison with normal weight group. While the results showed a high significant increase (p<0.0001) in the TSH levels in obese and overweight groups comparison with normal weight group, the results showed a significant decrease (p<0.001) in the Zn concentration in obese and overweight groups comparison with normal weight group, the results showed a high significant decrease (p<0.0001) in the Mg concentration in obese and overweight groups comparison with normal weight group. There is a high significant increase in the (cholesterol, TG, VLDL-c and LDL-c) levels in obese and overweight groups comparison with normal weight group (p<0.0001), while the results showed a high significant decrease (p<0.0001) in the HDL-c level in obese and overweight groups comparison with normal weight group. The results showed that there was a significant positive correlation between T3 and T4.While there was a significant negative correlation between T3 and LDL. There was a positive correlation between T4 and HDL. Whereas the there was a significant negative correlation between T4 and LDL. There was a significant positive correlation between TSH with Cholesterol, Triglyceride, LDL and VLDL. There was a significant negative correlation between TSH with HDL, and Mg. Conclusions: The results of (thyroid hormones and lipid profile) indicated highly associated with trace elements (Zn, Mg) levels and these correlations may be caused a risk of the obesity
Article Details

This work is licensed under a Creative Commons Attribution 4.0 International License.
Tikrit Journal of Pure Science is licensed under the Creative Commons Attribution 4.0 International License, which allows users to copy, create extracts, abstracts, and new works from the article, alter and revise the article, and make commercial use of the article (including reuse and/or resale of the article by commercial entities), provided the user gives appropriate credit (with a link to the formal publication through the relevant DOI), provides a link to the license, indicates if changes were made, and the licensor is not represented as endorsing the use made of the work. The authors hold the copyright for their published work on the Tikrit J. Pure Sci. website, while Tikrit J. Pure Sci. is responsible for appreciate citation of their work, which is released under CC-BY-4.0, enabling the unrestricted use, distribution, and reproduction of an article in any medium, provided that the original work is properly cited.
References
1. Morris MJ, Beilharz JE, Maniam J, Reichelt AC, and Westbrook RF: Why is obesity such a problem in the 21st century? The intersection of palatable food, cues and reward pathways, stress, and cognition. Neurosci. Biobehav. Rev., 2015; 58, 36–45.
2. Van Kruijsdijk R C, van der Wall E and Visseren F L; Obesity and cancer: the role of dysfunctional adipose tissue Cancer Epidemiol Biomarkers Prev, 2009; 18 2569-78.
3. Hajer G R, van Haeften T W and Visseren F L Adipose tissue dysfunction in obesity, diabetes, and vascular diseases Eur Heart J, 2008; 29 2959-71.
4. Torres-Leal F L, Fonseca-Alaniz M H, Rogero M M and Tirapegui J.; The role of inflamed adipose tissue in the insulin resistance Cell Biochem Funct, 2010; 28 623-31.
5. Brent GA: Mechanisms of thyroid hormone action. J Clin Invest, 2012; 122: 3035–43.
6. Jonklaas J, Bianco AC, Bauer AJ, et al: Guidelines for the treatment of hypothyroidism: prepared by the American Thyroid Association task force on thyroid hormone replacement. Thyroid, 2014; 24:1670–751.
7. Lobo JC, Torres JP, Fouque D. and Mafra D.; Zinc deficiency in chronic kidney disease: is there a relationship with adipose tissue and atherosclerosis? Biol Trace Elem Res, 2010; 135:16–21.
8. Saraymen R., Kilic E., Yazar S., Saraymen B.; Magnesium, Copper, Zinc, Iron and Chromium levels in Sweat of Boxers. JIUMF, 2003; 10(3):121-125.
9. Meyer JA, Spence DM: A perspective on the role of metals in diabetes: Past findings and possible future directions. Metallomics, 2009; 1, 32–41.
10. Pushparani DS. Anandan SN, Theagarayan P: Serum zinc and magnesium concentrations in type 2 diabetes mellitus with periodontitis. J. Indian Soc. Periodontol, 2014, 18, 187–193.
11. Meunier N, O’connor JM, Maiani G, Cashman KD, Secker DL, Ferry M et al: Importance of zinc in the elderly: the zenith study. Eur J Clin Nutr, 2005; 59: 1S-4S.
12. Gomez - García A, Hernandez - Salazar E, González-Ortiz M, and Martinez-Abundis E: Efecto de la administracion oral de zinc sobre sensibilidad a la insulina y niveles séricos de leptina yandrógenos en hombres con obesidad. Rev Méd Chile, 2006; 134: 279-84.
13. Palanivel R., Veluthakal R., McDonald P., Kowluru A.; Further evidence for the regulation of acetyl-CoA carboxylase activity by a glutamate- and magnesium-activated protein phosphatase in thepancreatic beta cell: defective regulation in the diabetic GK rat islet. Endocrine, 2005; 26(1):71-7.
14. Inoue I.; Lipid metabolism and magnesium. Clin Calcium, 2005; 15(11):65-76.
15. Barbagallo M., Dominguez LJ.; Magnesium metabolism in type 2 diabetes mellitus, metabolic syndrome and insulin resistance. Arch Biochem Biophys., 2007; 458(1):40-7.
16. Hordyjewska A., Pasternak K.; Magnesium role in cardiovascular diseases. Ann Univ Mariae Curie Sklodowska Med, 2004; 59(2):108-13.
17. Braverman LE., Utigen RD., Eds.; Werner and Ingbar's. 'The Thyroid – A Fundamental and Clinical Text'7th Ed. Philadelphia. Lippinscott –Raven, 1996.
18. Muzzaffari EL, Gharib H.; Thyroxine suppressive therapy in patients with nodular thyroid disease".Ann Inter Med, 1998; 128,386-394.
19. Spencer CA, et al; Interlaboratory / Intermethod differences in Functional Sensitivity of Immunometric Assays of Thyrotropin (TSH) and Impact on Reliability of Measurement of Subnormal Concentration of TSH. Clinical Chemistry, 1995; 41,367.
20. Tetsuo Makino, Chimica Clinica Acta, 1991; 197, 209-220.
21. Gindler E., Clin. Chem., 1971; 17,662.
22. Allian C.C. et al.; Estimation of Serum Cholesterol. Clin Chemistry, 1974; 470-475.
23. Trinder P. Ann. Estimation of Serum Triglyceride. Clin Biochem., 1969; 6: 27-29.
24. Burnestein M.; Estimation of Serum HDL-C. Journal of Lipid Research, 1970; 11:583-595.
25. Friedwald WT et al.; Estimation of Serum LDL-C. Clin Chem., 1972; 18:499.
26. Andreoli T. E., Carpenter J., Griggs R.C.; Cecil essentials of medicine: disorder of lipid metabolism. 5th ed Herbert P. N. Philadelphia W. B. Saunders Company, London, Tornto, 2001; 16: pp. 526-532.
27. Stipanuk M.H.; Biochemical and Physiological Aspects of human nutrition. Saunders, Philadelphia, 2000; pp: 763-775.
28. Choksi N.Y., Jahnka G.D., Hilaire C.S. and Shelby M.; Role of Thyroid Hormones in human and Laboratory Animal Reproductive Health. Dev. Reprod. Toxicol. B.D.R., 2003; 68: 479-491.
29. Krotkiewski M.; Thyroid hormones in the pathogenesis and treatment of obesity. Eur. J. Pharmacol, 2002; 440:85-98.
30. Reinehr T.; Obesity and thyroid function. Mol Cell Endocrinol, 2010; 316:165-17.
31. Villicev CS, Freitas FRS, Aoki MS, Taffarel C., Scanlan TS, Moriscot AS, Ribeiro MO, Bianco AC, Gouveia CH.; Thyroid hormone receptor β-specific agonist GC-1 increases energy expenditure and prevents fat-mass accumulation in rats. J. Endocrinol. 2007; 193:21-29.
32. A.S. de Rosa Araujo, M.F. Silva de Miranda, U.O. de Oliveira et al: Increased resistance to hydrogen peroxide-induced cardiac contracture is associated with decreased myocardial oxidative stress in hypothyroid rats. Cell Biochemistry and Function, 2010; vol.28, no.1, pp.38–44.
33. M.M. Estevez-Carmona, E. Melendez-Camargo, R. Ortiz Butron, M. Pineda-Reynoso, M. Franco-Colin, and E. Cano-Europa: Hypothyroidism maintained reactive oxygen species-steady state in the kidney of rats intoxicated with ethylene glycol: effect related to an increase in the glutathione that maintains
the redox environment. Toxicology and Industrial Health, 2013; vol.29, no.6, pp.555–566.
34. M.T. Elnakish, A.A.E. Ahmed, P.J. Mohler, and P.M. Janssen: Role of oxidative stress in thyroid hormone-induced cardiomyocyte hypertrophy and associated cardiacdysfunction: anundisclosedstory. Oxidative Medicine and Cellular Longevity, 2015;vol.2015,ArticleID854265, pages 16
35. N. Zhang, L. Wang, Q. Duan et al: Metallothionein - I/II knockoutmice aggravate mitochondrial superoxide production and peroxiredoxin 3 expression in thyroid after excessive iodide exposure. Oxidative Medicine and Cellular Longevity, 2015; vol.2015, Article ID 267027, pages 11.
36. Sun L, Yu Y, Huang T, An P, Yu D, Yu Z, Li H, Sheng H, Cai L, Xue J, Jing M, Li Y, Lin X, and Wang F: Associations between ionomic profile and metabolic abnormalities in human population. PLos One, 2012.
37. Mak IT, Kramer JH, Chen X, Chmielinska JJ, Spurney CF, Weglicki WB: Mg supplementation attenuates ritonavir - induced hyperlipidemia, oxidative stress, and cardiac dysfunction in rats. Amer. J Physiol., 2013; 305, 1102–1111.
38. Bao S, et al: Zinc modulates the innate immune response in vivo to polymicrobial sepsis through regulation of NF-kappaB. Am J Physiol Lung Cell Mol Physiol, 2010; 298(6): p. L744-54.
39. Osama M. Al-Sabaawy: The Relationship between Serum Lipid Profile and Selected Trace Elements for Adult Men in Mosul City. Oman Medical J., 2012; 4: 300-303.
40. Gunasekara P, Hettiarachchi M, Liyanage C, Lekamwasam S: Effects of zinc and multi mineral vitamin supplementation on glycemic and lipid control in adult diabetes. Diabetes Metab Syndr Obes, 2011; 4:53-60.