Journal Technologies of Living Systems №2 for 2020 г.
Article in number:
Assessment of patterns of hair essential and toxic trace elements content in overweight and obese adults
Type of article: scientific article
DOI: 10.18127/j20700997-202002-03
UDC: 616-056.52
Authors:

A.A. Tinkov – Ph.D. (Med.), Yaroslavl State University; 

I.M. Sechenov First Moscow State Medical University (Sechenov University) E-mail: tinkov.a.a@gmail.com

Abstract:

Statement of the problem. Alteration of metal-ligand homeostasis is associated with development of obesity and associated metabolic disturbances, although the particular patterns of such alterations are insufficiently studied.

Aim of the work – to assess characteristic patterns of hair essential and toxic element content in adults in relation to increased body mass index (BMI). A total of 556 men and 754 women aged 20-60 y.o. were examined. Assessment of hair trace element content was performed using inductively-coupled plasma mass-spectrometry.

Results. The obtained data demonstrate that only hair selenium (Se)(p = 0.006) and especially zinc (Zn)(p < <0.001) were characterized by a significant BMI-related increase. Particularly, hair Zn content in overweight and obese adults exceeded that in low- and normal-weight subjects by 16% and 8%, and 20% and 11%, respectively. At the same time, increased BMI was associated with a significant (p<0,01) elevation of hair arsenic (As), cadmium (Cd), lead (Pb), tin (Pb), and especially mercury (Hg) content. Hair Hg content in overweight and obese subjects exceeded that in normal-weight adults by 33% and 51%. Multiple linear regression analysis demonstrated that only hair As, Hg, Pb, Sn, and Zn levels were significantly associated with BMI. Principal component (PC) analysis (PCA) demonstrated that PC1 and PC2 being responsible for 57% BMI variability contained values on hair Pb and As, and Sn and Hg content, respectively.

Practical significance. The obtained data demonstrate increased risk of obesity under conditions of toxic metal overexposure, whereas adequate zinc supply may possess protective effect, that may be used as targets of preventive strategies.  

Pages: 31-38
For citation

Tinkov A.A. Assessment of patterns of hair essential and toxic trace elements content in overweight and obese adults. Technologies of living systems. 2020. V. 17. № 2. P. 31–38. DOI: 10.18127/j20700997-202002-03 (In Russian).

References
  1. Gregg E.W., Shaw J.E. Global health effects of overweight and obesity.  N. Engl. J. Med. 2017. V. 377(1). P. 80–81.
  2. Abdelaal M., le Roux C.W., Docherty N.G. Morbidity and mortality associated with obesity. Ann. Transl. Med. 2017. V. 5. № 7. P. 161.
  3. Lubrano C., Genovesi G., Specchia P., Mariani S., Petrangeli E., Lenzi A., Gnessi L. Obesity and metabolic comorbidities: environmental diseases?. Oxid Med. Cell. Longev. 2013. 640673. https://doi.org/10.1155/2013/640673.
  4. García O.P., Long K.Z., Rosado J.L. Impact of micronutrient deficiencies on obesity. Nutr. Rev. 2009. V. 67(10). P. 559–572.
  5. Nikonorov A.A., Skalnaya M.G., Tinkov A.A., Skalny A.V. Mutual interaction between iron homeostasis and obesity pathogenesis. J. Trace Elem. Med. Biol. 2015. V. 30. P. 207–214.
  6. Tinkov A.A., Sinitskii A.I., Popova E.V., Nemereshina O.N., Gatiatulina E.R., Skalnaya M.G., Skalny A.V., Nikonorov A.A. Alteration of local adipose tissue trace element homeostasis as a possible mechanism of obesity-related insulin resistance. Med. Hypotheses. 2015. V. 85(3). P. 343–347.
  7. Wang X., Mukherjee B., Park S.K. Associations of cumulative exposure to heavy metal mixtures with obesity and its comorbidities among US adults in NHANES 2003–2014. Environ. Int. 2018. V. 121. P. 683–694.
  8. Tinkov A.A., Ajsuvakova O.P., Skalnaya M.G., Popova E.V., Sinitskii A.I., Nemereshina O.N., Gatiatulina E.R., Nikonorov A.A., Skalny A.V. Mercury and metabolic syndrome: a review of experimental and clinical observations. Biometals. 2015. V. 28(2). P. 231–254.
  9. Ceja-Galicia Z.A., Daniel A., Salazar A.M., Pánico P., Ostrosky-Wegman P., Díaz-Villaseñor A. Effects of arsenic on adipocyte metabolism: Is arsenic an obesogen? Mol. Cell. Endocrinol. 2017. V. 452. P. 25–32.
  10. Tinkov A.A., Filippini T., Ajsuvakova O.P., Aaseth J., Gluhcheva Y.G., Ivanova J.M., Björklund G., Skalnaya M.G., Gatiatulina E.R., Popova E.V., Nemereshina O.N., Vinceti M., Skalny A.V. The role of cadmium in obesity and diabetes. Sci. Total Environ. 2017. V. 601. P. 741–755.
  11. Park S.S., Skaar D.A., Jirtle R.L., Hoyo C. Epigenetics, obesity and early-life cadmium or lead exposure. Epigenomics. 2017. V. 9(1). P. 57–75.
  12. Tinkov A. A., Ajsuvakova O.P., Skalnaya M.G., Skalny A.V., Aschner M., Suliburska J., Aaseth J. Organotins in obesity and associated metabolic disturbances. J. Inorg. Biochem. 2019. V. 191. P. 49–59.
  13. Shin Y.Y., Ryu I.K., Park M.J., Kim S.H. The association of total blood mercury levels and overweight among Korean adolescents: analysis of the Korean National Health and Nutrition Examination Survey (KNHANES) 2010–2013. Korean. J. Pediatr. 2018. V. 61(4). P. 121.
  14. Park J.S., Ha K.H., He K., Kim D.J. Association between blood mercury level and visceral adiposity in adults. Diabetes Metab. J. 2017. V. 41(2). P. 113–120.
  15. Rizzetti D.A., Corrales P., Piagette J.T., Uranga-Ocio J.A., Medina-Gomez G., Peçanha F.M., Vassallo D.V., Miguel M., Wiggers G.A. Chronic mercury at low doses impairs white adipose tissue plasticity. Toxicology. 2019. V. 418. P. 41–50.
  16. Caito S.W., Newell-Caito J., Martell M., Crawford N., Aschner M. Methylmercury Induces Metabolic Alterations in Caenorhabditis elegans: Role for C/EBP Transcription Factor. Toxicol. Sci. 2019. https://doi.org/10.1093/toxsci/kfz244.
  17. Su C.T., Lin H.C., Choy C.S., Huang Y.K., Huang S.R., Hsueh Y.M. The relationship between obesity, insulin and arsenic methylation capability in Taiwan adolescents. Sci. Total Environ. 2012. V. 414. P. 152–158.
  18. Yadav S., Anbalagan M., Shi Y., Wang F., Wang H. Arsenic inhibits the adipogenic differentiation of mesenchymal stem cells by down-regulating peroxisome proliferator-activated receptor gamma and CCAAT enhancer-binding proteins. Toxicol. In Vitro. 2013. V. 27(1). P. 211–219.
  19. Vallascas E., De Micco A., Deiana F., Banni S., Sanna E. Adipose tissue: another target organ for lead accumulation? A study on Sardinian children (Italy). Am. J. Human Biol. 2013. V. 25(6). P. 789–794.
  20. Beier E.E., Maher J.R., Sheu T.J., Cory-Slechta D.A., Berger A.J., Zuscik M.J., Puzas J.E. Heavy metal lead exposure, osteoporotic-like phenotype in an animal model, and depression of Wnt signaling. Environ. Health Perspect. 2012. V. 121(1). P. 97–104.
  21. Grün F., Blumberg B. Environmental obesogens: organotins and endocrine disruption via nuclear receptor signaling. Endocrinolog. 2006. V. 147. P. s50-s55.
  22. Milton F.A., Lacerda M.G., Sinoti S.B., Mesquita P.G., Prakasan D., Coelho M.S., de Lima C.L., Martini A.G., Pazzine G.T., de F. Borin M., Amato A.A., de A. R. Neves F. Dibutyltin compounds effects on PPARγ/RXRα activity, adipogenesis, and inflammation in mammalians cells. Front. Pharmacol. 2017. V. 8. P. 507.
  23. Gu K., Xiang W., Zhang Y., Sun K., Jiang X. The association between serum zinc level and overweight/obesity: a meta-analysis. Eur. J. Nutr. 2018. P. 1–12.
  24. Tinkov A.A., Popova E.V., Gatiatulina E.R., Skalnaya A.A., Yakovenko E.N., Alchinova I.B., Karganov M.Y., Skalny A.V., Nikonorov A.A. Decreased adipose tissue zinc content is associated with metabolic parameters in high fat fed Wistar rats. Acta Sci. Pol. Technol. Aliment. 2016. V. 15(1). P. 99–105.
  25. Olechnowicz J., Tinkov A., Skalny A., Suliburska J. Zinc status is associated with inflammation, oxidative stress, lipid, and glucose metabolism. J. Physiol. Sci. 2018. V. 68(1). P. 19–31.
  26. Wiernsperger N., Rapin J. Trace elements in glucometabolic disorders: an update. Diabetol. Metab. Syndr. 2010. V. 2(1). P. 70.
Date of receipt: 23 января 2020 г