Skip to main content

Advertisement

Log in

Sex differences in the relationship between blood mercury concentration and metabolic syndrome risk

  • Original Article
  • Published:
Journal of Endocrinological Investigation Aims and scope Submit manuscript

Abstract

Background

Mercury exposure enhances free radical production and reduces activity of anti-oxidant enzymes, resulting in detrimental health effects. Some researchers have reported an association between blood mercury and increased risk of metabolic syndrome (MetS); however, sex differences in the relationship were not fully considered.

Aim

To examine the sex differences in the relationship between blood mercury concentration and the increased risk of MetS in Korean men and women.

Materials and methods

A nationwide cross-sectional study was conducted to examine the relationship between blood mercury concentration and MetS in 2,976 men and 3,074 women over 19 years of age (aged 19–87 years), using data from the 2010–2012 Korean National Health and Nutrition Examination Survey (KNHANES-V). Multiple logistic regression analysis was used to assess the relationship between blood mercury concentration and the prevalence risk of MetS after adjusting for confounding variables.

Results

Compared to the lowest quartile of blood mercury concentration, the OR (95 % CI) for MetS of the highest quartile in men was 1.62 (1.15–2.28) after adjusting for age, smoking status, alcohol consumption, regular exercise, and BMI. Similarly, in multiple logistic regression analysis using log2-transformed blood mercury as a continuous variable, the OR (95 % CI) for having MetS with doubling of blood mercury was 1.20 (1.05–1.36) after adjusting for the same co-variables. However, the relationship was not observed in women after adjusting for the same co-variables.

Conclusions

Blood mercury concentration was independently associated with an increased risk of MetS in men.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

Similar content being viewed by others

Abbreviations

MetS:

Metabolic syndrome

ROS:

Radical oxygen species

RNS:

Reactive nitrogen species

KNHANES:

Korean National Health and Nutrition Examination Survey

IPAQ:

The International Physical Activity Questionnaire

HOMA-IR:

The Homeostasis Model Assessment estimate of Insulin Resistance

BMI:

Body mass index

WC:

Waist circumference

References

  1. Grundy SM, Brewer HB Jr, Cleeman JI, Smith SC Jr, Lenfant C (2004) Definition of metabolic syndrome: report of the National Heart, Lung, and Blood Institute/American Heart Association conference on scientific issues related to definition. Arterioscler Thromb Vasc Biol 24:e13–e18

    Article  CAS  PubMed  Google Scholar 

  2. Salonen JT, Seppanen K, Nyyssonen K et al (1995) Intake of mercury from fish, lipid peroxidation, and the risk of myocardial infarction and coronary, cardiovascular, and any death in eastern Finnish men. Circulation 91:645–655

    Article  CAS  PubMed  Google Scholar 

  3. Fortuño A, San José G, Moreno MU, Beloqui O, Díez J, Zalba G (2006) Phagocytic NADPH oxidase overactivity underlies oxidative stress in metabolic syndrome. Diabetes 55:209–215

    Article  PubMed  Google Scholar 

  4. Romeo GR, Lee J, Shoelson SE (2012) Metabolic syndrome, insulin resistance, and roles of inflammation-mechanisms and therapeutic targets. Arterioscler Thromb Vasc Biol 32:1771–1776

    Article  CAS  PubMed  Google Scholar 

  5. Jeong HS, Lee DB, Cho YC (1991) A study on the blood lead and cadmium concentration levels of rural residents. Res Rep Environ Sci 9:61–73

    Google Scholar 

  6. Lee BK (1999) The role of biological monitoring in the health management of lead- exposed workers. Toxicol Lett 108:149–160

    Article  CAS  PubMed  Google Scholar 

  7. Auger N, Oscar K, Tom K, Ben A (2005) Low-level methylmercury exposure as a risk factor for neurologic abnormalities in adults. Neurotoxicity 26:149–157

    Article  CAS  Google Scholar 

  8. Cranmer M, Gilbert S, Cranmer J (1996) Neurotoxicity of mercury-indicators and effects of low-level exposure: overview. Neurotoxicology 17:9–14

    CAS  PubMed  Google Scholar 

  9. Murata K, Mineshi S, Kunihiko N et al (2006) Subclinical effects of prenatal methylmercury exposure on cardiac autonomic function in Japanese children. Int Arch Occup Environ Health 79:379–386

    Article  CAS  PubMed  Google Scholar 

  10. Houston MC (2007) The role of mercury and cadmium heavy metals in vascular disease, hypertension, coronary heart disease, and myocardial infarction. Altern Ther Health Med 13:S128–S133

    PubMed  Google Scholar 

  11. Kim YS, Lee EJ, Bae SH, Ohtsuka R, Suzuki T (1982) Mercury concentrations in pregnant women’s hair in the Seoul area. Korean J Environ Health 18:105–111

    Google Scholar 

  12. Magos L, Clarkson TW, Sparrow S, Hudson AR (1987) Comparison of the protection given by selenite, selenomethionine and biological selenium against the renotoxicity of mercury. Arch Toxicol 60:422–426

    Article  CAS  PubMed  Google Scholar 

  13. Ratcliffe HE, Swanson GM, Fischer LJ (1996) Human exposure to mercury: a critical assessment of the evidence of adverse health effects. J Toxicol Environ Health 49:221–270

    CAS  PubMed  Google Scholar 

  14. Salonen JT, Seppanen K, Lakka TA, Salonen R, Kaplan GA (2000) Mercury accumulation and accelerated progression of carotid atherosclerosis: a population-based prospective 4-year follow-up study in men in eastern Finland. Atherosclerosis 148:265–273

    Article  CAS  PubMed  Google Scholar 

  15. Eom SY, Choi SH, Ahn SJ, Kim DK, Kim DW, Lim JA et al (2014) Reference levels of blood mercury and association with metabolic syndrome in Korean adults. Int Arch Occup Environ Health 87:501–513

    Article  CAS  PubMed  Google Scholar 

  16. Watanabe T, Akishita M, Toba K et al (2000) Influence of sex and age on serum nitrite/nitrate concentration in healthy subjects. Clin Chim Acta 301:169–179

    Article  CAS  PubMed  Google Scholar 

  17. Taskiran D, Kutay FZ, Sozmen E, Pogun S (1997) Sex differences in nitrite/nitrate levels and antioxidant defense in rat brain. Neuro Rep 8:881–884

    CAS  Google Scholar 

  18. Thomas DJ, Fisher HL, Sumler MR, Mushak P, Hall LL (1987) Sexual differences in the excretion of organic and inorganic mercury by methyl mercury-treated rats. Environ Res 43:203–216

    Article  CAS  PubMed  Google Scholar 

  19. Glass DC, Gray CN (2001) Estimating mean exposures from censored data exposure to benzene in the Australian petroleum industry. Ann Occup Hyg 25:275–282

    Article  Google Scholar 

  20. Kim NS, Lee BK (2011) National estimates of blood lead, cadmium, and mercury levels in the Korean general adult population. Int Arch Occup Environ Health 84:53–63 (Korean)

    Article  CAS  PubMed  Google Scholar 

  21. Lee SY, Park HS, Kim DJ et al (2007) Appropriate waist circumference cutoff points for central obesity in Korean adults. Diabetes Res Clin Pract 75:72–80

    Article  PubMed  Google Scholar 

  22. Rhee SY, Hwang YC, Woo JT et al (2013) Blood lead is significantly associated with metabolic syndrome in Korean adults: an analysis based on the Korea National Health and Nutrition Examination Survey (KNHANES), 2008. Cardiovasc Diabetol 12:9

    Article  PubMed Central  PubMed  Google Scholar 

  23. Lee BK, Kim Y (2013) Blood cadmium, mercury, and lead and metabolic syndrome in South Korea: 2005–2010 Korean National Health and Nutrition Examination Survey. Am J Ind Med 56:682–692

    Article  CAS  PubMed  Google Scholar 

  24. Rungby J, Ernst E (1992) Experimentally induced lipid peroxidation after exposure to chromium, mercury or silver: interactions with carbon tetrachloride. Pharmacol Toxicol 70:205–207

    Article  CAS  PubMed  Google Scholar 

  25. Salonen JT, Seppanen K, Nyyssonen K et al (1995) Intake of mercury from fish, lipid peroxidation, and the risk of myocardial infarction and coronary, cardiovascular, and any death in eastern Finnish men. Circulation 91:645–655

    Article  CAS  PubMed  Google Scholar 

  26. Insug O, Datar S, Koch CJ, Shapiro IM, Shenker BJ (1997) Mercuric compounds inhibit human monocyte function by inducing apoptosis: evidence for formation of reactive oxygen species, development of mitochondrial membrane permeability transition and loss of reductive reserve. Toxicology 124:211–224

    Article  CAS  PubMed  Google Scholar 

  27. Jansson G, Harms-Ringdahl M (1993) Stimulating effects of mercuric- and silver ions on the superoxide anion production in human polymorphonuclear leukocytes. Free Radic Res Commun 8:87–98

    Article  Google Scholar 

  28. Elnakish MT, Hassanain HH, Janssen PM, Angelos MG, Khan M (2013) Emerging role of oxidative stress in metabolic syndrome and cardiovascular disease: important role of Rac/NADPH oxidase. J Pathol 231:290–300

    CAS  PubMed  Google Scholar 

  29. Evans JL, Maddux BA, Goldfine ID (2005) The molecular basis for oxidative stress induced insulin resistance. Antioxid Redox Signal 7:1040–1052

    Article  CAS  PubMed  Google Scholar 

  30. Thomas DJ, Fisher HL, Sumler MR, Marcus AH, Mushak P, Hall LL (1986) Sexual differences in the distribution and retention of organic and inorganic mercury in methyl mercury-treated rats. Environ Res 41:219–234

    Article  CAS  PubMed  Google Scholar 

  31. Hultman P, Nielsen JB (2001) The effect of dose, gender, and non-H-2 genes in murine mercury-induced autoimmunity. J Autoimmun 17:27–37

    Article  CAS  PubMed  Google Scholar 

  32. Borrás C, Sastre J, García-Sala D, Lloret A, Pallardó FV, Viña J (2003) Mitochondria from females exhibit higher antioxidant gene expression and lower oxidative damage than males. Free Radic Biol Med 34:546–552

    Article  PubMed  Google Scholar 

  33. Olivieri G, Novakovic M, Savaskan E et al (2002) The effects of beta-estradiol on SHSY5Y neuroblastoma cells during heavy metal induced oxidative stress, neurotoxicity and beta-amyloid secretion. Neuroscience 113:849–855

    Article  CAS  PubMed  Google Scholar 

  34. Mahaffey KR, Clickner RP, Bodurow CC (2004) Blood organic mercury and dietary mercury intake: National Health and Nutrition Examination Survey, 1999 and 2000. Environ Health Perspect 112:562–570

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  35. Mahaffey KR (2005) Mercury exposure: medical and public health issues. Trans Am Clin Climatol Assoc 116:127–153

    PubMed Central  PubMed  Google Scholar 

  36. Schulz C, ConRad A, Becker K, Kolossa-Gehring M, Seiwert M, Seifert B (2007) Twenty years of the German Environmental Survey (GerES): human biomonitoring-temporal and spatial (West Germany/East Germany) differences in population exposure. Int J Hyg Environ Health 210:271–297

    Article  CAS  PubMed  Google Scholar 

Download references

Conflict of interest

The authors declare no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Yong-Jae Lee.

Additional information

J.-Y. Chung and M.-S. Seo contributed equally to this work.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Chung, JY., Seo, MS., Shim, JY. et al. Sex differences in the relationship between blood mercury concentration and metabolic syndrome risk. J Endocrinol Invest 38, 65–71 (2015). https://doi.org/10.1007/s40618-014-0132-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s40618-014-0132-3

Keywords

Navigation