Relationship between hair cadmium levels, indoor ETS exposure and wheezing frequency in children
Published in Allergol Immunopathol (Madr). 2012;40:51-9. - vol.40 núm 01
Abstract
Background
Cadmium (Cd) is a toxic heavy metal and the components of tobacco and scalp hair effectively reflect a long-term environmental exposure.
Objective
The aim of this study was to assess the concentration of Cd levels in the hair of children with recurrent wheezing, and to evaluate the predictors of elevated Cd levels with a focus on anthropometric, environmental, and dietary factors.
Methods
In this case-control study, scalp hair was obtained from 65 children with recurrent wheezing (RW) and from 65 healthy children (HC). Hair Cd concentrations were determined by ICP-MS.
Results
Median (IQR) hair Cd levels were 0.22μg/kg (0.10–0.35) in RW group and 0.12μg/kg (0.04–0.23) in HC group (p=0.013). Multivariable logistic regression model results showed that being a child with RW (OR=6.28; p=0.001), ETS exposure at home (OR=22.56; p<0.001), and mother's education level (OR=0.49; p=0.020), are the major predictor variables for elevated hair Cd levels (cut off >0.17μg/kg). In RW group, multivariable logistic regression results showed that hair Cd levels of >0.17μg/kg was significantly predictive of having three or more wheezing episodes in RW group after adjustment for ETS exposure at home (OR=5.48; p=0.012).
Conclusion
We demonstrated that the more children are exposed to ETS at home, the more they are exposed to heavy metals like Cd. Especially children who have had three or more wheezing attacks over the last six months are much more susceptible than the other asthmatic and non-asthmatic children, and Cd exposure aggravates their asthmatic status.
Key words: Asthma. Wheezing. Indoor air pollution. Hair toxic metals. Hair Cd.
Introduction
Introduction
Heavy metal pollution has become a serious health concern in recent years. Cadmium (Cd) is a toxic heavy metal and the components of tobacco, together with water and food contamination, represent the main sources of non-occupational exposure in the general population.1, 2 Cd enters the human body mainly after inhalation of environmental tobacco smoke (ETS) and also via gastrointestinal absorption. Inhalation is the major means of cadmium absorption for children.3, 4 Continuous exposure to low levels of Cd may result in bioaccumulation and can cause a variety of adverse health effects on human beings, depending on the level and the duration of exposure, among which kidney dysfunction, lung diseases and disturbed calcium metabolism and bone defects are the most prominent.5, 6
However, trace element and toxic heavy metal concentrations in biological samples are affected by environmental and geographical factors. Therefore, considerable variations can occur between specific subgroups of the populations.6 Another difficulty in assessing the effects of toxic heavy metals for past and long-term exposure is to find a reliable biological indicator.7 Cd in blood is widely used as indices for current or recent exposure.8, 9 Compared to other types of clinical specimens, scalp hair has different uses and even advantages over blood or urine,8 and each centimetre of scalp hair reflects approximately one month of past exposure.9 A considerable number of studies have revealed that head hair better reflects a long-term environmental exposure than does blood and/or urine for toxic metals like Cd (as biomarker), and children's head hair may...
Bibliography
1. Hossny E, Mokhtar G, El-Awady M, Ali I, Morsy M, Dawood A. Environmental exposure of the pediatric age groups in Cairo City and its suburbs to cadmium pollution. Sci Total Environ. 2001; 273:135-46.
Pubmed
2. Jarup L, Berglund M, Elinder CG, Nordberg G, Vahter M. Health effects of cadmium exposure: a review of the literature and a risk estimate. Scand J Work Environ Health. 1998; 24(Suppl. 1):1-51.
Pubmed
3. Ryan D, Levy B, Levy BS, Pollack S, Walker B. Protecting children from lead poisoning and building healthy communities. Am J Public Health. 1999; 89:822-4.
Pubmed
4. Tuthill RW. Hair lead levels related to children's classroom attention deficit behavior. Arch Environ Health. 1996; 1:214-21.
5. Goyers RA. Toxic effects of metals. In: Klaassen CD, Amdur MO, Doull J, editors. Casarett and Doull's toxicology: the basic science of poisons. 5th ed. New York: Mc Graw-Hills; 1996. p. 691–736.
6. Mortada WI, Sobh MA, El-Defrawy MM, Farahat SE. Reference intervals of cadmium, lead and mercury in blood, urine, hair and nails among residents in Mansoura city, Nile Delta, Egypt. Environ Res. 2002; 90:104-10.
Pubmed
7. Krejpdo Z, Olejnik D, Wójciak RW, Gawęcki J. Comparison of trace elements in the hair of children inhabiting areas of different environmental pollution types. Polish J Environ Stud. 1999; 8:227-9.
8. Bass DA. Trace element analysis in hair: factors determining accuracy, precision, and reliability—statistical data included. Altern Med Rev. 2001; 6:472-81.
Pubmed
9. Al-Delaimy WK, Crane J, Woodward A. Is the hair nicotine level a more accurate biomarker of environmental tobacco smoke exposure than urine cotinine?. J Epidemiol Community Health. 2002; 56:66-71.
Pubmed
10. Fréry N, Girard F, Moreau T, Blot P, Sahuquillo J, Hajem S. Validity of hair cadmium in detecting chronic cadmium exposure in general populations. Bull Environ Contam Toxicol. 1993; 50:736-43.
Pubmed
11. Chlopicha J, Zadrodzki P, Zachwieja Z, Krooeniak M, Flota M. Use of pattern recognition methods in the interpretation of heavy metal content (lead and cadmium) in children's scalp hair. Analyst. 1995; 120:943-6.
Pubmed
12. Özden TA, Gökçay G, Ertem HV, Süoğlu ÖD , Kılıç A, Sökücü S. Elevated hair levels of cadmium and lead in school children exposed to smoking and in highways near schools. Clin Biochem. 2007; 40:52-6.
Pubmed
13. Nowak B. Contents and relationship of elements in human hair for a nonindustrialised population in Poland. Sci Total Environ. 1998; 8:59-68.
14. Granero S, Vicente M, Aguilar V, Martínez-Para MC, Domingo JL. Effects of beer as a source of dietary silicon on aluminium absorption and retention in mice. Trace Elem Electrolytes. 2004; 21:28-32.
15. Friedman LS, Lukyanova EM, Kundiev YI, Shkiryak-Nizhnyk ZA, Chislovska NV, Mucha A. Anthropometric, environmental, and dietary predictors of elevated blood cadmium levels in Ukrainian children: Ukraine ELSPAC group. Environ Res. 2006; 102:83-9.
Pubmed
16. Taylor J, DeWoskin R, Ennever FK. Toxicological profile for cadmium. US Department of Health and Human Services, Public Health Service. Agency for Toxic Substances and Disease Registry. 1999; 1-97.
17. Schmitt CJ. National contaminant biomonitoring program: concentrations of arsenic, cadmium, copper, lead, mercury, selenium and zinc in US freshwater fish, 1976–1984. Arch Environ Contam Toxicol. 1990; 19:731-47.
Pubmed
18. Gartrell MJ, Craun JC, Podrebarac DS, Gunderson EL. Pesticides, selected elements, and other chemicals in adult total diet samples, October 1980–March 1982. J Assoc Off Anal Chem. 1986; 69:146-61.
Pubmed
19. Mannino DM, Holguin F, Greves HM, Savage-Brown A, Stock AL, Jones RL. Urinary cadmium levels predict lower lung function in current and former smokers: data from the Third National Health and Nutrition Examination Survey. Thorax. 2004; 59:194-8.
Pubmed
20. Weyermann M, Brenner H. Alcohol consumption an smoking habits determinants of blood lead levels in a national population sample from Germany. Arch Environ Health. 1997; 52:233-9.
Pubmed
21. Nnorom IC, Asıbanjo O, Ojı-Nnorom CG. Cadmium determination in cigarettes available in Nigeria. Afr J Biotechnol. 2005; 1128-32.
22. Kosanovic M, Jokanovic M. The association of exposure to cadmium through cigarette smoke with pregnancy-induced hypertension in a selenium deficient population. Environ Toxicol Pharm. 2007; 24:72-8.
23. Willers S, Attewell R, Bensryd I, Schütz A, Skarping G, Vahter M. Exposure to environmental tobacco smoke in the household and urinary cotinine excretion, heavy metals retention, and lung function. Arch Environ Health. 1992; 47:357-63.
Pubmed
24. Sukumar A, Subramanian R. Relative element levels in the paired samples of scalp hair and fingernails of patients from New Delhi. Sci Total Environ. 2007; 372:474-9.
Pubmed
25. Willers S, Gerhardsson L, Lundh T. Environmental tobacco smoke (ETS) exposure in children with asthma-relation between lead and cadmium, and cotinine concentrations in urine. Respir Med. 2005; 99:1521-7.
Pubmed
26. Landsberger S, Wu D. The impact of heavy metals from environmental tobacco smoke on indoor air quality as determined by Compton suppression neutron activation analysis. Sci Total Environ. 1995; 173:323-37.
Pubmed
27. Baker RR, da Silva JRP, Smith G. The effect of tobacco ingredients on smoke chemistry. Part I: Flavourings and additives. Food Chem Toxicol. 2004; 42(Suppl.):S3-S37.
Pubmed
28. Rickert WS, Kaiserman MJ. Levels of lead, cadmium, and mercury in Canadian cigarette tobacco as indicators of environmental change: results of a 21-year study (1968–1988). Environ Sci Technol. 1994; 28:924-7.
Pubmed
29. Paako P, Kokkonen P, Anttila S, Kalliomaki PL. Cadmium and chromium as markers of smoking in human lung tissue. Environ Res. 1989; 49:197-207.
Pubmed
30. Gairola CG, Wagner GJ. Cadmium accumulation in the lung, liver, and kidney of mice and rats chronically exposed to cigarette smoke. J Appl Toxicol. 1991; 11:355-8.
Pubmed
31. Hemdan NY, Emmrich F, Sack U, Wichmann G, Lehmann J, Adham K. The in vitro immune modulation by cadmium depends on the way of cell activation. Toxicology. 2006; 222:37-45.
Pubmed
32. Mulligan MS, Warner RL, McDuffie JE, Bolling SF, Sarma JV, Ward PA. Regulatory role of Th-2 cytokines, IL-10 and IL-4 in cardiac allograft rejection. Exp Mol Pathol. 2000; 69:1-9.
Pubmed
33. Oettgen HC, Geha RS. IgE regulation and roles in asthma pathogenesis. J Allergy Clin Immunol. 2001; 107:429-40.
Pubmed
34. Lawrence DA, Mc Cabe MJ. Immunomodulation by metals. Int Immunopharmacol. 2002; 2:293-302.
Pubmed
35. Ribeiro SA, Furuyama T, Schenkman S, Jardim JR. Atopy, passive smoking, respiratory infections and asthma among children from kindergarten and elementary school. Sao Paulo Med J. 2002; 120(July (4)):109-12.
Pubmed
36. Kirschvink N, Martin N, Fievez L, Smith N, Marlin D, Gustin P. Airway inflammation in cadmium-exposed rats is associated with pulmonary oxidative stress and emphysema. Free Radic Res. 2006; 40:241-50.
Pubmed
37. Morrison D, Rahman I, Lannan S, MacNee W. Epithelial permeability, inflammation, and oxidant stress in the air spaces of smokers. Am J Respir Crit Care Med. 1999; 159:473-9.
Pubmed
38. Balharry D, Sexton K, BéruBé KA. An in vitro approach to assess the toxicity of inhaled tobacco smoke components: nicotine, cadmium, formaldehyde and urethane. Toxicology. 2008; 244:66-76.
Pubmed
39. Lampe BJ, Park SK, Robins T, Mukherjee B, Litonjua AA, Amarasiriwardena C, et-al. Association between 24-hour urinary cadmium and pulmonary function among community-exposed men: the VA normative aging study. Environ Health Perspect. 2008; 116:1226-30.
Pubmed
40. Hart BA. Cellular and biochemical response of the rat lung to repeated inhalation of cadmium. Toxicol Appl Pharmacol. 1986; 82:281-91.
Pubmed
41. Lai YL, Diamond L. Cigarette smoke exposure does not prevent cadmium-induced alterations in rat lungs. J Toxicol Environ Health. 1992; 35:63-76.
Pubmed
Razi, C.H.a; Akın, K.O.b; Harmancı, K.c; Özdemir, O.d; Abacı, A.d; Hızlı, Ş.d; Renda, R.d; Çelik, A.d
aKecioren Education and Research Hospital, Department of Pediatric Allergy, Turkey
bKecioren Education and Research Hospital, Department of Biochemistry, Turkey
cDışkapı Pediatric Education and Research Hospital, Department of Pediatric Allergy, Turkey
dKecioren Education and Research Hospital, Department of Pediatry, Turkey