the effect of age, sex, smoking habit and hair color on the composition of hair
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Environmental Toxicology and Pharmacology 22 (2006) 5257
The effect of age, sex, smoking habit and hair coloron the composition of hair
K. Chojnacka , H. Gorecka, H. Gorecki
Institute of Inorganic Technology and Mineral Fertilizers, Wrocaw University of Technology, ul. Smoluchowskiego 25, 50-372 Wrocaw, Poland
Received 10 October 2005; accepted 23 November 2005
Available online 7 February 2006
Abstract
Hairsamples(N= 83)werecollected between theyears 1996 and2003 from inhabitants of Wrocaw, a city located in Lower Silesia,south-westernPoland (urbanized and industrialized region). The concentrations of 33 elements: Ca, Mg, Na, K, Cu, Zn, P, Fe, Mn, Cr, Se, B, Co, Mo, Si, V, Ni, Be,
Hg, Cd, Al, Pb, As, Ba, Au, Pt, Ag, Sr, Sn, Ti, W, Sb and Zr in hair were determined by inductively coupled plasma-mass spectrometry (ICP-MS)
and inductively coupled plasma-atomic emission spectrometry (ICP-AES) techniques. The effect of age, sex, smoking habits and hair color on the
elemental composition of hair was investigated. Also, the obtained results were compared with literature data. It was found that the composition of
hair varied with age, sex, hair color and smoking habits. This concerned the majority of elements except Ti, Se, Mn, Ni, Hg, Cd, As, Co (in the case
of effect of age), Al, Cd, Co (sex), Cd, K, Ag, Ca, Co, Be (smoking habit), P, Fe, Al, Mn and Cr (hair color). Therefore, reference valuesfor the level
of the remaining elements should be normalized according to age, sex, smoking habit and hair color. This would make hair analysis more reliable.
2006 Published by Elsevier B.V.
Keywords: Smoking habit; Hair color; Hair analysis
1. Introduction
Human hair has recently been used as a tool that enabled
to assess the environmental exposure to heavy metals (as
biomarker) and metabolic status of an organism concerning
essential trace elements (Bencko, 1995; Ashraf and Jaffar, 1997;
Ashraf et al., 1995). Several advantages of this method were
found, although several limitations were encountered in the
application of hair analysis in, for instance, clinical medicine
(Rodushkin and Axelssom, 2000). The main problems that arose
were related to theinterpretation of theresults,sincethe extentto
which elements are accumulated in hair could be a characteristic
of an individual person.
Undoubtedly, hair analysis is a non-invasive method of diag-nosis. Hair can be easily sampled, collected, stored and trans-
ported. Moreover, it provides a long-term information. Also, the
concentration of elements in hair is high when compared with
body tissues or fluids (Nowak, 1998).
Release of elements from body tissues and fluids to hair is a
method of detoxification of an organism. The excess of a given
Corresponding author. Tel.: +48 71 3203902; fax: +48 71 3203469.
E-mail address:[email protected] (K. Chojnacka).
element, either essential or toxic, can be safely deposited in hair.However, if the content of a given element in hair is elevated, it
does notnecessarilymean that a personsuffersfrom high content
of this element. It simply means that this element entered an
organism and was deposited in hair. This process occurs during
hair growthand thus thecompositionof hair provides a historical
insight of individual exposure andmineral statusof an organism.
Difficulties with the proper interpretation of results of hair
analysis are due to the absence of well defined reference concen-
tration ranges, problems associated with differentiating between
endogenous and exogenous deposition, inconsistency of hair
concentration anomalies with nutritional status and clinical
symptoms (Rodushkin and Axelssom, 2000).The difficulties in
establishing normal or reference ranges are also due to the nat-
ural variance of hair composition as a possible consequence of
age, sex, hair color, ethnical and geographic origin, dietary fac-
tors, etc. (Miekeley et al., 1998; Sharma et al., 2004; Batzevich,
1995).
The aim of the present work was to investigate the composi-
tion of hair of the population group living in an urbanized and
industrialized region of south-western Poland (Wrocaw). The
dependence of hair content on age, sex, tobacco smoking habits
and hair color was examined.
1382-6689/$ see front matter 2006 Published by Elsevier B.V.
doi:10.1016/j.etap.2005.11.006
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K. Chojnacka et al. / Environmental Toxicology and Pharmacology 22 (2006) 5257 53
2. Materials and methods
2.1. Hair samples
The studied material was sampled in the years 19962003 from 83 subjects
living in an urban population group in south-western Poland (Wrocaw). Hair
(directly after washing with shampoo and drying) was sampled from nape of the
neck. Samples were washed using acetone and distilled water (Nowak, 1998).
Hair was digested and afterwards underwent multielemental analysis with ICP-
MS and ICP-AES.
2.2. Digestion of samples
Hair samples were digested in Microwave Digestion System CEM 2000
(USA) in closed Teflon bombs. Hair (ca. 1.3 g) was mineralized with concen-
trated nitric acid (7.5 ml). The reagent and digestion conditions were chosen in
Fig. 1. (ah) Concentrations of elements in human hair for 015 years (N= 8), 1525 years (N= 21), 2545 years (N= 29) and 4565 years (N= 25) of age (mg/kg).
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order to achieve complete mineralization and decomposition of solid phase into
liquid phase. All the used reagents were of trace pure grade (from Merck). After
digestion, the solutions were filled up to 75 ml with deionized water.
2.3. Analytical methods
The concentrations of 33 elements: Ca, Mg, Na, U, Cu, Zn, P, Fe, Mn, Cr,
Se, B, Co, Mo, Si, V, Ni, Be, Hg, Cd, Al, Pb, As, Ba, Au, Pt, Ag, Sr, Sn,
Ti, W, Sb and Zr in hair were determined. Multielemental analysis of digested
hairsampleswas performedwith inductively coupled plasma massspectrometry
(ICP-MS;VarianUltraMass 700, Australia) forthe elements,exceptalkalimetals
and alkaline earth metals, that were analyzed with inductively coupled plasma-
atomic emission spectrometry (ICP-AES; PU 7000 from Philips, Cambridge,
UK) connectedwith ultrasonic nebulizer CETAC (USA). The analytical process
was controlled by the use of matrix standard NCS Reference MaterialHuman
Hair NCS ZC81002 from China National Analysis Center. The samples were
Fig. 2. (ah) Concentrations of elements in female (F, N= 41) and male (M,N= 42) hair as well as in hair of non-smokers (N-S,N= 63) and smokers (S,N=20)
(mg/kg).
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K. Chojnacka et al. / Environmental Toxicology and Pharmacology 22 (2006) 5257 55
Fig. 2. (Continued).
analyzed in three repeats (the relative standard deviation of the measurement
was as accepted for Certified Reference Material). Mercury was analyzed with
an atomic absorption mercury analyzer (AMA 254, Czech Republic).
3. Results and discussion
Hair analysis of 83 individualsliving in south-western Poland
was carried out. The statistical analysis, including multi-variant
analysis, was shown previously (Chojnacka et al., 2005). Table 1
presents mean values and standard deviations of the concen-
tration of 33 elements in hair (Chojnacka et al., 2005). When
comparing with reference ranges elaborated for an unexposed
population(Rodushkin and Axelssom, 2000), the concentrations
of Ag, Al, Ca and Na elements were higher in the examined sub-
jects.The studied population was divided into four age groups:
015 years (N= 8), 1525 years (N= 21), 2545 years (N=29)
and 4565 years (N= 25).Fig. 1shows mean concentration of
elements for each studied group. It was found that the level of
the majority of elements differed significantly between the age
groups (when comparing the average levels). Moreover, tenden-
cies of the variation in the content of elements were observed.
For this reason, the elements could be classified into the follow-
ing categories (years):
- (Ca) High level at
1545
Low level at 45
- (Na, K) High level at 45
Low level at 1545
- (P, Al, B, Pb, Fe, Cr,
Au, Pt, Sb, Be, W)
High level at 15
- (Cu, V, Sn) High level at >45 Low level at 25 Low level at
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children (
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