1. Introduction
Accumulation of toxic metals in infants and children is of serious concern worldwide, from the viewpoint of their harmful effects on normal growth and development of infants and children [
1,
2,
3,
4,
5,
6,
7,
8]. The pathogenic roles of some toxic metals have been interested in various neurodegenerative diseases [
9,
10], and mercury, lead, aluminum, and cadmium were reported to cause some fractions of neurodevelopmental disabilities [
4,
5,
6,
7,
8] and retardation of children’s growth [
11,
12]. In addition, we demonstrated zinc- and magnesium deficiency and toxic metal burdens such as aluminum, cadmium, lead, arsenic and mercury in autistic children [
4,
5,
13,
14], particularly in the infantile subjects aged 0–3 years, and statistically significant inverse relationship between zinc and lead, between zinc and cadmium, and between zinc and aluminum concentrations in these children, indicating the presence of “Infantile Time Window” in neurodevelopment disorders and for intervention [
4,
5,
14]. Cusick and Georgirff pointed out the importance of micronutrients including iron and zinc in early childhood before the age of 3 years in brain development [
15]. The critical role of zinc deficiency in etiology of autism has been suggested by recent studies that estimated fetal and postnatal exposure profiles of toxic metals and essential minerals [
6,
7,
16], and that investigated AMPA (α-amino-3-hydroxy-5-methyl-4-isoxazolepropionicacid) receptor subunit switch controlled by zinc and Shank in developing neurons [
17,
18]. Hagmeyer et al. [
19] suggested the beneficial effects of zinc supplementation in treatment of autism and Phelan McDermid Syndrome.
This study was undertaken to investigate the incidence and extent of accumulation of toxic metals in infants/children and to examine whether their toxic metal burdens are affected by those in their mothers. In addition, the concentrations of 13-kind essential minerals in the same subjects were determined simultaneously and the possible relationship between toxic metal burden and deficiency in some essential metals was examined.
3. Results
Metallomics analysis of 26-kind of trace bio-elements including toxic metals in scalp hair samples of 77 pair subjects of Japanese infants/children (28 males and 49 females; 0–11 year-old; mean age: 5.2 years old) and their mothers (mean age: 38.4 years old) were investigated in this study. Geometric mean concentration of mercury in infants/children was not statistically different from that in their mothers, and a high-significant close correlation (β = 0.758, r = 0.539,
p < 0.0001) was observed between mothers and infants/children (
Figure 1a), suggesting equivalent exposure to mercury in infants/children and mothers. A significant but less intimate mother/child relationship was observed for arsenic (β = 0.301, r = 0.433), lead (β = 0.444, r = 0.471), and aluminum (β = 0.379, r = 0.451) (
Figure 1b–e), and these mean burden levels in infants/children were significantly higher than those in their mothers (
Table 1). In particular, for lead, cadmium and aluminum, these mean burden levels in infants/children were approximately three times higher than those in their mothers, and the burden levels in some individuals exhibited several tens of times higher than those in their mothers. Namely the maximum values for lead, cadmium, and aluminum in infants/children were 11,930 (1-year-old girl), 241 (2-year-old boy) and 40,740 ng/g (2-year-old boy), which were 35, 41, and 12 times higher than mean levels in the mothers, respectively (
Table 1).
Infants/children were divided into three groups by age; 0–3, 4–9, and 10–11 year-old, and mean concentrations of the five toxic metals in each group were calculated and compared to their mothers (
Figure 2). The mean burden levels of lead, cadmium, and aluminum in infant group of 0–3 year-olds were highest, high-significantly different from their mothers (
p < 0.0001) and declined with age (
Figure 2c–e), while such an age-dependency was not observed in those of mercury and arsenic (
Figure 2a,b).
Among essential minerals, the levels of some elements, such as chromium, molybdenum, manganese, iron, and iodine in infants/children were significantly nearly two times higher than those in their mothers as well as for the above toxic metals. In contrast, the limited three elements of zinc, magnesium and calcium in infants/children were significantly lower than those in their mothers (
p < 0.0001) (
Table 2), and 29, 9 and 8 individuals (37.7, 11.7 and 10.4 %) in the infants/children group were estimated to be zinc-, magnesium- and calcium-deficient, respectively. There were a few or no individuals with deficiency in iron, copper, manganese, chromium, and molybdenum.
The mutual relationship of these toxic metals and essential minerals were examined by multiple regression analysis, and the correlation coefficients between some metal-metal combinations are shown in
Table 3. In infants/children, statistically significant positive correlations were observed between cadmium and lead (r = 0.616,
p < 0.0001), aluminum and lead (r = 0.347,
p = 0.002), and aluminum and iron (r = 0.601,
p < 0.0001). In their mothers, similar positive relationships were observed in each metal-metal combination (r = 0.438,
p < 0.0001; r = 0.273,
p = 0.016; r = 0.426,
p = 0.0001, respectively). About iron element, not only these toxic metals but also various metals such as manganese, cobalt, chromium, molybdenum, and nickel so on positively correlate with iron (data not shown), suggesting co-burdens of iron with a variety of heavy metals.
In contrast, statistically significant inverse correlations were observed between zinc and lead (r = −0.267,
p = 0.019), between magnesium and arsenic (r = −0.514,
p < 0.0001) and between zinc and molybdenum (r = −0.331,
p = 0.003) in infants/children, and in mothers between magnesium and arsenic (r = −0.649,
p < 0.0001). It is emphasized that zinc element is only one heavy essential metal exhibiting inverse relationship between various heavy metals, as previously reported [
4,
5,
20]. Among minerals, the highest positive correlation is observed between calcium and magnesium in both the infants/children and mothers group (r = 0.871 and 0.820, respectively,
p < 0.0001).
Representative metallome profiles of four individuals with high burdens of some toxic metals and/or with deficiency in essential metals are shown in
Figure 3, together with those of their mothers. The first (
Figure 3a) and second (
Figure 3b) cases showed a marked zinc deficiency with high burdens of cadmium and lead, while concentrations of these three metals in the mothers were almost normal levels. In the first case, a marked high burden of vanadium was also observed, and its burden level was nearly four times higher than that of her mother. The third and fourth cases, whose mother had a habit of smoking, showed high accumulation of not only cadmium and lead, but also vanadium, copper or lithium than the respective mother, while zinc levels were normal (
Figure 3c,d).
4. Discussion
The pathogenic roles of some toxic metals such as mercury, lead, aluminum, or cadmium have been interested in various neurodegenerative diseases [
1,
2,
3,
8,
9,
10]. These toxic metals are also known to cause some fraction of neurodevelopmental disabilities [
4,
5,
6,
7,
14]. Gardner et al. [
11] reported that early-life cadmium exposure had the strongest and most consistent inverse association with children’s growth in terms of weight and height. Choi et al. [
12] demonstrated that post-birth weight gain was negatively associated with blood levels of lead, and similar negative association for current head circumference with arsenic and lead.
In this study, the geometric mean concentration of mercury in infants/children was of similar level to that in their mothers (
Table 1), and statistically high-significant close correlation between mothers and infants/children was observed (
Figure 1a), suggesting equivalent exposure to mercury in infants/children and mothers due to their common lifestyles. A significant but less intimate mother/child relationship was observed for arsenic, lead and aluminum (
Figure 1b–e), and the proportion of infants/children with higher burdens than mother was larger than that of mercury, and these mean burden levels in infants/children were significantly higher than those in their mothers (
Table 1). Remarkably, the mean burden levels of lead, cadmium and aluminum in infants/children were found to be approximately three times higher than those in their mothers, the differences being statistically high-significant (
Table 1). The burden levels of these three toxic metals in some infants/children were several tens of times higher than those in mothers (
Figure 1c–e). It should be noted that the burden levels of lead, cadmium and aluminum in mothers, whose infants/children showed maximal or sub-maximal levels, were not so high. These findings indicate that these three toxic metals are liable to accumulate in infants/children more than in their mothers.
The burden levels of lead, cadmium, and aluminum in infants of 0–3 year-old were highest and declined with age inversely, while such an inverse age-dependency was not observed in those of mercury and arsenic (
Figure 2). These results are coincident with our previous study, suggesting that the three toxic metals of lead, cadmium and aluminum are characteristic liable to accumulate in infants and different from mercury and arsenic which have a character accumulating in adults age-dependently [
3]. In addition, statistically significant positive correlations were observed between cadmium and lead, and between aluminum and lead in both infants/children and mothers (
Table 3), suggesting that the mechanisms of distribution, detoxification, and excretion of these three toxic metals are different from those of mercury and arsenic. High close correlation between aluminum and iron in infants/children (
Table 3) seems to suggest multiple pollutions with some related-metals such as manganese and chromium, as shown in
Table 2.
In contrast to toxic metals, the mean concentrations of magnesium, calcium and zinc in infants/children were significantly lower than those in their mothers, and 29 and 9 individuals (37.7 and 11.7%) in the 77 child subjects were estimated to be zinc- and magnesium-deficient, respectively (
Table 2). In addition, statistically significant inverse correlations were observed between concentrations of zinc and lead, and between magnesium and arsenic in infants/children (
Table 3). A significant inverse correlation between magnesium and arsenic was also observed in their mothers, but not between zinc and lead, suggesting characteristic interaction between zinc and lead in infants/children [
4,
5,
14]. No significant correlation between zinc and cadmium or between zinc and aluminum was observed in this study, but our previous study for larger number of autistic children has revealed high burdens of lead, cadmium and aluminum accompanied by deficiency in zinc and magnesium, and significant relationships between these toxic metal burdens and zinc deficiency [
3,
4,
5,
14,
20]. It is, therefore, speculated that the relative and absolute deficiency in antagonistic metals such as zinc and magnesium are associated with the accumulation of toxic metals as observed in this study.
In fact, dietary restriction-induced zinc deficiency has been reported to up-regulate intestinal zinc-importer (Zip4) and induce the increase in Zip4 protein located to the plasma membrane of enterocytes [
21,
22,
23,
24]. This adaptive response to zinc deficiency is known to induce increasing in the risk of high uptake of toxic metals such as cadmium and lead [
25]. Thus, infants with zinc deficiency are liable to be exposed to increased risk of absorbing high amount of toxic metals and retaining them in their body. In addition, maternal cigarette smoking was reported to be associated with lower zinc and higher cadmium and lead concentrations in their neonates [
26]. Because of their high distribution property to bone tissue, during pregnancy and lactation, these toxic metals accumulated in the maternal bone matrix are co-transferred with calcium and magnesium to fetal and newborn bodies through increased bone-resorption [
27,
28].
As shown in
Figure 1, toxic metal burden levels in infants appear to be affected profoundly by those in their mothers through placental transfer during pregnancy and breastfeeding after birth, which are affected by foods/drinks, smoking, or passive smoking and other environmental factors. High contents of toxic metals (cadmium, lead and aluminum) in tobacco and high exposure to these toxic metals in smokers and their family members have been reported [
29,
30,
31,
32]. Toxic metal burdens in infants are also affected by infant formulas or weaning foods: higher concentration of cadmium in soy-based and cereal-based formulas than cow’s milk formulas and high content of aluminum in infant formulas and vaccine preparations have been reported [
33,
34,
35,
36,
37].
It is known that breast-fed infants are prone to develop trace element deficiency and that alopecia and dermatitis are attributable to zinc deficiency. Furthermore, “follow-up milk” formulas (nutritional supplement for infants aged over 6-month) used in Japan contain practically iron and calcium fortified but neither zinc nor copper, and the dependence on the follow-up milk formulas as the main source of nutrition is reported to be associated with a high risk of zinc deficiency [
38].
Recently, Fiore et al. [
8] reported that there was a negative, significant association between hair zinc level and severity of autistic symptoms (defective functional play and creativity and increase of stereotyped behavior), and lead, molybdenum and manganese hair levels were inversely correlated with cognitive level (full intelligence quotient) in autism spectrum disorder (ASD) individuals.
Thus, it is suggested that supplementation of deficient essential metals such as zinc and magnesium in early period of infant/child is expected to ameliorate the body metal imbalances and probably the clinical symptoms related to their deficiencies and toxic metal burdens in the early neurodevelopment period, named “Infantile Time Window” or “First 1000 Days” [
4,
5,
13,
14,
15,
19,
39,
40].
Arnold et al. [
41] reported that mean serum zinc levels were significantly lower in both autism and attention deficit/hyperactivity disorder (ADHD) groups, and that serum zinc level correlated inversely with parent- and teacher-rated inattention in ADHD children. Furthermore, it is reported that zinc supplementation reduces symptoms of hyperactivity, impulsivity, and impaired socialization in ADHD patients [
42,
43]. Other preliminary human study showed that zinc supplement as an adjunct to methylphenidate has favorable effects in the treatment of ADHD children [
44]. The critical role of zinc deficiency in etiology of ASD has been suggested by recent studies showing high uptake of neurotoxin lead and reduced uptake of essential minerals manganese and zinc during specific developmental windows [
4,
5,
6] and disruption of zinc-copper rhythmicity [
7] in those children. Furthermore, it has been suggested that zinc signaling through Shank2 and Shank3 controls the AMPA receptor subunit switch in developing neurons, and that zinc deficiency may impair synaptic maturation and circuit formation that underlie ASD etiology [
17,
18,
19]. Recently, Miyake et al. [
45] found the association between maternal smoking and DNA hypo-methylation of zinc-dependent Shank2 synaptic scaffolding gene in cord blood, suggesting the epigenetic and unfavorable effect of smoking on neurodevelopment in infants and fetus.
Kozielec et al. [
46] reported that in hyperactive children with ADHD, magnesium deficiency was found in the 95% of the subjects and reported that a significant decrease of hyperactivity and increase in hair magnesium contents has been achieved in the group of ADHD children given six months of magnesium supplementation [
47]. Mousain-Bosc et al. [
48] also reported that 52 hyper-excitable children have low intra-erythrocyte magnesium levels with normal serum magnesium values and that magnesium/vitamin B6 supplementation can restore the erythrocyte magnesium levels to normal and improve their abnormal behaviors. They also reported that 33 children with clinical symptoms of pervasive developmental disorder (PDD) or autism exhibit significantly lower red blood cell magnesium values and that the combination therapy with magnesium/vitamin B6 for six months improved significantly PDD symptoms with concomitant increases in intra-erythrocyte magnesium values [
49].
Such an evidence-based nutritional approach supplementing deficient nutrients and detoxifying accumulated toxic metals is of great importance for normal growth and development of infants and children, and probably yields a new pathway into prevention and treatment of neurodevelopment disorders such as ASD, ADHD and also learning disorders [
4,
5,
13,
19,
50].
The present study was cross-sectional, and detailed information about health conditions, dietary habits and environmental factors of the subjects was lacking. Nevertheless, a careful assessment and monitoring of such infants and children suffered from some essential metal deficiencies and/or toxic metal burdens revealed in this study would be essential, and if necessary, supplementing deficient metals should be considered. Therefore, it is expected that larger epidemiological and intervention studies will clarify the pathogenic relationship between infantile metal imbalances described above and neurodevelopment disorders and thereby provide reasonable and essential procedures for their normal growth and neurodevelopment. In addition, clinical metallomics (or “mineralomics”) analysis with another micronutrient omics “vitaminomics” analysis will be used as an essential tool for personalized precision medicine in the near future.