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Research Article

Materials and Methods Top

The study was conducted according to the Helsinki II Declaration (World Medical Association 2000) after informed oral and written consent of the parents. The ethical committees (Finland: 7/1996; Denmark: KF01-030/97) and the Danish Data Protection Agency (1997-1200-074) approved the study.

Study population

We obtained breast milk samples and placentas from a joint prospective, longitudinal cohort study performed 1997–2001 at Turku University Hospital, Turku, Finland, and the National University Hospital (Rigshospitalet, Hvidovre Hospital), Copenhagen, Denmark. This binational study aimed at establishing contemporary prevalence rates for cryptorchidism and hypospadias and evaluating risk factors by means of questionnaires and biological samples (blood, placentas, breast milk). Exposure measurements were prospectively planned to include persistent and nonpersistent chemicals, some of which have been previously reported (Damgaard et al. 2006; Main et al. 2006a; Shen et al. 2005, 2006, 2007). Recruitment strategy, inclusion criteria, and clinical examination of the children (i.e., the identification of cryptorchidism) have been previously described (Boisen et al. 2004; Main et al. 2006b; Suomi et al. 2006) and were strictly standardized. Boys with normally descended testes, including retractile testes, were used as controls in this study under the terms “controls” or “healthy boys.” Boys with undescended testes (nonpalpable, inguinal, suprascrotal, high scrotal), either uni- or bilaterally at birth, were included in the group of cryptorchid boys.

All boys were examined at birth and at 3 months of age before the results of chemical analyses were known. Birth weight and length were obtained from hospital records. The supine length of the children was measured with infantometers (Denmark: Kidimeter, Raven Equipment Ltd., Essex, United Kingdom; Finland: Pedihealth Ky, Oulu, Finland). Weight was measured on a digital scale (Baby scale model; Solotop Oy, Helsinki, Finland). Weight for gestational age was calculated using national standards as percent deviation from the expected mean (Marsál et al. 1996; Pihkala et al. 1989), −22% being equivalent to −2 SDs.

Biological samples

In Denmark biological samples were collected from all participants (case–cohort design). In Finland, due to lack of storage space, biological samples were collected from boys with cryptorchidism at birth and matched controls [matching criteria: parity, maternal smoking (yes/no), diabetes (yes/no), gestational age (± 7 days), and date of birth (± 14 days)] as a nested case–control design.

From this bio-bank, we selected 280 placentas (168 Danish/112 Finnish) and 130 breast milk samples (65 Danish/65 Finnish) for PBDE measurements; this number was determined by funding. Birth examination data were used for classification of cryptorchid and healthy boys.

In Finland, placentas were selected from 56 case–control pairs, in which both placentas were available. In Denmark, all available placentas from cryptorchid boys were chosen (n = 39). Control placentas were selected randomly from the total Danish cohort (n = 129).

Hereafter, 65 breast milk samples were selected for each country, with the aims, if possible, of having equal numbers of samples from boys with and without cryptorchidism and of including the same mothers as for placenta analyses. Only samples with a volume > 125 mL were included to ensure that all chemicals could be analysed. Milk from mothers of 29 cryptorchid boys and 36 randomly chosen control boys was included in Denmark. In Finland, milk samples were chosen from mothers of cryptorchid boys (n = 33), matched controls (n = 18), or random controls (n = 14).

For 86 boys, milk and placentas could be selected from the same mother–child pair (10 Danish boys with cryptorchidism, 33 Danish controls, 20 Finnish boys with cryptorchidism, 23 Finnish controls).

Collection of samples

Whole placentas were collected by the midwives and frozen immediately in two layers of polyethylene bags (−20°C). Placentas were not bled before storage.

Each mother collected one breast milk sample. We wished to assess the average concentration of PBDEs during the period preceding the endogenous hormone surge in infants. Thus, each sample consisted of several small aliquots collected over successive feedings over several weeks and frozen in household freezers in 250-mL Pyrex glass bottles (1515/06D; Bibby Sterilin, Staffordshire, UK) with Teflon coated caps. The mothers were instructed orally and in writing to feed the baby, and then to sample aliquots (hind milk), beginning 1 month after birth. We chose this start point after discussion with the ethics committee for human subject studies to ensure that breast-feeding had been well established. Mothers were instructed to collect samples into a clean household glass or porcelain container, avoiding, if possible, the use of breast pumps, and to freeze every portion immediately. Breast milk was delivered frozen to the hospital at the 3 months’ examination and stored at −20°C. In 57 of the 65 Danish mothers, but no Finnish mothers, information on breast pump use was obtained at sample delivery; 26 (46%) had used a pump on one or more occasions. No information was obtained on the type of breast pump (glass or plastic).

Blood samples

Venous nonfasting blood samples (4 mL) were drawn from the infants at the 3 months’ examination (median age, 3.0 months; range, 2.4–4.1); the overall success rate of obtaining a sample in the study was 74%. After clotting, the blood samples were centrifuged and the sera were separated and stored at −20°C. All samples were analysed as duplicates and blinded for the technician at one laboratory (Rigshospitalet, Denmark) for reproductive hormones. Each run contained samples of both cryptorchid and healthy boys from both countries (up to 160 samples per analysis) to minimize any effect of interassay variation.

Hormone analyses

We analyzed serum follicle-stimulating hormone (FSH), luteinizing hormone (LH), and sex hormone–binding globulin (SHBG) using time-resolved immunofluorometric assays (Delfia, Wallac Inc., Turku, Finland). Detection limits were 0.06 and 0.05 IU/L for FSH and LH, respectively, and 0.23 nmol/L for SHBG. The intra- and interassay coefficients of variation (CV) were < 5% in both gonadotropin assays and < 6% for SHBG. We measured serum testosterone by radioimmunoassay (Coat-a-Count; Diagnostic Products Corp., Los Angeles, CA, USA), with a detection limit of 0.23 nmol/L and intra- and interassay CVs < 10%. Free testosterone index was calculated: (testosterone × 100)/SHBG. We analyzed serum inhibin B by a double antibody enzyme-immunometric assay (Main et al. 2006b). The detection limit was 20 pg/mL, and intra- and interassay CVs were < 15 % and < 18 %, respectively. Ratios between hormones were calculated: LH/testosterone, LH/free testosterone, FSH/inhibin B.

Analysis of PBDE

All PBDE analyses for both milk and placenta were performed at the laboratory at the Department of Environmental Health in Kuopio, Finland. Placentas were defrosted, and the umbilical cord and all readily removable membranes were discarded. Whole placentas were homogenized in a mixer (Büchi Mixer B-400; Büchi Laboratories AG, Flawil, Switzerland), and 75 g of the homogenate was lyophilized. Dried homogenate was pulverized in a mortar and slurry was made by adding dichloromethane and cyclohexane (1:1 vol/vol) and concentrated sulphuric acid. This slurry was spiked with six ¹³C-labeled PBDE internal standards (BDEs 28, 47, 77, 99, 153, and 183) (Wellington Laboratories Inc., Guelph, Canada). Fat was not determined, and fat-based results were relying on the gravimetrically measured fat contents obtained from a German partner in this European Commission project (Shen et al. 2005, 2006, 2007).

Breast milk samples (average volume, 70 mL) were thawed in sample bottles in a water bath (40°C) for 1 hr and homogenized. Fat was extracted with a mixture of diethyl ether and hexane (1:1.4 vol/vol) after addition of sodium oxalate solution and ethanol (1:5 vol/vol). Fat content was determined gravimetrically after exchange of the solvent to hexane. An average 1.5 g of fat was spiked with the same set of internal standards used with placenta.

The procedure for decomposition of fat and sample cleanup has been described previously (Kiviranta et al. 2004). We quantified 14 PBDE analytes (BDEs 28, 75, 71, 47, 66, 77, 100, 119, 99, 85, 154, 153, 138, and 183) by selective-ion recording using a high resolution mass spectrometer (Autospec Ultima; Micromass Inc., Manchester, UK) at resolution 10,000. Gas chromatographic separation of the PBDEs was performed with a Hewlett Packard 6890 gas chromatograph with fused silica capillary column (DB5-MS, 60 m, 0.25 mm, 0.25 μm; J&W Scientific, Folsom, CA, USA). As a recovery standard for internal PBDE standards polychlorinated biphenyl congener 159 was used.

In the analysis of PBDEs at the Department of Environmental Health (National Public Health Institute, Kuopio, Finland), the technicians and chemists were blinded. Laboratory and cross-sample contamination was monitored by analyzing procedural blank samples. The concentrations of these blank samples were much lower than the concentrations in placenta and breast milk—on average, 3.6 and 2.6% of the average sum of PBDEs in placenta and milk, respectively.

Recoveries of individual internal PBDE standards were > 60%. Median limit of quantification (LOQ) for placentas corresponding to a signal to noise ratio of 3:1, was 0.006 ng/g fat (range, 0.004–0.14 ng/g fat). Corresponding LOQs for breast milk were 0.004 ng/g fat (range, 0.0003–0.12 ng/g fat). In placenta, CVs for individual congeners were 10–20%, and > 20% at concentration levels 0.1–1 ng/g fat and < 0.1 ng/g fat, respectively. In breast milk samples corresponding values were < 10%, 10–20%, and > 20% at concentrations levels > 1 ng/g fat, 0.1–1 ng/g fat, and < 0.1 ng/g fat, respectively. Concentrations below the LOQ were considered to be equal to nil (lower bound results). The laboratory has successfully participated in interlaboratory comparison studies of PBDEs in different biological matrices including breast milk (Becher et al. 2001; Småstuen and Becher 2004; Småstuen and Becher 2005). The Finnish Accreditation Service (FINAS; Espoo, Finland) has verified the competence of the laboratory (testing laboratory T077) in performing PBDE analyses in biological samples according to the European Standard (EN ISO/IEC 17025).

Statistics Top

Population characteristics are given as medians and percentiles (2.5th, 97.5th). Differences between boys with and without cryptorchidism and between Danish and Finnish populations were analysed by Mann-Whitney U-test. Eighty-six boys participated with both breast milk and placenta samples.

We tested country differences for (log-transformed) PBDE concentrations in breast milk and placenta by multiple linear regression including maternal age, parity (1, 2 and ≥ 3) and prepregnancy body mass index (BMI; kilograms per square meter) in the model.

Correlations between individual PBDE congener concentrations, and between PBDE concentrations and date of childbirth within the Danish and Finnish cohort, respectively, were tested by Spearman correlation on non-transformed data. For each country the date of birth for the first child was set at zero; the date of birth for all consecutive children was then calculated as number of days elapsed since the first child of the same country-specific cohort. This variable was applied to control for any time trends in flame-retardant concentration in the study period 1997–2001.

We tested differences in PBDE concentrations between boys with and without cryptorchidism in a multiple regression model, including as covariates maternal age, parity, maternal prepregnancy BMI, and date of childbirth within the cohort (days) to control for factors that could affect PBDE concentrations in the sample. Prematurity and small size for gestational age (SGA) are well-known risk factors for cryptorchidism. Because the number of premature (5 Danish, 3 Finnish) and SGA children (3 Danish, 1 Finnish) was small in this study, analyses were carried out both with and without inclusion of these parameters. Analyses were carried out only for the most abundant seven congeners in breast milk (and their sum) and for the most abundant five congeners in placenta.

We used multiple linear regression analysis to assess the correlation between serum levels of reproductive hormones (log-transformed LH, FSH, SHBG, inhibin B), square root–transformed serum testosterone or free testosterone index, and log-transformed PBDE concentrations in breast milk. Covariates included in these analyses were country of origin, testicular position (cryptorchidism/control), and age at blood sampling (months).

Results Top

There were no significant differences in maternal age, reported smoking, and parity between cryptorchid and control boys (Tables 1 and 2). Gestational age and birth weight were slightly lower in cryptorchid Danish (but not Finnish) boys than in controls. Diabetes was more prevalent in Finnish (but not Danish) mothers of cryptorchid boys than in their controls, because we could not always find controls matched by this criterion. The date of childbirth within the study period did not differ significantly between cryptorchid boys and controls (Denmark, p = 0.327; Finland, p = 0.949).

Danish mothers were slightly older than Finnish [30.6 years; 95% confidence interval (CI), 23.6–38.8 vs. 28.7 years; 95% CI, 21.4–39.7; p < 0.011], had a lower parity (p < 0.033) and smoked more frequently (p < 0.04). The prevalence of diabetes mellitus was higher among Finnish women (p < 0.004), but BMI before pregnancy (p = 0.678) did not differ significantly between the countries (p = 0.225).

Breast milk

Seven PBDEs were measurable in all breast milk samples (Table 3). Median concentrations were higher in Danish but not Finnish cryptorchid boys than in controls, reaching statistical significance for BDEs 47, 100, 28, 66, and 154. The sum of all seven congeners was significantly higher in cryptorchid boys than in controls if both countries were analyzed together (p < 0.007) (Figure 1), also if prematurity and SGA were included in the model (p < 0.035). Similar results were obtained for PBDE expressed as nanograms per liter (data shown only for the sum of all 14 congeners; Table 3). Table 4 shows the remaining seven congeners, which were below the detection limit in a substantial number of samples, and the sum of all 14 congeners.

The concentrations of PBDE congeners in milk samples showed large variations between congeners and individuals (Figure 2). Individual congener concentrations were positively correlated with one another (r = 0.178–0.955, p < 0.0001).

There were no significant country differences in the sum of all congeners [Denmark, 3.52 ng/g (95% CI, 1.26–14.2) vs. Finland, 3.44 ng/g (95% CI, 1.25–13.94), p = 0.754] or the sum of the most prevalent seven congeners, BDEs 47, 153, 99, 100, 28, 66, and 154 [Denmark, 3.24 ng/g (95% CI, 1.26–51.1) vs. Finland, 3.23 ng/g (95% CI, 1.26–51.0), p = 0.629]. Similar results were obtained if we analyzed only milk samples from mothers of healthy boys (data not shown). The estimated daily intake of PBDEs (sum of all) for an infant at 3 months of age (median infant body weight 6.58 kg, consuming 120 mL breast milk/kg) was a median of 16 ng/kg/day (range, 6–121 ng/kg/day). Breast milk lipid (percent wet weight) differed significantly between the countries (mean ± SD = 2.99 ± 1.38 in Denmark, 4.52 ± 1.56 in Finland; p < 0.0001). The lipid content was not significantly correlated with the sum of PBDE congeners (data not shown).

The pattern of congener distribution differed between the countries. BDE-28 was significantly higher in Finland than in Denmark (p < 0.021), with a similar tendency for BDE-47 (p < 0.077), which was the most prevalent congener. BDE-153 (p < 0.0001), BDE-66 (p < 0.026), and BDE-183 (p < 0.022) were significantly higher in Denmark than in Finland, with a similar tendency for BDE-99 (p < 0.073). For congeners at very low concentrations, the percentage of measurable samples was higher in Denmark than in Finland (Table 4). There was no significant effect of breast pump use during collection of samples on the concentration of any BDE congener in the Danish breast milk samples.

In the Danish but not the Finnish samples, the date of childbirth within the cohort was significantly correlated with the concentration of BDE-154 (r = −0.346, p < 0.005), BDE-85 (r = −0.434, p < 0.0001) and BDE-75 (r = 0.376, p < 0.002) with similar tendencies for BDE-66 (r = −0.211, p = 0.092) and BDE-77 (r = −0.214, p = 0.087).

Serum LH levels correlated positively with the sum of seven PBDEs in breast milk (r = 0.218, p < 0.033) as well as with individual congeners BDE-47 (r = 0.227, p < 0.027), BDE-100 (r = 0.293, p < 0.004), and BDE-154 (r = 0.203, p < 0.048). Country-specific analyses showed significant associations between serum LH and the above listed PBDEs and their sum for Finnish milk samples, but not Danish (data not shown). No other reproductive hormones or their ratios were significantly correlated with the concentration of PBDEs.

Placentas

The average levels of 14 PBDE congeners per gram fat in placentas were lower than in breast milk (Table 5), and more samples were nondetectable. Therefore, the sum of five congeners was used instead of the seven congeners used for milk. This had a minor influence on the total, because the sums of the five and the 14 congeners were very close.

The distribution of congeners resembled the distribution in breast milk, with BDE-47 and BDE-153 constituting the main fraction of PBDEs. There was no significant country difference for the sum of all 14 congeners (p = 0.198) or the sum of five (BDE-47, BDE-153, BDE-99, BDE-100, and BDE-28; p = 0.192). This was also true when only placentas from healthy boys were analyzed (data not shown). The concentrations of the five most prevalent congeners were positively correlated with each other (r = 0.171–0.827, p < 0.0001). Placenta lipid content (percent wet weight) differed significantly between the countries (mean ± SD = 1.09 ± 0.17 in Denmark, 1.21 ± 0.13 in Finland; p < 0.0001). Placenta lipid content was not significantly correlated with the sum of PBDE congeners (data not shown).

The date of childbirth within the cohort was significantly correlated in the Danish placentas with the concentration of BDE-66 (r = −0.246, p < 0.001), and in the Finnish placentas with BDE-85 (r = 0.239, p < 0.01) and BDE-153 (r = 0.275, p < 0.003).

There was no significant difference in the placenta concentration of the five most prevalent PBDEs between cryptorchid boys and healthy boys in Denmark (p = 0.10–0.976) or Finland (p = 0.09–0.835) or for their sum (p = 0.312 and p = 0.128, respectively). The results remained nonsignificant if prematurity and SGA were included in the model. There were no correlations between placental PBDEs and serum reproductive hormones in 3-month-old infants.

Paired samples

The median concentrations (nanograms per gram fat) of the 14 congeners in placenta were lower than the concentration found in the paired breast milk samples (n = 86) (Table 6), but there were significant correlations between the measurements, except for BDE-85 and BDE-138.

The sum of all congeners in milk was 3.39 (95% CI, 1.43–48.2) for boys with cryptorchidism and 3.15 (95% CI, 1.07–24.9) for controls (p = 0.228), and in placenta 1.22 (95% CI, 0.64–9.32) for boys with cryptorchidism and 1.17 (95% CI, 0.49–5.46) for controls (p = 0.871). Infant reproductive hormones at 3 months of age (27 Danish, 35 Finnish boys) were not correlated to PBDE concentrations in placenta or milk in this data subset.

Discussion Top

To our knowledge, this is the first study describing an association between congenital cryptorchidism in humans and exposure to PBDEs. An association was found for the sum of seven PBDEs (BDEs 47, 153, 99, 100, 28, 66, 154) in breast milk as well as for the individual congeners BDEs 47, 100, 28, 66, and 154. Concentrations of BDEs 47, 100, and 154 were also positively correlated with increasing serum LH values. This suggested that a higher gonadotropin drive was necessary to ensure normal testosterone production by the Leydig cells (Suomi et al. 2006), and thus a subtle primary testicular disfunction.

In this study we assessed infant exposure by measuring the concentration of PBDEs in breast milk, which reflects the accumulated body burden of the mother (Inoue et al. 2006; Jensen and Slorach 1991; Waliszewski et al. 2001). It also is a proxy for prenatal fetal exposure because PBDEs, especially the lower brominated compounds, can cross the placenta (Bi et al. 2006; Mazdai et al. 2003) and are transferred to breast milk during lactation (Darnerud and Risberg 2006). However, when we assesssed exposure by measuring PBDE in placenta, the results did not support the above findings, despite the fact that 86 mother–child pairs were represented with both milk and placenta samples. At present, it is not clear why this is the case.

The concentration of all PBDE congeners per gram fat in placenta was considerably lower than in milk, and more congeners were nondetectable. These differences did not have any remarkable influence on analytical errors, because the amount of fat used for analysis was similar for placentas and milk samples. In theory, placenta should be a better proxy for fetal exposure than breast milk, because it represents the direct route of chemical transfer during pregnancy. The number of placentas analyzed in this study was larger than the number of milk samples, and should thus better represent the pool of cases and controls. We could not establish any obvious selection bias of milk donors. On the other hand, due to higher concentrations, milk analyses were somewhat more reliable toward the lower end of concentration. This should not be important, because the main group differences were seen at the higher end of PBDE concentrations. It is currently unknown whether PBDEs accumulate in placenta, but our paired samples indicated that this may not be the case. We found positive correlations between measurements in placenta and breast milk, but three to four times lower absolute concentrations in placenta. Placenta concentrations may resemble measurements in single blood samples, and thus reflect the situation at delivery but not the long-term exposure.

There is some controversy as to whether the placental transport of PBDEs may differ between lower and higher brominated PBDEs. An American study reported a strong correlation of lipid-adjusted BDE concentrations in maternal serum at term and cord blood (Mazdai et al. 2003), whereas studies from countries with a generally lower exposure level found weaker correlations and higher values in maternal than in fetal samples (Bi et al. 2006). Segregation from serum into breast milk samples did not always follow a 1:1 pattern. The congener distribution appeared to be similar for lower brominated BDEs (Bi et al. 2006; Mazdai et al. 2003), whereas higher brominated BDEs such as BDE-209 were 10 times higher in serum than in breast milk (Inoue et al. 2006). Thus, the relative distribution of congeners between placenta and breast milk may also depend on the fat composition of these two matrices causing different solubility. We found significantly higher fat concentrations in the Finnish than in the Danish samples, which may reflect dietary habits in the two countries, because both long-term and short-term diet as well as the nutritional status may influence content and composition of breast milk lipids (Ortiz-Olaya et al.1996).

Current knowledge about human reproductive health consequences after exposure to PBDEs is very limited (Agency for Toxic Substances and Disease Registry 2004). A study from Taiwan showed an association between the sum of 12 PBDE congeners in breast milk, 10 of which were the same as in our study, and lower birth weight and length (Chao et al. 2007). Recently, a Swedish case–control study found higher values of PBDEs (sum of BDEs 47, 153, and 99) in blood samples from mothers of young men with testicular cancer than in age-matched controls (Hardell et al. 2006). However, maternal PBDE exposure was assessed 15–25 years after the critical time period—that is, at the time of the cancer diagnosis—which considerably weakens the possibility to establish a causal link between exposure and outcome. Also in this study (Hardell et al. 2006), exposures to other persistent chemicals occurred simultaneously, and it cannot be determined how these substances interact in their effect on reproductive development. Testicular cancer is the most severe clinical symptom of the testicular dysgenesis syndrome (TDS), which also encompasses impaired semen quality, congenital cryptorchidism, and hypospadias (Skakkebæk et al. 2001). TDS may be caused by genetic, hormonal, or environmental factors (Sharpe 2006; Skakkebæk et al. 2001). Prenatal exposure to PBDEs may have an adverse effect on testicular growth and differentiation in utero.

In animal studies, penta-brominated PBDEs showed antiandrogenic activity (Stoker et al. 2005). A peripubertal single-dose exposure to a commercial mixture of penta-BDEs delayed the onset of puberty in male and female rats (Stoker et al. 2004) and suppressed the growth of the seminal vesicles and ventral prostate. In adult rats, a single-dose exposure significantly increased LH concentration in serum (Stoker et al. 2005). Our observation of an association between PBDE levels in breast milk and serum LH in infants at 3 months of age is in line with these animal data. Gestational exposure of rats to BDE-99 caused a shortening of the anogenital distance in male and female rats, reduction in primordial and secondary ovarian follicles, a lower sperm count, and lower estradiol and testosterone levels in adulthood (Kuriyama et al. 2005; Lilienthal et al. 2006). In vitro assays showed a competitive androgen receptor binding for BDEs 47, 99, and 100. BDEs 47, 71, and 100 inhibited dihydrotestosterone-induced transcriptional activity (Stoker et al. 2005). Because testicular descent is highly androgen-dependent (Toppari 2003), the adverse effect of PBDE on testicular descent could be caused by their antiandrogenic properties.

In addition, BDEs 47, 100, 75, and 51, particularly their hydroxylated metabolites, are weakly estrogenic, and BDEs 153, 166, and 190 are antiestrogenic in vitro (Legler and Brouwer 2003; Meerts et al. 2001). Exposure of female rats to BDE-99 led to the formation of abundant vesicles and vacuolization of the ovary (Talsness et al. 2005), which showed signs of compromised steroidogenesis. Prenatal female exposure to BDE-99 in rats affected estrogen target genes in the uterus (Ceccatelli et al. 2006). Thus, the delicate balance between androgens and estrogens in the fetus may become altered by PBDE exposure. In mice, the metabolism of BDE-47 was highly dependent on the developmental stage of the animal, being slowest in pups (Staskal et al. 2006). Whether this also plays a role for human fetal development is currently unknown. Most exposure doses used in animal studies are several orders of magnitude higher than the levels of PBDEs found in breast milk in our study. However, there is emerging evidence that also low-dose exposure to, for example, BDE-99 close to levels found in human adipose tissue may have an adverse effect on the reproductive health of the offspring (Anonymous 2005; Kuriyama et al. 2005).

The distribution pattern of BDE congeners in breast milk corresponded to the distribution of BDE congeners in commercially available mixtures of PBDEs (Alaee et al. 2006; Darnerud et al. 2001; Law et al. 2006; Lilienthal et al. 2006). The absolute concentrations found in our study are within the same order of magnitude as reported from other Nordic and European countries (Jaraczewska et al. 2006; Kalantzi et al. 2004; Lind et al. 2003; Strandman et al. 2000) as well as China (Bi et al. 2006) and Japan (Eslami et al. 2006; Inoue et al. 2006). There are, however, significant geographic differences between and within these countries, which point toward differences in general contamination levels. In our study, the total amount of PBDEs did not differ between Finnish and Danish milk or placenta samples, but the pattern of congener distribution varied, which indicated different sources and timing of exposure. PBDE levels reported from American studies of breast milk appear to be considerably higher (Betts 2002). In contrast, the previous exponential increase in penta-PBDEs in Swedish breast milk samples since the 1970s has reversed since the late 1990s (Law et al. 2006; Meironyte et al. 1999; Sjödin et al. 2003), when penta-BDEs were gradually phased out. The collection of breast milk samples in our study covered a 5-year period, and we found a negative correlation between the level of PBDEs in breast milk and the infant date of birth. This is in line with the expected decline in the use of penta-PBDEs in the two regions. The high variability in PBDE concentrations among individual mothers has been described also for other human matrices (McDonald 2002), and may reflect variability in both exposure and metabolism. Deca-BDE can be converted through sunlight exposure into lower brominated BDEs, which are more readily absorbed from the intestine and bioaccumulate due to their longer half-life than deca-BDE (Watanabe and Tatsukawa 1987). However, it is as yet unknown how much this process contributes to human environmental exposure to lower brominated PBDEs.

Exposure to PBDEs cannot explain the observed geographic difference in the prevalence of cryptorchidism between Denmark and Finland. Breast milk contains significant levels of other persistent and nonpersistent chemical compounds (Damgaard et al. 2006; Main et al. 2006a), which can affect perinatal testicular development. Mothers with high levels of PBDE exposure also may be exposed to high levels of other persistent chemicals. Thus, the combined exposure to multiple environmental factors may cause the association between congenital cryptorchidism and PBDE concentration in breast milk (Koppe et al. 2006). In addition, other lifestyle factors and genetic susceptibility may play a role (Damgaard et al. 2007; Sharpe 2006; Virtanen et al. 2006). In our total study population, the geographic difference in the prevalence of cryptorchidism was observed mainly for mild forms of undescended testes, which had a high degree of spontaneous postnatal descent (Boisen et al. 2004). This pattern was also seen in this subpopulation, in which PBDEs was analyzed. However, also mild and transient forms of cryptorchidism are associated with a subtle impairment of primary testicular function (Suomi et al. 2006).

In conclusion, we used two different biological matrices in this study to assess infant perinatal exposure. Breast milk, but not placenta, showed an association with congenital cryptorchidism. There are valid arguments for either matrix, and risk assessment will require more scrutiny. The association between PBDE contamination levels in breast milk and congenital cryptorchidism is still of concern because exposure to PBDEs is considerable in some areas.

Figures and Tables Top

Figure 1.

Sum of the 7 most prevalent PBDEs in breast milk samples (BDEs 47, 153, 99, 100, 28, 66, 154, log-transformed values) from Denmark and Finland in boys with cryptorchidism (n = 62, blue) and healthy boys (n = 68, white). The box plot shows medians and interquartile ranges.

Figure 2.

Concentration (percentiles) of the sum of all PBDEs, BDE-47, and BDE-100 (ng/g fat) in human breast milk samples from Denmark (n = 65) and Finland (n = 65), 1997–2001. Note the differences in absolute values in the y-axis.

Table 1.

Population characteristics [median (2.5th–97.5th percentiles)] for breast milk samples.

Table 2.

Population characteristics [median (2.5th–97.5th percentiles)] for placentas.

Table 3.

Seven PBDEs, detectable in all breast milk samples from Danish and Finnish boys with and without cryptorchidism [median (2.5th–97.5th percentiles)].

Table 4.

Seven less-prevalent PBDEs in breast milk samples from Danish and Finnish boys with and without cryptorchidism.

Table 5.

PBDEs in placentas from Danish and Finnish boys with and without cryptorchidism [median (2.5th–97.5th percentiles)].

Table 6.

Correlations between PBDE measurements in paired placenta and breast milk samples (ng/g fat) of 43 Danish and 43 Finnish boys [median (95% CI).

References Top

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