Association between the Concentrations of Metallic Elements in Maternal Blood during Pregnancy and Prevalence of Abdominal Congenital Malformations: The Japan Environment and Children’s Study
by
, , ,
Chihiro Miyashita
1, 
Yasuaki Saijo
2,
Yoshiya Ito
3,
Atsuko Ikeda-Araki
1,4,
Sachiko Itoh
1,
Keiko Yamazaki
1,
Sumitaka Kobayashi
1,
Yu Ait Bamai
1,
Hideyuki Masuda
1,
Naomi Tamura
1,
Mariko Itoh
1,
Takeshi Yamaguchi
1,
Shin Yamazaki
5,
Reiko Kishi
1,* and
The Japan Environment and Children’s Study Group
† 1
Center for Environmental and Health Sciences, Hokkaido University, North-12, West-7, Kita-ku, Sapporo 060-0812, Japan
2
Department of Social Medicine, Asahikawa Medical University, Midorigaoka-higashi 2-1-1-1, Asahikawa 078-8510, Japan
3
Faculty of Clinical Medicine, Japanese Red Cross Hokkaido College of Nursing, 664-1 Akebono-cho, Kitami 090-0011, Japan
4
Faculty of Health Sciences, Hokkaido University, North-12, West-5, Kita-ku, Sapporo 060-0812, Japan
5
National Center for the Japan Environment and Children’s Study, National Institute for Environmental Sciences, 16-2 Onogawa, Tsukuba 305-8506, Japan
*
Author to whom correspondence should be addressed.
†
The complete membership of the author groups can be found in the Appendix A.
Int. J. Environ. Res. Public Health 2021, 18(19), 10103; https://0-doi-org.brum.beds.ac.uk/10.3390/ijerph181910103
Submission received: 2 July 2021
/
Revised: 14 September 2021
/
Accepted: 16 September 2021
/
Published: 26 September 2021
(This article belongs to the Section Global Health)
Abstract
:Abdominal congenital malformations are responsible for early mortality, inadequate nutrient intake, and infant biological dysfunction. Exposure to metallic elements in utero is reported to be toxic and negatively impacts ontogeny. However, no prior study has sufficiently evaluated the effects of exposure to metallic elements in utero on abdominal congenital malformations. The aim of the present study was to evaluate associations between metallic elements detected in maternal blood during pregnancy and congenital abdominal malformations. Data from participants in the Japan Environment and Children’s Study was used in the present study, and contained information on singleton and live birth infants without congenital abnormalities (control: n = 89,134) and abdominal malformations (case: n = 139). Heavy metals such as mercury (Hg), lead (Pb), cadmium (Cd), and trace elements of manganese (Mn) and selenium (Se) were detected in maternal serum samples during mid- and late-gestation. Infant congenital abnormalities were identified from delivery records at birth or one month after birth by medical doctors. In a multivariate analysis adjusted to account for potential confounders, quartiles of heavy metals and trace elements present in maternal blood were not statistically correlated to the prevalence of abdominal congenital malformations at birth. This study is the first to reveal the absence of significant associations between exposure levels to maternal heavy metals and trace elements in utero and the prevalence of abdominal congenital malformations in a large cohort of the Japanese population. Further studies are necessary to investigate the impact of exposure to heavy metals and trace elements via maternal blood in offspring after birth.
1. Introduction
Congenital anomalies are responsible for 11% of neonatal mortality worldwide [1]. In Japan, congenital anomalies, including congenital malformations, morphological anomalies, and chromosome aberrations, have been the main causes of neonatal mortality since 1990 and are responsible for 40.3% of domestic neonatal mortality [2]. Some of the causes of congenital anomalies are chromosomal abnormalities, single gene disorders, maternal infection, and medications during pregnancy; however, the majority of the causes remain unclear.
Heavy metals such as lead (Pb), cadmium (Cd), mercury (Hg), and trace elements of selenium (Se) and manganese (Mn) are ingested by the mother through daily food intake, and inhalation by air pollutants that cross the placenta and reach their fetus. Maternal heavy metals and trace elements are associated with fetal cell differentiation and development, oxidative stress, and metabolic function. Prenatal exposure to heavy metals and trace elements may play a role as genetic toxicants in fetal immature organs and developing tissues that could relate to the development of congenital anomalies [3,4,5,6]. In the past, genetic toxicants in methylmercury poisoning accidents have been reported to have severe harmful effects on the fetus, including stillbirth, fetal growth retardation, and congenital malformations [7].
Several human studies have evaluated the risk of congenital heart defects, cleft lip and palate, and neural tube defects due to maternal exposure to heavy metals and trace elements [8]. However, only a limited number of human studies have targeted abdominal malformation. Abdominal congenital malformations are responsible for early mortality, inadequate nutrient intake, and biological dysfunction in infants. Previous studies on the topic have either not adequately assessed the concentrations of metals and trace elements in the maternal body or had small sample sizes, hindering effective comparisons between cases and controls. Therefore, at present, there is insufficient evidence linking the concentrations of metals and trace elements in maternal blood to abdominal congenital malformations.
The present study used data and biological samples from participants in the Japan Environment and Children’ s Study (JECS). The difference in metal and trace element concentrations between the JECS study participants, North Americans and Europeans can be attributed to maternal smoking and alcohol drinking behavior, body size, socio-economic status, and a food preference for rice and fish/seafood in East Asians. Blood Pb and Cd levels decrease with time; however, recent studies specifically investigating their effects on the health of human offspring are limited. In fact, the JECS has reported adverse effects of maternal Cd and Mn on early preterm birth and birth size [9,10]. The aim of the present study was to evaluate any associations between maternal heavy metals and congenital abdominal malformations.
2. Materials and Methods
2.1. Participants and Data Collection in JECS
The JECS is a nationwide and government-funded birth cohort study that aims to investigate the effect of the environment on child health and development. The study design and baseline profile of JECS participants have been previously described [11,12]. Briefly, in the recruitment period from January 2011 to March 2014, a total of 103,060 pregnancies were recorded, of which 100,304 were live births. Maternal self-administered questionnaires were completed at mothers’ first gestations, and once again during their mid- to late-gestations. The maternal questionnaires included maternal and paternal data such as smoking and drinking habits, paternal smoking habits, maternal and paternal educational duration, and household income. A total of 51,402 male partners provided paternal consent forms during their female partner’s pregnancy, and provided data on paternal age at registration, of which 46,929 had female partners who were delivering live births.
2.2. Ethical Statement
The JECS protocol was approved by the Ministry of the Environment’s Institutional Review Board on Epidemiological Studies and the ethics committees of each participating institution (Appendix A) (ethical project identification code: Kanken19–117). All participants gave written informed consent for inclusion before they participated in the study. The study was conducted in accordance with the Declaration of Helsinki (sixth version).
2.3. Identified Congenital Abnormalities
Details of the collection of delivery records, categorization, and prevalence of congenital malformations have been published elsewhere [13]. Briefly, delivery records at birth or one month after birth were collected by transcription of medical records, which included data regarding maternal pre-pregnancy weight, height, pregnancy complications, infant birth weight, height, sex, and congenital abnormalities. Infants’ congenital abnormalities were identified from the delivery records at birth or one month after birth by medical doctors at each co-operating health care provider. Abdominal congenital malformations included seven types of anomalies: omphalocele, gastroschisis, esophageal atresia with or without fistula, duodenal atresia, intestinal atresia, anorectal atresia, and diaphragmic hernia [13].
2.4. Measurements of the Blood Content of Five Metallic Elements
Maternal blood was collected from mid-late trimesters and stored at −80 °C until the time of analysis. Detailed information on the analytic process and quality control has been previously described elsewhere [14]. The blood content level of five metallic elements (ME), mercury (Hg), lead (Pb), cadmium (Cd), manganese (Mn) and selenium (Se), were measured using inductively coupled plasma mass spectrometry (ICP-MS) analyses of maternal serum samples from 96,696 participants.
The JECS protocol was approved by the Ministry of the Environment’s Institutional Review Board on Epidemiological Studies, and the ethics committees of all participating institutions, listed as follows: the National Institute for Environmental Studies, the National Center for Child Health and Development, Hokkaido University, Sapporo Medical University, Asahikawa Medical College, Japanese Red Cross Hokkaido College of Nursing, Tohoku University, Fukushima Medical University, Chiba University, Yokohama City University, University of Yamanashi, Shinshu University, University of Toyama, Nagoya City University, Kyoto University, Doshisha University, Osaka University, Osaka Medical Center and Research Institute for Maternal and Child Health, Hyogo College of Medicine, Tottori University, Kochi University, University of Occupational and Environmental Health, Kyushu University, Kumamoto University, University of Miyazaki, and University of the Ryukyu. The JECS was conducted in accordance with the Declaration of Helsinki and other nationally valid regulations. Written informed consent was obtained from all participants. The present study used the JECS dataset “jecs-ta-20190930,” which was released in October 2019. The present study also used the jecs-ag-20160424 dataset, which was released in June 2016 and revised in October 2016, along with the supplementary dataset, jecs-ag-20160424-sp1.
2.5. Selected Participants in Present Study
The flowchart in Figure 1 illustrates when the various types of data were collected from participants. Concentrations of ME in maternal blood from 96,696 participants in their mid- and late-trimesters were analyzed. Of these, 94,661 sets of participant data contained the following: self-administered questionnaires, birth records without missing data on maternal age, maternal smoking and drinking habits, paternal smoking habits, birth year of infant, and sex of infant. We excluded infants with chromosomal abnormalities, congenital malformations without abdominal anomalies, miscarriages, and those that were stillbirths or from multiple births, but included singleton and live birth infants without congenital abnormalities (control: n = 89,134) and abdominal malformations (n = 139).
2.6. Statistical Analysis
The differences in the concentrations of ME detected in maternal blood, parental characteristics, and infant characteristics between abdominal malformed infants and non-abdominal malformed infants were analyzed using Pearson’s chi-square tests, Student’s t-tests, Spearman’s rank correlation test, Mann–Whitney U-test, and Kruskal–Wallis test (Table 1, Table 2, Table 3 and Table 4).
The participants were divided into quartiles according to distributed concentrations of each of the five ME. In a multivariable logistic regression analysis, with abdominal malformation as the dependent variable, the odds ratio (OR) and 95% confidence interval (CI) of abdominal malformation for the second, third, and fourth quartiles of the concentrations of ME present in maternal blood, compared with the lowest quartile as reference, were calculated. To evaluate the dose–response relationship, a p-trend was calculated for the quartile groups of categorized concentrations of ME in maternal blood, as an ordinal variable (Figure 2, Table 5, Table 6 and Table 7). Outcomes of all abdominal malformations and each of the seven types of anomalies, including omphalocele, gastroschisis, esophageal atresia with or without fistula, duodenal atresia, intestinal atresia, anorectal atresia, and diaphragmic hernia were used in a multivariable logistic regression analysis, adjusted for potential confounders. These confounders comprised factors from the present study or those previously reported to be significantly associated with maternal ME and abdominal congenital malformations, such as maternal age at delivery (categorical) and maternal smoking habit (never, quit, smoking during pregnancy), drinking habit (never, quit, drinking during pregnancy), paternal smoking habit (never, quit, smoking during pregnancy), birth year of infants, and sex of infants.
Statistical significance was set at p < 0.05. Statistical analyses were performed using SPSS software for Windows (version 21.0J; IBM, Armonk, NY, USA).
3. Results
Parental Characteristics
For 89,273 participants in the present study, the median concentrations of maternal ME, including Pb, Cd, Hg, Se, and Mn, were 5.84 ng/g, 0.661 ng/g, 3.64 ng/g, 168.0 ng/g, and 15.3 ng/g, respectively. There were no significant differences in the concentrations of maternal ME between infants with and without malformation (Table 1). Abdominal congenital malformations were observed in 139 infants, included in the current study by transcription of medical records at birth or one month after birth (Table 2). Parental and infant characteristics are shown in Table 3 and Table 4, respectively. The prevalence of abdominal congenital malformations significantly differed according to maternal smoking habit, type of delivery, sex of infants, gestational age, and birth weight, but not maternal age, drinking habit, educational duration, and household income (Table 3 and Table 4). Concentrations of maternal ME were significantly different between maternal, paternal, and infant characteristics.
Logistic regression analysis revealed no statistically significant (p < 0.05) associations between maternal ME and any abdominal congenital malformations (Figure 2 and Table 5). In relation to specific abdominal congenital malformations, compared with the lowest quartile (p-trend = 0.089), the third quartile of Hg, adjusted for ORs of diaphragmatic hernia, was significantly increased (OR (95% CI): 3.22 (1.05, 9.90)) (Table 6 and Table 7). A significant inverse trend was observed for diaphragmatic hernia throughout the quartiles of Mn (p-trend = 0.010). The highest (OR (95% CI): 0.15 (0.03, 0.68)) of Mn, adjusted for ORs of diaphragmatic hernia, were significantly decreased, compared with the lowest quartiles (Table 6 and Table 7). A significant inverse trend was observed for omphalocele throughout the quartiles of Pb (p-trend = 0.033). The second (OR (95% CI): 9.96 (1.27, 77.88)) and third quartiles (OR (95% CI): 10.06 (1.28, 78.77)) of Se, adjusted for ORs of omphalocele, were significantly increased, compared with the lowest quartiles (Table 6 and Table 7). We found no significant associations between maternal ME and specific abdominal congenital malformations, including gastroschisis, esophageal atresia with or without fistula, duodenal atresia/stenosis, intestinal atresia/stenosis, and anorectal atresia/stenosis (Table 6 and Table 7).
Table 5.
Odds ratios for all abdominal congenital malformations according to the concentrations of metallic elements detected in maternal blood at mid-late trimester.
Table 5.
Odds ratios for all abdominal congenital malformations according to the concentrations of metallic elements detected in maternal blood at mid-late trimester.
| Cd | Case /Control (n) | Adjusted OR (95% CI) | Pb | Case /Control (n) | Adjusted OR (95% CI) | Hg | Case /Control (n) | Adjusted OR (95% CI) | Se | Case /Control (n) | Adjusted OR (95% CI) | Mn | Case /Control (n) | Adjusted OR (95% CI) |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Q1 | 34/23,117 | 1 | Q1 | 37/22,571 | 1 | Q1 | 37/22,268 | 1 | Q1 | 36/22,348 | 1 | Q1 | 40/22,507 | 1 |
| Q2 | 44/21,323 | 1.46 (0.93, 2.29) | Q2 | 44/22,174 | 1.19 (0.76, 1.84) | Q2 | 29/22,218 | 0.80 (0.49, 1.31) | Q2 | 34/22,717 | 0.93 (0.58, 1.49) | Q2 | 35/22,858 | 0.86 (0.55, 1.36) |
| Q3 | 26/22,951 | 0.80 (0.48, 1.35) | Q3 | 28/22,382 | 0.77 (0.47, 1.26) | Q3 | 41/22,335 | 1.13 (0.72, 1.77) | Q3 | 41/22,889 | 1.11 (0.71, 1.74) | Q3 | 33/22,080 | 0.83 (0.52, 1.32) |
| Q4 | 35/21,743 | 1.22 (0.75, 2.00) | Q4 | 30/22,007 | 0.85 (0.52, 1.38) | Q4 | 32/22,313 | 0.88 (0.55, 1.42) | Q4 | 28/21,180 | 0.80 (0.48, 1.32) | Q4 | 31/21,689 | 0.78 (0.48, 1.25) |
| p for trend | 0.997 | 0.233 | 0.963 | 0.585 | 0.296 | |||||||||
OR: odds ratio was adjusted for maternal age, smoking habit, drinking habit, paternal smoking habit, birth year of child, and sex of the child. Q1: first quartile, Q2: second quartile, Q3: third quartile, Q4: fourth quartile, CI: confidence interval.
Table 6.
Odds ratios for each abdominal congenital malformation (Diaphragmatic hernia, Omphalocele, and Gastroschisis) according to the concentrations of metallic elements detected in maternal blood at mid-late trimester.
Table 6.
Odds ratios for each abdominal congenital malformation (Diaphragmatic hernia, Omphalocele, and Gastroschisis) according to the concentrations of metallic elements detected in maternal blood at mid-late trimester.
| Cd | Case/ Control (n) | Adjusted OR (95% CI) | Pb | Case/ Control (n) | Adjusted OR (95% CI) | Hg | Case/ Control (n) | Adjusted OR (95% CI) | Se | Case/ Control (n) | Adjusted OR (95% CI) | Mn | Case/ Control (n) | Adjusted OR (95% CI) |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Diaphragmatic hernia | ||||||||||||||
| Q1 | 10/23,117 | 1 | Q1 | 9/22,571 | 1 | Q1 | 4/22,268 | 1 | Q1 | 7/22,348 | 1 | Q1 | 13/22,507 | 1 |
| Q2 | 11/21,323 | 1.24 (0.52, 2.93) | Q2 | 11/22,174 | 1.24 (0.51, 2.99) | Q2 | 8/222,18 | 2.00 (0.60, 6.64) | Q2 | 7/22,717 | 0.95 (0.33, 2.71) | Q2 | 11/22,858 | 0.80 (0.36, 1.79) |
| Q3 | 10/22,951 | 1.08 (0.44, 2.62) | Q3 | 8/22,382 | 0.89 (0.34, 2.31) | Q3 | 13/22,335 | 3.22 (1.05, 9.90) * | Q3 | 9/22,889 | 1.18 (0.44, 3.18) | Q3 | 9/22,080 | 0.68 (0.29, 1.60) |
| Q4 | 4/21,743 | 0.48 (0.15, 1.58) | Q4 | 7/22,007 | 0.81 (0.30, 2.20) | Q4 | 10/22,313 | 2.50 (0.78, 8.00) | Q4 | 12/21,180 | 1.68 (0.66, 4.31) | Q4 | 2/21,689 | 0.15 (0.03, 0.68) * |
| p for trend | 0.297 | 0.543 | 0.089 | 0.221 | 0.010 | |||||||||
| Omphalocele | ||||||||||||||
| Q1 | 7/23,117 | 1 | Q1 | 11/22,571 | 1 | Q1 | 7/22,268 | 1 | Q1 | 1/22,348 | 1 | Q1 | 7/22,507 | 1 |
| Q2 | 8/21,323 | 1.26 (0.45, 3.51) | Q2 | 8/22,174 | 0.72 (0.29, 1.81) | Q2 | 3/22,218 | 0.44 (0.11, 1.71) | Q2 | 10/22,717 | 9.96 (1.27, 77.88) * | Q2 | 8/22,858 | 1.14 (0.41, 3.16) |
| Q3 | 3/22,951 | 0.44 (0.11, 1.74) | Q3 | 4/22,382 | 0.35 (0.11, 1.12) † | Q3 | 10/22,335 | 1.50 (0.57, 3.96) | Q3 | 10/22,889 | 10.06 (1.28, 78.77) * | Q3 | 4/22,080 | 0.59 (0.17, 2.03) |
| Q4 | 9/21,743 | 1.42 (0.50, 4.00) | Q4 | 4/22,007 | 0.35 (0.11, 1.13) † | Q4 | 7/22,313 | 1.10 (0.38, 3.15) | Q4 | 6/21,180 | 6.56 (0.78, 54.75) † | Q4 | 8/21,689 | 1.22 (0.44, 3.37) |
| p for trend | 0.846 | 0.033 | 0.439 | 0.152 | 0.962 | |||||||||
| Gastroschisis | ||||||||||||||
| Q1 | 4/23,117 | 1 | Q1 | 0/22,571 | - | Q1 | 2/22,268 | 1 | Q1 | 4/22,348 | 1 | Q1 | 2/22,507 | 1 |
| Q2 | 2/21,323 | 0.55 (0.10, 3.03) | Q2 | 2/22,174 | 1 | Q2 | 4/22,218 | 2.06 (0.38, 11.26) | Q2 | 1/22,717 | 0.24 (0.03, 2.13) | Q2 | 4/22,858 | 1.92 (0.35, 10.49) |
| Q3 | 0/22,951 | - | Q3 | 2/22,382 | 1.00 (0.14, 7.09) | Q3 | 1/22,335 | 0.53 (0.05, 5.89) | Q3 | 3/22,889 | 0.72 (0.16, 3.25) | Q3 | 2/22,080 | 0.97 (0.14, 6.91) |
| Q4 | 3/21,743 | 0.88 (0.18, 4.28) | Q4 | 5/22,007 | 2.63 (0.50, 13.70) | Q4 | 2/22,313 | 1.07 (0.15, 7.71) | Q4 | 1/21,180 | 0.26 (0.03, 2.34) | Q4 | 1/21,689 | 0.47 (0.04, 5.26) |
| p for trend | 0.935 | 0.212 | 0.717 | 0.317 | 0.431 | |||||||||
OR: odds ratio was adjusted for maternal age, smoking habit, drinking habit, paternal smoking habit, birth year of child, and sex of the child. Q1: first quartile, Q2: second quartile, Q3: third quartile, Q4: fourth quartile, CI: confidence interval. † p < 0.1, * p < 0.05. - no cases of abdominal malformation (number of case = 0), rather than OR value.
Table 7.
Odds ratios for each abdominal congenital malformation (Esophageal atresia with or without fistula, Duodenal atresia/stenosis, Intestinal atresia/stenosis, and Anorectal atresia/stenosis) according to the concentrations of metallic elements detected in maternal blood at mid-late trimester.
Table 7.
Odds ratios for each abdominal congenital malformation (Esophageal atresia with or without fistula, Duodenal atresia/stenosis, Intestinal atresia/stenosis, and Anorectal atresia/stenosis) according to the concentrations of metallic elements detected in maternal blood at mid-late trimester.
| Cd | Case/ Control (n) | Adjusted OR (95% CI) | Pb | Case/ Control (n) | Adjusted OR (95% CI) | Hg | Case/ Control (n) | Adjusted OR (95% CI) | Se | Case/ Control (n) | Adjusted OR (95% CI) | Mn | Case/ Control (n) | Adjusted OR (95% CI) |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Esophageal atresia with or without fistula | ||||||||||||||
| Q1 | 3/23,117 | 1 | Q1 | 2/22,571 | 1 | Q1 | 3/22,268 | 1 | Q1 | 2/22,348 | 1 | Q1 | 3/22,507 | 1 |
| Q2 | 6/21,323 | 2.94 (0.59, 14.72) | Q2 | 2/22,174 | 0.49 (0.04, 5.43) | Q2 | 1/22,218 | 0.48 (0.04, 5.31) | Q2 | 3/22,717 | 1.67 (0.26, 10.97) | Q2 | 3/22,858 | 1.45 (0.24, 8.69) |
| Q3 | 0/22,951 | - | Q3 | 2/22,382 | 0.95 (0.13, 6.80) | Q3 | 3/22,335 | 1.39 (0.23, 8.36) | Q3 | 2/22,889 | 1.06 (0.14, 8.21) | Q3 | 4/22,080 | 1.98 (0.36, 10.84) |
| Q4 | 1/21,743 | 0.44 (0.04, 5.10) | Q4 | 4/22,007 | 1.88 (0.33, 10.50) | Q4 | 3/22,313 | 1.36 (0.23, 8.27) | Q4 | 3/21,180 | 1.29 (0.19, 8.84) | Q4 | 0/21,689 | - |
| p for trend | 0.362 | 0.346 | 0.527 | 0.946 | 0.424 | |||||||||
| Duodenal atresia/stenosis | ||||||||||||||
| Q1 | 3/23,117 | 1 | Q1 | 4/22,571 | 1 | Q1 | 3/22,268 | 1 | Q1 | 5/22,348 | 1 | Q1 | 0/22,507 | - |
| Q2 | 2/21,323 | 0.72 (0.12, 4.39) | Q2 | 1/22,174 | 0.25 (0.03, 2.27) | Q2 | 3/22,218 | 0.99 (0.20, 4.90) | Q2 | 2/22,717 | 0.39 (0.08, 2.02) | Q2 | 3/22,858 | 1 |
| Q3 | 3/22,951 | 0.98 (0.19, 5.05) | Q3 | 2/22,382 | 0.50 (0.09, 2.75) | Q3 | 2/22,335 | 0.64 (0.11, 3.82) | Q3 | 4/22,889 | 0.76 (0.20, 2.86) | Q3 | 4/22,080 | 1.37 (0.31, 6.14) |
| Q4 | 3/21,743 | 1.01 (0.19, 5.44) | Q4 | 4/22,007 | 0.99 (0.24, 4.06) | Q4 | 3/22,313 | 0.92 (0.18, 4.62) | Q4 | 0/21,180 | - | Q4 | 4/21,689 | 1.35 (0.30, 6.04) |
| p for trend | 0.915 | 0.910 | 0.812 | 0.666 | 0.702 | |||||||||
| Intestinal atresia/stenosis | ||||||||||||||
| Q1 | 3/23,117 | 1 | Q1 | 3/22,571 | 1 | Q1 | 3/22,268 | 1 | Q1 | 2/22,348 | 1 | Q1 | 4/22,507 | 1 |
| Q2 | 6/21,323 | 2.28 (0.56, 9.20) | Q2 | 4/22,174 | 1.40 (0.31, 6.29) | Q2 | 4/22,218 | 1.30 (0.29, 5.81) | Q2 | 5/22,717 | 2.41 (0.47, 12.47) | Q2 | 2/22,858 | 0.47 (0.09, 2.58) |
| Q3 | 2/22,951 | 0.73 (0.12, 4.46) | Q3 | 3/22,382 | 1.06 (0.21, 5.27) | Q3 | 4/22,335 | 1.26 (0.28, 5.64) | Q3 | 6/22,889 | 2.82 (0.56, 14.06) | Q3 | 2/22,080 | 0.49 (0.09, 2.68) |
| Q4 | 2/21,743 | 0.87 (0.14, 5.46) | Q4 | 3/22,007 | 1.12 (0.22, 5.64) | Q4 | 2/22,313 | 0.62 (0.10, 3.76) | Q4 | 0/21,180 | - | Q4 | 5/21,689 | 1.22 (0.33, 4.57) |
| p for trend | 0.575 | 0.989 | 0.643 | 0.215 | 0.717 | |||||||||
| Anorectal atresia/stenosis | ||||||||||||||
| Q1 | 5/23,117 | 1 | Q1 | 10/22,571 | 1 | Q1 | 11/22,268 | 1 | Q1 | 15/22,348 | 1 | Q1 | 12/22,507 | 1 |
| Q2 | 11/21,323 | 2.57 (0.89, 7.43) † | Q2 | 15/22,174 | 1.65 (0.74, 3.67) | Q2 | 6/22,218 | 0.54 (0.20, 1.47) | Q2 | 7/22,717 | 0.49 (0.20, 1.19) | Q2 | 5/22,858 | 0.41 (0.14, 1.15) † |
| Q3 | 9/22,951 | 2.02 (0.67, 6.11) | Q3 | 5/22,382 | 0.57 (0.19, 1.68) | Q3 | 10/22,335 | 0.90 (0.38, 2.12) | Q3 | 7/22,889 | 0.50 (0.20, 1.24) | Q3 | 7/22,080 | 0.58 (0.23, 1.47) |
| Q4 | 10/21,743 | 2.65 (0.88, 8.00) † | Q4 | 5/22,007 | 0.62 (0.21, 1.83) | Q4 | 8/22,313 | 0.69 (0.28, 1.73) | Q4 | 6/21,180 | 0.48 (0.18, 1.24) | Q4 | 11/21,689 | 0.93 (0.41, 2.11) |
| p for trend | 0.149 | 0.158 | 0.633 | 0.099 | 0.969 | |||||||||
OR: odds ratio was adjusted for maternal age, smoking habit, drinking habit, paternal smoking habit, birth year of child, and sex of the child. Q1: first quartile, Q2: second quartile, Q3: third quartile, Q4: fourth quartile, CI: confidence interval. † p < 0.1; no cases of abdominal malformation (number of case = 0), rather than OR value.
4. Discussion
We found no statistically significant associations between maternal ME and any abdominal congenital malformations. However, significant positive or inverse associations were observed among maternal Pb, Mn, Hg, and Se and specific abdominal congenital malformations, including diaphragmatic hernia and omphalocele, with a wide range in 95% CI, due to the small sample size. The results indicated that presence of maternal ME was not a definite risk factor for congenital malformation in the offspring. This is the first study to show that exposure to ME via maternal blood is unlikely to cause fetal abdominal congenital malformations.
Direct comparison of results between previous studies and the present study is difficult, because there are no previous studies assessing the effects of ME in maternal blood. In North Carolina, a human study was conducted to evaluate the association between metal concentrations in private well water and birth defect prevalence, including heat defects, cleft palate/lip, hypospadias, pyloric stenosis, and gastroschisis. Individual exposure was designated as the average metal concentrations in the census tract encompassing the geocoded maternal residence. No association was observed between abdominal congenital malformation and Mn and Cd, excluding the inverse association between Cd and prevalence of pyloric stenosis (RR: 0.4 95% CI: 0.3–0.7) [15]. In another study, based on the classification of exposure to emissions from municipal solid waste incinerators, data from exposed (n = 194) and unexposed (n = 2678) settlement populations was used to evaluate the relative risks of congenital malformations. The rate of congenital anomalies, including diaphragmatic hernia and gastroschisis, was not significantly higher in exposed than unexposed communities [16]. In a recent study, metal concentrations in maternal blood from 140 pregnant women living in industrial areas were measured; however, Cd was detected in urine samples from only two pregnant women who birthed infants without congenital anomalies (detection rate: 1.4%, median: 5.3 µg/L), which means that the effect on congenital anomalies could not be effectively statistically evaluated [17]. While the three afore-mentioned studies described inadequate and weak effects of ME, our present study provides more tangible results contending that maternal exposure to ME via maternal blood (at levels detected in this study) are unlikely to cause fetal abdominal congenital malformation.
Adjusted ORs for infant diaphragmatic hernia and omphalocele increased the upper Hg and Se. The potential biological mechanisms are that Hg can disturb cell differentiation and growth, and Se can affect fetal growth, because the normal range of Se is very narrow. Moreover, previously reported exposure concentrations of Hg among JECS participants estimated that almost 30% of the participants had blood Hg levels within the range where detrimental health effects cannot be excluded with adequate certainty [14]. On the other hand, we cannot exclude the possibility that this result was due to chance, because there is no evidence of the toxicity of Hg and Se on the specific biological mechanisms of diaphragmatic hernia and omphalocele, gastroschisis, esophageal atresia with or without fistula, duodenal atresia/stenosis, intestinal atresia/stenosis, or anorectal atresia/stenosis. Conversely, the ORs of infantile omphalocele and diaphragmatic hernia decreased in the upper Pb and Mn. A previous JECS study reported a positive correlation between maternal Pb and abstinence from alcohol during pregnancy. Another study among Japanese women reported that the major contribution rates to the total estimated uptake of Mn were Japanese tea (33.9%), rice (23.7%), and vegetables (13.6%) [18]. Therefore, our study suggests that Pb and Mn concentrations in maternal blood were at levels that did not negatively impact fetal development, and that high-quality nutritional intake may safeguard against anomalous fetal development.
In a previous JECS study on congenital anomalies, which defined an index scaling of occurrence per 10,000 pregnancies, prevalence for diaphragmatic hernia was 1.9, omphalocele was 2.6, gastroschisis was 1.5, esophageal atresia with or without fistula was 1.5, and duodenal atresia/stenosis was 1.1, intestinal atresia/stenosis was 0.8, and anorectal atresia/stenosis was 2.9 [13]. Applying the same index scaling to the present study targeting infants who were singleton and live births, the prevalence of abdominal congenital malformations was lower in all participants [13]. In the present study, malformed abdominal infants had lower gestational ages and birth weights than non-malformed infants (Table 4), which is consistent with reports from previous human studies [19]. Congenital anomalies begin to develop in the early onset of fetal development and involve risk factors common to structural abnormalities and fetal growth retardation, such as prenatal complications, chromosomal anomalies, placental insufficiency, and polyhydramnios [19]. Maternal smoking is a known risk factor for birth defects [20]. However, in the present study, mothers with malformed abdominal infants had a lower frequency of smoking during pregnancy and a higher frequency of quitting smoking before pregnancy than those without abdominal malformed infants. The results suggest that maternal smoking during pregnancy cannot be responsible for abdominal malformed infants, and mothers may behave in a protective manner according to maternal awareness of self-risk of birth defects such as older childbearing age. Previously, associations between maternal alcohol consumption and malformed abdominal infants were weak [21]. In the present study, maternal alcohol consumption during pregnancy was not associated with malformed abdominal infants, a finding consistent with previous studies that reported that maternal alcohol consumption during pregnancy has a weak effect on the risk of cryptorchidism [22] and congenital heart defects [23].
5. Strengths and Limitations
The strengths of this study are that basic data on early gestations in participants have been prospectively collected using a national cohort study, which had a large sample size and included a sizable geographic proportion of Japan. ME in maternal blood were detected at a comprehensive detection rate. Cases of abdominal malformation were identified from hospital records by the obstetrician, which minimalized miscalculation bias. Our study did have some limitations. Firstly, we have no data on the history of abdominal congenital malformation in participating parents. Unobserved potential confounders may also be associated with maternal ME and abdominal malformations. Further studies are needed to evaluate the effect of exposure to maternal ME in utero on offspring health outcomes, including growth and development.
6. Conclusions
To our knowledge, this study is the first to reveal no significant associations between exposure levels in utero of maternal ME such as Hg, Pb, Cd, Mn, and Se, and the prevalence of abdominal congenital malformations in a large cohort of the Japanese population. However, there is a possibility that maternal ME may indeed have adverse effects on fetal development and subsequent health in children. Further studies with follow-up of children are necessary to investigate the effects of maternally present heavy metals on offspring after birth.
Author Contributions
C.M., Y.S., Y.I., A.I.-A., S.I., K.Y., S.Y. and R.K. conceived the idea and de-signed the study; S.K., Y.A.B., H.M., N.T., M.I. and T.Y. contributed to analysis and interpretation of data; C.M. wrote the initial draft of the manuscript; Y.S., Y.I., A.I.-A., S.I., K.Y., S.Y. and R.K. critically reviewed the manuscript. All authors have read and agreed to the published version of the manuscript.
Funding
The Japan Environment and Children’s Study was funded by the Ministry of Environment, Japan. The findings and conclusions of this article are solely the responsibility of the authors and do not represent the official views of the above government.
Institutional Review Board Statement
The study was conducted according to the guidelines of the Declaration of Helsinki. The JECS protocol was approved by the Ministry of the Environment’s Institutional Review Board on Epidemiological Studies (no.100406001), and approved by the ethics committees of all participating institutions (i.e., Asahikawa Medical College, Chiba University, Doshisha University, Fukushima Medical University, Hokkaido University, Hyogo College of Medicine, Japanese Red Cross Hokkaido College of Nursing, Kochi University, Kumamoto University, Kyoto University, Kyushu University, Nagoya City University, National Center for Child Health and Development, National Institute for Environmental Studies, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka University, Sapporo Medical University, Shinshu University, Tohoku University, Tottori University, University of Occupational and Environmental Health, University of Miyazaki, University of the Ryukyu, University of Toyama, University of Yamanashi, and Yokohama City University).
Informed Consent Statement
Written informed consent has been obtained from the participants to publish this paper.
Data Availability Statement
Data are available on reasonable request. Data are unsuitable for public deposition due to ethical restrictions and legal framework of Japan. It is prohibited by the Act on the Protection of Personal Information (Act No. 57 of 30 May 2003, amendment on 9 September 2015) to publicly deposit the data containing personal information. Ethical Guidelines for Medical and Health Research Involving Human Subjects enforced by the Japan Ministry of Education, Culture, Sports, Science and Technology and the Ministry of Health, Labour and Welfare also restricts the open sharing of the epidemiologic data. All inquiries about access to data should be sent to: [email protected]. The person responsible for handling enquiries sent to this email address is Dr Shoji F. Nakayama, JECS Programme Office, National Institute for Environmental Studies.
Acknowledgments
We would like to express our gratitude to all the JECS study participants and the Co-operating health care providers.
Conflicts of Interest
The authors declare no conflict of interest.
Appendix A
Members of the JECS as of 2021: Michihiro Kamijima (principal investigator, Nagoya City University, Nagoya, Japan), Shin Yamazaki (National Institute for Environmental Studies, Tsukuba, Japan), Yukihiro Ohya (National Center for Child Health and Development, Tokyo, Japan), Reiko Kishi (Hokkaido University, Sapporo, Japan), Nobuo Yaegashi (Tohoku University, Sendai, Japan), Koichi Hashimoto (Fukushima Medical University, Fukushima, Japan), Chisato Mori (Chiba University, Chiba, Japan), Shuichi Ito (Yokohama City University, Yokohama, Japan), Zentaro Yamagata (University of Yamanashi, Chuo, Japan), Hidekuni Inadera (University of Toyama, Toyama, Japan), Takeo Nakayama (Kyoto University, Kyoto, Japan), Hiroyasu Iso (Osaka University, Suita, Japan), Masayuki Shima (Hyogo College of Medicine, Nishinomiya, Japan), Youichi Kurozawa (Tottori University, Yonago, Japan), Narufumi Suganuma (Kochi University, Nankoku, Japan), Koichi Kusuhara (University of Occupational and Environmental Health, Kitakyushu, Japan), and Takahiko Katoh (Kumamoto University, Kumamoto, Japan).
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Figure 1.
Flowchart of participant data-collection procedures.
Figure 2.
Associations between the quartiles of maternal metallic elements (mercury (Hg), lead (Pb), cadmium (Cd), manganese (Mn), and selenium (Se)) (x-axes), and odds ratios and 95% confidence interval for all abdominal congenital malformations (y-axes), compared with the Q1, in a multivariable logistic regression analysis, adjusted for maternal age at delivery and maternal smoking habit, drinking habit, paternal smoking habit, birth year of infants, and sex of infants. Trend correlation was calculated using quartile group of maternal metallic elements, which were analyzed as ordinal variables. Q1: first quartile, Q2: second quartile, Q3: third quartile, Q4: fourth quartile. (A), (B), (C), (D) and (E) show associations between all abdominal congenital malformations and metallic elements; Cd, Pb, Hg, Se, and Mn, respectively.
Figure 2.
Associations between the quartiles of maternal metallic elements (mercury (Hg), lead (Pb), cadmium (Cd), manganese (Mn), and selenium (Se)) (x-axes), and odds ratios and 95% confidence interval for all abdominal congenital malformations (y-axes), compared with the Q1, in a multivariable logistic regression analysis, adjusted for maternal age at delivery and maternal smoking habit, drinking habit, paternal smoking habit, birth year of infants, and sex of infants. Trend correlation was calculated using quartile group of maternal metallic elements, which were analyzed as ordinal variables. Q1: first quartile, Q2: second quartile, Q3: third quartile, Q4: fourth quartile. (A), (B), (C), (D) and (E) show associations between all abdominal congenital malformations and metallic elements; Cd, Pb, Hg, Se, and Mn, respectively.
Table 1.
Concentrations of metallic elements in maternal blood at mid-late trimester.
| Metallic Elements | All (n = 89,273) | Normal (n = 89,134) | Abdominal Congenital Malformations (n = 139) | p | ||||
|---|---|---|---|---|---|---|---|---|
| Minimum | 25th Percentile | Median | 75th Percentile | Maximum | Median (IQR) | Median (IQR) | ||
| Pb (ng/g) | 1.2 | 4.7 | 5.84 | 7.32 | 110 | 5.85 (4.70, 7.32) | 5.53 (4.59, 7.00) | 0.094 |
| Cd (ng/g) | 0.0951 | 0.494 | 0.661 | 0.902 | 5.33 | 0.66 (0.49, 0.90) | 0.62 (0.50, 0.92) | 0.546 |
| Hg (n/g) | 0.182 | 2.55 | 3.64 | 5.2 | 58.8 | 3.64 (2.55, 5.20) | 3.69 (2.45, 5.01) | 0.827 |
| Se (ng/g) | 82.8 | 156 | 168 | 182 | 976 | 168.00 (156.00, 182.00) | 168.00 (155.00, 180.00) | 0.773 |
| Mn (ng/g) | 3.06 | 12.6 | 15.3 | 18.6 | 60.8 | 15.30 (12.60, 18.60) | 14.90 (12.20, 18.20) | 0.458 |
p by Mann–Whitney U test, with significance at p < 0.05. IQR: interquartile range.
Table 2.
Cases of congenital abdominal malformations.
| Abdominal Congenital Malformations | ICD-10 Code | All | Male | Female | Unknown |
|---|---|---|---|---|---|
| N | N (%) | N (%) | N (%) | ||
| Diaphragmatic hernia | Q79.0 | 35 | 16 (45.7) | 19 (54.3) | 0 (0.0) |
| Omphalocele | Q79.2 | 27 | 11 (40.7) | 16 (59.3) | 0 (0.0) |
| Gastroschisis | Q79.3 | 9 | 6 (66.7) | 3 (33.3) | 0 (0.0) |
| Esophageal atresia with or without fistula | Q39.0 Q39.1 | 10 | 5 (50.0) | 4 (40.0) | 1 (10.0) |
| Duodenal atresia/stenosis | Q41.0 | 11 | 7 (63.6) | 4 (36.4) | 0 (0.0) |
| Intestinal atresia/stenosis | Q41.1–Q41.9 | 13 | 6 (46.2) | 7 (53.8) | 0 (0.0) |
| Anorectal atresia/stenosis | Q42.0–Q42.9 | 35 | 21 (60.0) | 14 (40.0) | 0 (0.0) |
ICD-10 code: Transcriptions of both the ICD-10 code and congenital anomaly names in medical records were collected during the data collection phase.
Table 3.
Parental characteristics for births with/without abdominal congenital malformations.
| Characteristics | All | Non-Malformed | Abdominal Congenital Malformations | |
|---|---|---|---|---|
| Maternal Characteristics | ||||
| Age at delivery (years old) | N or N (%) | Mean ± SD | N (%) | N (%) |
| <25 | 10,265 (11.50) | 10,244 (11.49) | 21 (15.11) | |
| 25 to <30 | 26,545 (29.73) | 26,507 (29.74) | 38 (27.34) | |
| 30 to <35 | 31,260 (35.02) | 31,216 (35.02) | 44 (31.65) | |
| ≥35 | 21,203 (23.75) | 21,167 (23.75) | 36 (25.90) | |
| Mean ± SD | Mean ± SD | |||
| Pre-pregnancy weight | 89,234 | 53.12 ± 8.85 | 53.11 ± 8.85 | 53.59 ± 9.01 |
| Height | 89,253 | 158.12 ± 5.35 | 158.12 ± 5.35 | 158.57 ± 4.95 |
| Parity | N or N (%) | N (%) | N (%) | |
| Nulliparous | 43,097 (48.44) | 43,022 (48.43) | 75 (54.35) | |
| Multiparous | 45,870 (51.56) | 45,807 (51.57) | 63 (45.65) | |
| Smoking habit | ||||
| Never | 51,924 (58.16) | 51,846 (58.17) | 78 (56.12) | |
| Quit before pregnancy | 21,217 (23.77) | 21,172 (23.75) | 45 (32.37) | |
| Smoking during pregnancy | 16,132 (18.07) | 16,116 (18.08) | 16 (11.51) | |
| Drinking habit | ||||
| Never | 30,825 (34.53) | 30,773 (34.52) | 52 (37.41) | |
| Quit before pregnancy | 49,330 (55.26) | 49,252 (55.26) | 78 (56.12) | |
| Drinking during pregnancy | 9118 (10.21) | 9109 (10.22) | 9 (6.47) | |
| Educational duration (year) | ||||
| <10 | 4137 (4.69) | 4129 (4.68) | 8 (5.84) | |
| 10–<13 | 27,892 (31.59) | 27,855 (31.60) | 37 (27.01) | |
| 13–<15 | 37,288 (42.23) | 37,218 (42.22) | 70 (51.09) | |
| 15–<17 | 18,977 (21.49) | 18,955 (21.50) | 22 (16.06) | |
| Paternal characteristics | ||||
| Age at entry (years old) | N or N (%) | N (%) | N (%) | |
| <25 | 3385 (7.22) | 3379 (7.22) | 6 (8.57) | |
| 25 to <30 | 11,210 (23.92) | 11,194 (23.92) | 16 (22.86) | |
| 30 to <35 | 15,516 (33.11) | 15,485 (33.09) | 31 (44.29) | |
| ≥35 | 16,753 (35.75) | 16,736 (35.77) | 17 (24.29) | |
| Smoking habit | ||||
| Never | 24,084 (26.98) | 24,051 (26.98) | 33 (23.74) | |
| Quit before pregnancy | 20,753 (23.25) | 20,713 (23.24) | 40 (28.78) | |
| Smoking during pregnancy | 44,436 (49.78) | 44,370 (49.78) | 66 (47.48) | |
| Educational duration (year) | ||||
| <10 | 6430 (7.31) | 6423 (7.31) | 7 (5.11) | |
| 10–<13 | 32,538 (36.98) | 32,489 (36.99) | 49 (35.77) | |
| 13–<15 | 19,880 (22.60) | 19,850 (22.60) | 30 (21.90) | |
| 15–<17 | 29,132 (33.11) | 29,081 (33.11) | 51 (37.23) | |
| Household income (million yen) | ||||
| <2 | 4622 (5.59) | 4614 (5.59) | 8 (6.30) | |
| 2–<4 | 28,705 (34.73) | 28,663 (34.74) | 42 (33.07) | |
| 4–<6 | 27,334 (33.08) | 27,290 (33.07) | 44 (34.65) | |
| 6–<8 | 13,115 (15.87) | 13,092 (15.87) | 23 (18.11) | |
| 8–<10 | 5359 (6.48) | 5351 (6.48) | 8 (6.30) | |
| ≥10 | 3507 (4.24) | 3505 (4.25) | 2 (1.57) | |
SD, standard deviation.
Table 4.
Infant characteristics for births with/without abdominal congenital malformations.
| All | Non-Malformed | Abdominal Congenital Malformations | p | ||
|---|---|---|---|---|---|
| Infant characteristics | |||||
| N or N (%) | Mean ± SD | Mean ± SD | Mean ± SD | p a | |
| Gestational weeks | 89235 | 38.87 ± 1.46 | 38.87 ± 1.46 | 37.76 ± 2.68 | <0.001 |
| Birth weight | 89183 | 3033.77 ± 402.47 | 3034.21 ± 401.95 | 2743.65 ± 594.58 | <0.001 |
| N (%) | N (%) | p b | |||
| Vaginal delivery | 72,701 (81.65) | 72,612 (81.68) | 89 (64.96) | <0.001 | |
| Cesarean section | 16,339 (18.35) | 16,291 (18.32) | 48 (35.04) | ||
| Sex | |||||
| Male | 45,662 (51.15) | 45,591 (51.15) | 71 (51.08) | <0.001 | |
| Female | 43,609 (48.85) | 43,542 (48.85) | 67 (48.20) | ||
| Unknown | 2 (0.00) | 1 (0.00) | 1 (0.72) | ||
| Birth year | |||||
| 2011 | 8713 (9.76) | 8696 (9.76) | 17 (12.23) | 0.807 | |
| 2012 | 25,335 (28.38) | 25,297 (28.38) | 38 (27.34) | ||
| 2013 | 31,815 (35.64) | 31,767 (35.64) | 48 (34.53) | ||
| 2014 | 23,410 (26.22) | 23,374 (26.22) | 36 (25.90) | ||
SD, standard deviation. p a; T test, p b; χ2 test.
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Miyashita, C.; Saijo, Y.; Ito, Y.; Ikeda-Araki, A.; Itoh, S.; Yamazaki, K.; Kobayashi, S.; Ait Bamai, Y.; Masuda, H.; Tamura, N.; et al. Association between the Concentrations of Metallic Elements in Maternal Blood during Pregnancy and Prevalence of Abdominal Congenital Malformations: The Japan Environment and Children’s Study. Int. J. Environ. Res. Public Health 2021, 18, 10103. https://0-doi-org.brum.beds.ac.uk/10.3390/ijerph181910103
AMA Style
Miyashita C, Saijo Y, Ito Y, Ikeda-Araki A, Itoh S, Yamazaki K, Kobayashi S, Ait Bamai Y, Masuda H, Tamura N, et al. Association between the Concentrations of Metallic Elements in Maternal Blood during Pregnancy and Prevalence of Abdominal Congenital Malformations: The Japan Environment and Children’s Study. International Journal of Environmental Research and Public Health. 2021; 18(19):10103. https://0-doi-org.brum.beds.ac.uk/10.3390/ijerph181910103
Chicago/Turabian StyleMiyashita, Chihiro, Yasuaki Saijo, Yoshiya Ito, Atsuko Ikeda-Araki, Sachiko Itoh, Keiko Yamazaki, Sumitaka Kobayashi, Yu Ait Bamai, Hideyuki Masuda, Naomi Tamura, and et al. 2021. "Association between the Concentrations of Metallic Elements in Maternal Blood during Pregnancy and Prevalence of Abdominal Congenital Malformations: The Japan Environment and Children’s Study" International Journal of Environmental Research and Public Health 18, no. 19: 10103. https://0-doi-org.brum.beds.ac.uk/10.3390/ijerph181910103
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