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Article

Patterns and Determinants of Essential and Toxic Elements in Chinese Women at Mid-Pregnancy, Late Pregnancy, and Lactation

1
Institute of Reproductive and Child Health/Ministry of Health Key Laboratory of Reproductive Health, Peking University, Beijing 100191, China
2
Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing 100191, China
3
Department of Laboratorial Science and Technology, School of Public Health, Peking University, Beijing 100191, China
4
Medical and Health Analysis Center, School of Public Health, Peking University, Beijing 100191, China
5
Vaccine Research Center, School of Public Health, Peking University, Beijing 100191, China
*
Author to whom correspondence should be addressed.
Nutrients 2021, 13(2), 668; https://doi.org/10.3390/nu13020668
Submission received: 20 January 2021 / Revised: 6 February 2021 / Accepted: 12 February 2021 / Published: 19 February 2021
(This article belongs to the Section Micronutrients and Human Health)

Abstract

:
Maternal status of essential and toxic elements affects the health of the mother, developing fetus, or breastfeeding infant. However, few studies have examined the patterns of these elements and their determinants in pregnant or lactating women. Plasma samples of 1211 healthy mid-pregnant, late pregnant, and lactating women enrolled in coastland, lakeland, and inland areas of China from May–July 2014, were analyzed for concentrations of 15 elements, using inductively coupled plasma mass spectrometry. The adjusted median concentrations of elements varied by physiologic stage and region. Lactating versus pregnant women showed higher concentrations of Zn, Cr, Mo, Ni, Sb, Cd and Pb, but lower concentrations of Cu, I, Al and Hg. In pregnant women, the concentrations of Fe, Zn, I, Mo, Ni, Al, Hg and Cd were higher in mid- versus late-pregnancy. Overall, the highest concentrations were observed in Zn, I, Mn, Al, and Pb in coastland, in Hg in lakeland, and in Fe in inland area. Element concentrations varied by maternal age, pre-pregnancy BMI, education, parity, delivery mode, feeding practice, and intakes of aquatic products and mutton. In conclusion, essential and toxic elements coexisted in pregnant and lactating women, and their concentrations varied by physiologic stages, regions, maternal socio-demographic characteristics and dietary factors.

1. Introduction

Essential trace elements such as zinc, copper, chromium, and manganese, acting as co-factors in enzyme reactions and playing roles in energy metabolism and cellular activities, are essential for human physiological functions [1,2]. Deficiency in these elements is relatively common among pregnant and lactating women [2], due to their increased demands. On the other hand, excessive accumulation might occur, especially when multi-micronutrient supplementations are inappropriately taken. In addition, maternal exposure to toxic elements, such as mercury, cadmium, and lead, is also concerned [3,4]. In the vulnerable periods of pregnancy and lactation, deficiency and overload of essential trace elements as well as excessive accumulation of toxic elements might co-exist, likely increasing risks of maternal complications [5,6], stillbirth [7], birth defects [8,9], fetal growth restriction [10,11,12], or long-term low neurobehavioral functions [13,14,15].
Essential and toxic elements exist in water, diet, soil, air, and commercial products, with ingestion, inhalation and dermal contact as dominant pathways of exposure. The elements’ status in pregnant and lactating women might relate to environmental, dietary, and maternal socio-demographic characteristics [16,17], suggesting that element status may differ among women from different areas. Moreover, the status may change concurrently with the rapidly changing metabolism during pregnancy and lactation [18,19]. For example, mobilization of lead from bone stores to blood likely occur alongside altered calcium metabolism during the stages [20,21].
In China, pregnant women are generally recommended to take folic acid supplements, iron-rich foods, and iodized salt at their first prenatal care visit, and to increase intake of milk, fish, poultry, eggs, and lean meat during late pregnancy. Lactating women are recommended to take iodized salt, marine products and animal source foods. A complete understanding of essential and toxic elements status in Chinese pregnant and lactating women is important to develop effective public health strategies. However, data on element concentrations in lactating women are sparse [22], and have been limited in terms of geographic coverage in pregnant women [22,23]. Given the marked diversity of geography, environment, and diet throughout China, estimates are likely to be sensitive to the area sampled. Most previous studies compared the element status between pregnant and non-pregnant women [19,23,24,25,26,27], but few focused on the comparison between pregnant and lactating women [22,28], even though the status is a continuum throughout pregnancy and lactation [2]. In addition, little is known about determinants of element status in pregnant or lactating women.
The main objectives of the present study were to describe the plasma concentrations and patterns of essential and toxic elements in pregnant and lactating women who were living in typically representative coastland, lakeland, and inland areas of China, and to identify geographic, dietary, and socio-demographic determinants of element status.

2. Materials and Methods

2.1. Study Population

A cross-sectional study was carried out in women at mid-pregnancy (15–19 weeks of gestation), late pregnancy (37–41 weeks of gestation), and lactation (35–49 days postpartum) in the Weihai, Yueyang, and Baotou cities of China from May to July 2014 [29,30,31]. Weihai, prevailing a monsoon climate with a latitude of 37°25′ N, is a coastland city located in Shandong Province of China. Yueyang, prevailing a subtropical monsoon climate with a latitude of 29°37′ N, is a lakeside city located in Hunan Province. Moreover, Baotou, prevailing a temperate continental monsoon climate with a latitude of 40°15′ N, is an inland city located in the Inner Mongolia Autonomous Region. The main manufacturing industries are agricultural and sideline food processing industry in Weihai, petrochemical industry in Yueyang, and metallurgical and rare-earth industry in Baotou.
All participants were recruited at local maternal and child health centers, when they underwent prenatal or postpartum clinic visit. Important inclusion criteria for all participants were as follows: 18 to 35 years old, the absence of comorbidities, local residents in the study areas, and willingness to comply with the study protocol. Additional inclusion criteria for pregnant women included a singleton pregnancy and no pregnancy-induced complications, and for lactating women included having a singleton live birth and currently exclusive or partial breastfeeding their infants. Among 1254 women initially recruited, 43 were excluded due to age >35 years (n = 23) or not being in the predetermined mid-, late-pregnancy or lactation stages (n = 20), leaving 1211 in the final analyses. The 1211 women were recruited approximately equally in mid-pregnancy, late pregnancy, and lactation by the three regions, with an average 135 women in each physiological period per region.
The study protocol was reviewed and approved by the Institutional Review Board /Human Subjects Committee (IRB00001052-14012; date of approval: 22 April 2014). Informed consent was obtained from all participants before their recruitment into the study.

2.2. Data Collection

Information about maternal socio-demographic characteristics including maternal age, ethnicity, education status, annual family income per capita, height and weight before pregnancy, parity, and gestational age at enrollment or delivery was collected using a structured questionnaire. Information about delivery mode and feeding practice was further collected for lactating women.
Dietary information in the previous month was collected using a semiquantitative, tablet-based food frequency questionnaire (FFQ) by trained obstetricians or nurses. Given that the primary aim of the original study was to assess the maternal docosahexaenoic acid (DHA) status, only DHA-specific foods were contained in the FFQ, as detailed previously [30,31]. In the present analysis, information on freshwater aquatic products (38 items, such as carp, shrimp, and river crab), marine aquatic products (75 items, such as mackerel, lobster, and crab), mutton, and formula which probably contain multiple elements was used. For each food item, a standard portion size with 9 options ranging from 25 g to 250 g, and consumption frequency with 12 options ranging from “once per month” to “three times per day” were collected. The average daily intake was calculated as multiplying the frequency of consumption in the previous month by the average amount consumed per time, and then dividing by 30 days.

2.3. Blood Sample Collection, Processing, and Analysis

About 5 mL of fasting venous blood was drawn from each woman at enrollment by experienced phlebotomists. Blood samples were collected into ethylene diamine tetraacetic acid-containing tubes, placed into a refrigerator at 5 °C for at least 30 min, and then processed to separate plasma aliquots within 4 h. These aliquots were stored in cryostat tubes at −20 °C at local hospitals for about 10 days, before being sent on day ice to the National Health Commission Key Laboratory of Reproductive Health at Peking University Health Science Center in China, and then stored at −80 °C until analysis.
A total of 15 elements in the plasma including copper (Cu), iron (Fe), zinc (Zn), chromium (Cr), iodine (I), manganese (Mn), cobalt (Co), molybdenum (Mo), boron (B), nickel (Ni), aluminum (Al), antimony (Sb), mercury (Hg), cadmium (Cd), and lead (Pb) were determined using inductively coupled plasma mass spectrometry (ICP-MS) (ELan DRC II; PerkinElmer, Waltham, MA, USA). A sample volume of 0.1 mL was diluted 20 times by mixing with 1.8 mL of 1% nitric acid solution and 0.1 mL of internal standards (Indium and Rhenium) in a 2-mL centrifuge tube. The operating conditions of ICP-MS for analysis were the following: 0.96 L/min atomized gas flow rate, 1.87 L/min auxiliary gas flow rate, 17.1 L/min plasma gas flow rate, 1000 W radio frequency power, 50–100 ms duration of stay, 1.1 mL/min sample lift, single point peak hopping scanning mode, and 0.7–0.9 amu resolution.
The analytical accuracy was verified by repeated analysis of Certified Reference Materials (CRMs) ClinChek®-Plasma Control samples (Level II, 8884). For Pb and B, standard pork liver samples (GBW10051) were used as the CRMs. The measured values of the CRMs for all elements were ranging from 95.5% to 103.0%. The limit of detection (LOD) was calculated as 3 times the standard deviation of the blank concentration. Data on CRMs and LODs are presented in Table S1. The element analysis was completed in the Central Laboratory of Biological Elements at Peking University Health Science Center in China, with the operational procedure approved by China Metrology Accreditation.

2.4. Statistical Analysis

Medians and interquartile ranges (IQRs) were used to summarize the concentrations of elements because of their abnormal distribution, according to the Kolmogorov-Smirnov D tests (all p values < 0.01). Adjusted medians and adjusted IQRs were estimated using multivariable quantile regression models, by considering covariates including physiologic stage (mid-pregnancy, late pregnancy, and lactation), geographic region (coastland, lakeland, and inland), maternal age (≤25, 26 to 30, and 31 to 35 years), parity (nulliparous, and multiparous), ethnicity (Han, and others), education status (middle school or less, high school, and college or higher), annual family income per capita (<30,000, 30,000 to 49,999, 50,000 to 99,999, and ≥100,000 Yuan), pre-pregnancy body mass index (BMI; underweight <18.5 kg/m2, normal weight 18.5 to <25 kg/m2, and overweight/obese ≥25 kg/m2), and dietary intake (the lowest and middle tertiles, and the highest tertile) of aquatic products, mutton, and formula. Pre-pregnancy BMI was calculated as the pre-pregnancy weight in kilograms divided by the squared height in meters. Regarding the estimates for lactating women, delivery mode (vaginal delivery, and cesarean delivery) and feeding practice (exclusive breastfeeding, and partial breastfeeding) were additionally adjusted. The differences of adjusted median concentrations between pregnant and lactating women, or other dichotomous variables were tested using the Mann-Whitney tests; and the differences across geographic regions or other polytomous variables were tested using the Kruskal-Wallis tests, followed by Bonferroni corrected Mann-Whitney tests for multiple comparisons. In addition, multivariable quantile regression models with stepwise selection were used to examine potential determinants of elements concentrations.
All statistical analyses were performed using SPSS 24.0 software (SPSS Inc., Chicago, IL, USA). p values were two-sided, and statistical significance was set at p < 0.05.

3. Results

The maternal characteristics of the pregnant and lactating women analyzed in this study have been presented elsewhere. [29,31] In brief, the average (standard deviation) age of the women was 27.8 (3.0) years, and average pre-pregnancy BMI was 20.9 (2.9) kg/m2. Among the 1211 women, those at mid-pregnancy, late pregnancy, and lactation periods accounted for 33.6% (n = 407), 32.8% (n = 397), and 33.6% (n = 407), respectively. Women in different periods were recruited approximately equally from the coastland (32.9%), lakeland (33.2%), and inland (33.9%) regions. Most women were of Han ethnicity (95.2%), had college or higher educational status (65.7%), and had an annual per capita family income of less than 50,000 Yuan (71.4%). The average intake of freshwater aquatic products, marine aquatic products, mutton, and formula were 43.4 (88.8) g/d, 29.7 (46.0) g/d, 9.3 (42.3) g/d, and 0.7 (2.1) tsp/d, respectively (Table S2).
Crude and adjusted median concentrations of plasma essential and toxic elements among pregnant and lactating women are presented in Table 1. For essential elements, lactating women had lower levels of Cu (1300 vs. 2025 ng/mL) and I (56.5 vs. 97.9 ng/mL), but higher levels of Zn (1064 vs. 929 ng/mL), Cr (0.43 vs. 0.38 ng/mL), and Mo (3.81 vs. 2.97 ng/mL), as compared with pregnant women. For toxic elements, lactating women had higher concentrations of Ni (16.4 vs. 12.9 ng/mL), Sb (6.42 vs. 6.03 ng/mL), Cd (1.21 vs. 0.98 ng/mL), and Pb (1.59 vs. 1.34 ng/mL), but lower concentrations of Al (65.0 vs. 75.5 ng/mL) and Hg (0.59 vs. 0.73 ng/mL).
In pregnant women, concentrations of almost all elements differed between stage of pregnancy, except Sb (Table 2). The concentrations of Fe, Zn, I, Mo, Ni, Al, Hg, and Cd were higher, while the concentrations of Cu, Cr, Mn, Co, B, and Pb were lower in mid- versus late-pregnancy. The concentrations varied significantly by geographic region, both in pregnant (Table 2) and lactating women (Table 3). The concentrations of Zn, I, Mn, Al, and Pb were highest in coastland area, followed by lakeland, and lowest in inland. The Fe concentration was highest in inland area, followed by lakeland and coastland area. The Hg concentration was highest in lakeland area, followed by coastland, and lowest in inland.
Element concentrations of pregnant and lactating women differed by maternal socio-demographic characteristics (Table 2 and Table 3). For example, in pregnant women, the concentrations of Cu and Mn increased with increasing maternal age, and the concentrations of Fe, Cr, Sb, and Cd increased with increasing pre-pregnancy BMI; in lactating women, the concentrations of Fe, Cr, Mo, and B increased with increasing maternal age, and the concentrations of Cu, Zn, Co, B, Ni, and Pb increased with increasing pre-pregnancy BMI. Pregnant women with higher versus lower education had higher concentrations of Fe and Mo, and lower concentration of Pb. In addition, the concentrations of Cu, Zn, Cr, Mo, B, Cd, and Pb varied by parity in pregnant women (Table 2), and the concentrations of Cu, Zn, Cr, I, B, Al, Ni, Sb, Hg, and Cd varied by delivery mode and feeding practice in lactating women (Table 3).
Element concentrations were also determined by dietary intakes of pregnant and lactating women (Table 4). For example, women in the highest tertile of marine aquatic product had higher concentrations of Cu, Zn, I, Mn, Co, Hg, and Pb, women in the highest tertile of mutton had a higher concentration of Fe, and women in the highest tertile of freshwater aquatic products had a higher level of Hg, as compared to those in the lowest and middle tertiles.
The multivariable quantile regression models on the association between median concentrations of elements and the potential determinants showed similar results, with physiological period and geographic region as the most influential determinants (Tables S4 and S5).

4. Discussion

In this large cross-sectional study conducted in coastland, lakeland, and inland regions of China, we found that the essential and toxic elements coexisted in pregnant and lactating women. Moreover, the concentrations of elements varied significantly by pregnancy and lactation stages, geographic regions, maternal socio-demographic characteristics, as well as dietary intakes.
Maternal element status is a continuum from pregnancy through lactation with varying trends [2], but few studies have explored the trends between pregnant and lactating women [22,28]. In our study, lactating women had higher concentrations of essential trace elements including Zn, Cr, and Mo, as well as toxic elements including Ni, Sb, Cd, and Pb. This finding was similar to that from North Norwegian women [28], which also found that concentrations of Zn, Mn, Cd, and Pb were higher postpartum than during pregnancy. The concentrations of Cu and I were lower in lactating women than in pregnant women in this study, similar to another Chinese study which showed that the concentration of urine I was lower in lactating than in pregnant women (194 vs. 206 μg/L) [33]. Additionally, data from New Zealand showed that the urine I concentration was consistently lower in lactating than in pregnant women before (34 vs. 47 μg/L) or after (74 vs. 85 μg/L) taking iodine supplements [34]. These findings indicate that lactating women might need more iodine to meet the demands of both the mother and the growing infant. Iodine is one of “priority” nutrients for lactating women, because maternal iodine status likely affects its amount secreted in the breast milk, subsequently affecting infants’ health [2]. The health effect of maternal iodine status on offspring warranted further study, particularly given that about 80% of infants were breastfed at 4 months with an average duration of 10 months in China [35].
Most element concentrations in pregnant women of our study were in the reference range for Chinese pregnant women derived from the China Nutrition and Health Survey (CNHS) 2010–2012 [36]. The concentrations of almost all elements varied by stages of pregnancy; the concentrations of Cu, Cr, Mn, Co, B, and Pb were higher, while the concentrations of Fe, Zn, I, Mo, Al, Ni, Hg, and Cd were lower in women at late pregnancy, compared to those at mid-pregnancy. These trends by pregnancy stages were consistent with previous studies, as maternal Cu, Mn, and Co concentrations increased while the Fe and Zn concentrations decreased as pregnancy progressed [24,36,37]. The increasing Cu and Mn concentrations were possibly due to maternal increased intestinal absorption and the increased estrogen and progesterone concentrations during pregnancy [37,38]. Cu is necessary for normal fetal hematopoiesis, and Cu deficiency during fetal development can result in structural and biochemical abnormalities [39] while high level of Cu might be linked to congenital heart defects [8]. Mn is essential for normal development and cellular function during pregnancy, but also toxic particularly neurotoxic at high exposures [40]. The decreasing concentrations of Fe and Zn were mainly due to hemodilution, fetal and placental growth, and increasing physiological requirements as pregnancy progress. Maternal zinc status is critical for the development of fetus and infant, and iron status during pregnancy is associated with pregnancy outcomes and strongly affects the iron stores of the infant at birth [2], although delayed cord clamping is recommended to improve iron stores in infancy [41]. Thus, adequate intakes of iron and zinc are important, particularly given that they are typically less well absorbed trace elements [42].
Consistent with the findings from Norwegian women [28], we observed an increasing Pb concentration from mid-pregnancy (1.27 ng/mL) to late pregnancy (1.36 ng/mL), and to lactation (1.59 ng/mL), possibly due to the mobilization of cumulative maternal Pb from bones to blood during pregnancy and lactation [20,21]. We also observed a decreasing trend in maternal Hg concentration as expected, with the highest in mid-pregnancy (0.75 ng/mL), following by late pregnancy (0.70 ng/mL), and the lowest in lactation (0.59 ng/mL), possibly because of the increasing blood volume during pregnancy and the faster blood clearance half-life of Hg during lactation [43]. Hg and Pb mainly affect central nervous system, such as impairing infant cognitive and behavioral development, and the risk effect of Pb for fetus and infant is higher and lasts longer than Hg [44]. While the relatively higher Hg status in pregnant women requires further study, given that maternal exposure to Hg is more important during fetal development than during breastfeeding [44].
The concentrations of elements differed markedly across geographic regions, possibly due to the distinct dietary patterns. Maternal Fe concentration was highest in inland compared to lakeland and coastland areas, possibly because inland women consumed more mutton (24.9 g/d vs. 0 and 2.8 g/d). As a kind of red meat, mutton likely provides considerable amounts of iron in highly bioavailable heme form [45]. Consistently, a higher Fe concentration was observed in women having more mutton in this study. Concentrations of Zn, I, and Mn were highest in coastland compared to lakeland and inland areas, possibly since women in coastland area consume more aquatic foods (98.5 g/d vs. 81.5 g/d and 39.9 g/d), particularly marine aquatic foods (62.5g/d, vs. 14.2 g/d and 12.9 g/d). Consistently, higher concentrations of Zn, I, Mn were observed in women having more marine aquatic foods. The highest concentration of Hg was observed in lakeland area, consistent to the finding of a higher Hg concentration in women having more freshwater aquatic foods.
It is challenging to make direct comparisons of element concentrations in pregnant or lactating women from different studies, because the concentrations were determined using different assay methods with various specimen types. However, some comparable studies on plasma elements for pregnant women were found in the literature. Cu status in our study was comparable to that in American women [19]. However, the level of Zn we observed was slightly higher than that of American women [19], and markedly higher than that of Korean women [24]. The concentrations of Pb and Cd were higher but the Hg concentration was lower in pregnant women in our study as compared to those in Japan [46].
This study comprehensively described the concentrations and patterns of essential and toxic elements and some of its determinants in both pregnant and lactating women, providing important information concerning element status of vulnerable populations in China. However, limitations of this study should be taken into account. Women in mid-pregnancy, late pregnancy, and lactation stages in this study were cross-sectionally selected, rather than longitudinally followed up a cohort of the population. However, the estimates, after multivariable adjustments, can largely reflect the variations in element status at different stages of pregnancy or lactation. Women in early pregnancy or non-pregnant women within the reproductive age were not included in this study, thus we could not make a complete comparison from pre-pregnancy through postpartum. Cord blood samples were not collected in the study, so fetal exposure could not be assessed. In addition, only healthy women in urban areas were enrolled in this study, therefore generalization of our findings to other pregnant or lactating women needs caution. Dietary information was not fully collected, and only data on the DHA-specific foods containing essential trace elements or toxic elements were analyzed in this study. Furthermore, although we briefly depicted the variations of element concentrations by dietary intakes, our data do not provide a bioavailable picture of the elements, which varies widely by food components, dietary interactions, and individual nutritional status [42].

5. Conclusions

This large cross-sectional study presented concentrations of essential and toxic elements among Chinese pregnant and lactating women, and the results were partly representing proxies for fetal and infant exposures. The concentrations differed markedly across physiologic stages, geographical regions, maternal socio-demographic characteristics, and dietary intakes. The concentration differences by physiologic periods were mainly due to the metabolism changes during the pregnancy and lactation stages, while the differences by geographic regions were mainly due to distinct dietary patterns. Our findings illustrate the coexistence of essential and toxic elements, and the complex impacts of maternal characteristics on element status, indicating that a comprehensive assessment of element status is needed before formulation of public health strategies. Additional research is needed to establish more reliable bioavailability of trace elements in pregnant and lactating women.

Supplementary Materials

The following are available online at https://www.mdpi.com/2072-6643/13/2/668/s1, Table S1: Data on the Certified Reference Materials (CRM) and limit of detection (LOD), Table S2: Dietary intakes for participants (n = 1208), Table S3: Dietary reference intakes of essential trace elements, Table S4: Quantile regression results from the adjusted models for median concentrations (ng/mL) of essential elements for pregnant and lactating women, Table S5: Quantile regression results from the adjusted models for median concentrations (ng/mL) of toxic elements for pregnant and lactating women.

Author Contributions

J.L. conceived, designed and supervised the study, critically revised the manuscript, and takes responsibility for the integrity of the data and has full access to all of the data in the study. Y.Z. designed the study, collected the data, did the analysis, interpreted the data, and drafted the manuscript. L.Y. and Y.L. analyzed the samples, interpreted the data, and critically reviewed and revised the manuscript. H.L. designed the study, collected the data, and critically reviewed and revised the manuscript. X.L. analyzed the samples, and reviewed and revised the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the National Natural Science Foundation of China, grant number 81801542; and the Wyeth Nutrition Science Center, project number 14.10.CN.INF.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Institutional Review Board/Human Subjects Committee (IRB00001052-14012; date of approval: 22 April 2014).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

The data presented in this study are available on request from the corresponding author. The data are not publicly available due to containing identifiable personal information.

Acknowledgments

We thank all physicians, nurses and other staff members from Weihai Maternal and Child Health Hospital, Yueyang Maternal and Child Health Hospital, The First Affiliated Hospital of Baotou Medical School, and The Third Hospital of Baogang Group for their outstanding assistance with the field work. We thank Ya-li Zhang, Lin-lin Wang and Zhao-xia Xiong from Institute of Reproductive and Child Health of Peking University for their contribution to data collection. We are also indebted to all women who participated in this study for their cooperation.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

References

  1. Mertz, W. The essential trace elements. Science 1981, 213, 1332–1338. [Google Scholar] [CrossRef] [Green Version]
  2. Allen, L.H. Multiple micronutrients in pregnancy and lactation: An overview. Am. J. Clin. Nutr. 2005, 81, 1206S–1212S. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Shah, S.; Jeong, K.S.; Park, H.; Hong, Y.C.; Kim, Y.; Kim, B.; Chang, N.; Kim, S.; Kim, Y.; Kim, B.N.; et al. Environmental pollutants affecting children’s growth and development: Collective results from the MOCEH study, a multi-centric prospective birth cohort in Korea. Environ. Int. 2020, 137, 105547. [Google Scholar] [CrossRef]
  4. Zhou, F.; Yin, G.; Gao, Y.; Liu, D.; Xie, J.; Ouyang, L.; Fan, Y.; Yu, H.; Zha, Z.; Wang, K.; et al. Toxicity assessment due to prenatal and lactational exposure to lead, cadmium and mercury mixtures. Environ. Int. 2019, 133, 105192. [Google Scholar] [CrossRef]
  5. Liu, T.; Zhang, M.; Guallar, E.; Wang, G.; Hong, X.; Wang, X.; Mueller, N.T. Trace Minerals, Heavy Metals, and Preeclampsia: Findings from the Boston Birth Cohort. J. Am. Heart Assoc. 2019, 8, e012436. [Google Scholar] [CrossRef]
  6. Zhang, C.; Rawal, S. Dietary iron intake, iron status, and gestational diabetes. Am. J. Clin. Nutr. 2017, 106, 1672S–1680S. [Google Scholar] [CrossRef] [Green Version]
  7. WHO/UNICEF/ICCIDD. Assessment of Iodine Deficiency Disorders and Monitoring Their Elimination: A Guide for Programme Manager. 2007. Available online: https://apps.who.int/iris/bitstream/handle/10665/43781/9789241595827_eng.pdf;sequence=1 (accessed on 17 December 2020).
  8. Hu, H.; Liu, Z.; Li, J.; Li, S.; Tian, X.; Lin, Y.; Chen, X.; Yang, J.; Deng, Y.; Li, N.; et al. Correlation between Congenital Heart Defects and maternal copper and zinc concentrations. Birth Defects Res. Part A Clin. Mol. Teratol. 2014, 100, 965–972. [Google Scholar] [CrossRef] [PubMed]
  9. Pi, X.; Qiao, Y.; Wei, Y.; Jin, L.; Li, Z.; Liu, J.; Zhang, Y.; Wang, L.; Liu, Y.; Xie, Q.; et al. Concentrations of selected heavy metals in placental tissues and risk for neonatal orofacial clefts. Environ. Pollut. 2018, 242, 1652–1658. [Google Scholar] [CrossRef]
  10. Everson, T.M.; Kappil, M.; Hao, K.; Jackson, B.P.; Punshon, T.; Karagas, M.R.; Chen, J.; Marsit, C.J. Maternal exposure to selenium and cadmium, fetal growth, and placental expression of steroidogenic and apoptotic genes. Environ. Res. 2017, 158, 233–244. [Google Scholar] [CrossRef]
  11. Goldenberg, R.L.; Tamura, T.; Neggers, Y.; Copper, R.L.; Johnston, K.E.; Dubard, M.B.; Hauth, J.C. The Effect of Zinc Supplementation on Pregnancy Outcome. JAMA 1995, 274, 463–468. [Google Scholar] [CrossRef]
  12. Scholl, T.O. Iron status during pregnancy: Setting the stage for mother and infant. Am. J. Clin. Nutr. 2005, 81, 1218S–1222S. [Google Scholar] [CrossRef] [PubMed]
  13. Chung, S.E.; Cheong, H.-K.; Ha, E.-H.; Kim, B.-N.; Ha, M.; Kim, Y.; Hong, Y.-C.; Park, H.; Oh, S.-Y. Maternal Blood Manganese and Early Neurodevelopment: The Mothers and Children’s Environmental Health (MOCEH) Study. Environ. Health Perspect. 2015, 123, 717–722. [Google Scholar] [CrossRef] [Green Version]
  14. Do Nascimento, S.N.; Barth, A.; Goethel, G.; Baierle, M.; Charão, M.F.; Brucker, N.; Moro, A.M.; Bubols, G.B.; Sobreira, J.S.; Sauer, E.; et al. Cognitive deficits and ALA-D-inhibition in children exposed to multiple metals. Environ. Res. 2015, 136, 387–395. [Google Scholar] [CrossRef]
  15. Hynes, K.L.; Otahal, P.; Hay, I.; Burgess, J.R. Mild Iodine Deficiency During Pregnancy Is Associated with Reduced Educational Outcomes in the Offspring: 9-Year Follow-up of the Gestational Iodine Cohort. J. Clin. Endocrinol. Metab. 2013, 98, 1954–1962. [Google Scholar] [CrossRef] [Green Version]
  16. Bocca, B.; Ruggieri, F.; Pino, A.; Rovira, J.; Calamandrei, G.; Mirabella, F.; Ángeles Martí, M.; Domingo, J.L.; Alimonti, A.; Schuhmacher, M. Human biomonitoring to evaluate exposure to toxic and essential trace elements during pregnancy. Part B: Predictors of exposure. Environ. Res. 2020, 182, 109108. [Google Scholar] [CrossRef]
  17. Caspersen, I.H.; Thomsen, C.; Haug, L.S.; Knutsen, H.K.; Brantsæter, A.L.; Papadopoulou, E.; Erlund, I.; Lundh, T.; Alexander, J.; Meltzer, H.M. Patterns and dietary determinants of essential and toxic elements in blood measured in mid-pregnancy: The Norwegian Environmental Biobank. Sci. Total. Environ. 2019, 671, 299–308. [Google Scholar] [CrossRef]
  18. Almeida, A.A.; Lopes, C.M.; Silva, A.M.; Barrado, E. Trace elements in human milk: Correlation with blood levels, inter-element correlations and changes in concentration during the first month of lactation. J. Trace Elem. Med. Biol. 2008, 22, 196–205. [Google Scholar] [CrossRef]
  19. Watson, C.V.; Lewin, M.; Ragin-Wilson, A.; Jones, R.; Jarrett, J.M.; Wallon, K.; Ward, C.; Hilliard, N.; Irvin-Barnwell, E. Characterization of trace elements exposure in pregnant women in the United States, NHANES 1999–2016. Environ. Res. 2020, 183, 109208. [Google Scholar] [CrossRef]
  20. Silbergeld, E.K. Lead in bone: Implications for toxicology during pregnancy and lactation. Environ. Health Perspect. 1991, 91, 63–70. [Google Scholar] [CrossRef] [PubMed]
  21. Téllez-Rojo, M.M.; Hernández-Avila, M.; Lamadrid-Figueroa, H.; Smith, D.; Hernández-Cadena, L.; Mercado, A.; Aro, A.; Schwartz, J.; Hu, H. Impact of Bone Lead and Bone Resorption on Plasma and Whole Blood Lead Levels during Pregnancy. Am. J. Epidemiol. 2004, 160, 668–678. [Google Scholar] [CrossRef]
  22. Liu, J.; Yang, H.; Shi, H.; Shen, C.; Zhou, W.; Dai, Q.; Jiang, Y. Blood Copper, Zinc, Calcium, and Magnesium Levels during Different Duration of Pregnancy in Chinese. Biol. Trace Elem. Res. 2010, 135, 31–37. [Google Scholar] [CrossRef]
  23. Zhang, Z.; Yuan, E.; Liu, J.; Lou, X.; Jia, L.; Li, X.; Zhang, L. Gestational age-specific reference intervals for blood copper, zinc, calcium, magnesium, iron, lead, and cadmium during normal pregnancy. Clin. Biochem. 2013, 46, 777–780. [Google Scholar] [CrossRef] [PubMed]
  24. Choi, R.; Sun, J.; Yoo, H.; Kim, S.; Cho, Y.Y.; Kim, H.J.; Kim, S.W.; Chung, J.H.; Oh, S.-Y.; Lee, S.-Y. A Prospective Study of Serum Trace Elements in Healthy Korean Pregnant Women. Nutrients 2016, 8, 749. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Kassu, A.; Yabutani, T.; Mulu, A.; Tessema, B.; Ota, F. Serum Zinc, Copper, Selenium, Calcium, and Magnesium Levels in Pregnant and Non-Pregnant Women in Gondar, Northwest Ethiopia. Biol. Trace Elem. Res. 2008, 122, 97–106. [Google Scholar] [CrossRef] [PubMed]
  26. Nwagha, U.I.; Ogbodo, S.O.; Nwogu-Ikojo, E.E.; Ibegbu, D.M.; Ejezie, F.E.; Nwagha, T.U.; Dim, C.C. Copper and selenium status of healthy pregnant women in Enugu, southeastern Nigeria. Niger. J. Clin. Pract. 2011, 14, 408–412. [Google Scholar] [CrossRef]
  27. Sengupta, S.; Bhaskar, M.V.; Haq, I. A study of micronutrient status in pregnancy. J. Indian Med. Assoc. 2010, 108, 817–822. [Google Scholar] [PubMed]
  28. Hansen, S.; Nieboer, E.; Sandanger, T.M.; Wilsgaard, T.; Thomassen, Y.; Veyhe, A.S.; Odland, J.Ø. Changes in maternal blood concentrations of selected essential and toxic elements during and after pregnancy. J. Environ. Monit. 2011, 13, 2143–2152. [Google Scholar] [CrossRef] [PubMed]
  29. Li, Y.; Li, H.-T.; Trasande, L.; Ge, H.; Yu, L.-X.; Xu, G.-S.; Bai, M.-X.; Liu, J.-M. DHA in Pregnant and Lactating Women from Coastland, Lakeland, and Inland Areas of China: Results of a DHA Evaluation in Women (DEW) Study. Nutrients 2015, 7, 8723–8732. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  30. Liu, M.-J.; Li, H.-T.; Yu, L.-X.; Xu, G.-S.; Ge, H.; Wang, L.-L.; Zhang, Y.-L.; Zhou, Y.-B.; Li, Y.; Bai, M.-X.; et al. A Correlation Study of DHA Dietary Intake and Plasma, Erythrocyte and Breast Milk DHA Concentrations in Lactating Women from Coastland, Lakeland, and Inland Areas of China. Nutrients 2016, 8, 312. [Google Scholar] [CrossRef] [Green Version]
  31. Zhou, Y.-B.; Li, H.-T.; Trasande, L.; Wang, L.-L.; Zhang, Y.-L.; Si, K.-Y.; Bai, M.-X.; Liu, J.-M. A Correlation Study of DHA Intake Estimated by a FFQ and Concentrations in Plasma and Erythrocytes in Mid- and Late Pregnancy. Nutrients 2017, 9, 1256. [Google Scholar] [CrossRef] [Green Version]
  32. Nielsen, F. Nickel. Adv. Nutr. 2020, 12, 281–282. [Google Scholar] [CrossRef]
  33. Meng, F.; Zhao, R.; Liu, P.; Liu, L.; Liu, S. Assessment of Iodine Status in Children, Adults, Pregnant Women and Lactating Women in Iodine-Replete Areas of China. PLoS ONE 2013, 8, e81294. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Brough, L.; Jin, Y.; Shukri, N.H.; Wharemate, Z.R.; Weber, J.L.; Coad, J. Iodine intake and status during pregnancy and lactation before and after government initiatives to improve iodine status, in Palmerston North, New Zealand: A pilot study. Matern. Child Nutr. 2015, 11, 646–655. [Google Scholar] [CrossRef] [PubMed]
  35. Li, Q.; Tian, J.; Xu, F.; Binns, C. Breastfeeding in China: A Review of Changes in the Past Decade. Int. J. Environ. Res. Public Health 2020, 17, 8234. [Google Scholar] [CrossRef] [PubMed]
  36. Liu, X.; Zhang, Y.; Piao, J.; Mao, D.; Li, Y.; Li, W.; Yang, L.; Yang, X. Reference Values of 14 Serum Trace Elements for Pregnant Chinese Women: A Cross-Sectional Study in the China Nutrition and Health Survey 2010–2012. Nutrients 2017, 9, 309. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Takser, L.; Lafond, J.; Bouchard, M.; St-Amour, G.; Mergler, D. Manganese levels during pregnancy and at birth: Relation to environmental factors and smoking in a Southwest Quebec population. Environ. Res. 2004, 95, 119–125. [Google Scholar] [CrossRef]
  38. McArdle, H. The metabolism of copper during pregnancy—A review. Food Chem. 1995, 54, 79–84. [Google Scholar] [CrossRef]
  39. Keen, C.L.; Uriu-Hare, J.Y.; Hawk, S.N.; A Jankowski, M.; Daston, G.P.; Kwik-Uribe, C.L.; Rucker, R.B. Effect of copper deficiency on prenatal development and pregnancy outcome. Am. J. Clin. Nutr. 1998, 67, 1003S–1011S. [Google Scholar] [CrossRef] [Green Version]
  40. O’Neal, S.L.; Zheng, W. Manganese Toxicity upon Overexposure: A Decade in Review. Curr. Environ. Health Rep. 2015, 2, 315–328. [Google Scholar] [CrossRef] [Green Version]
  41. American College of Obstetricians and Gynecologists. Delayed Umbilical Cord Clamping after Birth. ACOG Committee Opinion. Obstet. Gynecol. 2020, 136, e100–e106. [Google Scholar] [CrossRef]
  42. Fairweather-Tait, S.; Hurrell, R.F. Bioavailability of Minerals and Trace Elements. Nutr. Res. Rev. 1996, 9, 295–324. [Google Scholar] [CrossRef] [Green Version]
  43. Greenwood, M.R.; Clarkson, T.W.; Doherty, R.A.; Gates, A.H.; Amin-Zaki, L.; Elhassani, S.; Majeed, M.A. Blood clearance half-times in lactating and nonlactating members of a population exposed to methylmercury. Environ. Res. 1978, 16, 48–54. [Google Scholar] [CrossRef]
  44. Dorea, J.G.; Donangelo, C.M. Early (in uterus and infant) exposure to mercury and lead. Clin. Nutr. 2006, 25, 369–376. [Google Scholar] [CrossRef]
  45. Cook, J.D.; Monsen, E.R. Food iron absorption in human subjects. III. Comparison of the effect of animal proteins on nonheme iron absorption. Am. J. Clin. Nutr. 1976, 29, 859–867. [Google Scholar] [CrossRef]
  46. Nakayama, S.F.; The Japan Environment and Children’s Study Group; Iwai-Shimada, M.; Oguri, T.; Isobe, T.; Takeuchi, A.; Kobayashi, Y.; Michikawa, T.; Yamazaki, S.; Nitta, H.; et al. Blood mercury, lead, cadmium, manganese and selenium levels in pregnant women and their determinants: The Japan Environment and Children’s Study (JECS). J. Expo. Sci. Environ. Epidemiol. 2019, 29, 633–647. [Google Scholar] [CrossRef] [Green Version]
Table 1. Concentrations (ng/mL) of plasma essential and toxic elements among pregnant and lactating women.
Table 1. Concentrations (ng/mL) of plasma essential and toxic elements among pregnant and lactating women.
ElementsOverall (n = 1211)Pregnant Women (n = 804)Lactating Women (n = 407)p2
Crude Median
(IQR)
Adjusted 1 Median
(IQR)
Crude Median
(IQR)
Adjusted 1 Median
(IQR)
Crude Median
(IQR)
Adjusted 1 Median
(IQR)
Essential elements 3
Cu1810
(1409, 2133)
1949
(1760, 2167)
2024
(1804, 2281)
2025
(1809, 2292)
1306
(1165, 1454)
1300
(1194, 1441)
<0.001
Fe2392
(2077, 2702)
2374
(2115, 2699)
2395
(2057, 2716)
2372
(2093, 2709)
2383
(2124, 2674)
2348
(2087, 2639)
0.879
Zn962
(843, 1101)
979
(907, 1074)
935
(816, 1077)
929
(849, 1032)
1012
(899, 1141)
1064
(974, 1166)
<0.001
I82.1
(61.7, 104.4)
88.9
(77.3, 102.2)
96.4
(80.7, 112.5)
97.9
(84.5, 109.5)
57.5
(50.1, 66.6)
56.5
(51.2, 62.8)
<0.001
Cr0.39
(0.31, 0.53)
0.39
(0.30, 0.51)
0.38
(0.30, 0.52)
0.38
(0.29, 0.52)
0.42
(0.33, 0.59)
0.43
(0.34, 0.55)
<0.001
Mn2.00
(1.59, 2.64)
1.91
(1.62, 2.50)
2.03
(1.63, 2.66)
1.95
(1.71, 2.55)
1.96 (1.52, 2.63)1.80
(1.43, 2.41)
0.059
Co1.69
(1.32, 2.21)
1.70
(1.41, 2.12)
1.70
(1.35, 2.10)
1.67
(1.46, 1.99)
1.67
(1.26, 2.44)
1.63
(1.28, 2.39)
0.501
Mo3.22
(2.68, 3.90)
3.22
(2.76, 3.82)
3.07
(2.58, 3.60)
2.97
(2.60, 3.35)
3.63
(3.04, 4.32)
3.81
(3.12, 4.43)
<0.001
B 465.3
(41.9, 94.4)
60.4
(42.9, 92.6)
65.7
(44.3, 88.7)
65.2
(52.5, 88.2)
64.5
(38.7, 113) b
60.1
(38.2, 101.0)
0.167
Toxic elements
Ni 514.7
(9.7, 25.2)
15.8
(11.6, 24.1)
13.4
(9.1, 21.7)
12.9
(10.5, 19.6)
20.1
(11.1, 31.4)
16.4
(11.2, 29.8)
<0.001
Al72.6
(59.9, 93.0)
71.8
(61.4, 84.6)
75.5
(61.1, 99.0)
75.5
(64.1, 88.5)
68.6
(58.5, 84.1)
65.0
(58.7, 73.5)
<0.001
Sb6.14
(5.34, 6.98)
6.20
(5.31, 6.93)
6.04
(5.37, 6.72)
6.03
(5.52, 6.57)
6.46
(5.27, 7.58)
6.42
(5.49, 7.39)
<0.001
Hg0.69
(0.50, 0.89)
0.68
(0.54, 0.84)
0.71
(0.52, 0.90)
0.73
(0.60, 0.89)
0.65
(0.48, 0.87)
0.59
(0.48, 0.73)
0.021
Cd1.07
(0.85, 1.30)
1.06
(0.88, 1.27)
1.00
(0.82, 1.22)
0.98
(0.82, 1.20)
1.20
(0.99, 1.45)
1.21
(0.99, 1.45)
<0.001
Pb1.60
(1.14, 2.23)
1.46
(1.13, 2.12)
1.53
(1.08, 2.16)
1.34
(1.06, 2.06)
1.70
(1.33, 2.45)
1.59
(1.34, 2.17)
<0.001
1 Estimated from multivariable quantile regression models adjusted for physiologic stage, geographic region, maternal age, parity, ethnicity, education status, annual family income per capita, pre-pregnancy BMI, and dietary intake of aquatic products, mutton, and formula; delivery mode and feeding practice were also included in the models for lactating women; 2 The statistical differences in the plasma element concentrations between pregnant and lactating women were tested using Mann-Whitney tests; statistical significance was set at p < 0.05; 3 Dietary reference intakes of essential elements were presented in Table S3; 4 Although B was classified as an essential element, neither a recommended dietary allowance nor an adequate intake has been established for boron; 5 Ni is generally not considered an essential nutrient for humans at present, while evidence from experimental animals indicated the beneficial effects of Ni on metabolic processes and enzyme functions [32]; IQR, interquartile range.
Table 2. Adjusted median concentrations (ng/mL) of plasma essential and toxic elements by characteristics of pregnant women (n = 804) 1.
Table 2. Adjusted median concentrations (ng/mL) of plasma essential and toxic elements by characteristics of pregnant women (n = 804) 1.
Characteristicsn (%)Essential ElementsToxic Elements
CuFeZnICrMnCoMoBNiAlSbHgCdPb
Pregnancy stage
Mid-pregnancy407 (51)1948 a2515 b1026 b107.3 b0.37 a1.89 a1.55 a3.02 b59.3 a13.1 b78.9 b6.040.75 b1.00 b1.27 a
Late-pregnancy397 (49)2096 b2184 a895 a94.2 a0.38 b2.00 b1.91 b2.84 a73.6 b12.1 a72.9 a6.020.70 a0.90 a1.36 b
Geographic region
Coastland263 (33)2056 b2297 a1088 c109.9 c0.36 a2.44 c1.69 b2.87 a87.0 c13.0 b100.4 c6.03 b0.74 b0.93 b1.89 b
Lakeland267 (33)2069 b2371 b935 b101.6 b0.39 b1.96 b1.94 c2.84 a67.3 b21.2 c75.5 b5.55 a0.85 c0.90 a1.27 a
Inland274 (34)1993 a2518 c813 a84.1 a0.38 b1.59 a1.34 a3.58 b43.1 a9.07 a62.5 a6.55 c0.49 a1.12 c1.26 a
Age (years)
≤25 140 (17)1988 a2341 a91696.50.39 b1.94 a1.822.9156.8 a20.1 b72.9 a5.64 a0.760.961.33
26 to 30491 (61)2005 a2383 b96999.70.37 a1.95 a1.652.9772.5 b12.5 a78.0 b6.04 b0.730.991.33
31 to 35173 (22)2091b2356 a92095.00.39 b2.06 b1.623.0563.7 a13.2 a76.3 b6.03 b0.721.001.41
Pre-pregnancy BMI
Underweight147 (18)2032 a2362 a90897.90.37 a1.901.77 b2.9164.512.774.85.90 a0.740.96 a1.35
Normal weight591 (74)2017 a2368 a95798.50.38 a1.991.69 b2.9767.613.076.36.04 b0.730.98 a1.33
Overweight/obese66 (8)2090 b2395 b91489.30.43 b1.951.54 a3.1659.311.575.56.34 b0.661.04 b1.37
Parity
Primiparous665 (83)2015 a2390968 b98.50.38 a1.991.692.97 b69.3 b12.876.36.040.730.99 b1.35 b
Multiparous139 (17)2066 b2315886 a94.20.39 b1.911.602.78 a56.4 a14.072.25.960.800.94 a1.27 a
Ethnicity
Han764 (95)2032 b2364 a967 b98.5 b0.38 b1.97 b1.70 b2.95 a68.1 b13.0 b76.36.02 a0.750.98 a1.35 b
Others40 (5)1937 a2597 b845 a87.9 a0.37 a1.62 a1.28 a3.55 b40.4 a9.1 a68.76.89 b0.621.20 b1.15 a
Education
College or higher523 (65)2018 a2390 c91594.3 a0.38 a1.951.62 a2.98 b64.512.1 a74.0 a6.09 b0.721.00 b1.33 b
High school175 (22)2069 b2360 b969105.9 b0.38 a1.951.91 b2.94 b60.513.6 b74.7 a5.85 a0.730.96 a1.24 a
Middle school or less106 (13)2035 a2264 a95798.6 a0.40 b2.041.62 a2.78 a69.713.5 b81.3 b5.93 a0.770.93 a1.68 c
Annual family income per capita (Yuan 2)
<30,000296 (37)2034 a2294 a96998.50.37 a1.951.87 b2.9163.019.7 b77.36.090.710.981.30 a
30,000 to <50,000231 (29)2023 a2408 c98599.80.38 a2.031.59 a2.9975.613.1 a77.36.090.740.981.54 b
50,000 to <100,000191 (24)2052 b2327 b92997.20.38 a2.001.58 a2.9772.512.4 a75.16.040.790.971.30 a
≥100,00030 (4)2029 a2569 d92887.70.42 b1.941.42 a2.7973.712.0 a68.96.510.580.991.70 c
1 Estimated from multivariable quantile regression models adjusted for physiologic stage, geographic region, maternal age, parity, ethnicity, education status, annual family income per capita, pre-pregnancy BMI, and dietary intake of aquatic products, mutton, and formula; delivery mode and feeding practice were also included in the models for lactating women. Values not sharing the same superscript letter (a, b, c, d) denote significant differences across characteristics of women: concentrations of a < b < c < d; statistical significance was set at p < 0.01 due to multiple comparisons.2 Eighty three women (10%) missed information on annual family income per capita.
Table 3. Adjusted median concentrations (ng/mL) of plasma essential and toxic elements by characteristics of lactating women (n = 407) 1.
Table 3. Adjusted median concentrations (ng/mL) of plasma essential and toxic elements by characteristics of lactating women (n = 407) 1.
Characteristicsn (%)Essential ElementsToxic Elements
CuFeZnICrMnCoMoBNiAlSbHgCdPb
Geographic region
Coastland136 (33)1335 b2333 a1106 c65.8 b0.42 b2.29 c2.43 c3.01 a114.8 c30.4 c88.5 c5.23 a0.58 b1.09 a2.16 c
Lakeland135 (33)1246 a2316 a1074 b53.9 a0.38 a1.73 b1.31 a4.01 c40.7 a13.4 a64.1 b7.63 c0.90 c1.31 c1.57 b
Inland136 (33)1316 b2569 b867 a54.7 a0.52 c1.64 a1.63 b3.86 b59.9 b15.8 b61.5 a6.42 b0.48 a1.25 b1.41 a
Age (years)
≤25 61 (15)1189 a2242 a105456.60.40 a1.861.40 a3.75 a43.2 a13.3 a63.46.630.661.241.55
26 to 30253 (62)1324 b2347 b106757.00.42 a1.761.63 b3.81 a60.4 b16.8 b65.36.500.581.191.64
31 to 3593 (23)1298 b2364 c107255.30.45 b1.841.60 b4.01 b60.6 b16.6 b65.66.180.591.291.59
Pre-pregnancy BMI
Underweight80 (20)1251 a23261044 a57.10.441.771.41 a4.00 b46.5 a14.6 a64.56.74 c0.621.31 b1.58 a
Normal weight287 (70)1312 b23481072 b56.20.421.811.63 b3.81 a60.6 b16.4 b65.06.41 b0.641.18 a1.58 a
Overweight/obese40 (10)1317 b24101079 b61.00.442.072.26 b3.25 a101.9 b27.3 b84.45.46 a0.661.19 a2.12 b
Ethnicity
Han389 (96)13002348106756.8 b0.42 a1.791.633.80 a60.416.465.06.410.601.20 a1.58 a
Others18 (4)1278235792750.0 a0.58 b1.951.584.57 b55.816.968.26.790.551.47 b2.02 b
Education
College or higher273 (67)13012361 b1060 a56.50.421.771.633.9260.416.465.46.410.691.25 b1.59
High school92 (23)12832288 a1059 a57.30.431.851.563.6756.615.663.46.270.601.19 b1.58
Middle school or less42 (10)13042232 a1100 b56.60.441.861.503.7944.316.765.76.690.541.09 a1.65
Annual family income per capita (Yuan 2)
<30,000238 (58)1317 b23351084 b56.30.411.821.633.8260.6 b16.9 b66.3 b6.40 a0.611.221.58 b
30,000 to <50,000100 (25)1250 a23481033 a55.40.431.731.553.8360.1 b13.9 a62.3 b6.37 a0.571.251.49 a
50,000 to <100,00037 (9)1334 b23751098 b56.00.431.791.503.9048.6 a14.3 a57.3 a7.07 b0.551.211.51 a
≥100,0005 (1)1381 b24081020 a61.00.321.561.284.1141.9 a12.0 a56.7 a7.73 b0.821.181.99 b
Delivery mode
Vaginal delivery243 (60)129823391089 b60.6 b0.41 a1.982.333.2796.4 b24.8 b67.4 b5.93 a0.611.16 a1.61
Cesarean delivery164 (40)13012377934 a53.0 a0.51 b1.691.344.0853.3 a14.1 a62.1 a6.66 b0.581.28 b1.58
Feeding practice
Exclusive breastfeeding240 (59)1267 a2336105955.1 a0.41 a1.821.753.8960.416.7 b64.2 a6.450.66 b1.211.59
Partial breastfeeding167 (41)1320 b2359108158.0 b0.44 b1.761.543.7455.714.5 a66.2 b6.370.61 a1.221.59
1 Estimated from multivariable quantile regression models adjusted for physiologic stage, geographic region, maternal age, parity, ethnicity, education status, annual family income per capita, pre-pregnancy BMI, and dietary intake of aquatic products, mutton, and formula; delivery mode and feeding practice were also included in the models for lactating women. Values not sharing the same superscript letter (a, b, c) denote significant differences across groups of women: concentrations of a < b < c; statistical significance was set at p < 0.01 due to multiple comparisons. 2 Twenty seven women (7%) missed information on annual family income per capita.
Table 4. Adjusted median concentrations (ng/mL) of plasma essential and toxic elements by dietary intakes of pregnant and lactating women (n = 1208) 1.
Table 4. Adjusted median concentrations (ng/mL) of plasma essential and toxic elements by dietary intakes of pregnant and lactating women (n = 1208) 1.
Dietary Intakesn (%)Essential ElementsToxic Elements
CuFeZnICrMnCoMoBNiAlSbHgCdPb
Pregnant women
Freshwater aquatic product
Lowest and middle tertiles580 (72)20202345931 a97.3 a0.37 a1.97 b1.62 a3.05 b69.112.6 a75.6 b6.10 b0.68 a1.00 b1.43 b
Highest tertile223 (28)20362395943 b99.2 b0.38 b1.94 a1.87 b2.87 a63.021.0 b75.1 a5.55 a0.83 b0.93 a1.26 a
Marine aquatic product
Lowest and middle tertiles494 (62)2015 a2398 b892 a92.6 a0.38 b1.86 a1.67 a3.05 b57.5 a13.8 b72.4 a6.070.70 a1.00 b1.30 a
Highest tertile309 (38)2054 b2296 a1000 b102.5 b0.37 a2.32 b1.70 b2.87 a80.6 b13.0 a94.7 b6.030.74 b0.94 a1.84 b
Mutton
Lowest and middle tertiles531 (66)2037 b2339 a994 b102.5 b0.37 a2.01 b1.862.89 a72.9 b19.7 b78.4 b5.78 a0.79 b0.94 a1.38 b
Highest tertile272 (34)2013 a2386 b853 a86.9 a0.38 b1.64 a1.493.43 b48.0 a9.2 a65.2 a6.44 b0.52 a1.06 b1.30 a
Formula
No 610 (76)2005 a236693798.30.381.90 a1.62 a3.05 b62.3 a12.5 a75.36.09 b0.68 a1.00 b1.39 b
Yes194 (24)2109 b233093397.60.382.01 b1.87 b2.87 a71.8 b20.8 b75.65.61 a0.81 b0.91 a1.30 a
Lactating women
Freshwater aquatic product
Lowest and middle tertiles231 (57)13142417 b105556.40.45 b1.821.63 b3.75 a60.816.9 b63.3 a6.24 a0.55 a1.19 a1.62
Highest tertile174 (43)13032313 a106156.50.40 a1.851.48 a3.87 b53.715.7 a66.7 b6.71 b0.69 b1.24 b1.65
Marine aquatic product
Lowest and middle tertiles310 (77)1301 a2375 b1048 a55.0 a0.431.78 a1.51 a3.87 b54.7 a15.4 a64.0 a6.50 b0.591.23 b1.57 a
Highest tertile95 (23)1329 b2297 a1075 b64.9 b0.422.16 b2.36 b3.13 a107.7 b28.1 b87.9 b5.27 a0.611.13 a2.10 b
Mutton
Lowest and middle tertiles282 (70)1292 a2321 a1077 b58.1 b0.40 a1.90 b1.47 a3.77 a54.916.467.0 b6.61 b0.67 b1.191.71 b
Highest tertile123 (30)1339 b2512 b894 a54.2 a0.52 b1.64 a1.62 b3.85 b60.116.862.2 a6.24 a0.50 a1.231.47 a
Formula
No 356 (87)13072352106456.90.43 b1.89 b1.64 b3.75 a61.0 b17.1 b65.6 b6.22 a0.59 a1.19 a1.67 b
Yes51 (13)12992397103554.90.41 a1.61 a1.35 a4.07 b44.0 a13.5 a62.6 a7.66 b0.84 b1.28 b1.53 a
1 Estimated from multivariable quantile regression models adjusted for physiologic stage, geographic region, maternal age, parity, ethnicity, education status, annual family income per capita, pre-pregnancy BMI, and dietary intake of aquatic products, mutton, and formula; delivery mode and feeding practice were also included in the models for lactating women. Values not sharing the same superscript letter (a, b) denote significant differences across characteristics of women: concentrations of a < b. A total of 1208 participants were included in the analyses for dietary intakes, because 3 missed dietary information.
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Zhou, Y.; Yan, L.; Li, H.; Li, X.; Liu, Y.; Liu, J. Patterns and Determinants of Essential and Toxic Elements in Chinese Women at Mid-Pregnancy, Late Pregnancy, and Lactation. Nutrients 2021, 13, 668. https://doi.org/10.3390/nu13020668

AMA Style

Zhou Y, Yan L, Li H, Li X, Liu Y, Liu J. Patterns and Determinants of Essential and Toxic Elements in Chinese Women at Mid-Pregnancy, Late Pregnancy, and Lactation. Nutrients. 2021; 13(2):668. https://doi.org/10.3390/nu13020668

Chicago/Turabian Style

Zhou, Yubo, Lailai Yan, Hongtian Li, Xiucui Li, Yaqiong Liu, and Jianmeng Liu. 2021. "Patterns and Determinants of Essential and Toxic Elements in Chinese Women at Mid-Pregnancy, Late Pregnancy, and Lactation" Nutrients 13, no. 2: 668. https://doi.org/10.3390/nu13020668

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