Background: The impact of prenatal exposure to cadmium (Cd) on birth outcomes is an area of concern. This study aimed to assess an impact of prenatal Cd exposure on birth outcomes in distinct coastal populations of South Africa. Methods: Cadmium was measured in maternal blood (CdB) (n = 641), cord blood and in maternal urine (n = 317). This investigation assessed the associations between CdB (non-transformed) and birth outcomes across the 25th, 50th, and 75th percentile for birth weight, birth length and head circumference, to test for a linear trend. Associations between natural log-transformed maternal CdB, size at birth and other factors were further evaluated using linear mixed-effects modelling with random intercepts. Results: The average gestational age in the total sample was 38 weeks; 47% of neonates were female, average birth weight was 3065 g and 11% were of low birth weight (< 2500 g). The geometric mean (GM) of the maternal CdB level was 0.25 μg/L (n = 641; 95% CI, 0.23- 0.27). The cord blood Cd level was 0.27 μg/L (n = 317; 95% CI, 0.26-0.29) and urine (creatinine- corrected) Cd level was 0.27 μg/L (n = 318; 95% CI, 0.24-0.29). The CdB cord:maternal ratio in the sub-cohort was 1, suggesting that the placenta offers no protective mechanism to the foetus. An inverse association was found between CdB and the lower birth weight percentile in female neonates only (β = – 0.13, p = 0.047). Mothers who reported eating vine vegetables daily had lower levels of CdB (β = – 0.55, p = 0.025). Maternal smoking was associated with an elevation in natural log-transformed CdB levels in both male and female cohorts. Discussion: Significant inverse associations between prenatal Cd exposure and birth anthropometry were found in female neonates but not in male neonates, suggesting potential sex differences in the toxico-kinetics and toxico-dynamics of Cd.
A total of five sites were included in the study: three sites were situated along the Indian Ocean coast of the KwaZulu Natal (KZN) Province, and two sites were situated along the Atlantic Ocean coast of the Western Cape Province of South Africa (Fig 1). Figure is identical but sites locations were added, and is therefore for representative purposes only. https://www.cia.gov/library/publications/resources/cia-maps-publications/South%20Africa.html. All three sites along the Indian Ocean coast can be defined as rural with varying degrees of agricultural activities. However, their geographical location may predispose them to environmental pollution emanating from mining and industrial activities (site 1); aluminium smelting, mining, coal terminals and ports (site 2); and small industrial activities (site 3). Along the Atlantic Ocean coast, one study site is the urban city of Cape Town, which is surrounded by commercial, industrial and port activities (site 4); and the second site is considered to be rural (site 5), where commercial agriculture and fishing activities dominate. Potential study candidates were recruited by a health worker on duty, from women who were admitted for delivery at the local maternity sections of public hospitals. A trained research assistant briefly explained the objectives of the study and distributed a detailed information sheet about the project. All women who agreed to participate signed an informed consent form and agreed to donate blood before delivery. Participants agreed to answer a socio-demographic questionnaire which also included the topics of diet, lifestyle, and health status. Participants also consented to access and use of hospital birth outcome data for research purposes. The socio-demographic questionnaire was not specifically designed for Cd exposure, but for exposure to environmental pollutants in general. The dietary part of the questionnaire recorded the intake frequency of various basic foods during pregnancy. After delivery, records from hospital files were extracted, including maternal and neonate characteristics such as weight, length and head circumference, gestational age, as well as any birth complications, if any. In total, 650 delivering women participated in the study, of which 641 women, who delivered singleton infants of gestation of more than 20 weeks, were included. Due to financial constraints, the collection of additional samples (pre-partum urine samples and post-partum cord blood samples) was limited to women residing in Sites 1, 2 and 3 (n = 317). From each woman, a volume of 10 ml of venous blood was collected before delivery into BD Vacutainer tube (10 ml capacity and containing EDTA). Participants from the sub-cohort (n = 317) also donated 30 ml of urine before delivery, and 10 ml of umbilical cord blood post-partum. The analyses for Cd content in whole blood and urine were performed using an Inductively Coupled Plasma-Mass Spectrometer (ICP-MS) instrument (Agilent 7500ce ICP-MS with an Octopole Reaction System). Contamination-free vessels and procedures were used throughout, and validation of results was accomplished by including certified standards, as well as certified references quality controls, in the analyses. Briefly, the whole blood samples (0.5ml volumes) were digested with 1 ml nitric acid (Fluka, Trace Select Ultra for trace analysis) at 90°C for 2 hours. After cooling, the internal standard was added and samples were diluted with water to a final volume of 7 ml. Cd was measured in ‘no gas’ acquisition mode with 115In and 197Au as internal standards. Aliquots of each sample were analysed in triplicate. The detection limits (three times the standard deviation of all blank samples) for Cd was 0.03μg/L. For quality assurance, two certified reference controls, viz. Seronorm ™Trace Elements (Sero LTD., Billingstad, Norway) in whole blood (Levels 1 and 2), were analysed with every analytical run, at intervals between every 10 samples. Urine samples (1 ml volumes) were digested with 0.1 ml of 65% ultrapure nitric acid ((Fluka, Trace Select Ultra for trace analysis). An internal standard solution containing 72Ge, 115In and 197Au was added (50 μl) to all samples, reagent blanks, reference controls and calibration standards and made up to 5 ml (5 times sample dilution). Urinary Cd (CdU) levels were measured in ‘no gas’ acquisition mode and percentage recovery, when using certified standards (Seronorm Urine Blank and Lyphchek Level 1&2), was 108.8% and 111.5% for level 1 and 2, respectively. The sample analyses were conducted by the Johannesburg National Institute for Occupational Health (NIOH) laboratory, which participates in the Wadsworth Center—New York State Department of Health Proficiency testing scheme for whole blood and urine. The results obtained are consistently accepted with no indication of bias. Covariate information was obtained during the questionnaire-based interview and from medical records. Maternal weight and height were recorded at the hospital on admission. From the medical records, the following newborn characteristics were retrieved: birth weight (grams), birth length (cm), head circumference (cm) and gestational age (weeks). Preterm labour was defined as mothers giving birth at less than 37 weeks gestational age. Education was categorised as no education, completed primary school, completed secondary school and any level of tertiary education reached. Maternal tobacco smoking was defined as ever or never. Exposure to environmental tobacco smoke (ETS) was defined as exposure to tobacco smoke from smoking by others in the household. A binary classification was used for exposure to indoor smoke from the burning of fossil fuel (wood and coal) for the purpose of heating or cooking, separating women into those exposed to fossil fuel and those not exposed (for example, electricity). Dietary questions relating to vine, root and leafy vegetable intake were assessed and classified as daily, at least once a week and seldom. The statistical analyses were performed using STATA (StataCorp, 2013. Stata Statistical Software: Release 13. College Station, TX: StataCorp LP). The distribution of Cd levels in maternal blood and urine and in cord blood, were skewed and were log transformed. Bivariate analyses between Cd exposure, sizes at birth and covariates were evaluated by Spearman’s correlation coefficient. The non-parametric Wilcoxon rank-sum (Mann-Whitney) and Kruskal-Wallis rank tests were used where appropriate, to make categorical comparisons of the maternal CdB distribution (n = 641) and demographic, dietary, and environmental characteristics. The 25th percentile (lowest quintile), 50th percentile (median quintile), and 75th percentile (highest quintile) were assessed for birth outcomes (birth weight, birth length and head circumference). Furthermore, associations between CdB (non-transformed) and size at birth across the quintiles were assessed using a non-parametric test (nptrend in Stata) to test for linear trend. Linear mixed-effect models with random intercepts were used to identify significant predictors (p < 0.1) of natural logarithm—transformed blood Cd levels and to estimate the amount of variability in measured levels explained by the model. Potential explanatory variables were identified from questionnaire data that were associated with blood Cd levels with a p < 0.2 during univariate analyses: vegetable intake, smoking history, burning of fossil fuel, environmental tobacco smoke exposure, gestational age, parity, size at birth (birth weight, birth length and head circumference), and gender of the newborn. Model fit was compared using log likelihood and Akaike Information Criterion (AIC) statistics. Ethics approval for the study was obtained from the Human Research Ethics Committee of the University of Witwatersrand in Johannesburg (Protocol no. {"type":"entrez-nucleotide","attrs":{"text":"M10742","term_id":"147973"}}M10742), and from the relevant provincial Departments of Health. The sites along the Indian Ocean coast (sites 1 to 3) fall under the Provincial Department of Health of KwaZulu Natal, which issued ethical consent for each site and requested the CEOs of the respective hospitals to allow this research to take place. Each CEO confirmed that he/she allowed the research work to proceed. The sites along the Atlantic Ocean coast (sites 4 and 5) fall under the Western Cape Provincial Department of Health; identical procedures were followed in terms of obtaining consent for the study. Confidentiality was maintained by assigning identification numbers to all study participants. During the informed consent process, it was emphasised that participation was voluntary and could be withdrawn at any time.