Fetal exposure to mercury and lead from intrauterine blood transfusions

Abstract

Background

Mercury (Hg) and lead (Pb) exposure during childhood is associated with irreversible neurodevelopmental effects. Fetal exposure to Hg and Pb from intrauterine blood transfusion (IUBT) has not been reported.

Methods

Fetal exposure was estimated based on transfusion volume and metal concentration in donor packed red blood cell (PRBCs). As biomarkers to quantify prenatal exposure are unknown, Hg and Pb in donor PRBCs were compared to estimated intravenous (IV) RfDs based on gastrointestinal absorption.

Results

Three pregnant women received 8 single-donor IUBTs with volumes ranging from 19 to 120 mL/kg. Hg and Pb were present in all donor PRBC units. In all, 1/8 IUBT resulted in Hg dose five times higher than the estimated IV RfD. Median Pb dose in one fetus who received 5 single-donor IUBTs between 20–32 weeks gestation was 3.4 μg/kg (range 0.5–7.9 μg/kg). One donor unit contained 12.9 μg/dL of Pb, resulting in a fetal dose of 7.9 μg/kg, 40 times higher than the estimated IV RfD at 20 weeks gestation.

Conclusion

This is the first study documenting inadvertent exposure to Hg and Pb from IUBT and quantifying the magnitude of exposure. Screening of donor blood is warranted to prevent toxic effects from Hg and Pb to the developing fetus.

Introduction

Exposure to the heavy metals mercury (Hg) and lead (Pb) has adverse effects to the developing brain, in addition to detrimental effects to the reproductive, renal, and cardiovascular health.1 Pb exposure can affect nearly every system in the body with irreversible effects.1 While no safe blood Pb level in children has been identified, even low levels of Pb in blood have been shown to affect learning, memory, attention, cognitive function, and academic achievement.2,3 The Center for Disease Control (CDC) recommends public health actions be initiated when blood Pb levels exceed 5 µg/dL.4 The current focus is on primary prevention and to prevent Pb exposure before it occurs. Thereafter protection from exposure to heavy metals starting from the period of conception is important to lifelong good health.

Both Hg and Pb are known neurotoxins that impact fetal brain development, resulting in adverse neurodevelopmental outcomes in children exposed prenatally.5,6 Hg and Pb are both lipid-soluble heavy metals that bind hemoglobin, concentrate in red blood cells, and readily cross the blood–brain barrier.2,7 Hg and Pb have been found consistently in blood samples collected annually by the U.S. Center for Disease Control (CDC) National Health and Nutrition Examination Survey.5,8 Blood products including whole blood, donor packed red blood cells (PRBCs), platelets, and plasma, routinely used for neonatal transfusions, are known sources of Pb and Hg exposure to infants.9,10 Our previous studies have shown that very premature infants at <30 weeks of gestation are exposed to the heavy metal Pb through RBC transfusions and that Pb exposure from RBC transfusion may exceed established safety limits.11,12

Prenatal exposure to Hg and Pb from intrauterine blood transfusion (IUBT) has never before been studied. Currently, donor PRBCs that are used for IUBT are not prescreened for heavy metals. Thus IUBT, a lifesaving treatment for fetal anemia, could potentially expose the fetus to these metals during critical periods of fetal brain development. Ours is the first study to investigate and estimate the burden of fetal heavy metal exposure from IUBT.

Methods

Following approval of the study protocol by The University of Maryland School of Medicine institutional review board, this study was conducted between October 2014 and May 2015 at the University of Maryland Medical Center.

IUBT practice

Top-up intravascular fetal transfusion was performed for all of the IUBTs. The volume of blood for each IUBT was determined based on the measured fetal hemoglobin/hematocrit, the target hematocrit of the fetus, the hematocrit of the transfused RBCs, and estimated fetal weight (EFW). After identifying fetuses at risk for moderate-to-severe anemia by both hematocrit and middle cerebral artery peak systolic velocity, consent was obtained for the IUBT procedure. In the operating room and under intravenous (IV) sedation, the position of the fetus, placenta, and the cord insertion site on the placenta were identified by ultrasound. A 21-gauge needle was introduced into the fetal umbilical vein at the placental insertion site. For posterior placentas or where the fetus is interposed between abdominal insertion site and the cord insertion site of the placenta, the fetus was first given a single dose of Vecuronium 0.1 mg/kg EFW. Compatible cytomegalovirus-negative, irradiated, leukoreduced, and washed PRBCs were then transfused through the needle into the fetal umbilical vein. Fetal heart rate was intermittently monitored by ultrasound throughout the procedure. When infusion was completed, another fetal blood sample was obtained to check the post-transfusion hematocrit. A medical record review was performed to determine gestational age (GA) in weeks at the time of IUBT, transfusion volume (ml), and EFW (g).

Determination of metal content in PRBC unit

After a request for IUBT with PRBCs to correct fetal anemia secondary to immune hemolytic anemia, 1 mL of donor PRBCs was collected as a segment in the blood bank from the designated donor PRBC unit for IUBT use. Samples from 8 single donors were collected and stored at −20 °C. Metal content in donor PRBC segments was measured as total concentration of Hg (μg/L) and Pb (μg/dL) using inductively coupled plasma mass spectroscopy (ICP-MS, Elan DRC-II, Perkin-Elmer, Waltham, MA). The lower limit of detection for both metals was 0.1 μg/L. Accuracy and precision of metal analysis was tested using the external quality control program of the CDC (Wisconsin State Laboratory of Hygiene).

Reference doses (RfDs) for Hg and Pb

Biomarkers to quantify prenatal exposure to Hg and Pb have not been established. Moreover, no exposure to Pb can be considered safe and no safe intake level for Pb currently exists. RfD, a measure to define thresholds of exposure, is defined as an estimate (with uncertainty spanning perhaps an order of magnitude) of a daily exposure to humans (including sensitive subgroups) that is likely to be without an appreciable risk of deleterious effects during one’s lifetime.13 In order to quantify fetal Hg and Pb exposure from PRBC transfusions based on donor PRBC concentration, each IUBT was considered as an IV dose of Hg and Pb. As IV RfDs have not been characterized, we used estimated IV RfDs that were calculated from oral RfDs based on gastrointestinal (GI) absorption as previously published by Elabiad et al.14 The U.S. Environmental Protection Agency has established an oral RfD of 0.1 µg/kg/day for Hg.15 The higher oral Pb intake of 1.9 µg/kg/day, defined by the Joint Food and Agriculture Organization/World Health Organization Expert Committee on Food Additives to be of concern due to a population decrease of 3 IQ points,16 was used as the oral RfD to compare Pb doses given with each blood transfusion.14 With 95% of oral Hg intake and 10% of oral Pb intake being absorbed,15,17 the corresponding estimated IV RfDs would be 0.095 µg/kg/day for Hg and 0.19 µg/kg/day for Pb10 in children, respectively, as shown in Fig. 1.

Fig. 1
figure1

Calculation of estimated intravenous (IV) reference doses (RfD) for Hg and Pb from oral RfD based on gastrointestinal absorption of heavy metals

Estimating Hg and Pb dose per IUBT

We initially determined the fetal metal dose in donor RBC based on the measured concentration of Hg (µg/L) and Pb (µg/dL) content in donor PRBCs by ICP-MS. Metal dose per transfusion was subsequently calculated with the following equation: volume of blood transfused (ml) × PRBC metal level (µg/L)/estimated fetal weight (kg) = estimated IV metal dose (μg/kg/day). Finally, we quantified the burden of Hg and Pb exposure from IUBT by comparing the result of the calculated fetal IV metal dose per transfusion with the estimated IV RfD for Hg and Pb.10,14

Results

Three pregnant women received a total of 8 single-donor IUBTs (n = 5, 2, and 1 IUBT per fetus, respectively) for treatment of fetal anemia secondary to immune hemolytic anemia. At the time of IUBT, fetal GA ranged from 20 to 34 weeks and EFW was 396–2568 g (Table 1). The etiology of hemolytic anemia in fetus 1 was anti-Kell alloimmunization, while fetuses 2 and 3 required IUBT for treatment of Rh isoimmunization. IUBT volume ranged from 19 to 120 mL/kg, based on EFW (Table 1). Hg and Pb were present in all 8 donor PRBC units. Median donor Hg concentration was 1.8 μg/L (range 0.7–3.7), while median donor Pb concentration was 3.7 μg/dL (range 0.9–12.9) (Table 1).

Table 1 Demographics, Donor Metal Concentration, Estimated Fetal Dose, and Magnitude of Exposure to Hg and Pb from Each Fetal Transfusion

Exposure to IUBT resulted in a median estimated fetal IV dose of 0.07 μg/kg (range 0.04–0.44; Fig. 2a) for Hg and 1.1 μg/kg (range 0.5–7.9; Fig. 2b) for Pb. In these IUBTs, 1/8 and 8/8 contained doses of Hg and Pb that were greater than the estimated IV RfDs (Fig. 2a, b).

Fig. 2
figure2

Fetal doses of Hg (a) and Pb (b) as compared to estimated intravenous reference dosesfrom eight single-donor intrauterine blood transfusions of packed red blood cells

Magnitude of exposure in fetus 1

Fetus 1 received a total of 5 IUBTs between 20 and 32 weeks GA from 5 single donors. In this fetus, the median Pb dose among the 5 IUBTs was 3.4 μg/kg (range 0.5–7.9 μg/kg). At 22 weeks GA and an EFW of 500 g, a single IUBT of 120 mL/kg resulted in concurrent fetal doses of Hg of 0.45 μg/Kg (5 times the IV RfD) and Pb of 4.4 μg/kg (23 times the IV RfD) (Table 1). Of added concern, this fetus received an additional single-donor IUBT at 28 weeks GA (61 mL/kg) with almost 13 μg/dL of Pb (Table 1). This represents an estimated IV Pb dose of 8 µg/kg, >40 times the estimated IV RfD (Table 1).

Discussion

This is the first study to quantify in utero exposure to Hg and Pb as early as 20 weeks gestation from an IUBT procedure. In this study, all eight single-donor PRBC units utilized for IUBT contained Hg and Pb. Multiple IUBT procedures resulted in delivering substantial higher concentrations of Hg and Pb that is much greater than the estimated IV RfD, with one instance of Pb exposure >40 times the estimated IV RfD. This magnitude of exposure is much higher and much more significant than previously shown in the literature that evaluated Hg and Pb exposure from PRBC transfusions in premature infants.11,18

The fetus is highly susceptible to neurotoxins during periods of rapid neuronal cell division and proliferation. While organogenesis is complete in most organ systems by 8 weeks GA, central nervous system development is not complete until well into infancy and beyond.19 Fetal central nervous system remains vulnerable to teratogens across fetal development and following birth. Exposure to neurotoxins such as Hg and Pb may impact neuronal differentiation, proliferation, migration, and myelination leading to permanent neuronal loss and impaired neurodevelopment.20

The primary source of methyl Hg (organic Hg) is dietary, through ingestion of fish.21 Fetal exposure to methyl Hg has been linked to neurocognitive and neurosensory impairment and neurobehavioral disorders such as attention-deficit/hyperactivity disorder (ADHD).5,20 Hg levels tend to be higher in cord blood than in maternal blood.22 Hg, well known to cross the placenta, is effluxed through glutathione conjugation to be transported primarily toward the fetal side.23 The fetal brain is more susceptible to Hg-induced injury than the adult brain, as Hg inhibits the division and migration of neuronal cells that result in disruption of the developing brain cyto-architecture.24 Prenatal methyl Hg exposure as determined from Hg analyses of cord blood, cord tissue, and maternal hair has been significantly associated with deficits in motor, attention, and verbal tests at 14 years of age.25

Pb is a potent neurotoxic heavy metal; the central and peripheral nervous systems are highly vulnerable to the toxic effects of Pb.20 Fetal central nervous system exposure to Pb is associated with neurocognitive impairment, altered executive functioning, developmental disorders of scholastic skills, and other social and neurobehavioral disorders, including ADHD.5,20 Pb has been shown to have detrimental effects on brain development through alteration of neurite outgrowth26; substitution for calcium in critical enzymatic processes, including metal transport, energy metabolism, apoptosis, protein maturation, and genetic regulation27,28; and inhibiting neurite initiation through alteration of enzyme protein kinase C (calcium-dependent enzyme) resulting in blockade of voltage-dependent calcium channels and disruption of neuronal activity.2 Deleterious effects from infantile Pb exposure that result in severe motor and cognitive impairments are far greater in children than in adults.29,30 Increasing levels of blood Pb were found inversely associated with cognitive performance and neuropsychological development through the first 7 years of life.31

Blood Pb is a representative of soft tissue lead and is the primary biomarker most commonly used for the assessment of Pb exposure, both for screening and diagnostic purposes and for biomonitoring body burden.2 Pb moves freely from erythrocyte into the plasma and to the various body compartments including umbilical cord blood; brain; bone; and soft tissues such as hair, nail, saliva, tooth, and urine. The half-life of Pb varies from about a month in blood, about 2 years in the brain, to about 25–30 years in the bone.27 As plasma fraction of Pb is rapidly exchangeable in the blood, toxic effects of Pb are assumed to be associated with plasma Pb. But accurate determination of plasma Pb is challenging due to shift of Pb into the plasma from erythrocyte hemolysis.32 The blood Pb concentration that actually relates to brain extracellular concentration is not known. Maternal blood Pb concentration is highly correlated with umbilical cord Pb, suggesting trans-placental transfer of Pb to the fetus.33 In fact, Pb readily crosses the placenta both by passive diffusion and actively transported by divalent metal ion transporters.34,35,36 Pb has been measured in the fetal brain as early as the end of the first trimester (13 weeks).34,37 Following exposure, potentially via IUBT, these lipid-soluble metals cross the immature blood–brain barrier and can bioaccumulate in the fetal brain.38

A major excretory route for heavy metal is through the GI tract.39,40 In contrast to the newborn, the fetus has minimal Gl excretory abilities, which potentially could contribute to further bioaccumulation of Hg and Pb in the fetal compartment.

In conclusion, while IUBT is a life-saving therapy for fetal anemia, this is the first study to report fetal exposure to Hg and Pb of variable amounts exceeding estimated IV RfDs that could potentially have extremely harmful consequences. This study further confirms and only complements what is already known for decades regarding blood products as a known source of Hg and Pb exposure in infants. Biomarkers in blood to quantify in utero exposure to Hg and Pb have not been established, and toxic threshold levels to the developing fetal brain are unknown. Until biomarkers of Hg and Pb in blood are identified, screening of donor blood for these known neurotoxins is imperative and must be a priority for this highly specialized and vulnerable population.

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Acknowledgements

We gratefully acknowledge the contribution of the late Dr. Prince A.K. Kassim for assistance with the blood sample analysis for heavy metals.

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Substantial contributions to conception and design, acquisition of data, or analysis and interpretation of data—all authors. Drafting the article or revising it critically for important intellectual content—AJF and SS. Final approval of the version to be published—all authors.

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Correspondence to Alison J. Falck.

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Falck, A.J., Sundararajan, S., Al-Mudares, F. et al. Fetal exposure to mercury and lead from intrauterine blood transfusions. Pediatr Res 86, 510–514 (2019). https://doi.org/10.1038/s41390-019-0463-z

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