Skip to main content
Environmental Health Perspectives logoLink to Environmental Health Perspectives
. 2024 Mar 27;132(3):037704. doi: 10.1289/EHP13567

Maternal and Umbilical Cord Blood Lead Levels in Selected Informal Settlements in Nairobi, Kenya: A Cross-Sectional Study

Edith A Lumumba 1, Anne M Riederer 2, John O Onyatta 1, Sarah Benki-Nugent 3, Catherine J Karr 2,4, Faridah H Were 1,
PMCID: PMC10970993  PMID: 38536883

Introduction

Lead (Pb) is a well-characterized neurodevelopmental toxicant that can cross the placenta.1 In prior Nairobi-based studies, the prevalence of blood lead levels (BLLs) >10μg/dL was 70% in pregnant women2 and 30% in children 2–20 years of age.3 To our knowledge, no prior studies have reported umbilical cord BLLs in Nairobi and data more recent than one to two decades ago on maternal BLLs in sub-Saharan Africa (SSA) are lacking.

In 2020–2021, we measured Pb in maternal and cord blood in a convenience sample of mothers delivering at a hospital that caters to women from the Nairobi informal settlements, Dandora and Kariobangi. Dandora is home to Nairobi’s main dumpsite; studies of environmental samples show heavy contamination with Pb.4 Kariobangi is clustered with cottage industries, including informal lead acid battery recycling.5 We aimed to characterize current maternal Pb exposures in these communities and explore associations between potential Pb sources and BLLs.

Methods

Mothers delivering at Pumwani Hospital, 18 years of age, residing in Dandora or Kariobangi for >1 y, with singleton pregnancy and no known pregnancy complications, were recruited/eligible. Of 150 enrolled mothers with informed consent, 100 were included in the analysis; those excluded were due to refusal (22), new pregnancy complications or fetal/infant death (20), and sample mislabeling (8). Kenyatta National Hospital–University of Nairobi–Ethics and Research Committee (P835/10/2019) approved this study.

At delivery, a nurse drew 2mL of maternal venous and 1mL of umbilical cord blood into trace element-free dipotassium ethylenediaminetetraacetic acid Vacutainer tubes (BD).6 For every 20 samples, a field blank was collected. Samples and blanks were stored at 4 Degrees Celsius,2 then digested using 4mL of 69% nitric acid (HNO3) on a hot plate inside a fume hood for 3 h at 100°C as described.6 One distilled–deionized water blank was digested each day along with the samples.

Working Pb standards of 10, 20, 30, 40, and 50 ppb were prepared from a stock standard traceable to ISO 17025 (Reagecon). Assays for total Pb were done in triplicate using an inductively coupled plasma mass spectrometer (ICP-MS) (Thermo Scientific, ICAP RC model) at the Government Chemist Laboratory (Nairobi), with the mean used for analysis. Trace metals grade HNO3 (Thermo Fisher Scientific) and the clean procedures described by Benoit et al.7 were used.

The method detection limit (MDL) was set at the lowest calibrant concentration. Pb was not detected in any blanks. Machine values were used for six cord blood samples with Pb concentrations < MDL (range 0.7180.913μg/dL). Accuracy was evaluated using matrix spikes and certified reference material (CRM) ClinChek Whole Blood Control, lyophilized, for Trace Elements, Level I, II, III (RECIPE Chemicals + instruments GmbH).

After delivery, a trained nurse administered a brief standardized questionnaire regarding demographics and potential sources of Pb adapted from Were et al.8 and World Health Organization recommendations on environmental risk factors surveys for pregnant women.

We calculated descriptive statistics and evaluated bivariate associations between BLLs and demographic and Pb exposure characteristics using R/RStudio (version 2022.07; Posit). We used multivariable linear regression to evaluate associations between natural log-transformed maternal BLLs and age, education, and potential exposure sources (yes/no). A reduced model including only age and a full model containing all variables were fit to the data and evaluated by examining residual plots and the adjusted R2. The same approach was used with natural log-transformed cord BLLs. We exponentiated regression coefficients (β), used the formula [exp(β)1]×100 to express results as a percentage change in BLL per predictor increment, and considered predictors without 0 in their 95% confidence interval (CI) statistically significant.

Results and Discussion

Maternal BLLs ranged from 4.0 to 91.2μg/dL (mean 27.3±15.5μg/dL), and cord BLLs ranged from 0.7 to 9.9μg/dL (mean 2.7±1.9μg/dL) (Table 1). Maternal and cord BLLs were positively correlated (ρSpearman=0.65, p<0.0001); 23% and 100%, respectively, of the cord and maternal BLLs exceeded the US Centers for Disease Control and Prevention’s blood Pb reference value of 3.5μg/dL.9

Table 1.

Demographic and potential characteristics related to lead (Pb) exposure and blood lead levels in participants (N=100) delivering at Pumwani Maternity Hospital (Nairobi, Kenya) in 2020–2021.

Characteristic n
Maternal age [y (median)] 30.5
Residence location
 Dandora 52
 Kariobangi 48
Maternal highest level of education
 Primary school 30
 Secondary school or higher 65
 No formal education 5
Maternal occupation
 Housewife 18
 Business 11
 Cleaner 10
 Other service jobsa 58
 Battery recycling/smelting 3
 Other jobs with potential Pb exposureb 0
Years in this occupation
 0–5 78
>5 to 10 22
Live in a painted house
 No 13
 Yes 87
  House paint peeling or chipping
   No 29
   Yes 58
  Median years living in this house 2
Live in a building undergoing renovation or construction
 No 80
 Yes 20
Live or work near (within 1-km radius) an active lead smelter/battery recycling plant
 No 52
 Yes 48
Drinking water passes through old pipes and fixtures
 No 47
 Yes 53
Use old painted pottery or glazed pottery at home
 No 43
 Yes 57
Live near a dumpsite (within 1-km radius)
 No 44
 Yes 56
Ingested non-food items such as soil or stones in pregnancy (pica)
 No 60
 Yes 40
Aware of Pb as a toxicant or Pb poisoning
 No 100
 Yes 0
Maternal blood Pb (μg/dL)
Mean±SD 27.3±15.5
 Max (min) 91.2 (4.0)
 Percentile
  25th 14.6
  50th 26.7
  75th 33.9
Cord blood Pb (μg/dL)
Mean±SD 2.7±1.9
 Max (min) 9.9 (0.7)
 Percentile
  25th 1.6
  50th 2.1
  75th 3.2
Excluding 3 highly Pb-exposed battery recycling workers (n=97)
Maternal blood Pb (μg/dL)
Mean±SD 26.2±12.9
 Max (min) 64.3 (4.0)
 Percentile
  25th 14.7
  50th 26.6
  75th 33.2
Cord blood Pb (μg/dL)
Mean±SD 2.6±1.7
 Max (min) 9.9 (0.7)
 Percentile
  25th 1.6
  50th 2.1
  75th 3.1

Note: All characteristics besides blood lead levels were self-reported. Max, maximum; min, minimum; SD, standard deviation.

a

Bus conductor, carpenter, cook, grocery attendant, street vendor, money transfer attendant, nanny, salon worker, security, and shop attendant.

b

Construction, electronics recycling/repair, garbage collection/burning, house painting, and welding.

Three mothers reported working as battery recyclers and had maternal (cord) BLLs of 91.2μg/dL (9.8μg/dL), 86.0μg/dL (9.2μg/dL), and 13.8μg/dL (1.5μg/dL). We considered them highly Pb-exposed workers and excluded them from the regressions. In the reduced models, each maternal age year was associated with 11% (95% CI: 9%, 12%) and 5% (3%, 8%) increases in maternal and cord BLL, respectively. Living in a painted house was also significantly associated with maternal and cord BLLs in bivariate analyses. In the full models (Figure 1), each maternal age year was associated with 9% (95% CI: 7%, 11%), or 0.07 (0.06,0.09)μg/dL, and 4% (1%, 6%), or 0.015 (0.004,0.02)μg/dL, increases in maternal and cord BLLs, respectively. Living in a painted house with no peeling/chipping paint was associated with 58% (95% CI: 19%, 109%), or 0.5 (0.2,0.9)μg/dL increases in maternal BLL and 75% (18%, 161%), or 0.3 (0.07,0.6)μg/dL, increase in cord BLLs, compared with not living in a painted house, whereas living in a painted house with peeling/chipping paint was associated with 76% (95% CI: 36%, 128%), or 0.6 (0.3,1.0)μg/dL increase in maternal and 87% (30%, 169%), or 0.3 (0.1,0.6)μg/dL, increase in cord BLLs. Living near battery recycling (vs. not) was associated with a 16% (95% CI: 1%, 34%), or 0.1 (0.01,0.3)μg/dL, increase in maternal BLL but was not significantly associated with cord BLLs. Education level, home renovation, proximity to dumpsite, pica, drinking from old pipes, and using glazed pottery were not significantly associated with BLLs in the maternal or cord blood models.

Figure 1.

Figures 1A and 1B are forest plots titled Maternal blood and Cord Blood, plotting predictor, ranging as 57 cases of use glazed pottery, 40 cases of do not use glazed pottery (reference), 53 cases of drink from old pipes, 44 cases of do not dink from old pipes, 41 cases of pica in pregnancy, 56 cases of no pica in pregnancy (reference), 46 cases of live within 1 kilometer of battery recycling, 51 cases of do not live within 1 kilometer of battery recycling (reference), 54 cases of live within 1 kilometer of dumpsite, 43 cases of do not live within 1 kilometer of dumpsite (reference), 48 cases of house renovation or construction, 49 cases of no house renovation or construction (reference), 55 cases of painted house with peeling or chipping, 29 cases of painted house, no peeling or chipping, 13 cases of do not live in painted house (reference), 65 cases of secondary school or higher, 27 cases of primary school, 5 cases of no formal education, and maternal age (per year increase) (y-axis) across coefficient estimate (95 percent confidence interval), ranging from 0.0 to 1.0 in increments of 0.5 (x-axis), respectively.

Associations between demographic or environmental factors and natural log-transformed (A) maternal and (B) cord blood lead levels in multivariable linear regression models using data from 97 participants delivering at Pumwani Maternity Hospital (Nairobi, Kenya) in 2020–2021 (adjusted R2: maternal blood model 0.72, cord blood model 0.30; points indicate coefficient estimates, error bars indicate 95% CIs). Three participants employed at a battery recycling facility were excluded. Numeric data are available at https://github.com/anneried/Lumumba-et-al/tree/main. Note: CI, confidence interval; Ref, reference category.

These high Pb levels are concerning, considering the neurodevelopmental effects associated with even very low levels of BLL (<5μg/dL).9 Furthermore, they reveal a global disparity, where BLLs are declining in high-income countries (HICs), such as the United States, but remain high in low and middle-income countries (LMICs).10 A 2018 systematic review reported a weighted mean BLL of 26.24μg/dL in pregnant women in SSA comprising data from 14 surveys from 1997–2013.10 One included study, from a comparable community in Nairobi in 1998, reported a mean BLL of 28.4μg/dL,2 similar to our data. It should be noted that a legal limit was established in 2018 to phase out lead in paint in Kenya, although the implementation process is quite slow, particularly in the informal settlements with poor housing conditions.5 Persistent lead exposure may occur during sweeping and dusting in houses painted with lead-based paints.

Multilevel strategies have been adopted in HICs, including policy changes to remove lead from gasoline, restrict lead in residential paint, regulate airborne lead emissions, address lead in water infrastructure, and limit lead in some foods and children’s products. Although leaded gasoline was banned in Kenya in 20068 and actions on leaded paints are in progress, screening and surveillance are nonexistent and medical system and public education on lead hazards are absent. Kenya and other LMICs should consider implementing established strategies to reverse the increasing global disparity in lead exposure.

Acknowledgments

We thank the Department of Chemistry of the University of Nairobi for the research facility and technical support, Dr. Shar Samy of the University of Washington Environmental Health Laboratory for technical guidance and the collaboration with the Government Chemist Department; special thanks to Mr. Ali Gakweli, Mr. Stephen Matinde, Dr. Mwendo, Mr. Geoffrey Anyona, Mr. Daniel Boit, and Ms. Felista Henry from the Government Chemist. We also thank Pumwani Maternity Hospital and all study participants.

Grant 1R01ES032153 and P3ES007033 from the US National Institute of Environmental Health Sciences (to S.B.N. and C.J.K., respectively) supported research that included A.R. and the purchase of the ClinChek CRMs.

Code for data processing/analysis and files with the Figure 1 numeric data are available in a GitHub repository (https://github.com/anneried/Lumumba-et-al/tree/main).

References


Articles from Environmental Health Perspectives are provided here courtesy of National Institute of Environmental Health Sciences

RESOURCES