A longitudinal study of rural Bangladeshi children with long-term arsenic and cadmium exposures and biomarkers of cardiometabolic diseases
Creators
- 1. Infectious Diseases Division, icddr,b, Dhaka, 1212 (Bangladesh)
- 2. Department of Community Health Sciences and Epidemiology, Fielding School of Public Health, University of California Los Angeles (United States)
- 3. Institute of Environmental Medicine, Karolinska Institutet, SE- 171 77, Stockholm (Sweden)
- 4. Department of Women's and Children's Health, Uppsala University, SE-751 85, Uppsala (Sweden)
- 5. Department of Clinical Trial and Clinical Epidemiology, Faculty of Medicine, University of Tsukuba, Tsukuba (Japan)
Description
Highlights: • Early signs of detrimental influence of metal(loid)s on fat metabolism in children. • Early life cadmium exposure was associated with increased preadolescent blood pressure. • Early life arsenic or cadmium exposure was associated with decreased plasma lipoproteins. • Childhood cadmium exposure was inversely associated with kidney function (eGFR). There is growing interest in understanding the contribution of environmental toxicant exposure in early life to development of cardiometabolic diseases (CMD) in adulthood. We aimed to assess associations of early life exposure to arsenic and cadmium with biomarkers of CMD in children in rural Bangladesh. From a longitudinal mother-child cohort in Matlab, Bangladesh, we followed up 540 pairs. Exposure to arsenic (U–As) and cadmium (U–Cd) was assessed by concentrations in urine from mothers at gestational week 8 (GW8) and children at ages 4.5 and 9 years. Blood pressure and anthropometric indices were measured at 4.5 and 9 years. Metabolic markers (lipids, glucose, hemoglobin A1c, adipokines, estimated glomerular filtration rate (eGFR) were determined in plasma/blood of 9 years old children. In linear regression models, adjusted for child sex, age, height-for-age z score (HAZ), BMI-for-age z score (BAZ), socioeconomic status (SES) and maternal education, each doubling of maternal and early childhood U–Cd was associated with 0.73 and 0.82 mmHg increase in systolic blood pressure (SBP) respectively. Both early and concurrent childhood U–Cd was associated with diastolic (D)BP (β = 0.80 at 4.5 years; β = 0.75 at 9 years). Each doubling of U–Cd at 9 years was associated with decrements of 4.98 mg/dL of total cholesterol (TC), 1.75 mg/dL high-density lipoprotein (HDL), 3.85 mg/dL low-density lipoprotein (LDL), 0.43 mg/dL glucose and 4.29 units eGFR. Each doubling of maternal U–Cd was associated with a decrement of 1.23 mg/dL HDL. Both maternal and childhood U–As were associated with decrement in TC and HDL. Multiple comparisons were checked with family-wise error rate Bonferroni-type-approach. The negative associations of arsenic and cadmium with biomarkers of CMD in preadolescent children indicated influence of both metal(loid)s on fat and carbohydrate metabolism, while cadmium additionally influenced kidney function and BP. Thus, fewer outcomes were associated with U–As compared to U–Cd at preadolescence.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.envpol.2020.116333Additional details
Identifiers
- DOI
- 10.1016/j.envpol.2020.116333;
- PII
- S0269749120370226;
Publishing Information
- Journal Title
- Environmental Pollution (1987)
- Journal Volume
- 271
- Journal Page Range
- vp.
- ISSN
- 0269-7491
- CODEN
- ENPOEK
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54036083
- Subject category
- S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- ARSENIC; BANGLADESH; BIOLOGICAL MARKERS; BLOOD PLASMA; BLOOD PRESSURE; CADMIUM; CHILDREN; CHOLESTEROL; ENVIRONMENTAL EXPOSURE; ERRORS; FATS; GLUCOSE; HEMOGLOBIN; KIDNEYS; LIPOPROTEINS; METABOLISM; URINE
- Descriptors DEC
- AGE GROUPS; ALDEHYDES; ANIMALS; ASIA; BIOLOGICAL MATERIALS; BIOLOGICAL WASTES; BLOOD; BODY; BODY FLUIDS; CARBOHYDRATES; CARBOXYLIC ACIDS; DEVELOPING COUNTRIES; ELEMENTS; GLOBINS; HETEROCYCLIC ACIDS; HETEROCYCLIC COMPOUNDS; HEXOSES; HUMANS; HYDROXY COMPOUNDS; LIPIDS; MAMMALS; MATERIALS; METALS; MONOSACCHARIDES; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANS; PIGMENTS; PORPHYRINS; PRIMATES; PROTEINS; SACCHARIDES; SEMIMETALS; STEROIDS; STEROLS; VERTEBRATES; WASTES
Optional Information
- Copyright
- Copyright (c) 2020 Elsevier Ltd. All rights reserved.