Cadmium exposure increases the risk of juvenile obesity: a human and zebrafish comparative study.

Published

Journal Article

OBJECTIVE: Human obesity is a complex metabolic disorder disproportionately affecting people of lower socioeconomic strata, and ethnic minorities, especially African Americans and Hispanics. Although genetic predisposition and a positive energy balance are implicated in obesity, these factors alone do not account for the excess prevalence of obesity in lower socioeconomic populations. Therefore, environmental factors, including exposure to pesticides, heavy metals, and other contaminants, are agents widely suspected to have obesogenic activity, and they also are spatially correlated with lower socioeconomic status. Our study investigates the causal relationship between exposure to the heavy metal, cadmium (Cd), and obesity in a cohort of children and in a zebrafish model of adipogenesis. DESIGN: An extensive collection of first trimester maternal blood samples obtained as part of the Newborn Epigenetics Study (NEST) was analyzed for the presence of Cd, and these results were cross analyzed with the weight-gain trajectory of the children through age 5 years. Next, the role of Cd as a potential obesogen was analyzed in an in vivo zebrafish model. RESULTS: Our analysis indicates that the presence of Cd in maternal blood during pregnancy is associated with increased risk of juvenile obesity in the offspring, independent of other variables, including lead (Pb) and smoking status. Our results are recapitulated in a zebrafish model, in which exposure to Cd at levels approximating those observed in the NEST study is associated with increased adiposity. CONCLUSION: Our findings identify Cd as a potential human obesogen. Moreover, these observations are recapitulated in a zebrafish model, suggesting that the underlying mechanisms may be evolutionarily conserved, and that zebrafish may be a valuable model for uncovering pathways leading to Cd-mediated obesity in human populations.

Full Text

Duke Authors

Cited Authors

  • Green, AJ; Hoyo, C; Mattingly, CJ; Luo, Y; Tzeng, J-Y; Murphy, SK; Buchwalter, DB; Planchart, A

Published Date

  • July 2018

Published In

Volume / Issue

  • 42 / 7

Start / End Page

  • 1285 - 1295

PubMed ID

  • 29511319

Pubmed Central ID

  • 29511319

Electronic International Standard Serial Number (EISSN)

  • 1476-5497

Digital Object Identifier (DOI)

  • 10.1038/s41366-018-0036-y

Language

  • eng

Conference Location

  • England