Altered cord blood mitochondrial DNA content and prenatal exposure to arsenic metabolites in low-arsenic areas

Author:

Qiu Feng1,Zhang Hongling2,Wang Xin1,Jia Zhenxian1,He Yujie1,Wu Yi1,Li Zhangpeng1,Zheng Tongzhang3,Xia Wei1,Xu Shunqing1,Li Yuanyuan4ORCID

Affiliation:

1. Huazhong University of Science and Technology Tongji Medical College

2. Wuchang University of Technology

3. Brown University

4. Tongji Medical College of Huazhong University of Science and Technology: Huazhong University of Science and Technology Tongji Medical College

Abstract

Abstract While mitochondria are susceptible to environmental detriments, little is known about potential associations between arsenic metabolites and mitochondria DNA copy number (mtDNAcn). We attempted to examine whether arsenic metabolism in different trimesters was related to cord blood mtDNAcn alteration. We included 819 mother-newborn pairs embedded in an in-progress birth cohort survey performed from April 2014 to October 2016 in Wuhan, China. We determined maternal urinary arsenic species concentrations in different trimesters using HPLC-ICPMS. We decided on cord blood mtDNAcn using quantitative real-time polymerase chain reaction. In covariate-adjusted models, each two-fold increment of dimethylated arsenic (DMA) and total arsenic (TAs) in the 3rd trimester were related to 8.43% (95% CI: 1.13%, 16.26%) and 12.15% (95% CI:4.35%, 20.53%) increases in mtDNAcn, respectively. The dose-response trend with statistical significance was observed across tertiles of DMA and TAs in the 3rd trimester with mtDNAcn. These findings may prove the relationships between arsenic species and mitochondrial dysfunction.

Publisher

Research Square Platform LLC

Reference85 articles.

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