Scientific publications

In Utero Exposure to Mercury Is Associated With Increased Susceptibility to Liver Injury and Inflammation in Childhood

Sep 1, 2021 | Magazine: Hepatology

Nikos Stratakis #  1 , Lucy Golden-Mason #  2 , Katerina Margetaki  1 , Yinqi Zhao  1 , Damaskini Valvi  3 , Erika Garcia  1 , Léa Maitre  4   5   6 , Sandra Andrusaityte  7 , Xavier Basagana  4   5   6 , Eva Borràs  5   8 , Mariona Bustamante  4   5   6 , Maribel Casas  4   5   6 , Serena Fossati  4   5   6 , Regina Grazuleviciene  7 , Line Småstuen Haug  9 , Barbara Heude  10 , Rosemary R C McEachan  11 , Helle Margrete Meltzer  9 , Eleni Papadopoulou  9 , Theano Roumeliotaki  12 , Oliver Robinson  13 , Eduard Sabidó  5   8 , Jose Urquiza  4   5   6 , Marina Vafeiadi  12 , Nerea Varo  14 , John Wright  11 , Miriam B Vos  15   16 , Howard Hu  1 , Martine Vrijheid  4   5   6 , Kiros T Berhane  17 , David V Conti  1 , Rob McConnell  1 , Hugo R Rosen  2 , Lida Chatzi  1


Background and aims: Nonalcoholic fatty liver disease (NAFLD) is the most prevalent cause of liver disease in children. Mercury (Hg), a ubiquitous toxic metal, has been proposed as an environmental factor contributing to toxicant-associated fatty liver disease.

Approach and results: We investigated the effect of prenatal exposure to Hg on childhood liver injury by combining epidemiological results from a multicenter mother-child cohort with complementary in vitro experiments on monocyte cells that are known to play a key role in liver immune homeostasis and NAFLD.

We used data from 872 mothers and their children (median age, 8.1 years; interquartile range [IQR], 6.5-8.7) from the European Human Early-Life Exposome cohort. We measured Hg concentration in maternal blood during pregnancy (median, 2.0 μg/L; IQR, 1.1-3.6).

We also assessed serum levels of alanine aminotransferase (ALT), a common screening tool for pediatric NAFLD, and plasma concentrations of inflammation-related cytokines in children. We found that prenatal Hg exposure was associated with a phenotype in children that was characterized by elevated ALT (≥22.1 U/L for females and ≥25.8 U/L for males) and increased concentrations of circulating IL-1β, IL-6, IL-8, and TNF-α.

Consistently, inflammatory monocytes exposed in vitro to a physiologically relevant dose of Hg demonstrated significant up-regulation of genes encoding these four cytokines and increased concentrations of IL-8 and TNF-α in the supernatants.

Conclusions: These findings suggest that developmental exposure to Hg can contribute to inflammation and increased NAFLD risk in early life.

CITATION  Hepatology. 2021 Sep;74(3):1546-1559. doi: 10.1002/hep.31809. Epub 2021 Aug 30