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. 2015 Apr 8;2(2):195–203. doi: 10.1007/s40572-015-0049-9

Table 1.

Main characteristics of the studies (all three were cohort studies) conducted in humans analyzing associations between prenatal exposure to cadmium and epigenetic changes

First author, year Population; n Prenatal cadmium exposure, concentration (range) Epigenetic modification Tissue/s Expression changes Main outcomes in relation to cadmium exposure
Boeke CE, 2012 Massachusetts, USA; n = 557 mother-child pairs Estimated by FFQ (T1), AM: 15.38 μg/day (14.7–16.3) Global DNA methylation (LINE-1 methylation) Maternal blood (T1 and T3), cord blood Na Hypermethylation in maternal DNA (T1), hypomethylation in fetal DNA
Kippler M, 2013 Matlab, Bangladesh; n = 127 mother-child pairs Urine (GW8), M 0.77 μg/L (0.25–2.4); Blood (GW14), M 1.3 μg/kg (0.54–3.1) Genome-wide DNA methylation (450 K array) Cord blood, children blood (4.5 years) Na Sex-specific correlations with maternal blood cadmium: in boys, 96 % of 500 top CpG sites hypermethylated; in girls, 21 % hypermethylated
Sanders AP, 2014 North Carolina, USA; n = 17 mother-child pairs Blood (T3); AM: 0.44 μg/L (0–1.05) Genome-wide DNA methylation (MIRA, Affimetrix array) Maternal blood (T3), cord blood Na Maternal DNA: hypermethylation in 81 genes hypomethylation in 11 genes fetal DNA: hypermethylation in 90 genes hypomethylation in 1 gene

T1/T3 first/third trimester of pregnancy, M median, AM arithmetic mean, GW gestational week, FFQ food frequency questionnaire, LINE-1 long interspersed nuclear element-1, 450 K Illumina Infinium Human Methylation 450, MIRA methylated CpG island recovery assay; expression changes refer to the level of mRNA and/or protein