4.5 Review

Exposure to PFOA and PFOS and fetal growth: a critical merging of toxicological and epidemiological data

Journal

CRITICAL REVIEWS IN TOXICOLOGY
Volume 47, Issue 6, Pages 482-508

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/10408444.2016.1271972

Keywords

Birth weight; fetal growth; PFOA; PFOS; systematic review; meta-analysis; epidemiology; toxicology; perfluoroalkyls; reproduction; integration; evidence

Categories

Funding

  1. CEFIC Long Range Research Initiative [EMSG58]

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Toxicological and epidemiological evidence on the association between perfluorooctanoic acid (PFOA) or perfluorooctane sulfonic acid (PFOS) and birth/fetal weight was assessed. An extensive search for toxicological information in rats and mice, and a systematic search for epidemiological evidence were conducted. The linear regression coefficient (LRC) of birth weight (BrthW) on PFOA/PFOS was considered, and separate random effects meta-analyses for untransformed (i.e. not mathematically transformed) and log-transformed values were performed. Toxicological evidence: PFOA: 12 studies (21 datasets) in mice showed statistically significant lower birth/fetal weights from 5mg/kg body weight per day. PFOS: most of the 13 studies (19 datasets) showed lower birth/fetal weights following in utero exposure. Epidemiological evidence: Sixteen articles were considered. The pooled LRC for a 1 ng/mL increase in untransformed PFOA (12 studies) in maternal plasma/serum was -12.8 g (95% CI -23.2; 2.4), and -27.1 g (95% CI - 50.6; -3.6) for an increase of 1 log(e) ng/mL PFOA (nine studies). The pooled LRC for untransformed PFOS (eight studies) was -0.92 g (95% CI - 3.4; 1.6), and for an increase of 1 log(e) ng/mL was -46.1(95% CI - 80.3; -11.9). No consistent pattern emerged for study location or timing of blood sampling. Conclusions: Epidemiological and toxicological evidence suggests that PFOA and PFOS elicit a decrease in BrthW both in humans and rodents. However, the effective animal extrapolated serum concentrations are 10(2)-10(3) times higher than those in humans. Thus, there is no quantitative toxicological evidence to support the epidemiological association, thus reducing the biological plausibility of a causal relationship.

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