Pharmacological Research (Jul 2024)

The association between endocrine disrupting chemicals and nonalcoholic fatty liver disease: A systematic review and meta-analysis

  • Kai Pan,
  • Jie Xu,
  • Yuzhu Xu,
  • Chengxing Wang,
  • Jie Yu

Journal volume & issue
Vol. 205
p. 107251

Abstract

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Nonalcoholic fatty liver disease (NAFLD) is one of the leading causes of chronic liver disease worldwide. Epidemiological studies have reported that exposure of the population to environmental endocrine-disrupting chemicals (EDCs) is associated with NAFLD. However, EDCs are of different types, and there are inconsistencies in the relevant evidence and descriptions, which have not been systematically summarized so far. Therefore, this study aimed to determine the association between population exposure to EDCs and NAFLD. Three databases, including PubMed, Web of science, and Embase were searched, and 27 articles were included in this study. Methodological quality, heterogeneity, and publication bias of the included studies were assessed using the Newcastle–Ottawa scale, I2 statistics, Begg’s test, and Egger’s test. The estimated effect sizes of the included studies were pooled and evaluated using the random-effects model (I2 > 50 %) and the fixed-effects model ( I2 < 50 %). The pooled-estimate effect sizes showed that population exposure to Phthalates (PAEs) (OR = 1.18, 95 % CI:1.03–1.34), cadmium (Cd) (OR = 1.37, 95 % CI:1.09–1.72), and bisphenol A (OR = 1.43, 95 % CI:1.24–1.65) were positively correlated with the risk of NAFLD. Exposure to mercury (OR =1.46, 95 % CI:1.17–1.84) and Cd increased the risk of “elevated alanine aminotransferase”. On the contrary, no significant association was identified between perfluoroalkyl substances (OR =0.99, 95 % CI:0.93–1.06) and NAFLD. However, female exposure to perfluorooctanoic acid (OR =1.82, 95 % CI:1.01–3.26) led to a higher risk of NAFLD than male exposure. In conclusion, this study revealed that EDCs were risk factors for NAFLD. Nonetheless, the sensitivity analysis results of some of the meta-analyses were not stable and demonstrated high heterogeneity. The evidence for these associations is limited, and more large-scale population-based studies are required to confirm these findings.

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