» Articles » PMID: 32702804

Association of Bisphenol A or Bisphenol S Exposure with Oxidative Stress and Immune Disturbance Among Unexplained Recurrent Spontaneous Abortion Women

Overview
Journal Chemosphere
Date 2020 Jul 25
PMID 32702804
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

Human exposure to environmental chemicals might play a role in the pathogenesis of unexplained recurrent spontaneous abortion (URSA). Bisphenol A (BPA) and bisphenol S (BPS) have been suggested to affect reproductive health. However, the mechanism remains unclear. To explore the association between BPA and BPS exposure and oxidative stress and immune homeostasis, we conducted a cross-sectional study and revealed BPA and BPS levels in relation to these two factors which were supposed to be implicated in miscarriage. 111 URSA patients were recruited and we analyzed urinary BPA and BPS concentrations, oxidative stress biomarkers (8-hydroxydeoxyguanosine and 8-isoprostane) and serum immune balance biomarkers (IL-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12p70, IL-13, TNF-α, TGF-β and IFN-γ). Multivariable linear regression models were used to evaluate the correlation between bisphenols exposure and outcome biomarkers. After adjustment for age, BMI, menstrual cycle, and parity history, creatinine-adjusted BPA was significantly associated with increases in 8-isoprostane (β = 0.74, 95% CI = 0.07, 1.41; p = 0.031) and IFN-γ (β = 0.18, 95% CI = 0.00, 0.36; p = 0.046). No statistical correlation between BPS and biomarkers of oxidative stress or immune balance was observed when all participants were analyzed. Further analysis revealed that in the subgroup of BPS > limit of detection (0.01 ng/ml), creatinine-adjusted BPS was significantly associated with increases in IL-10 (β = 0.22, 95% CI = 0.00, 0.45; p = 0.048). Our findings suggested that BPA and BPS exposure might be related to oxidative stress and immune imbalance in URSA patients. Overall, our work might suggest potential pathogenic and aetiological associations among the bisphenols, biomarkers and URSA, which offers hypotheses for further studies.

Citing Articles

as a Model to Assess the Potential Risk to Human Health Associated with the Use of Bisphenol A and Its Substitutes.

Kaiglova A, Bardyova Z, Hockickova P, Zvolenska A, Melnikov K, Kucharikova S Int J Mol Sci. 2025; 26(5).

PMID: 40076635 PMC: 11900329. DOI: 10.3390/ijms26052013.


The Effect of Bisphenol and Its Cytotoxicity on Female Infertility and Pregnancy Outcomes: A Narrative Review.

Drakaki E, Stavros S, Dedousi D, Potiris A, Mavrogianni D, Zikopoulos A J Clin Med. 2025; 13(24.

PMID: 39768492 PMC: 11728370. DOI: 10.3390/jcm13247568.


The impact of Bisphenol-A on human reproductive health.

Salami E, Rotimi O Toxicol Rep. 2024; 13:101773.

PMID: 39526236 PMC: 11550589. DOI: 10.1016/j.toxrep.2024.101773.


Temporal and geographic variability of bisphenol levels in humans: A systematic review and meta-analysis of international biomonitoring data.

Acevedo J, Kahn L, Pierce K, Carrasco A, Singer Rosenberg M, Trasande L Environ Res. 2024; 264(Pt 1):120341.

PMID: 39522874 PMC: 11863187. DOI: 10.1016/j.envres.2024.120341.


Comparative in silico and in vitro evaluation of possible toxic effects of bisphenol derivatives in HepG2 cells.

Balci-Ozyurt A, Yirun A, Cakir D, Ozcelik I, Bacanli M, Ozkemahli G Toxicol Res (Camb). 2024; 13(4):tfae127.

PMID: 39132192 PMC: 11316955. DOI: 10.1093/toxres/tfae127.