Department of Preventive Medicine and Public Health, Shinshu University School of Medicine, Matsumoto, Japan.
Center for Perinatal, Pediatric, and Environmental Epidemiology, Shinshu University School of Medicine, Matsumoto, Japan.
Environ Health Perspect. 2024 Sep;132(9):97004. doi: 10.1289/EHP13617. Epub 2024 Sep 11.
Although recent experimental results have raised the question of whether maternal exposure to per- and polyfluoroalkyl substances (PFAS) may be a potential environmental risk factor for chromosomal abnormalities, epidemiological studies investigating these associations are lacking.
This study examined whether prenatal PFAS exposure is associated with a higher prevalence of chromosomal abnormalities among offspring.
We used data from the Japan Environment and Children's Study, a nationwide birth cohort study, and employed logistic regression models to examine the associations between maternal plasma PFAS concentrations in the first trimester and the diagnosis of chromosomal abnormalities in all births (artificial abortions, miscarriages, stillbirths, and live births) up to 2 years of age. In addition, we examined associations with mixtures of PFAS using multipollutant models.
The final sample consisted of 24,724 births with singleton pregnancies, of which 44 confirmed cases of chromosomal abnormalities were identified (prevalence: 17.8/10,000 births). When examined individually, exposure to perfluorononanoic acid (PFNA) and perfluorooctane sulfonic acid (PFOS) showed positive associations with any chromosomal abnormalities with age-adjusted odds ratios of 1.81 (95% CI: 1.26, 2.61) and 2.08 (95% CI: 1.41, 3.07) per doubling in concentration, respectively. These associations remained significant after Bonferroni correction, although they did not reach the adjusted significance threshold in certain sensitivity analyses. Furthermore, the doubling in all PFAS included as a mixture was associated with chromosomal abnormalities, indicating an age-adjusted odds ratio of 2.25 (95% CI: 1.34, 3.80), with PFOS as the predominant contributor, followed by PFNA, perfluoroundecanoic acid (PFUnA), and perfluorooctanoic acid (PFOA).
The study findings suggested a potential association between maternal exposure to PFAS, particularly PFOS, and chromosomal abnormalities in offspring. However, the results should be interpreted cautiously, because selection bias arising from the recruitment of women in early pregnancy may explain the associations. https://doi.org/10.1289/EHP13617.
尽管最近的实验结果提出了这样一个问题,即母体接触全氟和多氟烷基物质(PFAS)是否可能成为染色体异常的一个潜在环境风险因素,但缺乏对此类关联进行的流行病学研究。
本研究旨在检验产前 PFAS 暴露是否与后代染色体异常的发生率升高有关。
我们使用了日本环境与儿童研究(一项全国性的出生队列研究)的数据,采用逻辑回归模型,检验了妊娠早期母体血浆 PFAS 浓度与所有出生(人工流产、自然流产、死产和活产)至 2 岁时染色体异常诊断之间的关联。此外,我们还使用多污染物模型检验了 PFAS 混合物的关联。
最终的样本包括 24724 例单胎妊娠分娩,其中确认了 44 例染色体异常病例(发生率:17.8/10000 例)。当单独进行检验时,全氟壬酸(PFNA)和全氟辛烷磺酸(PFOS)的暴露与任何染色体异常均呈正相关,浓度每增加 1 个对数倍,其对应的年龄调整比值比(OR)分别为 1.81(95%置信区间:1.26,2.61)和 2.08(95%置信区间:1.41,3.07)。在 Bonferroni 校正后,这些关联仍然具有统计学意义,尽管在某些敏感性分析中,它们并未达到调整后的显著性阈值。此外,作为混合物的所有 PFAS 的浓度加倍与染色体异常相关,其对应的年龄调整比值比为 2.25(95%置信区间:1.34,3.80),其中 PFOS 是主要贡献者,其次是 PFNA、全氟十一酸(PFUnA)和全氟辛酸(PFOA)。
研究结果表明,母体接触 PFAS,尤其是 PFOS,与后代的染色体异常之间可能存在关联。然而,由于招募妊娠早期的女性可能会产生选择偏倚,因此应谨慎解释这些结果。https://doi.org/10.1289/EHP13617.