The U.S. PFAS exposure burden calculator for 2017–2018: Application to the HOME Study, with comparison of epidemiological findings from NHANES

IF 2.6 3区 医学 Q3 NEUROSCIENCES Neurotoxicology and teratology Pub Date : 2024-01-13 DOI:10.1016/j.ntt.2024.107321
Shelley H. Liu , Yitong Chen , Leah Feuerstahler , Aimin Chen , Anne Starling , Dana Dabelea , Xiaobin Wang , Kim Cecil , Bruce Lanphear , Kimberly Yolton , Joseph M. Braun , Jessie P. Buckley
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Abstract

Background

The 2017–2018 U.S. PFAS exposure burden calculator was designed to provide a summary exposure score for per- and polyfluoroalkyl substances (PFAS) mixtures using targeted PFAS analyte data. Its aim was to place PFAS burden score estimates onto a common scale based on nationally representative U.S. reference ranges from 2017 to 2018, enabling comparisons of overall PFAS burden scores across studies even if they did not measure the same set of PFAS analytes.

Objective

To use the U.S. PFAS exposure burden calculator for comparing the same mixture of PFAS compounds in similarly aged adolescents and their associations with cardiometabolic outcomes in the HOME Study and NHANES between 2015 and 2018.

Methods

We applied the PFAS burden calculator to 8 PFAS analytes measured in the serum of adolescents from the HOME Study (Cincinnati, Ohio; age range 11–14 years; years: 2016–2019; n = 207) and NHANES (US; age range 12–14 years; years 2015–2018; n = 245). We used the non-parametric Mann-Whitney U test and chi-squared test to compare the two study samples. In both studies, we examined associations of PFAS burden scores with the same cardiometabolic outcomes, adjusted for the same core set of covariates using regression analyses. We conducted sensitivity analyses to verify robustness of exposure-outcome associations, by accounting for measurement error of PFAS burden scores.

Results

PFAS burden scores were significantly different (p = 0.004) between the HOME Study (median: 0.00, interquartile range − 0.37, 0.34) and the NHANES samples (median: 0.04, IQR -0.11, 0.54), while no significant difference was found for PFAS summed concentrations (p = 0.661). In the HOME Study, an interquartile (IQR) increase in PFAS burden score was associated with higher total cholesterol [7.0 mg/dL, 95% CI: 0.6, 13.4]; HDL [2.8 mg/dL, 95% CI: 0.4, 5.2]; LDL [5.9 mg/dL, 95% CI: 0.5, 11.3], insulin [0.1 log(mIU/L), 95% CI: 0.01, 0.2], and HOMA-IR [0.1, 95% CI: 0.01, 0.2]. In NHANES, an IQR increase in PFAS burden score was associated with higher diastolic blood pressure [2.4 mmHg, 95% CI: 0.4, 4.4] but not with other outcomes. Sensitivity analyses in the HOME Study and NHANES were consistent with the main findings.

Conclusions

Performance of the U.S. PFAS exposure burden calculator was similar in a local versus national sample of adolescents, and may be a useful tool for the assessment of PFAS mixtures across studies.

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2017-2018年美国PFAS暴露负担计算器:应用于 "家庭 "研究,并与 NHANES 的流行病学研究结果进行比较
背景2017-2018年美国PFAS暴露负担计算器旨在利用有针对性的PFAS分析物数据,提供全氟和多氟烷基物质(PFAS)混合物的简要暴露得分。其目的是根据 2017 年至 2018 年具有全国代表性的美国参考范围,将 PFAS 负担分值估算值纳入一个通用量表,从而能够比较不同研究的总体 PFAS 负担分值,即使这些研究测量的 PFAS 分析物并不相同。方法我们将 PFAS 负担计算器应用于 HOME 研究(俄亥俄州辛辛那提市;年龄范围 11-14 岁;年份:2016-2019 年;n = 207)和 NHANES(美国;年龄范围 12-14 岁;年份 2015-2018 年;n = 245)青少年血清中测得的 8 种 PFAS 分析物。我们使用非参数曼-惠特尼 U 检验和卡方检验来比较这两项研究的样本。在这两项研究中,我们考察了 PFAS 负担得分与相同的心脏代谢结果之间的关联,并对相同的核心协变量进行了调整。通过考虑 PFAS 负担得分的测量误差,我们进行了敏感性分析,以验证暴露-结果关联的稳健性。结果PFAS 负担得分在 HOME 研究(中位数:0.00,四分位数间距 - 0.37,0.34)和 NHANES 样本(中位数:0.04,四分位数间距 -0.11,0.54)之间存在显著差异(p = 0.004),而 PFAS 总浓度则无显著差异(p = 0.661)。在 "居家 "研究中,PFAS 负担得分的四分位数(IQR)增加与总胆固醇[7.0 mg/dL,95% CI:0.6,13.4]、高密度脂蛋白[2.8毫克/分升,95% CI:0.4,5.2];低密度脂蛋白[5.9毫克/分升,95% CI:0.5,11.3];胰岛素[0.1 log(mIU/L),95% CI:0.01,0.2]和 HOMA-IR [0.1,95% CI:0.01,0.2]。在 NHANES 中,PFAS 负担得分的 IQR 增加与舒张压升高有关 [2.4 mmHg,95% CI:0.4,4.4],但与其他结果无关。结论美国 PFAS 暴露负担计算器在本地和全国青少年样本中的表现相似,可能是评估不同研究中 PFAS 混合物的有用工具。
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来源期刊
CiteScore
5.60
自引率
10.30%
发文量
48
审稿时长
58 days
期刊介绍: Neurotoxicology and Teratology provides a forum for publishing new information regarding the effects of chemical and physical agents on the developing, adult or aging nervous system. In this context, the fields of neurotoxicology and teratology include studies of agent-induced alterations of nervous system function, with a focus on behavioral outcomes and their underlying physiological and neurochemical mechanisms. The Journal publishes original, peer-reviewed Research Reports of experimental, clinical, and epidemiological studies that address the neurotoxicity and/or functional teratology of pesticides, solvents, heavy metals, nanomaterials, organometals, industrial compounds, mixtures, drugs of abuse, pharmaceuticals, animal and plant toxins, atmospheric reaction products, and physical agents such as radiation and noise. These reports include traditional mammalian neurotoxicology experiments, human studies, studies using non-mammalian animal models, and mechanistic studies in vivo or in vitro. Special Issues, Reviews, Commentaries, Meeting Reports, and Symposium Papers provide timely updates on areas that have reached a critical point of synthesis, on aspects of a scientific field undergoing rapid change, or on areas that present special methodological or interpretive problems. Theoretical Articles address concepts and potential mechanisms underlying actions of agents of interest in the nervous system. The Journal also publishes Brief Communications that concisely describe a new method, technique, apparatus, or experimental result.
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