Wu Jing, Zhang Xiaoqian, Wang Qiong, Ma Ning, Zheng Fangjieyi, Chen Kening, Niu Wenquan
Center for Evidence-Based Medicine, Capital Institute of Pediatrics, Beijing, China.
Graduate School, Beijing University of Chinese Medicine, Beijing, China.
Heliyon. 2024 Aug 24;10(17):e36894. doi: 10.1016/j.heliyon.2024.e36894. eCollection 2024 Sep 15.
Epidemiological studies linking metabolic syndrome (MetS) and exposure to perfluoroalkyl substances (PFASs) are limited, and the observations gleaned thus far are inconclusive. The study was performed to explore the association of serum PFASs both singly and in a mixed manner with MetS, and meanwhile to examine whether this association was mediated by serum albumin in a US national population.
Total 8108 participants from the National Health and Nutrition Examination Survey, 2007-2018 were included. Four PFASs - including perfluorohexane sulfonic acid (PFHxS), perfluorononanoic acid (PFNA), perfluoromethylheptane sulfonic acid (PFOS), and perfluorooctanoic acid (PFOA), were selected. Weighted quantile sum regression was used to evaluate mixed PFAS exposure and MetS. Multivariable logistic regression models were used to calculate odd ratio (OR) and 95 % confidence interval (95 % CI). Mediating analyses were used to evaluate the mediating effects of albumin.
Comparing the highest with lowest quartile yielded a multivariable-adjusted OR (95 % CI) of 1.40 (1.14-1.72) for PFHxS, 1.36 (1.09-1.70) for PFNA, 1.26 (1.00-1.58) for PFOA, and 1.50 (1.19-1.88) for PFOS when associating MetS. Per unit increment in ln-transformed PFHxS, PFNA, PFOA, and PFOS concentrations was significantly associated with 16 %, 17 %, 13 %, and 15 % increased risk of MetS, respectively. When stratified by sex, the significant association between four PFASs and MetS was only noted in females. Mixed PFAS exposure was inversely associated with MetS, and 8.1 % of this association was mediated by serum albumin ( < 0.001).
Our findings indicate a significant and independent association of serum PFASs with MetS, and importantly this association was dose-dependent, sex-specific, and possibly mediated by serum albumin.
将代谢综合征(MetS)与全氟烷基物质(PFASs)暴露联系起来的流行病学研究有限,目前所获得的观察结果尚无定论。本研究旨在探讨血清PFASs单独及混合暴露与MetS之间的关联,同时在美国全国人群中检验这种关联是否由血清白蛋白介导。
纳入了2007 - 2018年国家健康与营养检查调查中的8108名参与者。选取了四种PFASs,包括全氟己烷磺酸(PFHxS)、全氟壬酸(PFNA)、全氟甲基庚烷磺酸(PFOS)和全氟辛酸(PFOA)。采用加权分位数和回归来评估混合PFAS暴露与MetS。使用多变量逻辑回归模型计算比值比(OR)和95%置信区间(95%CI)。中介分析用于评估白蛋白的中介作用。
将最高四分位数与最低四分位数进行比较,在关联MetS时,PFHxS的多变量调整OR(95%CI)为1.40(1.14 - 1.72),PFNA为1.36(1.09 - 1.70),PFOA为1.26(1.00 - 1.58),PFOS为1.50(1.19 - 1.88)。ln转换后的PFHxS、PFNA、PFOA和PFOS浓度每单位增加分别与MetS风险增加16%、17%、13%和15%显著相关。按性别分层时,仅在女性中发现四种PFASs与MetS之间存在显著关联。混合PFAS暴露与MetS呈负相关,且这种关联的8.1%由血清白蛋白介导(P < 0.001)。
我们的研究结果表明血清PFASs与MetS之间存在显著且独立的关联,重要的是这种关联具有剂量依赖性、性别特异性,并且可能由血清白蛋白介导。