Xiao Wenwen, Jian Guojin, Ma Fei, Li Hong, Yang Xiaohong, Zhang Hengyang, Cao Yongping
Eastern Theater Command Centers for Disease Control and Prevention, Nanjing, China.
Department of Cardiology, PLA Joint Logistic Support Force 902 Hospital, Bengbu, China.
Front Cardiovasc Med. 2025 Jan 9;11:1487956. doi: 10.3389/fcvm.2024.1487956. eCollection 2024.
Polyfluoroalkyl chemicals (PFCs) present potential health risks due to their persistence and bioaccumulation. However, there is currently insufficient evidence regarding their impact on cardiovascular disease (CVD). Consequently, it is imperative to investigate the correlation between PFCs and CVD.
The data was collected from National Health and Nutrition Examination Survey in 2005-2012. Logistic regression models were employed to assess the association between single PFC and CVD. Generalized additive model (GAM) was used for evaluating nonlinear relationships. Subgroup analyses were conducted to explore interaction effects. Bayesian kernel machine regression (BKMR) and weighted quantile sum (WQS) models were used to evaluate the joint effect of PFC exposures on CVD.
In logistic regression, PFDE, MPAH, and PFUA were positively associated with CVD. In the GAM, there was a significant nonlinear relationship between MPAH and CVD. Subgroup analysis revealed the interaction of gender and race in the effects of PFCs and CVD. PFUA was positively correlated with CVD in males but show no significant difference in females. PFDE was positively associated with CVD among non-Hispanic white individual. The results of BKMR indicated that the impact of mixed PFCs on CVD increased initially and then weakened, showing an overall positive trend. The results of WQS suggested that PFDO contributed most to the effect.
Our study showed that serum PFDE, MPAH, and PFUA levels were positively correlated with CVD. PUFA was found to interact with gender and race in relation to CVD. A general positive correlation exists between mixed exposure to PFCs and CVD, with PFDO being the most contributory PFC. Our study provided important evidence for probing the impact of PFCs on CVD and laid a foundation for further mechanism research.
多氟烷基化合物(PFCs)因其持久性和生物累积性而存在潜在的健康风险。然而,目前关于它们对心血管疾病(CVD)影响的证据不足。因此,研究PFCs与CVD之间的相关性势在必行。
数据收集自2005 - 2012年的国家健康与营养检查调查。采用逻辑回归模型评估单一PFC与CVD之间的关联。使用广义相加模型(GAM)评估非线性关系。进行亚组分析以探索交互作用。采用贝叶斯核机器回归(BKMR)和加权分位数和(WQS)模型评估PFC暴露对CVD的联合效应。
在逻辑回归中,全氟二乙基醚(PFDE)、单甲基全氟辛烷磺酸(MPAH)和全氟十一酸(PFUA)与CVD呈正相关。在GAM中,MPAH与CVD之间存在显著的非线性关系。亚组分析揭示了性别和种族在PFCs与CVD效应中的交互作用。PFUA在男性中与CVD呈正相关,但在女性中无显著差异。PFDE在非西班牙裔白人个体中与CVD呈正相关。BKMR结果表明,混合PFCs对CVD的影响先增加后减弱,总体呈正趋势。WQS结果表明,全氟癸酸(PFDO)对该效应的贡献最大。
我们的研究表明,血清PFDE、MPAH和PFUA水平与CVD呈正相关。发现PFUA在CVD方面与性别和种族存在交互作用。PFCs混合暴露与CVD之间总体呈正相关,PFDO是最具贡献的PFC。我们的研究为探究PFCs对CVD的影响提供了重要证据,并为进一步的机制研究奠定了基础。