美国中老年人接触全氟和多氟烷基物质与老年性黄斑变性的关系

Habyeong Kang, Sung Kyun Park, Dong Hyun Kim, Yoon-Hyeong Choi
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引用次数: 0

摘要

尽管接触全氟烷基和多氟烷基物质(PFAS)会对健康产生各种影响,但尚未调查过接触 PFAS 与年龄相关性黄斑变性(AMD)之间的关系。我们利用参加 2005-2008 年全国健康与营养调查的 1722 名 40 岁以上美国成年人的数据,评估了 PFAS 暴露与老年性黄斑变性之间的关系,这些数据包含 PFAS 测量、老年性黄斑变性诊断和协变量的完整数据。研究人员测量了血清中 PFAS 的浓度,包括全氟辛酸 (PFOA)、全氟壬酸 (PFNA)、全氟己烷磺酸 (PFHxS) 和全氟辛烷磺酸 (PFOS)。采用项目反应理论评分法计算出 PFAS 负担总分。单个 PFAS 浓度和 PFAS 负担总分被分为低(参考值)、中和高三组。老年性视网膜病变的诊断基于视网膜图像检查。任何 AMD 都被定义为存在早期或晚期 AMD。在对潜在混杂因素进行调整后,采用调查加权逻辑回归法计算出根据 PFAS 暴露情况出现 AMD 的几率比 (OR) 和 95% 置信区间 (CI)。总体而言,132 人(6.5%)被诊断出患有任何老年性黄斑变性,其中 115 人(5.7%)患有早期老年性黄斑变性。血清中全氟辛烷磺酸浓度与任何老年性视网膜病变之间存在明显的剂量-反应关系(p-趋势=0.03),与参照组相比,高浓度组的OR值为1.99(95% CI:1.05,3.79)。全氟辛烷磺酸的总体负担与任何老年黄斑病变呈非单调关系,中度组的显着OR值为2.18(95% CI:1.18,4.04)。通过限制性立方样条分析可以观察到倒 U 型关系。此外,早期黄斑变性在全氟辛烷磺酸和全氟辛烷磺酸总体负荷中也显示出相似的模式,此外,在全氟萘烷中也显示出倒 U 型关联。我们的研究结果表明,根据血清全氟辛烷磺酸和全氟萘系物以及全氟辛烷磺酸总体负荷估算的全氟辛烷磺酸暴露量可能是中老年人群患老年性黄斑变性的风险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exposure to per- and polyfluoroalkyl substances and age-related macular degeneration in U.S. middle-aged and older adults
Despite various health effects of per- and polyfluoroalkyl substances (PFAS) exposure, the association between PFAS exposure and age-related macular degeneration (AMD) has not been investigated. We aimed to assess associations of PFAS exposure with AMD, using data from 1,722 U.S. adults aged 40 years or more participating in the National Health and Nutrition Examination Survey 2005–2008 with complete data on PFAS measurement, AMD diagnosis, and covariates. Serum concentrations of PFAS, including perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), perfluorohexane sulfonic acid (PFHxS), and perfluorooctane sulfonic acid (PFOS), were measured. An overall PFAS burden score was calculated using item response theory scoring. Individual PFAS concentration and overall PFAS burden score were categorized into low (reference), medium, and high groups. Diagnosis of AMD was based on retinal image examination. Any AMD was defined as the presence of early or late AMD. Survey-weighted logistic regression adjusted for potential confounders was used to calculate odds ratios (ORs) and 95% confidence intervals (CIs) for presence of AMD according to PFAS exposure. Overall, 132 (6.5%) individuals were diagnosed as any AMD, including 115 (5.7%) individuals with early AMD. A significant dose-response association was observed between serum PFOS concentration and any AMD (p-trend=0.03), with a significant OR of 1.99 (95% CI: 1.05, 3.79) for the high group compared to the reference. Overall PFAS burden showed a non-monotonic association with any AMD, with a significant OR of 2.18 (95% CI: 1.18, 4.04) for the medium. Inverted U-shaped associations were observed by restricted cubic spline analyses. Also, early AMD showed similar patterns in PFOS and overall PFAS burden and additionally an inverted U-shape association in PFNA. Our findings suggest that exposure to PFAS estimated by serum PFOS and PFNA as well as overall PFAS burden might be a risk factor for AMD in middle-aged and older population.
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