Chen Xiaodong, Li Jiaqi, Xu Ningda, Li Xuewei, Li Jiarui, Guo Qianwen, Zhang Jia, Miao Heng, Huang Lvzhen
Department of Ophthalmology, Eye Diseases and Optometry Institute, Peking University People's Hospital, Beijing, China.
Beijing Key Laboratory of Diagnosis and Therapy of Retinal and Choroid Diseases, Beijing, China.
PLoS One. 2025 Jan 31;20(1):e0317678. doi: 10.1371/journal.pone.0317678. eCollection 2025.
This study aims to investigate the connection between serum lipids, per- and polyfluoroalkyl substances (PFAS), and age-related macular degeneration (AMD) risk and assess whether serum lipids mediate the association between PFAS and AMD.
1605 participants were enrolled from NHANES 2005-2008. Four serum PFAS levels with high detective rates, including perfluorononanoic acid (PFNA), perfluorooctanoic acid (PFOA), perfluorooctane sulfonic acid (PFOS), and perfluorohexane sulfonic acid (PFHxS) were examined. Restricted cubic spline analysis (RCS) and weighted quantile sum (WQS) analysis were employed to detect nonlinear and mixed exposure effects.
PFOS level was associated with any AMD (OR, 1.54; 95% CI, 1.12 to 2.11; P = 0.011), early AMD (OR, 1.43; 95% CI, 1.06 to 1.95; P = 0.024), and late AMD (OR, 3.35; 95% CI, 1.55 to 7.23; P = 0.004) risk. PFHxS (OR, 1.72; 95% CI, 1.01 to 2.93; P = 0.045) and PFOA (OR, 2.10; 95% CI, 1.21 to 3.63; P = 0.011) levels were associated with late AMD risk. The RCS showed a nonlinear connection between PFOS exposure and AMD risk (P nonlinear = 0.006). WQS analysis indicated a positive relationship between mixed PFAS exposure and AMD risk (OR, 1.34; 95% CI, 1.03 to 1.75; P = 0.030). Serum total cholesterol (TC) and high-density lipoprotein (HDL) cholesterol were associated with AMD risk (ORTC, 1.005; 95% CI, 1.001 to 1.009; P = 0.026. ORHDL, 1.028; 95% CI, 1.014 to 1.042; P<0.001), and mediated the relationship of PFOS exposure and AMD risk, with mediation proportions of 5.73% (P = 0.020) and 7.27% (P = 0.032), respectively.
PFOS exposure was connected with AMD risk and serum TC and HDL mediated this relationship.
本研究旨在调查血清脂质、全氟和多氟烷基物质(PFAS)与年龄相关性黄斑变性(AMD)风险之间的联系,并评估血清脂质是否介导PFAS与AMD之间的关联。
从2005 - 2008年美国国家健康与营养检查调查(NHANES)中招募了1605名参与者。检测了四种检出率高的血清PFAS水平,包括全氟壬酸(PFNA)、全氟辛酸(PFOA)、全氟辛烷磺酸(PFOS)和全氟己烷磺酸(PFHxS)。采用受限立方样条分析(RCS)和加权分位数和(WQS)分析来检测非线性和混合暴露效应。
PFOS水平与任何AMD(比值比[OR],1.54;95%置信区间[CI],1.12至2.11;P = 0.011)、早期AMD(OR,1.43;95% CI,1.06至1.95;P = 0.024)和晚期AMD(OR,3.35;95% CI,1.55至7.23;P = 0.004)风险相关。PFHxS(OR,1.72;95% CI,1.01至2.93;P = 0.045)和PFOA(OR,2.10;95% CI,1.21至3.63;P = 0.011)水平与晚期AMD风险相关。RCS显示PFOS暴露与AMD风险之间存在非线性联系(P非线性 = 0.006)。WQS分析表明混合PFAS暴露与AMD风险之间存在正相关(OR,1.34;95% CI,1.03至1.75;P = 0.030)。血清总胆固醇(TC)和高密度脂蛋白(HDL)胆固醇与AMD风险相关(ORTC,1.005;95% CI,1.001至1.009;P = 0.026。ORHDL,1.028;95% CI,1.014至1.042;P<0.001),并介导了PFOS暴露与AMD风险的关系,中介比例分别为5.73%(P = 0.020)和7.27%(P = 0.032)。
PFOS暴露与AMD风险相关,血清TC和HDL介导了这种关系。