Department of Biostatistics and Epidemiology, University of Massachusetts Amherst, Amherst, MA, USA.
Center for Global Cardiometabolic Health, Departments of Epidemiology, Medicine and Surgery, Brown University, USA.
Int J Hyg Environ Health. 2021 May;234:113743. doi: 10.1016/j.ijheh.2021.113743. Epub 2021 Apr 1.
Recent experimental work has shown that phthalates may increase inflammation. Prior research has not examined the role of exposure to phthalates in relation to inflammatory status among postmenopausal women who are at higher risk of developing inflammation-related chronic disorders.
We aimed to examine the associations of urinary phthalate biomarker concentrations with circulating levels of c-reactive protein [CRP] and interleukin-6 [IL-6] among 443 postmenopausal women selected into a breast cancer case-control study nested within the Women's Health Initiative (WHI).
A total of 13 phthalate metabolites were measured in urine samples provided at WHI enrollment from 1993 to 1998. We also measured baseline levels of CRP and IL-6 in these women's serum or plasma samples. Multivariable linear models were used to investigate the role of each phthalate biomarker in relation to CRP and IL-6, adjusting for potential confounding factors and specifically evaluating the role of BMI.
In adjusted models we observed positive associations of monocarboxynonyl phthalate (MCNP) with CRP (β = 0.092; 95% CI 0.026, 0.158) and IL-6 (β = 0.108; 95% CI 0.013, 0.204). These positive associations were attenuated and non-significant, however, after further adjustment for body mass index (BMI). In contrast, we observed inverse associations of monoethyl phthalate (MEP) (β = -0.019; 95% CI -0.036, -0.001) and monobenzyl phthalate (MBzP) (β = -0.034; 95% CI -0.058, -0.010) with CRP levels only after adjustment for BMI. Other phthalate biomarkers examined were not significantly associated with either CRP or IL-6 levels.
Overall, these results do not suggest an important role for phthalates in promoting an inflammatory response. Future prospective studies are warranted to improve understanding of these associations, particularly in clarifying the role of BMI.
最近的实验工作表明,邻苯二甲酸酯可能会增加炎症。先前的研究并未检查接触邻苯二甲酸酯与处于更高风险的发展与炎症相关的慢性疾病的绝经后妇女的炎症状态之间的关系。
我们旨在研究 443 名绝经后妇女尿液中邻苯二甲酸酯生物标志物浓度与循环 C 反应蛋白 [CRP] 和白细胞介素 6 [IL-6] 水平之间的关联,这些妇女是从 1993 年至 1998 年参加妇女健康倡议(WHI)的乳腺癌病例对照研究中选择的。
在 WHI 登记时,从尿液样本中测量了 13 种邻苯二甲酸酯代谢物。我们还测量了这些妇女血清或血浆样本中的 CRP 和 IL-6 的基线水平。多变量线性模型用于研究每个邻苯二甲酸酯生物标志物与 CRP 和 IL-6 的关系,调整了潜在的混杂因素,并专门评估了 BMI 的作用。
在调整后的模型中,我们观察到单羧酸壬基邻苯二甲酸酯(MCNP)与 CRP(β=0.092;95%CI 0.026,0.158)和 IL-6(β=0.108;95%CI 0.013,0.204)呈正相关。然而,在进一步调整体重指数(BMI)后,这些正相关关系减弱且无统计学意义。相比之下,我们仅在调整 BMI 后观察到单乙基邻苯二甲酸酯(MEP)(β=-0.019;95%CI-0.036,-0.001)和单苄基邻苯二甲酸酯(MBzP)(β=-0.034;95%CI-0.058,-0.010)与 CRP 水平呈负相关。检查的其他邻苯二甲酸酯生物标志物与 CRP 或 IL-6 水平均无显著相关性。
总体而言,这些结果表明邻苯二甲酸酯在促进炎症反应方面没有重要作用。未来的前瞻性研究对于更好地了解这些关联是必要的,特别是在澄清 BMI 的作用方面。