Moderating effects of reduced morning and evening questionnaire scores on the association between urinary phthalate metabolites and inflammatory cytokines among Chinese young adults: A human biomonitoring study

IF 4.2 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES
Tingting Li , Shuman Tao , Tangjun Jiang , Wanyu Che , Liwei Zou , Yajuan Yang , Fangbiao Tao , Xiaoyan Wu
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引用次数: 0

Abstract

Although previous findings have suggested that phthalate exposure was related to inflammation in young adults, little is known about whether chronotype, measured by the reduced Morning and Evening Questionnaire (rMEQ), reflects a moderating or mediating effect of phthalate exposure on inflammation. To address these gaps, this study examined the correlation of phthalate metabolites with inflammatory cytokines in Chinese young adults and explored the moderating effects of rMEQ scores in this association. From April to May 2019, 1179 young adults were recruited from 2 universities in Hefei and Shangrao cities. Among them, 1135 completed valid self-administered questionnaires, 1012 provided sufficient urine samples for phthalate metabolites analysis, and 744 provided fasting blood samples for the determination of inflammatory cytokines levels. The high-performance liquid chromatography-tandem mass spectrometry was adopted to determine the concentration of urinary phthalate metabolites. A liquid-phase protein suspension chip detection instrument was utilized to detect the levels of inflammatory cytokines in the supernatant. The rMEQ was adopted as a measure of chronotype. The generalized linear model was established to determine the association of phthalate metabolites with inflammatory cytokines. Moderating analysis was used to examine whether rMEQ scores moderated the relationships of phthalate metabolites with inflammatory cytokines. The median concentrations of phthalate metabolites ranged from 2.74 to 107.22 ng/mL. The mean levels of tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) were 0.78 ± 0.21 pg/mL and 0.34 ± 0.26 pg/mL, respectively. The generalized linear model results revealed that monobutyl phthalate (MBP) was weakly but significantly positively correlated with TNF-α. According to gender and further stratified analysis, the results showed that MBP and mono(2-ethyl-5-oxohexyl) phthalate (MEOHP) were weakly but significantly positively correlated with TNF-α and IL-1β only among females. Furthermore, the moderating effects analysis results indicated that rMEQ scores have a negative moderating role among MBP, MEOHP and TNF-α. Phthalate exposure was significantly positively correlated with inflammatory cytokines in young adults, and rMEQ scores played a negative moderating role in this association. This study has the potential to offer useful insights for the prevention and control of chronic inflammation among young adults.
降低早晚问卷得分对中国年轻人尿邻苯二甲酸酯代谢物和炎症细胞因子之间关系的调节作用:一项人体生物监测研究
虽然先前的研究结果表明,邻苯二甲酸盐暴露与年轻人的炎症有关,但通过减少的早晚问卷(rMEQ)测量的时间类型是否反映了邻苯二甲酸盐暴露对炎症的调节或中介作用,我们知之甚少。为了解决这些空白,本研究考察了中国年轻人中邻苯二甲酸酯代谢物与炎症细胞因子的相关性,并探讨了rMEQ评分在这种关联中的调节作用。2019年4月至5月,从合肥和上饶两市的两所大学招募了1179名年轻人。其中1135人完成了有效的自填问卷,1012人提供了足够的尿液样本用于邻苯二甲酸盐代谢物分析,744人提供了空腹血液样本用于检测炎症细胞因子水平。采用高效液相色谱-串联质谱法测定尿中邻苯二甲酸酯代谢物浓度。采用液相蛋白悬液芯片检测仪检测上清液中炎性细胞因子水平。rMEQ被用来衡量时间类型。建立广义线性模型来确定邻苯二甲酸酯代谢物与炎症细胞因子的关系。使用调节分析来检查rMEQ评分是否调节邻苯二甲酸酯代谢物与炎症细胞因子的关系。邻苯二甲酸酯代谢物中位浓度为2.74 ~ 107.22ng/mL。肿瘤坏死因子-α (TNF-α)和白细胞介素-1β (IL-1β)的平均水平分别为0.78±0.21pg/mL和0.34±0.26pg/mL。广义线性模型结果显示,邻苯二甲酸一丁酯(MBP)与TNF-α呈微弱但显著的正相关。根据性别和进一步的分层分析,结果显示MBP和邻苯二甲酸单(2-乙基-5-氧己基)酯(MEOHP)仅在女性中与TNF-α和IL-1β呈弱但显著的正相关。此外,调节效应分析结果表明,rMEQ评分对MBP、MEOHP和TNF-α具有负向调节作用。在年轻人中,邻苯二甲酸盐暴露与炎症细胞因子显著正相关,rMEQ评分在这一关联中起负调节作用。这项研究有可能为年轻人慢性炎症的预防和控制提供有用的见解。
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来源期刊
CiteScore
7.00
自引率
4.70%
发文量
185
审稿时长
34 days
期刊介绍: Environmental Toxicology and Pharmacology publishes the results of studies concerning toxic and pharmacological effects of (human and veterinary) drugs and of environmental contaminants in animals and man. Areas of special interest are: molecular mechanisms of toxicity, biotransformation and toxicokinetics (including toxicokinetic modelling), molecular, biochemical and physiological mechanisms explaining differences in sensitivity between species and individuals, the characterisation of pathophysiological models and mechanisms involved in the development of effects and the identification of biological markers that can be used to study exposure and effects in man and animals. In addition to full length papers, short communications, full-length reviews and mini-reviews, Environmental Toxicology and Pharmacology will publish in depth assessments of special problem areas. The latter publications may exceed the length of a full length paper three to fourfold. A basic requirement is that the assessments are made under the auspices of international groups of leading experts in the fields concerned. The information examined may either consist of data that were already published, or of new data that were obtained within the framework of collaborative research programmes. Provision is also made for the acceptance of minireviews on (classes of) compounds, toxicities or mechanisms, debating recent advances in rapidly developing fields that fall within the scope of the journal.
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