From repellent to risk: DEET’s adverse effects on hormones and bone health in kids

IF 13 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Journal of Advanced Research Pub Date : 2025-03-21 DOI:10.1016/j.jare.2025.03.037
Xinyu Zhu , Wanlu Liu , Baihao Lin , Haixia Qian , Mengya Xu , Yuyu Zheng , Yansen Bai
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Abstract

Introduction

Early life bone accumulation, which predicts future fragility fracture risk, is intimately associated with sex hormones. N, N-diethyl-3-methylbenzamide (DEET) is the primary and most effective active ingredient widely used globally, especially among children and adolescents. However, the effects of DEET on sex hormones and bone mass remain unclear.

Objective

We aimed to explore the adverse effects of DEET exposure on bone mass and to elucidate the potential mediating roles of sex hormones in children and adolescents.

Methods

This cross-sectional study analyzed 864 children and adolescents from NHANES 2013–2016. Urinary 3-diethyl-carbamoyl benzoic acid (DCBA) was employed as a biomarker for DEET exposure. The study examined the relationships between DCBA, sex hormones, and bone mass, with a particular focus on evaluating the independent and serial mediation effects of sex hormones on DEET-bone mass associations.

Results

Increased DCBA was associated with decreased testosterone (TT), estrogen (E2), and free androgen index (FAI), alongside an increase in sex hormone-binding globulin (SHBG) levels, particularly pronounced among subjects < 12 years [β% (95 % CI) = −0.081 (−0.144, −0.017), −0.064 (−0.114, −0.013), −0.101 (−0.177, −0.024), and 0.020 (−0.009, 0.048), respectively] and non-overweight subjects [β% (95 % CI) = −0.160 (−0.234, −0.086), −0.103 (−0.158, −0.048), −0.195 (−0.282, −0.107), and 0.035 (0.012, 0.058), respectively]. Negative dose–response relationships between DCBA and bone mass were observed in non-overweight participants [β% (95 % CI) = −0.011 (−0.018, −0.005) and −0.027 (−0.041, −0.013) for total bone mineral density (BMD) and total bone mineral content (BMC), respectively], and in children < 12 years for total BMC [β% (95 % CI) = −0.012 (−0.024, 0.000)]. Additionally, TT, E2, and SHBG were found to significantly and independently mediate 15.41 % to 79.84 % of the relationship between DCBA and bone mass. Furthermore, serial mediation effects among sex hormones were detected between TT, E2, and SHBG.

Conclusions

DEET exerts a detrimental effect on bone health by interfering with sex hormones in children and adolescents, warranting heightened public concern.

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从驱虫剂到风险:避蚊胺对儿童激素和骨骼健康的不利影响
早期骨质积累与性激素密切相关,它可以预测未来的脆性骨折风险。N, N-二乙基-3-甲基苄胺(DEET)是全球广泛使用的主要和最有效的活性成分,特别是在儿童和青少年中。然而,避蚊胺对性激素和骨量的影响尚不清楚。目的探讨避蚊胺暴露对儿童和青少年骨量的不良影响,并阐明性激素在其中的潜在调节作用。方法本横断面研究分析了NHANES 2013-2016年的864名儿童和青少年。尿3-二乙基氨基甲酰苯甲酸(DCBA)被用作避蚊胺暴露的生物标志物。本研究考察了DCBA、性激素和骨量之间的关系,特别侧重于评估性激素对避蚊胺骨量关联的独立和系列中介作用。ResultsIncreased DCBA与降低睾酮(TT)、雌激素(E2)、和自由雄激素指数(FAI),除了增加性hormone-binding球蛋白(SHBG)水平,特别是主体间明显 & lt; 12 年[β%(95 % CI) = -0.081(−0.144−0.017)−0.064(−0.114−0.013)−0.101(−0.177−0.024),和0.020(−0.009,0.048),分别)和非超重受试者(β%(95 % CI) = -0.160(−0.234−0.086)−0.103(−0.158−0.048)−0.195(−0.282−0.107),和0.035(分别为0.012,0.058)。消极的剂量反应DCBA和骨密度之间的关系被观察到在非超重参与者[β%(95 % CI) = -0.011(−0.018−0.005)和−0.027(−0.041−0.013)总骨密度(BMD)和总骨矿物质含量(BMC),分别),和孩子 & lt; 12 年总BMC(β%(95 % CI) = -0.012(−0.024,0.000)]。此外,TT、E2和SHBG在DCBA和骨量之间的关系中有15.41 %至79.84 %的独立介导作用。此外,性激素在TT、E2和SHBG之间存在一系列的中介作用。结论避蚊胺通过干扰儿童和青少年性激素对骨骼健康产生不利影响,应引起公众高度关注。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Advanced Research
Journal of Advanced Research Multidisciplinary-Multidisciplinary
CiteScore
21.60
自引率
0.90%
发文量
280
审稿时长
12 weeks
期刊介绍: Journal of Advanced Research (J. Adv. Res.) is an applied/natural sciences, peer-reviewed journal that focuses on interdisciplinary research. The journal aims to contribute to applied research and knowledge worldwide through the publication of original and high-quality research articles in the fields of Medicine, Pharmaceutical Sciences, Dentistry, Physical Therapy, Veterinary Medicine, and Basic and Biological Sciences. The following abstracting and indexing services cover the Journal of Advanced Research: PubMed/Medline, Essential Science Indicators, Web of Science, Scopus, PubMed Central, PubMed, Science Citation Index Expanded, Directory of Open Access Journals (DOAJ), and INSPEC.
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