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2
Pharmacokinetics of bisphenol S in humans after single oral administration.人体单次口服双酚 S 的药代动力学。
Environ Int. 2018 Mar;112:127-133. doi: 10.1016/j.envint.2017.11.020. Epub 2017 Dec 19.
3
Clinical Practice Guideline for Screening and Management of High Blood Pressure in Children and Adolescents.临床实践指南:儿童和青少年高血压的筛查和管理。
Pediatrics. 2017 Sep;140(3). doi: 10.1542/peds.2017-1904. Epub 2017 Aug 21.
4
Environmental exposures and pediatric kidney function and disease: A systematic review.环境暴露与儿童肾功能及疾病:一项系统综述。
Environ Res. 2017 Oct;158:625-648. doi: 10.1016/j.envres.2017.06.029. Epub 2017 Jul 17.
5
Albuminuria, Proteinuria, and Renal Disease Progression in Children with CKD.慢性肾脏病患儿的白蛋白尿、蛋白尿与肾脏疾病进展
Clin J Am Soc Nephrol. 2017 Jun 7;12(6):912-920. doi: 10.2215/CJN.11971116. Epub 2017 May 25.
6
The safety of the use of bisphenol A in medical devices.医疗设备中双酚A使用的安全性。
Regul Toxicol Pharmacol. 2016 Aug;79:106-107. doi: 10.1016/j.yrtph.2016.01.014. Epub 2016 Feb 4.
7
Translational research in nephrology: chronic kidney disease prevention and public health.肾脏病学中的转化研究:慢性肾脏病预防与公共卫生
Clin Kidney J. 2015 Dec;8(6):647-55. doi: 10.1093/ckj/sfv082. Epub 2015 Aug 30.
8
Pharmacokinetics of bisphenol A in humans following a single oral administration.单次口服给药后双酚A在人体中的药代动力学。
Environ Int. 2015 Oct;83:107-15. doi: 10.1016/j.envint.2015.06.008. Epub 2015 Jun 24.
9
Bisphenol S and F: A Systematic Review and Comparison of the Hormonal Activity of Bisphenol A Substitutes.双酚S和双酚F:双酚A替代品激素活性的系统评价与比较
Environ Health Perspect. 2015 Jul;123(7):643-50. doi: 10.1289/ehp.1408989. Epub 2015 Mar 16.
10
Bisphenol-A induces podocytopathy with proteinuria in mice.双酚 A 可诱导小鼠足细胞病伴蛋白尿。
J Cell Physiol. 2014 Dec;229(12):2057-66. doi: 10.1002/jcp.24665.

儿童慢性肾脏病的肾功能与双酚 A 和邻苯二甲酸酯暴露。

Renal Function and exposure to Bisphenol A and phthalates in children with Chronic Kidney Disease.

机构信息

Department of Pediatrics, Divisions of Nephrology and Environmental Pediatrics, NYU Langone Medical Center, New York, NY, USA.

Wadsworth Center, New York State Department of Health, and Department of Environmental Health Sciences, School of Public Health, State University of New York at Albany, NY, USA.

出版信息

Environ Res. 2018 Nov;167:575-582. doi: 10.1016/j.envres.2018.08.006. Epub 2018 Aug 9.

DOI:10.1016/j.envres.2018.08.006
PMID:30172191
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7409562/
Abstract

RATIONALE AND OBJECTIVE

Exposure to Bisphenol A (BPA) and phthalates is ubiquitous among adults and children in the United States. Among children and adolescents, those with chronic kidney disease (CKD) are potentially at greater risk of adverse effects from BPA and phthalate exposure. The objective of this study was to evaluate BPA and phthalate exposure among children with CKD and evaluate associations with three measures of kidney function.

STUDY DESIGN

Cross sectional study.

SETTING, PARTICIPANTS, AND MEASUREMENTS: The CKD population was represented by the Chronic Kidney Disease in Children (CKiD) Study, a multicenter, prospective cohort study of children with impaired kidney function in the US. The main outcome was assessment of the relationship between chemical exposures and clinical laboratory findings at enrollment into CKiD. Data collected at baseline from participants 1 to 17 years old (N = 538) were analyzed. Urinary BPA and phthalate levels were evaluated at this time point. Data from the National Health and Nutrition Examination Survey (NHANES), a nationally representative pediatric population, were used for comparison to the CKiD cohort.

RESULTS

Urinary BPA and phthalate levels in the CKiD population were consistently lower than levels detected in healthy children. Additionally, BPA was not significantly associated with blood pressure, proteinuria, or estimated glomerular filtration rate (eGFR). Within the CKiD population, for select individual and combined phthalates, there was an inverse relationship with the urinary protein:creatinine ratio (LMW phthalates, - 9.53% change; 95% CI: - 14.21, - 4.21; p = 0.001), and in most cases, a positive relationship with eGFR (LMW phthalates, a 3.46 unit increase in eGFR, 95% CI: 1.85, 5.07; p < 0.001).

LIMITATIONS

Lack of longitudinal data, limited assessment of diet and nutritional status.

CONCLUSION

In the study cohort, children with CKD did not have increased exposure to BPA and phthalates. Longitudinal studies with repeated measures are likely to be more informative about the possible health effects of prolonged exposure to BPA and phthalates in pediatric patients with CKD.

摘要

背景和目的

双酚 A(BPA)和邻苯二甲酸酯在美国的成年人和儿童中普遍存在。在儿童和青少年中,患有慢性肾脏病(CKD)的儿童可能面临更大的 BPA 和邻苯二甲酸酯暴露的不良影响。本研究的目的是评估 CKD 儿童的 BPA 和邻苯二甲酸酯暴露情况,并评估其与三种肾功能指标的关系。

研究设计

横断面研究。

地点、参与者和测量:CKiD 研究代表了 CKD 人群,这是一项在美国进行的多中心、前瞻性队列研究,纳入了有肾功能受损的儿童。主要结局是评估化学暴露与 CKiD 入组时临床实验室发现之间的关系。分析了来自年龄在 1 至 17 岁(n=538)的参与者基线时的数据。此时评估了尿液中的 BPA 和邻苯二甲酸酯水平。使用来自全国健康和营养调查(NHANES)的数据与 CKiD 队列进行比较,NHANES 是一个具有全国代表性的儿科人群。

结果

CKiD 人群的尿液 BPA 和邻苯二甲酸酯水平始终低于健康儿童的检测水平。此外,BPA 与血压、蛋白尿或估计肾小球滤过率(eGFR)均无显著相关性。在 CKiD 人群中,对于特定的个体和组合邻苯二甲酸酯,与尿蛋白/肌酐比值呈负相关(LMW 邻苯二甲酸酯,-9.53%变化;95%CI:-14.21,-4.21;p=0.001),在大多数情况下,与 eGFR 呈正相关(LMW 邻苯二甲酸酯,eGFR 增加 3.46 个单位,95%CI:1.85,5.07;p<0.001)。

局限性

缺乏纵向数据,对饮食和营养状况的评估有限。

结论

在研究队列中,CKD 儿童的 BPA 和邻苯二甲酸酯暴露并未增加。具有重复测量的纵向研究可能更能提供有关儿科 CKD 患者长期暴露于 BPA 和邻苯二甲酸酯可能产生的健康影响的信息。