内分泌干扰物的发育毒性:挑战与未来方向

Q4 Pharmacology, Toxicology and Pharmaceutics
A. Pizent
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引用次数: 1

摘要

产妇接触各种内分泌干扰物的混合物可能对其后代的产后健康产生重大影响,并增加成年后健康失调和疾病的风险。近几十年来,为了更好地了解生命早期接触内分泌干扰物所带来的健康风险,研究工作有所增加。本文简要概述了目前研究人员在选择适当的流行病学方法和研究设计以识别内分泌干扰物并评估其在这一关键发育窗口期对健康的不利影响方面继续面临的挑战。主要的挑战涉及选择一种具有代表性的生物标志物,该生物标志物应反映生物活性化学品或其代谢物的胎儿内部剂量,这些物质可能与暴露的不同水平和持续时间以及暴露与失调/疾病表现之间的潜伏期有关,对健康产生不利影响。未来的研究应更多地关注确定导致对各种EDCs和其他毒物易感性的个体间差异的因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Developmental toxicity of endocrine-disrupting chemicals: Challenges and future directions
Maternal exposure to a mixture of various endocrine disruptors (EDCs) may have a substantial impact on postnatal health of her offspring(s) and increase the risk for health disorders and diseases in adulthood. Research efforts to better understand the health risk associated with endocrine disruptor exposures in early life have increased in recent decades. This paper provides a short overview of the current challenges that researchers continue to face in selecting appropriate epidemiologic methods and study designs to identify endocrine disruptors and evaluate their adverse health effects during this critical developmental window. Major challenges involve the selection of a representative biomarker that reflects the foetal internal dose of the biologically active chemical or its metabolite(s) that may be associated with adverse health effects with regard to variable level and duration of exposure and the latency between exposure and disorder/disease manifestation. Future studies should pay more attention to identifying factors that contribute to interindividual variability in susceptibility to various EDCs and other toxicants.
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来源期刊
Arhiv za Farmaciju
Arhiv za Farmaciju Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
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发文量
19
审稿时长
12 weeks
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