Sex difference of pre- and post-natal exposure to six developmental neurotoxicants on intellectual abilities: a systematic review and meta-analysis of human studies.

IF 5.3 2区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES Environmental Health Pub Date : 2023-11-17 DOI:10.1186/s12940-023-01029-z
Carly V Goodman, Rivka Green, Allya DaCosta, David Flora, Bruce Lanphear, Christine Till
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Abstract

Background: Early life exposure to lead, mercury, polychlorinated biphenyls (PCBs), polybromide diphenyl ethers (PBDEs), organophosphate pesticides (OPPs), and phthalates have been associated with lowered IQ in children. In some studies, these neurotoxicants impact males and females differently. We aimed to examine the sex-specific effects of exposure to developmental neurotoxicants on intelligence (IQ) in a systematic review and meta-analysis.

Method: We screened abstracts published in PsychINFO and PubMed before December 31st, 2021, for empirical studies of six neurotoxicants (lead, mercury, PCBs, PBDEs, OPPs, and phthalates) that (1) used an individualized biomarker; (2) measured exposure during the prenatal period or before age six; and (3) provided effect estimates on general, nonverbal, and/or verbal IQ by sex. We assessed each study for risk of bias and evaluated the certainty of the evidence using Navigation Guide. We performed separate random effect meta-analyses by sex and timing of exposure with subgroup analyses by neurotoxicant.

Results: Fifty-one studies were included in the systematic review and 20 in the meta-analysis. Prenatal exposure to developmental neurotoxicants was associated with decreased general and nonverbal IQ in males, especially for lead. No significant effects were found for verbal IQ, or postnatal lead exposure and general IQ. Due to the limited number of studies, we were unable to analyze postnatal effects of any of the other neurotoxicants.

Conclusion: During fetal development, males may be more vulnerable than females to general and nonverbal intellectual deficits from neurotoxic exposures, especially from lead. More research is needed to examine the nuanced sex-specific effects found for postnatal exposure to toxic chemicals.

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产前和产后接触六种发育性神经毒物对智力的性别差异:对人类研究的系统回顾和荟萃分析。
背景:儿童早期接触铅、汞、多氯联苯(PCBs)、多溴联苯醚(PBDEs)、有机磷农药(OPPs)和邻苯二甲酸盐与智商降低有关。在一些研究中,这些神经毒物对男性和女性的影响是不同的。我们的目的是通过系统回顾和荟萃分析来研究暴露于发育性神经毒物对智力(IQ)的性别特异性影响。方法:筛选2021年12月31日前发表在PsychINFO和PubMed上的摘要,对六种神经毒物(铅、汞、多氯联苯、多溴二苯醚、OPPs和邻苯二甲酸盐)进行实证研究:(1)使用个体化生物标志物;(2)产前或六岁前的暴露量;(3)按性别提供对一般、非语言和/或语言智商的影响估计。我们评估了每项研究的偏倚风险,并使用导航指南评估了证据的确定性。我们按性别和暴露时间进行了单独的随机效应荟萃分析,并按神经毒物进行了亚组分析。结果:51项研究被纳入系统评价,20项研究被纳入meta分析。产前接触发育性神经毒物与男性一般智商和非语言智商下降有关,尤其是铅。没有发现言语智商、产后铅暴露和一般智商有显著影响。由于研究数量有限,我们无法分析任何其他神经毒物的产后影响。结论:在胎儿发育过程中,男性可能比女性更容易受到神经毒性暴露,特别是铅的一般和非语言智力缺陷的影响。需要更多的研究来检验出生后接触有毒化学物质所产生的细微的性别特异性影响。
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来源期刊
Environmental Health
Environmental Health 环境科学-公共卫生、环境卫生与职业卫生
CiteScore
10.10
自引率
1.70%
发文量
115
审稿时长
3.0 months
期刊介绍: Environmental Health publishes manuscripts on all aspects of environmental and occupational medicine and related studies in toxicology and epidemiology. Environmental Health is aimed at scientists and practitioners in all areas of environmental science where human health and well-being are involved, either directly or indirectly. Environmental Health is a public health journal serving the public health community and scientists working on matters of public health interest and importance pertaining to the environment.
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