Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.
Stony Brook Cancer Center, Stony Brook University, Stony Brook, NY, USA.
Crit Rev Toxicol. 2024 Mar;54(3):174-193. doi: 10.1080/10408444.2023.2297751. Epub 2024 Mar 27.
An association between exposure to arsenic (As) and neurologic and behavioral effects has been reported in some studies, but no systematic review is available of the evidence linking As in drinking water and neurobehavioral effects after consideration of study quality and potential confounding, with focus on low-level circumstances of exposure. We conducted a systematic review and reported it in compliance with the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines, through a search of the databases PubMed, Web of Science, Scopus, and Embase. We included in the review the studies reporting results based on exposure from drinking water in humans. Endpoints were heterogeneous across studies, so we classified them into eight broad domains and developed an ad-hoc system to evaluate their methodological quality, based on three tiers. It was not possible to conduct meta-analysis because of the heterogeneity in exposure assessment and in the definition and assessment of outcomes. The search identified 18,518 articles. After elimination of duplicates and irrelevant articles, we retained 106 articles which reported results on As exposure and neurobehavioral effects, of which 22 reported risk estimates from exposure in drinking water (six among adults and 16 among children). None of the studies was conducted blindly. Among the studies in adults, two, which were conducted in highly exposed populations, were classified as high quality. These two studies were broadly consistent in reporting an association between exposure to As and decline in cognitive function; however, they provide no evidence of an association for exposure below 75 μg/L. The four lower-quality studies were based on populations with low exposure; these studies reported associations with inconsistent outcomes, few of which remained statistically significant after adjustment for multiple comparisons. Among the five high-quality studies of children, one reported an association between As in drinking water and intellectual function, whereas none of the other studies reported an association with different neurobehavioral indicators, after adjusting for potential confounders and multiple comparisons. Out of seven intermediate-quality studies, three reported an association with cognitive function or other outcomes; but sources of bias were not adequately controlled. The remaining studies were negative. The four low-quality studies did not contribute to the overall evidence because of methodological limitations. Our assessment of the available literature showed a lack of evidence for a causal association between exposure to As in drinking water and neurobehavioral effects. To clarify whether such an association exists, further studies prospectively evaluating changes in both the concentration of As in drinking water during the life course, and neurobehavioral outcomes, as well as appropriately controlling for potential confounders, are needed.
一些研究报告指出,砷(As)暴露与神经和行为影响之间存在关联,但没有系统综述考虑研究质量和潜在混杂因素后,将饮用水中的砷与神经行为影响联系起来的证据,重点关注低水平暴露情况。我们按照系统评价和荟萃分析的首选报告项目(PRISMA)指南进行了系统综述,并在 PubMed、Web of Science、Scopus 和 Embase 数据库中进行了搜索。我们将报告基于人类饮用水暴露结果的研究纳入综述。由于研究终点在不同研究之间存在异质性,因此我们将其分为八个广泛的领域,并根据三个层次制定了一个专门的系统来评估其方法学质量。由于暴露评估以及结局的定义和评估存在异质性,因此无法进行荟萃分析。搜索共确定了 18518 篇文章。消除重复项和不相关的文章后,我们保留了 106 篇报告砷暴露与神经行为影响结果的文章,其中 22 篇报告了饮用水暴露的风险估计值(成人中有 6 篇,儿童中有 16 篇)。没有一项研究是盲法进行的。在成人研究中,有两项在高暴露人群中进行的研究被评为高质量。这两项研究在报告砷暴露与认知功能下降之间的关联方面基本一致;然而,它们没有提供暴露低于 75μg/L 与关联的证据。四项低质量研究基于低暴露人群;这些研究报告了与不一致结局的关联,其中很少有在调整多重比较后仍具有统计学意义。在五项高质量的儿童研究中,有一项报告了饮用水中砷与智力功能之间的关联,而其他研究在调整潜在混杂因素和多重比较后,均未报告与不同神经行为指标的关联。在七项中等质量的研究中,有三项报告了与认知功能或其他结局的关联;但偏倚来源未得到充分控制。其余研究均为阴性。由于方法学限制,四项低质量研究对总体证据没有贡献。我们对现有文献的评估表明,饮用水中砷暴露与神经行为影响之间不存在因果关联的证据不足。为了澄清是否存在这种关联,需要进一步前瞻性研究评估整个生命周期中饮用水中砷浓度的变化以及神经行为结果,并适当控制潜在混杂因素。