识别产前酒精暴露和受其影响的儿童:生物标志物和筛选工具的综述

IF 6.8 1区 医学 Q1 SUBSTANCE ABUSE
Julie A Kable, Kenneth Lyons Jones
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引用次数: 1

摘要

目的:早期识别产前酒精暴露(PAE)和因这种暴露而需要服务的人是一个重要的公共卫生问题。本研究综述了PAE潜在的生物标志物和筛选工具及其影响的现有文献。检索方法:在电子数据库中检索1996年1月1日至2021年11月30日之间发表的文章,使用以下检索词:(“胎儿酒精”或“产前酒精”或“FASD”或“酒精相关神经发育障碍”或“ARND”或“ND-PAE”)和(“筛选”或“鉴定”或“生物标志物”)。重复的文章以电子方式删除。审查标题和摘要的适当性,并检索选定的文章作进一步分析。在评审文章中引用或从专家知识中确定的其他文章被添加。提取有关样本特征、生物标志物或筛选工具以及预测有效性结果数据的信息。然后对数据进行研究的叙述性分析。搜索结果:最初总共确定了3,813篇文章,其中1,215篇被删除为重复。在剩余的文章中,通过标题和摘要检查,182篇文章被确定在审查范围内,181篇文章被成功检索。其中,额外的文章被删除,因为它们是临床前的(3),仅描述性的(13),仅包括PAE的自我报告(42),仅包括平均组比较(17),额外的重复(2),关注成本分析(9),错过预测效度数据(24),或其他原因(23)。对其余48篇文献进行摘要。从这些文章中确定了另外13份手稿,另外两份来自专家知识。共有63篇文章参与了本次综述。讨论与结论:PAE的生物标志物和筛选工具及其影响缺乏理想的预测效度特征。许多用于识别PAE及其影响的生物标志物和筛选工具的特异性高于敏感性,这表明目前的方法仍然不能充分识别受PAE影响的所有个体。在最近的研究中发现了例外,这些研究使用了与生长和血管发育相关的microrna,与PAE相关的蛋白质组学变化,以及估计各种细胞因子水平的标记组合。需要在其他样本中重复这些发现,以确认有限的可用数据。未来对生物标志物和筛选工具的研究应关注实施的可行性和可扩展性。本文还建议一个系统的评估过程,以提高早期识别受PAE影响的个人,以便实施减少伤害和康复护理工作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Identifying Prenatal Alcohol Exposure and Children Affected by It: A Review of Biomarkers and Screening Tools.

Identifying Prenatal Alcohol Exposure and Children Affected by It: A Review of Biomarkers and Screening Tools.

Identifying Prenatal Alcohol Exposure and Children Affected by It: A Review of Biomarkers and Screening Tools.

Identifying Prenatal Alcohol Exposure and Children Affected by It: A Review of Biomarkers and Screening Tools.

Purpose: Early identification of prenatal alcohol exposure (PAE) and of those in need of services resulting from this exposure is an important public health concern. This study reviewed the existing literature on potential biomarkers and screening tools of PAE and its impact.

Search methods: Electronic databases were searched for articles published between January 1, 1996, and November 30, 2021, using the following search terms: ("fetal alcohol" or "prenatal alcohol" or "FASD" or "alcohol-related neurodevelopmental disorder" or "ARND" or "ND-PAE") and ("screening" or "identification" or "biomarker"). Duplicate articles were electronically eliminated. Titles and abstracts were reviewed for appropriateness, and selected articles were retrieved for further analysis. Additional articles were added that were referenced in the reviewed articles or identified from expert knowledge. Information about the characteristics of the sample, the biomarker or screening tool, and the predictive validity outcome data were abstracted. A narrative analysis of the studies was then performed on the data.

Search results: A total of 3,813 articles were initially identified, and 1,215 were removed as duplicates. Of the remaining articles, 182 were identified as being within the scope of the review based on title and abstract inspection, and 181 articles were successfully retrieved. Of these, additional articles were removed because they were preclinical (3), were descriptive only (13), included only self-report of PAE (42), included only mean group comparison (17), were additional duplicates (2), focused on cost analysis (9), missed predictive validity data (24), or for other reasons (23). The remaining articles (n = 48) were abstracted. An additional 13 manuscripts were identified from these articles, and two more from expert knowledge. A total of 63 articles contributed to the review.

Discussion and conclusions: Biomarkers and screening tools of PAE and its impact fall short of ideal predictive validity characteristics. Higher specificity than sensitivity was found for many of the biomarkers and screening tools used to identify PAE and its impact, suggesting that current methods continue to under-identify the full range of individuals impacted by PAE. Exceptions to this were found in recent investigations using microRNAs related to growth and vascular development, proteomic changes associated with PAE, and combinations of markers estimating levels of various cytokines. Replications of these findings are needed across other samples to confirm the limited data available. Future research on biomarkers and screening tools should attend to feasibility and scalability of implementation. This article also recommends a systematic process of evaluation to improve early identification of individuals impacted by PAE so that harm reduction and habilitative care efforts can be implemented.

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来源期刊
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期刊介绍: Alcohol Research: Current Reviews (ARCR) is an open-access, peer-reviewed journal published by the National Institute on Alcohol Abuse and Alcoholism (NIAAA) at the National Institutes of Health. Starting from 2020, ARCR follows a continuous, rolling publication model, releasing one virtual issue per yearly volume. The journal offers free online access to its articles without subscription or pay-per-view fees. Readers can explore the content of the current volume, and past volumes are accessible in the journal's archive. ARCR's content, including previous titles, is indexed in PubMed, PsycINFO, Scopus, and Web of Science.
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