儿童注意缺陷/多动障碍的精准医学:行为、神经生物学和遗传诊断生物标志物的系统综述。

IF 2.2 3区 医学 Q3 BEHAVIORAL SCIENCES
Marija Pranjić, Virginia Peisch, Nikolina Vukšić, Sambridhi Subedi, Anne B Arnett
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引用次数: 0

摘要

目的:注意缺陷/多动障碍(ADHD)是最常见的儿童精神障碍之一,也是儿科初级和发展性护理中常见的问题。然而,目前缺乏客观的诊断工具,导致延误和漏诊。当前的系统综述旨在确定客观指标是否可以作为儿童ADHD的诊断指标。方法:我们对客观的行为、神经生物学和遗传生物标志物进行了系统的回顾,这些生物标志物可以为儿科ADHD的精确医学诊断提供信息。根据PRISMA指南,我们检索了三个主要数据库(MEDLINE, PsycInfo和Scopus),检索了2012年至2024年间发表的以翻译为目的评估诊断性生物标志物的文章。结果:共有111项研究符合纳入标准,包括42项行为研究、44项神经影像学研究和25项遗传学研究。在行为研究中,身体活动的测量在良好到优秀的范围内达到了区别效度。当使用机器学习和多特征模型时,神经成像生物标志物最强。一个特别有前途的方向涉及以认知控制为目标的基于任务的近红外光谱范式。遗传研究的结果强调了ADHD遗传结构的复杂性,包括罕见和常见的变异,以及表观遗传机制。总体而言,MicroRNA和甲基化谱显示出最强的准确性。结论:我们的系统综述通过行为、神经影像学和遗传方法确定了有希望的ADHD候选诊断标记。多方法方法可能产生最强的诊断准确性。这些方法的复杂性和成本限制了在初级保健机构中实施精确医学方法来诊断小儿多动症的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Precision Medicine in Pediatric Attention-Deficit/Hyperactivity Disorder: A Systematic Review of Behavioral, Neurobiological and Genetic Diagnostic Biomarkers.

Objective: Attention-deficit/hyperactivity disorder (ADHD) is one of the most common childhood psychiatric disorders and a common presenting concern in primary and developmental pediatric care. However, objective diagnostic tools are currently not available, leading to delayed and missed diagnoses. The current systematic review aimed to determine whether objective indices can serve as diagnostic markers for pediatric ADHD.

Method: We conducted a systematic review of objective behavioral, neurobiological, and genetic biomarkers that could inform a precision medicine approach to diagnosis of pediatric ADHD. Following the PRISMA guidelines, we searched three major databases (MEDLINE, PsycInfo, and Scopus) for articles published between 2012 and 2024 that evaluated diagnostic biomarkers with a translational aim.

Results: A total of 111 studies met inclusion criteria, including 42 behavioral, 44 neuroimaging, and 25 genetic studies. Among behavioral studies, measures of physical activity achieved discriminant validity in the good to excellent range. Neuroimaging biomarkers were strongest when machine learning and multiple-features models were used. A particularly promising direction involved task-based NIRS paradigms targeting cognitive control. The results of the genetic studies underscored the complexity of the genetic architecture of ADHD, implicating rare and common variants, as well as epigenetic mechanisms. MicroRNA and methylation profiles demonstrated the strongest accuracy, overall.

Conclusion: Our systematic review identified promising candidate diagnostic markers for ADHD across behavioral, neuroimaging, and genetic methods. Multimethod approaches are likely to yield the strongest diagnostic accuracy. The complexity and cost of these approaches limits potential for implementation of a precision medicine approach to pediatric ADHD diagnosis in primary care settings.

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来源期刊
CiteScore
3.10
自引率
8.30%
发文量
155
审稿时长
6-12 weeks
期刊介绍: Journal of Developmental & Behavioral Pediatrics (JDBP) is a leading resource for clinicians, teachers, and researchers involved in pediatric healthcare and child development. This important journal covers some of the most challenging issues affecting child development and behavior.
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