MIND Institute, Department of Psychiatry and Behavioral Sciences, University of California Davis School of Medicine, Sacramento, California, USA.
Neurodevelopmental and Behavioral Phenotyping Service, National Institute of Mental Health, Bethesda, Maryland, USA.
Genes Brain Behav. 2022 Jun;21(5):e12803. doi: 10.1111/gbb.12803. Epub 2022 Mar 14.
Neurodevelopmental disorders (NDDs), including autism spectrum disorder (ASD) and intellectual disability (ID), are pervasive, often lifelong disorders, lacking evidence-based interventions for core symptoms. With no established biological markers, diagnoses are defined by behavioral criteria. Thus, preclinical in vivo animal models of NDDs must be optimally utilized. For this reason, experts in the field of behavioral neuroscience convened a workshop with the goals of reviewing current behavioral studies, reports, and assessments in rodent models. Goals included: (a) identifying the maximal utility and limitations of behavior in animal models with construct validity; (b) providing recommendations for phenotyping animal models; and (c) guidelines on how in vivo models should be used and reported reliably and rigorously while acknowledging their limitations. We concluded by recommending minimal criteria for reporting in manuscripts going forward. The workshop elucidated a consensus of potential solutions to several problems, including revisiting claims made about animal model links to ASD (and related conditions). Specific conclusions included: mice (or other rodent or preclinical models) are models of the neurodevelopmental insult, not specifically any disorder (e.g., ASD); a model that perfectly recapitulates a disorder such as ASD is untenable; and greater attention needs be given to validation of behavioral testing methods, data analysis, and critical interpretation.
神经发育障碍(NDDs),包括自闭症谱系障碍(ASD)和智力障碍(ID),是普遍存在的、往往是终身的障碍,缺乏针对核心症状的循证干预措施。由于没有既定的生物标志物,因此诊断是根据行为标准定义的。因此,必须最佳利用神经发育障碍的临床前体内动物模型。出于这个原因,行为神经科学领域的专家召开了一次研讨会,旨在回顾啮齿动物模型中的当前行为研究、报告和评估。目标包括:(a)确定具有构建有效性的动物模型中的行为的最大效用和局限性;(b)为表型动物模型提供建议;以及(c)关于如何可靠和严格地使用体内模型以及报告的指南,同时承认其局限性。我们最后建议在未来的手稿中报告最低标准。研讨会阐明了对几个问题的潜在解决方案的共识,包括重新审视有关动物模型与 ASD(和相关病症)联系的说法。具体结论包括:老鼠(或其他啮齿动物或临床前模型)是神经发育损伤的模型,而不是特定的任何病症(例如 ASD);完全再现 ASD 等病症的模型是不可行的;需要更加关注行为测试方法、数据分析和批判性解释的验证。