Luo Yuyang, Weibman Dana, Halperin Jeffrey M, Li Xiaobo
Department of Biomedical Engineering, New Jersey Institute of Technology, Newark, NJ, United States.
Department of Psychology, Queens College of the City University of New York, Flushing, NY, United States.
Front Hum Neurosci. 2019 Feb 11;13:42. doi: 10.3389/fnhum.2019.00042. eCollection 2019.
Attention-deficit/hyperactivity disorder (ADHD) is a neurodevelopmental disorder that affects approximately 8%-12% of children worldwide. Throughout an individual's lifetime, ADHD can significantly increase risk for other psychiatric disorders, educational and occupational failure, accidents, criminality, social disability and addictions. No single risk factor is necessary or sufficient to cause ADHD. The multifactorial causation of ADHD is reflected in the heterogeneity of this disorder, as indicated by its diversity of psychiatric comorbidities, varied clinical profiles, patterns of neurocognitive impairment and developmental trajectories, and the wide range of structural and functional brain anomalies. Although evidence-based treatments can reduce ADHD symptoms in a substantial portion of affected individuals, there is yet no curative treatment for ADHD. A number of theoretical models of the emergence and developmental trajectories of ADHD have been proposed, aimed at providing systematic guides for clinical research and practice. We conducted a comprehensive review of the current status of research in understanding the heterogeneity of ADHD in terms of etiology, clinical profiles and trajectories, and neurobiological mechanisms. We suggest that further research focus on investigating the impact of the etiological risk factors and their interactions with developmental neural mechanisms and clinical profiles in ADHD. Such research would have heuristic value for identifying biologically homogeneous subgroups and could facilitate the development of novel and more tailored interventions that target underlying neural anomalies characteristic of more homogeneous subgroups.
注意力缺陷多动障碍(ADHD)是一种神经发育障碍,全球约8%-12%的儿童受其影响。在个体一生中,ADHD会显著增加患其他精神障碍、教育和职业失败、事故、犯罪、社交障碍及成瘾的风险。没有单一风险因素是导致ADHD所必需或充分的。ADHD的多因素病因反映在该障碍的异质性上,这体现在其精神共病的多样性、不同的临床特征、神经认知损害模式和发育轨迹,以及广泛的大脑结构和功能异常。尽管循证治疗可在很大一部分受影响个体中减轻ADHD症状,但目前尚无治愈ADHD的疗法。已经提出了一些关于ADHD出现和发展轨迹的理论模型,旨在为临床研究和实践提供系统指导。我们对目前在理解ADHD在病因、临床特征和轨迹以及神经生物学机制方面的异质性的研究现状进行了全面综述。我们建议进一步的研究集中于调查病因风险因素的影响及其与ADHD发育神经机制和临床特征的相互作用。此类研究对于识别生物学上同质的亚组具有启发价值,并可促进开发针对更同质亚组特有的潜在神经异常的新型且更具针对性的干预措施。