首页> 外文期刊>Physiological Research >Novel Approach to Evaluate Central Autonomic Regulation in Attention Deficit/Hyperactivity Disorder (ADHD)
【24h】

Novel Approach to Evaluate Central Autonomic Regulation in Attention Deficit/Hyperactivity Disorder (ADHD)

机译:评估中枢性自主调节注意力缺陷/多动障碍(ADHD)的新方法

获取原文
获取原文并翻译 | 示例
           

摘要

Attention deficit/hyperactivity disorder (ADHD) is one of the most commonly diagnosed developmental disorders in childhood characterized by hyperactivity, impulsivity and inattention. ADHD manifests in the child's development by deficits in cognitive, executive and perceptor-motor functions, emotional regulation and social adaptation. Although the exact cause has not yet been known, the crucial role in the development of this disease plays the interaction of genetic, neurobiological and epigenetic factors. According to current knowledge, ADHD is defined as a biological dysfunction of central nervous system with genetically or organically defined deficits in noradrenergic and dopaminergic neurotransmission associated with structural abnormalities, especially in prefronto-striatal regions. In this context, a significant part of the difficulties could be due to a faulty control of fronto-striato-thalamo-cortical circuits important for attention, arousal and executive functions. Moreover, ADHD is associated with abnormal autonomic regulation. Specifically, reduced cardiac-linked parasympathetic activity associated with relative sympathetic dominance indexed by low heart rate variability can represent a noninvasive marker for prefrontal hypoactivity. However, the mechanisms underlying altered autonomic regulation in ADHD are still unknown. In this aspect, the evaluation of central autonomic regulation by noninvasive methods, namely pupillometry and eye-tracking, may provide novel information for better understanding of the neurobiological pathomechanisms leading to ADHD.
机译:注意力缺陷/多动障碍(ADHD)是儿童时期最常见的发育障碍之一,其特征在一起,其特征在于多动,冲动和疏忽。 ADHD在儿童的发展中表现在认知,行政和知情运动员功能,情感监管和社会适应中的赤字。虽然确切的原因尚未知道,但这种疾病发展中的至关重要作用发挥了遗传,神经生物学和表观遗传因素的相互作用。根据目前的知识,ADHD被定义为中枢神经系统的生物功能障碍,在丙炔病菌和多巴胺能神经递血中具有遗传或有机缺陷,与结构异常相关,特别是在前晶体区域中。在这种情况下,困难的重要部分可能是由于对关注,唤醒和行政功能重要的前端 - 泰拉米 - 皮质电路的错误控制。此外,ADHD与异常自主调节有关。具体而言,与低心率变异性指数的相对交感神经统治性相关的减少的心脏连接副交感度活性可以代表前额叶脱悬性的非侵入性标记。然而,ADHD中的自主调节改变的机制仍然未知。在这方面,通过非侵入性方法,即瞳孔测量和眼睛跟踪对中央自主调节的评估可以提供新颖的信息,以便更好地了解导致ADHD的神经生物学机制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号