Huss Michael, Chen Wai, Ludolph Andrea G
Child and Adolescent Psychiatry of the University Medicine Johannes Gutenberg University, Langenbeckstr. 1, 55131, Mainz, Germany.
Department of Child and Adolescent Psychiatry, School of Paediatrics and Child Health and School of Psychiatry and Clinical Neurosciences, Faculty of Medicine, Dentistry and Health Sciences, The University of Western Australia, Perth, WA, Australia.
Clin Drug Investig. 2016 Jan;36(1):1-25. doi: 10.1007/s40261-015-0336-0.
Children/adolescents with attention-deficit/hyperactivity disorder (ADHD) may have a poor or inadequate response to psychostimulants or be unable to tolerate their side-effects; furthermore, stimulants may be inappropriate because of co-existing conditions. Only one non-stimulant ADHD pharmacotherapy, the noradrenaline transporter inhibitor atomoxetine, is currently approved for use in Europe. We review recent advances in understanding of the pathophysiology of ADHD with a focus on the roles of catecholamine receptors in context of the α2A-adrenergic receptor agonist guanfacine extended release (GXR), a new non-stimulant treatment option in Europe. Neuroimaging studies of children/adolescents with ADHD show impaired brain maturation, and structural and functional anomalies in brain regions and networks. Neurobiological studies in ADHD and medication response patterns support involvement of monoaminergic neurotransmitters (primarily dopamine and noradrenaline). Guanfacine is a selective α2A-adrenergic receptor agonist that has been shown to improve prefrontal cortical cognitive function, including working memory. The hypothesized mode of action of guanfacine centres on direct stimulation of post-synaptic α2A-adrenergic receptors to enhance noradrenaline neurotransmission. Preclinical data suggest that guanfacine also influences dendritic spine growth and maturation. Clinical trials have demonstrated the efficacy of GXR in ADHD, and it is approved as monotherapy or adjunctive therapy to stimulants in Canada and the USA (for children and adolescents). GXR was approved recently in Europe for the treatment of ADHD in children and adolescents for whom stimulants are not suitable, not tolerated or have been shown to be ineffective. GXR may provide particular benefit for children/adolescents who have specific co-morbidities such as chronic tic disorders or oppositional defiant disorder (or oppositional symptoms) that have failed to respond to first-line treatment options.
患有注意力缺陷多动障碍(ADHD)的儿童/青少年可能对精神兴奋剂反应不佳或反应不足,或者无法耐受其副作用;此外,由于并存其他病症,兴奋剂可能并不适用。目前在欧洲,仅有一种非兴奋剂ADHD药物疗法,即去甲肾上腺素转运体抑制剂托莫西汀被批准使用。我们回顾了ADHD病理生理学理解方面的最新进展,重点关注在欧洲一种新型非兴奋剂治疗选择——缓释α2A肾上腺素能受体激动剂胍法辛(GXR)背景下儿茶酚胺受体的作用。对患有ADHD的儿童/青少年的神经影像学研究显示大脑成熟受损,以及大脑区域和神经网络存在结构和功能异常。ADHD的神经生物学研究及药物反应模式支持单胺能神经递质(主要是多巴胺和去甲肾上腺素)的参与。胍法辛是一种选择性α2A肾上腺素能受体激动剂,已被证明可改善前额叶皮质认知功能,包括工作记忆。胍法辛的假定作用模式集中在直接刺激突触后α2A肾上腺素能受体以增强去甲肾上腺素神经传递。临床前数据表明胍法辛还会影响树突棘的生长和成熟。临床试验已证明GXR对ADHD有效,并且在加拿大和美国它被批准作为单一疗法或兴奋剂的辅助疗法(用于儿童和青少年)。GXR最近在欧洲被批准用于治疗对兴奋剂不适用、不耐受或已证明无效的儿童和青少年ADHD。GXR可能对患有特定共病(如慢性抽动障碍或对立违抗障碍(或对立症状))且对一线治疗方案无反应的儿童/青少年特别有益。