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评估盐酸胍法辛在成年注意缺陷多动障碍(ADHD)患者中的治疗作用:设计、研发及治疗中的定位。

Evaluating Guanfacine Hydrochloride in the Treatment of Attention Deficit Hyperactivity Disorder (ADHD) in Adult Patients: Design, Development and Place in Therapy.

机构信息

Department of Psychiatry, Nara Medical University, Kashihara, Japan.

Faculty of Nursing, School of Medicine, Nara Medical University, Kashihara, Japan.

出版信息

Drug Des Devel Ther. 2021 May 11;15:1965-1969. doi: 10.2147/DDDT.S221126. eCollection 2021.

Abstract

Attention-deficit/hyperactivity disorder (ADHD) is characterized by age-inappropriate and impairing levels of inattention, hyperactivity, or impulsivity, or a combination of these characteristics. It is estimated to affect around 4% of adults worldwide. In the past few decades, prescriptions for ADHD drugs (psychostimulants and non-psychostimulants) have increased significantly. However, the efficacy and safety of adult ADHD medications remains controversial. Guanfacine extended-release (GXR) is a non-psychostimulant ADHD drug that is a selective α2A-adrenergic receptor agonist, first approved for treatment of adult ADHD in Japan in June 2019. Our aim was to provide an overview of GXR pharmacology and review the studies on efficacy and safety that have been conducted in adults with ADHD. The beneficial actions of guanfacine are thought to be attributed to the strengthening of prefrontal cortical network connections, which regulate attention, emotion, and behavior via the activity at post-synaptic α2A receptors. Current evidence of GXR efficacy and safety suggests that GXR is an effective monotherapy treatment option for adults with ADHD.

摘要

注意缺陷多动障碍(ADHD)的特征是注意力不集中、过度活跃或冲动,或这些特征的组合,这些症状与年龄不相符且对患者造成损害。据估计,全球约有 4%的成年人受其影响。在过去的几十年中,ADHD 药物(精神兴奋剂和非精神兴奋剂)的处方量显著增加。然而,成人 ADHD 药物的疗效和安全性仍存在争议。盐酸胍法辛缓释片(GXR)是一种非精神兴奋剂 ADHD 药物,作为选择性α2A-肾上腺素能受体激动剂,于 2019 年 6 月在日本首次被批准用于成人 ADHD 的治疗。我们旨在提供 GXR 药理学概述,并回顾在 ADHD 成人患者中进行的疗效和安全性研究。胍法辛的有益作用被认为归因于增强前额皮质网络连接,通过突触后α2A 受体的活性来调节注意力、情绪和行为。目前关于 GXR 疗效和安全性的证据表明,GXR 是治疗 ADHD 成人的有效单药治疗选择。

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