Viloxazine for the Treatment of Attention Deficit Hyperactivity Disorder.

IF 2 Q3 PSYCHOLOGY, CLINICAL Health Psychology Research Pub Date : 2022-09-23 eCollection Date: 2022-01-01 DOI:10.52965/001c.38360
Christopher L Robinson, Katelyn Parker, Saurabh Kataria, Evan Downs, Rajesh Supra, Alan D Kaye, Omar Viswanath, Ivan Urits
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Abstract

Purpose of review: Attention deficit hyperactivity disorder (ADHD) is a widely diagnosed neurodevelopmental disorder giving rise to symptoms of hyperactivity, impulsivity, and inattentiveness that can impair daily functioning. Stimulants, such as methylphenidate and amphetamines, are the mainstay of treatment for ADHD. However, nonstimulant drugs such as viloxazine, atomoxetine, guanfacine, and clonidine are becoming more popular due to minimal adverse effects when compared to stimulants.

Recent findings: Viloxazine is a selective norepinephrine reuptake inhibitor (NRI) originally used to treat depression in adults with activity in both the noradrenergic as well as serotonergic pathways. Studies have demonstrated its efficacy for its use in the treatment of ADHD. Unlike stimulants, viloxazine has a decreased chance of substance abuse, drug dependance, and withdrawal symptoms upon the cessation of therapy. Additionally, dopamine levels in the nucleus accumbens after treatment with viloxazine are elevated considerably less in comparison with traditional stimulant ADHD treatments. Viloxazine provides an alternative, nonstimulant approach to treating ADHD.

Summary: Viloxazine is a recently approved, non-stimulant medication functions by inhibiting the uptake of norepinephrine which has been seen to be decreased in patients with ADHD. When patients do not respond to first-line stimulants, cannot tolerate the side effects, or have contraindications to stimulants, viloxazine may be a nonstimulant option offering patients an increasing arsenal of medications to treat ADHD.

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维洛嗪治疗注意缺陷多动障碍。
综述目的:注意缺陷多动障碍(ADHD)是一种被广泛诊断的神经发育障碍,其症状包括多动、冲动和注意力不集中,可损害日常功能。兴奋剂,如哌甲酯和安非他明,是治疗多动症的主要药物。然而,非兴奋剂药物如维洛西嗪、阿托莫西汀、胍法辛和可乐定正变得越来越受欢迎,因为与兴奋剂相比,它们的副作用很小。最近发现:Viloxazine是一种选择性去甲肾上腺素再摄取抑制剂(NRI),最初用于治疗成人抑郁症,具有去甲肾上腺素能和血清素能两种途径的活性。研究已经证明了它在治疗多动症方面的有效性。与兴奋剂不同,维洛嗪在药物滥用、药物依赖和停止治疗后的戒断症状的机会减少。此外,与传统的兴奋剂治疗相比,维洛嗪治疗后伏隔核多巴胺水平的升高要少得多。维洛嗪为治疗多动症提供了另一种非兴奋剂的方法。摘要:Viloxazine是最近批准的一种非兴奋剂药物,其作用是抑制去甲肾上腺素的摄取,而去甲肾上腺素在ADHD患者中已被发现减少。当患者对一线兴奋剂没有反应,不能忍受副作用,或有兴奋剂禁忌症时,维洛嗪可能是一种非兴奋剂的选择,为患者提供了越来越多的治疗多动症的药物。
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来源期刊
Health Psychology Research
Health Psychology Research PSYCHOLOGY, CLINICAL-
CiteScore
2.90
自引率
0.00%
发文量
63
审稿时长
15 weeks
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