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法舒地尔在伴有谷氨酸能基因网络变异的 ADHD 青少年中的应用,这些变异会破坏 mGluR 神经递质信号传递。

Fasoracetam in adolescents with ADHD and glutamatergic gene network variants disrupting mGluR neurotransmitter signaling.

机构信息

Nemours, du Pont Hospital for Children, Wilmington, 19803, DE, USA.

Department of Pediatrics Sidney Kimmel Medical College of Thomas Jefferson University, Philadelphia, 19107, PA, USA.

出版信息

Nat Commun. 2018 Jan 16;9(1):4. doi: 10.1038/s41467-017-02244-2.

Abstract

The glutamatergic neurotransmitter system may play an important role in attention-deficit hyperactivity disorder (ADHD). This 5-week, open-label, single-blind, placebo-controlled study reports the safety, pharmacokinetics and responsiveness of the metabotropic glutamate receptor (mGluR) activator fasoracetam (NFC-1), in 30 adolescents, age 12-17 years with ADHD, harboring mutations in mGluR network genes. Mutation status was double-blinded. A single-dose pharmacokinetic profiling from 50-800 mg was followed by a single-blind placebo at week 1 and subsequent symptom-driven dose advancement up to 400 mg BID for 4 weeks. NFC-1 treatment resulted in significant improvement. Mean Clinical Global Impressions-Improvement (CGI-I) and Severity (CGI-S) scores were, respectively, 3.79 at baseline vs. 2.33 at week 5 (P < 0.001) and 4.83 at baseline vs. 3.86 at week 5 (P < 0.001). Parental Vanderbilt scores showed significant improvement for subjects with mGluR Tier 1 variants (P < 0.035). There were no differences in the incidence of adverse events between placebo week and weeks on active drug. The trial is registered at https://clinicaltrials.gov/ct2/show/study/NCT02286817 .

摘要

谷氨酸能神经递质系统可能在注意缺陷多动障碍(ADHD)中发挥重要作用。这项为期 5 周、开放标签、单盲、安慰剂对照的研究报告了代谢型谷氨酸受体(mGluR)激动剂法舒地尔(NFC-1)在 30 名年龄在 12-17 岁、患有 ADHD 且 mGluR 网络基因发生突变的青少年中的安全性、药代动力学和反应性。突变状态是双盲的。在第 1 周进行了单次剂量药代动力学分析,范围为 50-800mg,随后进行了单次盲法安慰剂治疗,第 2 周到第 4 周根据症状进行单盲剂量递增,每天 2 次,剂量为 400mg。NFC-1 治疗后显著改善。平均临床总体印象改善(CGI-I)和严重程度(CGI-S)评分分别为:基线时 3.79 分,第 5 周时 2.33 分(P < 0.001),基线时 4.83 分,第 5 周时 3.86 分(P < 0.001)。对于 mGluR 1 层变体的患者,父母范德比尔特评分显著改善(P < 0.035)。在安慰剂周和活性药物治疗周之间,不良事件的发生率没有差异。该试验在 https://clinicaltrials.gov/ct2/show/study/NCT02286817 上注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc30/5770454/d96127e6e917/41467_2017_2244_Fig1_HTML.jpg

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