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