确定 N-乙酰半胱氨酸对青少年非自杀性自伤的生物学特征。

Journal of psychiatry and brain science Pub Date : 2021-01-01 Epub Date: 2021-04-29 DOI:10.20900/jpbs.20210007
Siddhee A Sahasrabudhe, Thanharat Silamongkol, Young Woo Park, Alanna Colette, Lynn E Eberly, Bonnie Klimes-Dougan, Lisa D Coles, James C Cloyd, Gülin Öz, Bryon A Mueller, Reena V Kartha, Kathryn R Cullen
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引用次数: 0

摘要

非自杀性自伤(NSSI)在青少年中的发病率很高。然而,针对这一临床问题的循证治疗方法却很少。一项针对目标人群的开放标签试点研究显示,口服 N-乙酰半胱氨酸(NAC)(一种广泛使用的膳食补充剂)治疗与 NSSI 频率的降低有关。在准备进行生物学意义上的疗效试验设计时,一个关键的初步步骤是明确 NAC 的生物学特征,或其临床效果的基本机制。为此,我们建议分两个阶段对 NAC 在 NSSI 女性患者中的生物特征(谷胱甘肽 (GSH) 和/或谷氨酸 (Glu) 的变化)进行研究。第一阶段是一项双盲随机安慰剂对照研究,重点是确定最佳剂量,以便在对 36 名 16-24 岁女性 NSSI 患者进行短期(4 周)NAC 治疗期间,使谷胱甘肽和谷氨酸发生有意义的变化。决定研究是否进入第二阶段的 "去/不去 "标准包括预先指定的大脑和血液中 GSH 测量值的变化。脑部 GSH 的变化通过磁共振光谱(MRS)进行测量。第二阶段的剂量将根据第一阶段观察到的生物变化和耐受性来选择。第二阶段将在一个新的患者队列中进行为期 8 周的试验,试图复制生物特征研究结果,并研究生物特征、NAC 药代动力学和临床反应之间的关系。这个分两个阶段进行的项目是独一无二的,因为它将临床精神病学测量、定量 MRS 和药理学方法结合在一起,首次在患有 NSSI 的年轻女性中进行 NAC 的安慰剂对照临床试验:第 1 阶段试验方案已在 https://clinicaltrials.gov/ 上注册,ClinicalTrials.gov ID 为 "NCT04005053"(注册日期为 2019 年 7 月 2 日。网址:https://clinicaltrials.gov/ct2/show/NCT04005053)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Identifying Biological Signatures of N-Acetylcysteine for Non-Suicidal Self-Injury in Adolescents and Young Adults.

Identifying Biological Signatures of N-Acetylcysteine for Non-Suicidal Self-Injury in Adolescents and Young Adults.

The prevalence of non-suicidal self-injury (NSSI) is high in adolescents and young adults. However, there is a paucity of evidence-based treatments to address this clinical problem. An open-label, pilot study in the target population showed that treatment with oral N-acetylcysteine (NAC), a widely available dietary supplement, was associated with reduction in NSSI frequency. In preparation for a biologically informed design of an efficacy trial, a critical preliminary step is to clarify NAC's biological signatures, or measures of the mechanisms underlying its clinical effects. Toward that end, we propose a 2-stage project to investigate NAC's biological signatures (changes in glutathione (GSH) and/or glutamate (Glu)) in women with NSSI. The first stage; a double-blind randomized placebo-controlled study will focus on identifying the optimal dose to achieve meaningful change in GSH and Glu during short-term (4 weeks) NAC treatment in 36 women aged 16-24 years with NSSI. Go/No-go criteria to determine if the study will progress to the second stage include pre-specified changes in brain and blood measures of GSH. Changes in the brain GSH are measured through magnetic resonance spectroscopy (MRS). The dose for the stage 2 will be selected based on the biological changes and the tolerability observed in the stage 1. The stage 2 will seek to replicate the biological signature findings in an 8-week trial in a new patient cohort, and examine the relationships among biological signatures, NAC pharmacokinetics and clinical response. This 2-stage project is unique as it unifies clinical psychiatric measurements, quantitative MRS and pharmacological approaches in the first placebo-controlled clinical trial of NAC in young women with NSSI.

Trial registration: The stage 1 trial protocol has been registered on https://clinicaltrials.gov/ with ClinicalTrials.gov ID "NCT04005053" (Registered on 02 July 2019. Available from: https://clinicaltrials.gov/ct2/show/NCT04005053).

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