Cannabinoid type 1 receptor availability imaging in attention-deficit/hyperactivity disorder using [18F]MK-9470 positron emission tomography: study protocol of the CB1-ADHD study.

IF 1.7
Isabelle Miederer, Marina Louise Schofer, Christian Ruckes, Wolfgang Retz, Mathias Schreckenberger, Alexandra Sebastian
{"title":"Cannabinoid type 1 receptor availability imaging in attention-deficit/hyperactivity disorder using [<sup>18</sup>F]MK-9470 positron emission tomography: study protocol of the CB1-ADHD study.","authors":"Isabelle Miederer, Marina Louise Schofer, Christian Ruckes, Wolfgang Retz, Mathias Schreckenberger, Alexandra Sebastian","doi":"10.1186/s41824-026-00322-7","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Attention deficit/hyperactivity disorder (ADHD) is a neurodevelopmental disorder characterized by attentional deficits, hyperactivity and impulsivity that often persists into adulthood. While dysfunction of dopaminergic neurotransmitter systems has been observed, underlying mechanisms remain incompletely understood. Current treatments with methylphenidate and amphetamines show limited long-term effectiveness and do not address broader clinical needs. The endocannabinoid system represents a promising therapeutic target. Cannabinoid type 1 (CB1) receptors are highly concentrated in the prefrontal cortex and striatum, brain regions central to ADHD pathophysiology. The \"dual pathway model of ADHD\" describes deficits in inhibition-related executive functions and reward-related functions, both mediated by fronto-striatal networks. Striatal CB1 receptor availability correlates negatively with impulsivity. Given the interaction between dopaminergic and endocannabinoid systems, CB1 receptors may play a key role in ADHD pathogenesis.</p><p><strong>Methods: </strong>This controlled study will investigate CB1 receptor availability in ADHD using positron emission tomography (PET) with the CB1-selective radiotracer [<sup>18</sup>F]MK-9470. The primary outcome is the CB1 receptor distribution volume (V<sub>T</sub>) in the striatum. Secondary outcomes include CB1 receptor availability in prefrontal cortex and other ADHD-relevant brain regions, plasma concentrations of endocannabinoids (anandamide, 2-arachidonoylglycerol), and validated neuropsychological assessments of attention and impulsivity. We will compare three groups (n = 34 each): medication-naïve participants with ADHD, methylphenidate-treated participants with ADHD, and healthy controls. Statistical analysis will employ ANOVA with post-hoc comparisons and correlation analyses between neuroimaging and behavioral measures.</p><p><strong>Results: </strong>N/A, as this is a study protocol.</p><p><strong>Conclusions: </strong>This first investigation of the endocannabinoid system in ADHD will provide crucial insights into disease mechanisms and identify potential therapeutic targets. Results may inform development of novel cannabinoid-based treatments and improve evidence-based therapeutic strategies for ADHD management.</p><p><strong>Trial registration: </strong>German Clinical Trials Register (DRKS-ID: DRKS00037526, Registration date: 25 September 2025).</p>","PeriodicalId":519909,"journal":{"name":"EJNMMI reports","volume":"10 1","pages":""},"PeriodicalIF":1.7000,"publicationDate":"2026-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13569728/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"EJNMMI reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s41824-026-00322-7","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Attention deficit/hyperactivity disorder (ADHD) is a neurodevelopmental disorder characterized by attentional deficits, hyperactivity and impulsivity that often persists into adulthood. While dysfunction of dopaminergic neurotransmitter systems has been observed, underlying mechanisms remain incompletely understood. Current treatments with methylphenidate and amphetamines show limited long-term effectiveness and do not address broader clinical needs. The endocannabinoid system represents a promising therapeutic target. Cannabinoid type 1 (CB1) receptors are highly concentrated in the prefrontal cortex and striatum, brain regions central to ADHD pathophysiology. The "dual pathway model of ADHD" describes deficits in inhibition-related executive functions and reward-related functions, both mediated by fronto-striatal networks. Striatal CB1 receptor availability correlates negatively with impulsivity. Given the interaction between dopaminergic and endocannabinoid systems, CB1 receptors may play a key role in ADHD pathogenesis.

Methods: This controlled study will investigate CB1 receptor availability in ADHD using positron emission tomography (PET) with the CB1-selective radiotracer [18F]MK-9470. The primary outcome is the CB1 receptor distribution volume (VT) in the striatum. Secondary outcomes include CB1 receptor availability in prefrontal cortex and other ADHD-relevant brain regions, plasma concentrations of endocannabinoids (anandamide, 2-arachidonoylglycerol), and validated neuropsychological assessments of attention and impulsivity. We will compare three groups (n = 34 each): medication-naïve participants with ADHD, methylphenidate-treated participants with ADHD, and healthy controls. Statistical analysis will employ ANOVA with post-hoc comparisons and correlation analyses between neuroimaging and behavioral measures.

Results: N/A, as this is a study protocol.

Conclusions: This first investigation of the endocannabinoid system in ADHD will provide crucial insights into disease mechanisms and identify potential therapeutic targets. Results may inform development of novel cannabinoid-based treatments and improve evidence-based therapeutic strategies for ADHD management.

Trial registration: German Clinical Trials Register (DRKS-ID: DRKS00037526, Registration date: 25 September 2025).

[18F]MK-9470正电子发射断层扫描在注意缺陷/多动障碍中的大麻素1型受体可用性成像:CB1-ADHD研究方案。
背景:注意缺陷/多动障碍(ADHD)是一种以注意缺陷、多动和冲动为特征的神经发育障碍,通常持续到成年。虽然已经观察到多巴胺能神经递质系统的功能障碍,但其潜在机制仍不完全清楚。目前使用哌甲酯和安非他明的治疗显示出有限的长期有效性,并且不能满足更广泛的临床需求。内源性大麻素系统是一个很有前景的治疗靶点。大麻素1型(CB1)受体高度集中于前额叶皮层和纹状体,这是ADHD病理生理的核心大脑区域。ADHD的“双通路模型”描述了与抑制相关的执行功能和与奖励相关的功能缺陷,两者都是由额纹状体网络介导的。纹状体CB1受体可用性与冲动性呈负相关。考虑到多巴胺能和内源性大麻素系统之间的相互作用,CB1受体可能在ADHD发病中起关键作用。方法:本对照研究将使用CB1选择性放射性示踪剂[18F]MK-9470的正电子发射断层扫描(PET)研究CB1受体在ADHD中的可用性。主要结果是纹状体中CB1受体分布体积(VT)。次要结局包括前额皮质和其他adhd相关脑区CB1受体的可用性,内源性大麻素(anandamide, 2-花生四烯醇甘油)的血浆浓度,以及验证的注意力和冲动的神经心理学评估。我们将比较三组(每组n = 34): medication-naïve ADHD患者、服用哌甲酯治疗的ADHD患者和健康对照组。统计分析将采用方差分析与事后比较和神经影像学和行为测量之间的相关性分析。结果:N/A,因为这是一个研究方案。结论:对ADHD内源性大麻素系统的首次研究将为疾病机制提供重要见解,并确定潜在的治疗靶点。结果可能为开发新的基于大麻素的治疗方法提供信息,并改善ADHD管理的循证治疗策略。试验注册:德国临床试验注册(DRKS-ID: DRKS00037526,注册日期:2025年9月25日)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书