Suppr超能文献

去甲肾上腺素能控制人类暴食障碍和肥胖症的神经行为(NOBEAD):一项整合分子脑成像的智能手机支持的行为情绪调节干预研究方案。

Noradrenergic control of neurobehavior in human binge-eating disorder and obesity (NOBEAD): A smartphone-supported behavioral emotion regulation intervention study protocol integrating molecular brain imaging.

机构信息

Department of Nuclear Medicine, University of Leipzig Medical Center, Leipzig, Germany.

Integrated Research and Treatment Center (IFB) Adiposity Diseases, Leipzig University Medical Centre Leipzig, Leipzig, Germany.

出版信息

Int J Eat Disord. 2024 Jan;57(1):206-220. doi: 10.1002/eat.24080. Epub 2023 Nov 8.

Abstract

OBJECTIVE

The neurobehavioral underpinnings of binge-eating disorder (BED), co-occurring with obesity (OB), are largely unknown. This research project conceptualizes BED as a disorder with dysfunctional emotion regulation (ER) linked with changes in central noradrenaline (NA) transmission and NA-modulated neuronal networks.

METHODS

We expect abnormalities in NA activity in both BED and OB, but most pronounced in BED. We expect these abnormalities to be modifiable through state-of-the-art ER intervention, specifically in BED. To assess the role of NA transmission, we will quantify changes in NA transporter (NAT) availability using the highly NAT-specific [ C]methylreboxetin (MRB) and positron emission tomography-magnetic resonance imaging (PET-MRI) that allows measuring molecular and neuronal changes before and after an ER intervention. Individual 12-session smartphone-supported acceptance-based behavioral therapy will be conducted to improve ER. Thirty individuals with OB and BED (OB + BED), 30 individuals with OB without BED (OB - BED), and 20 individuals with normal weight will undergo assessments of NAT availability and neuronal network activity under rest and stimulated conditions, clinical interviews, self-report questionnaires on eating behavior, ER, mental and physical health, and quality of life, and neuropsychological tests on executive function. Afterwards, in an experimental randomized-controlled design, individuals with OB + BED and OB - BED will be allocated to smartphone-supported ER intervention versus a waitlist and re-assessed after 10 weeks.

DISCUSSION

By obtaining biological and behavioral markers, the proposed study will disentangle the involvement of NAT and the central NA system in the modulation of emotion-supporting neuronal networks that influence eating behavior. Neurobehavioral mechanisms of change during an ER intervention will be determined.

TRIAL REGISTRATION

German Clinical Trials Register (DRKS): DRKS00029367.

PUBLIC SIGNIFICANCE

This study investigates the central noradrenaline system by using hybrid brain imaging in conjunction with emotion regulation as a putative core biological mechanism in individuals with obesity with or without binge-eating disorder that is targeted by emotion regulation intervention. The results will provide a molecular signature beyond functional imaging biomarkers as a predictive biomarker toward precision medicine for tailoring treatments for individuals with binge-eating disorders and obesity.

摘要

目的

暴食症(BED)伴肥胖(OB)的神经行为基础在很大程度上尚不清楚。本研究项目将 BED 概念化为一种功能失调的情绪调节(ER)障碍,与中枢去甲肾上腺素(NA)传递和 NA 调节的神经元网络变化有关。

方法

我们预计 BED 和 OB 中都会出现 NA 活性异常,但在 BED 中更为明显。我们预计这些异常可以通过最先进的 ER 干预来改变,特别是在 BED 中。为了评估 NA 传递的作用,我们将使用高度特定于 NA 转运体(NAT)的 [C]甲基reboxetine(MRB)和正电子发射断层扫描-磁共振成像(PET-MRI)来量化 NAT 可用性的变化,该方法允许在进行 ER 干预之前和之后测量分子和神经元变化。将进行 12 次个体智能手机支持的基于接受的行为治疗,以改善 ER。30 名 OB 伴 BED(OB+BED)、30 名 OB 不伴 BED(OB-BED)和 20 名体重正常的个体将接受 NAT 可用性和神经元网络活动的评估在休息和刺激条件下,临床访谈,关于饮食行为、ER、精神和身体健康以及生活质量的自我报告问卷,以及执行功能的神经心理学测试。之后,在实验性随机对照设计中,将 OB+BED 和 OB-BED 个体分配到智能手机支持的 ER 干预与候补组,并在 10 周后重新评估。

讨论

通过获得生物学和行为学标志物,拟议的研究将阐明 NAT 和中枢 NA 系统在调节影响饮食行为的情绪支持神经元网络中的作用。将确定 ER 干预期间的神经行为变化机制。

试验注册

德国临床试验注册处(DRKS):DRKS00029367。

公众意义

本研究通过使用混合脑成像结合情绪调节,调查中枢去甲肾上腺素系统,作为一种潜在的核心生物学机制,针对肥胖伴或不伴暴食症个体的情绪调节干预。结果将提供超越功能成像生物标志物的分子特征,作为针对精准医学的预测生物标志物,用于为暴食症和肥胖症个体量身定制治疗方法。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验