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赖氨酸安非他明对注意力缺陷多动障碍常见精神共病作用的评估:对暴饮暴食症和抑郁症的机制性见解

evaluation of the role of lisdexamfetamine on attention-deficit/hyperactivity disorder common psychiatric comorbidities: mechanistic insights on binge eating disorder and depression.

作者信息

Gutiérrez-Casares José Ramón, Segú-Vergés Cristina, Sabate Chueca Juncal, Pozo-Rubio Tamara, Coma Mireia, Montoto Carmen, Quintero Javier

机构信息

Unidad Ambulatoria de Psiquiatría y Salud Mental de la Infancia, Niñez y Adolescencia, Hospital Perpetuo Socorro, Badajoz, Spain.

Anaxomics Biotech, Barcelona, Spain.

出版信息

Front Neurosci. 2023 Jun 30;17:1118253. doi: 10.3389/fnins.2023.1118253. eCollection 2023.

Abstract

Attention-deficit/hyperactivity disorder (ADHD) is a psychiatric condition well recognized in the pediatric population that can persist into adulthood. The vast majority of patients with ADHD present psychiatric comorbidities that have been suggested to share, to some extent, the pathophysiological mechanism of ADHD. Lisdexamfetamine (LDX) is a stimulant prodrug approved for treating ADHD and, in the US, also for binge eating disorder (BED). Herein, we evaluated, through a systems biology-based method, the efficacy of a virtual model of LDX (vLDX) as ADHD treatment to improve five common ADHD psychiatric comorbidities in adults and children, and we explored the molecular mechanisms behind LDX's predicted efficacy. After the molecular characterization of vLDX and the comorbidities (anxiety, BED, bipolar disorder, depression, and tics disorder), we created a protein-protein interaction human network to which we applied artificial neural networks (ANN) algorithms. We also generated virtual populations of adults and children-adolescents totaling 2,600 individuals and obtained the predicted protein activity from Therapeutic Performance Mapping System models. The latter showed that ADHD molecular description shared 53% of its protein effectors with at least one studied psychiatric comorbidity. According to the ANN analysis, proteins targeted by vLDX are predicted to have a high probability of being related to BED and depression. In BED, vLDX was modeled to act upon neurotransmission and neuroplasticity regulators, and, in depression, vLDX regulated the hypothalamic-pituitary-adrenal axis, neuroinflammation, oxidative stress, and glutamatergic excitotoxicity. In conclusion, our modeling results, despite their limitations and although requiring or validation, could supplement the design of preclinical and potentially clinical studies that investigate treatment for patients with ADHD with psychiatric comorbidities, especially from a molecular point of view.

摘要

注意缺陷多动障碍(ADHD)是一种在儿科人群中广为人知的精神疾病,可持续至成年期。绝大多数ADHD患者存在精神共病,这些共病在一定程度上被认为与ADHD共享病理生理机制。赖右苯丙胺(LDX)是一种被批准用于治疗ADHD的兴奋剂前体药物,在美国还被用于治疗暴饮暴食症(BED)。在此,我们通过一种基于系统生物学的方法,评估了LDX虚拟模型(vLDX)作为ADHD治疗手段改善成人和儿童五种常见ADHD精神共病的疗效,并探讨了LDX预测疗效背后的分子机制。在对vLDX和共病(焦虑症、BED、双相情感障碍、抑郁症和抽动障碍)进行分子特征分析后,我们创建了一个蛋白质-蛋白质相互作用的人类网络,并应用人工神经网络(ANN)算法。我们还生成了总计2600名成人和儿童-青少年的虚拟人群,并从治疗性能映射系统模型中获得预测的蛋白质活性。后者表明,ADHD的分子描述与至少一种研究的精神共病共享53%的蛋白质效应器。根据ANN分析,vLDX靶向的蛋白质被预测极有可能与BED和抑郁症相关。在BED中,vLDX被建模为作用于神经传递和神经可塑性调节因子,而在抑郁症中,vLDX调节下丘脑-垂体-肾上腺轴、神经炎症、氧化应激和谷氨酸能兴奋性毒性。总之,我们的建模结果尽管存在局限性,且尽管需要验证,但可以补充针对患有精神共病的ADHD患者治疗的临床前研究以及潜在的临床研究设计,特别是从分子角度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee94/10347683/8da1a3d95447/fnins-17-1118253-g001.jpg

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