| Issue |
BIO Web Conf.
Volume 237, 2026
2026 8th International Conference on Biotechnology and Biomedicine (ICBB 2026)
|
|
|---|---|---|
| Article Number | 01009 | |
| Number of page(s) | 11 | |
| Section | Molecular and Cellular Pathophysiology | |
| DOI | https://doi.org/10.1051/bioconf/202623701009 | |
| Published online | 10 June 2026 | |
Sugar Addiction and BED: Elucidating Pathological Mechanisms and Therapeutic Strategies
1 School of Clinical Medicine, Bengbu Medical University, Bengbu city, 233030, China
2 School of Food Science and Technology, Jiangnan University, Wuxi city, 214122, China
3 School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing city, 210023, China
a This email address is being protected from spambots. You need JavaScript enabled to view it.
Corresponding author:b* This email address is being protected from spambots. You need JavaScript enabled to view it.
c This email address is being protected from spambots. You need JavaScript enabled to view it.
Abstract
Given the lack of systematic comparisons of neurobiological mechanisms and translatable therapeutic strategies between sugar addiction and binge eating disorder (BED), and the urgent need to address sugar-related metabolic and psychiatric comorbidities, this review aims to fill this gap and highlight the clinical and public health relevance of this comparison. This review examined the neurobiological parallels between sugar addiction and binge eating disorder (BED), highlighting shared dysregulations in dopaminergic, opioid, and GLP-1 systems, particularly within prefrontal-striatal-limbic circuits. Based on shared dysregulations in reward circuitry , opioid system downregulation , and hypothalamic POMC neuron dysfunction, we discussed the potential of repurposing investigational BED pharmacotherapies—such as lisdexamfetamine, naltrexone/bupropion, GLP-1 receptor agonists, and topiramate-for sugar addiction treatment. These agents are proposed to modulate neurotransmitter release, receptor activity, and neural network function to reduce cravings, impulsive feeding, and reward-seeking behaviors. Despite its high prevalence and significant adverse health consequences, sugar addiction remains unrecognized in major diagnostic systems (e.g., DSM-5 or ICD-11), limiting targeted therapeutic development. We underscore the necessity for additional mechanistic investigations and stringently designed clinical trials to transform these initial observations into validated, evidence-based treatment approaches. Future work should incorporate biotechnology-enabled approaches, such as neurocircuit-specific intervention strategies, biomarker-guided patient stratification, and rigorously designed clinical trials, to validate and translate these preliminary findings into evidence-based treatments.
© The Authors, published by EDP Sciences, 2026
This is an Open Access article distributed under the terms of the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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