{"title":"Neuroimaging in narcolepsy","authors":"Yuefan Ding, Fei Zhang, Minglin Li, Jiahe Wang","doi":"10.1016/j.imed.2024.11.005","DOIUrl":null,"url":null,"abstract":"<div><div>Narcolepsy is a chronic neurological disorder that disrupts the sleep-wake cycle and manifests in symptoms like excessive daytime sleepiness (EDS), cataplexy, and rapid transitions into rapid eye movement (REM) sleep. Its variable prevalence, genetics, and clinical presentations pose considerable challenges in diagnosis and management. Here, we synthesized the advances in neuroimaging techniques and their substantial contributions to the narcolepsy complex pathology. We analyzed the structural magnetic resonance imaging (MRI) scan findings that highlight gray matter reductions and cortical thinning in patients with narcolepsy. Additionally, we explored findings from diffusion tensor imaging (DTI) scans that shed light on compromises in white matter integrity. Functional MRI and positron emission tomography (PET) scan studies further illuminated neurochemical deficits and altered brain connectivity. The implications of these findings extend beyond diagnosis, suggesting potential targets for neuromodulation therapies and calling for larger, more standardized studies to enhance both our understanding and treatment approaches for narcolepsy. Despite such advances, this field continues to meet challenges, including limitations in sample size and the need for comprehensive longitudinal and multimodal studies. This review highlighted the potential of neuroimaging combined with machine learning and advanced analytics, which help to discover novel biomarkers, refine the comprehension of narcolepsy and its neurochemical intricacies, and improve the therapeutic strategies.</div></div>","PeriodicalId":73400,"journal":{"name":"Intelligent medicine","volume":"5 3","pages":"Pages 195-208"},"PeriodicalIF":6.9000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Intelligent medicine","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667102625000567","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS","Score":null,"Total":0}
引用次数: 0
Abstract
Narcolepsy is a chronic neurological disorder that disrupts the sleep-wake cycle and manifests in symptoms like excessive daytime sleepiness (EDS), cataplexy, and rapid transitions into rapid eye movement (REM) sleep. Its variable prevalence, genetics, and clinical presentations pose considerable challenges in diagnosis and management. Here, we synthesized the advances in neuroimaging techniques and their substantial contributions to the narcolepsy complex pathology. We analyzed the structural magnetic resonance imaging (MRI) scan findings that highlight gray matter reductions and cortical thinning in patients with narcolepsy. Additionally, we explored findings from diffusion tensor imaging (DTI) scans that shed light on compromises in white matter integrity. Functional MRI and positron emission tomography (PET) scan studies further illuminated neurochemical deficits and altered brain connectivity. The implications of these findings extend beyond diagnosis, suggesting potential targets for neuromodulation therapies and calling for larger, more standardized studies to enhance both our understanding and treatment approaches for narcolepsy. Despite such advances, this field continues to meet challenges, including limitations in sample size and the need for comprehensive longitudinal and multimodal studies. This review highlighted the potential of neuroimaging combined with machine learning and advanced analytics, which help to discover novel biomarkers, refine the comprehension of narcolepsy and its neurochemical intricacies, and improve the therapeutic strategies.