Yalan Liao, Linqiong Sang, Qiannan Wang, Pengyue Li, Li Wang, Ye Zhang, Mingguo Qiu, Jingna Zhang
{"title":"Alterations in Functional Connectivity Density in Patients With Phantom Limb Pain","authors":"Yalan Liao, Linqiong Sang, Qiannan Wang, Pengyue Li, Li Wang, Ye Zhang, Mingguo Qiu, Jingna Zhang","doi":"10.1002/cne.70058","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Phantom limb pain (PLP) is prevalent and challenging to treat in amputees, which likely stems from maladaptive cortical reorganization, but the precise mechanisms remain unclear. This study aimed to comprehensively investigate the cortical remodeling patterns in amputees experiencing PLP, pinpointing key brain regions and neural circuits directly associated with the pain. Eighteen PLP patients and 20 healthy participants were recruited for resting-state functional magnetic resonance imaging (rs-fMRI). The functional connectivity density (FCD) mapping method was used to identify PLP-related abnormal local and global signaling hubs. FCD changes were observed within the sensorimotor, pain-processing, and visual stream networks in PLP patients, with the precentral gyrus (PreCG), insula (INS), precuneus (PCUN), and middle occipital gyrus (MOG) identified as key hubs correlated with the visual analog scale (VAS) pain ratings. A voxel-wise functional connectivity (FC) analysis was further performed between the VAS-correlated FCD hubs and the rest of the brain. FC was significantly decreased between the hubs and widespread brain regions. In contrast, increased FC was revealed between the hubs and subregions of the dorsolateral prefrontal cortex (DLPFC) (the dorsolateral superior frontal gyrus [SFGdor] and middle frontal gyrus [MFG]). FC of the SFGdor-INS and MFG-PCUN pathways was negatively correlated with VAS pain ratings specifically, likely playing crucial roles in PLP. These results provide novel insights into the critical neural mechanisms of PLP, highlighting valuable targets for developing long-term effective neuromodulation modalities.</p>\n </div>","PeriodicalId":15552,"journal":{"name":"Journal of Comparative Neurology","volume":"533 5","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2025-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Comparative Neurology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cne.70058","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Phantom limb pain (PLP) is prevalent and challenging to treat in amputees, which likely stems from maladaptive cortical reorganization, but the precise mechanisms remain unclear. This study aimed to comprehensively investigate the cortical remodeling patterns in amputees experiencing PLP, pinpointing key brain regions and neural circuits directly associated with the pain. Eighteen PLP patients and 20 healthy participants were recruited for resting-state functional magnetic resonance imaging (rs-fMRI). The functional connectivity density (FCD) mapping method was used to identify PLP-related abnormal local and global signaling hubs. FCD changes were observed within the sensorimotor, pain-processing, and visual stream networks in PLP patients, with the precentral gyrus (PreCG), insula (INS), precuneus (PCUN), and middle occipital gyrus (MOG) identified as key hubs correlated with the visual analog scale (VAS) pain ratings. A voxel-wise functional connectivity (FC) analysis was further performed between the VAS-correlated FCD hubs and the rest of the brain. FC was significantly decreased between the hubs and widespread brain regions. In contrast, increased FC was revealed between the hubs and subregions of the dorsolateral prefrontal cortex (DLPFC) (the dorsolateral superior frontal gyrus [SFGdor] and middle frontal gyrus [MFG]). FC of the SFGdor-INS and MFG-PCUN pathways was negatively correlated with VAS pain ratings specifically, likely playing crucial roles in PLP. These results provide novel insights into the critical neural mechanisms of PLP, highlighting valuable targets for developing long-term effective neuromodulation modalities.
期刊介绍:
Established in 1891, JCN is the oldest continually published basic neuroscience journal. Historically, as the name suggests, the journal focused on a comparison among species to uncover the intricacies of how the brain functions. In modern times, this research is called systems neuroscience where animal models are used to mimic core cognitive processes with the ultimate goal of understanding neural circuits and connections that give rise to behavioral patterns and different neural states.
Research published in JCN covers all species from invertebrates to humans, and the reports inform the readers about the function and organization of nervous systems in species with an emphasis on the way that species adaptations inform about the function or organization of the nervous systems, rather than on their evolution per se.
JCN publishes primary research articles and critical commentaries and review-type articles offering expert insight in to cutting edge research in the field of systems neuroscience; a complete list of contribution types is given in the Author Guidelines. For primary research contributions, only full-length investigative reports are desired; the journal does not accept short communications.