Degeneration of peripheral nerves causes neuropathic pain. Previous studies have documented structural and functional brain alterations in peripheral neuropathy, which may be attributed to maladaptive plasticity following chronic neuropathic pain. Nevertheless, the effects of peripheral neuropathic pain on the macroscale organization of the cerebral cortex have not been explored. This study investigated altered surface morphology and topographic hierarchy of the cerebral cortex in patients with neuropathic pain due to peripheral neuropathy. T1-weighted magnetic resonance imaging data were acquired from 52 patients with peripheral neuropathic pain and 50 age- and sex-matched healthy controls. Cortical morphometric features including thickness and gyrification index were obtained using surface-based morphometry. A topographic gradient encoding interregional similarity in cortical thickness was extracted using a machine-learning technique named diffusion map embedding. Compared with controls, patients with neuropathic pain exhibited cortical thinning in the frontal and sensorimotor cortices, with the severity increasing with greater neuropathic pain. The patients also showed decreased gyrification in the insula, with a greater reduction in gyrification linked to more severe skin nerve degeneration. Moreover, the patients exhibited altered topographic organization of the cerebral cortex, where the direction of the topographic gradient deviated from the occipital-to-frontal axis observed in the controls in this study and reported in the literature. Our findings provided a novel perspective for macroscale cortical structural reorganization after neuropathic pain, showing thinning and gyral flattening in pain-related areas and deviation from the normal topographic axis of the cerebral cortex.
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http://dx.doi.org/10.1097/j.pain.0000000000003557 | DOI Listing |
Int J Biol Macromol
March 2025
Department of Rheumatism and Immunology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei 050000, China.
Chronic pain is a significant public health concern that diminishes patients' quality of life and imposes considerable socioeconomic costs. Effective pharmacological treatments for ongoing pain are limited. Recent studies have indicated that various models of chronic pain-such as neuropathic pain, inflammatory pain, and pain associated with cancer-have abnormal levels of long noncoding RNAs (lncRNAs).
View Article and Find Full Text PDFNeurosci Lett
March 2025
Department of Pharmacy, Nanjing Drum Tower Hospital, the Affiliated Hospital of Nanjing University Medical School, Nanjing 210008 Jiangsu, China. Electronic address:
Vincristine (VCR) is a commonly used clinical anti-cancer drug, but it can also induce neurotoxicity and cause vincristine-induced neuropathic pain (VINP). The metabotropic glutamate receptor 5 (mGluR5) within spinal dorsal horn neurons regulates the transmission of pain mediated by glutamate. In this study, we investigated for the first time the role of mGluR5 in the transmission of noxious information in VINP.
View Article and Find Full Text PDFJ Immunol
February 2025
Orthopedics Department, Central Hospital of Ezhou, Ezhou, China.
Diabetic nephropathy is a severe chronic complication characterized by cytotoxicity, inflammation, and fibrosis, ultimately leading to renal failure. This study systematically investigated the effects of the PARP1 inhibitor PJ-34 on high glucose-induced cytotoxicity, inflammation, and fibrosis in HK-2 cells, as well as its improvement on neuropathic pain response and transforming growth factor β (TGFβ) expression in a type 1 diabetes mellitus diabetic nephropathy mouse model. Through cellular and animal experiments, we observed that PJ-34 significantly enhanced the proliferative capacity of cells damaged by high glucose, reduced apoptosis, and decreased the release of proinflammatory factors TGFα, interleukin-6, and interleukin-1β.
View Article and Find Full Text PDFDentomaxillofac Radiol
March 2025
Radiology Center, Division of Integrated Facilities, Institute of Science Tokyo Hospital, 1-5-45 Yushima, Bunkyo-ku, Tokyo, Japan.
Objective: To quantitatively and qualitatively compare directly two types of cisternography images for diagnosing trigeminal neuralgia (TN) using 3-T magnetic resonance imaging.
Methods: This prospective study recruited 64 patients with a clinical diagnosis or suspicion of TN. Patients were examined through the three-dimensional (3D) Constructive Interference in Steady State (CISS) and Sampling Perfection with Application-optimized Contrasts using different flip angle Evolutions (SPACE) sequences.
J Neurogenet
March 2025
Department of Neurology, Faculty of Medicine, Universitas Udayana/Ngoerah Hospital, Bali, Indonesia.
Painful diabetic neuropathy (PDN) is a common complication in patients with type 2 diabetes mellitus (T2DM) with disruption of vitamin D (VD) activity as one of the risk factors. Active VD exerts its biological functions through the vitamin D receptor (VDR), which polymorphisms in the VDR gene can impair. This study aims to establish VDR FokI and ApaI polymorphisms as risk factors for PDN.
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