Yanqiao Zhao , Chen Gong , Pan Zhu , Suimin Guo , Yangyang Lin , Yafei Wang , Beibei Feng , Xiaochun Meng , Yuling Wang
{"title":"前额叶皮层在慢性腰痛伴抑郁症中的作用:静息状态fMRI研究。","authors":"Yanqiao Zhao , Chen Gong , Pan Zhu , Suimin Guo , Yangyang Lin , Yafei Wang , Beibei Feng , Xiaochun Meng , Yuling Wang","doi":"10.1016/j.brainresbull.2025.111408","DOIUrl":null,"url":null,"abstract":"<div><div>Patients with chronic low back pain (CLBP) experience comorbid depression. However, the central neural processing profile of CLBP with comorbid depression remains unclear. Therefore, this study aimed to investigate specific brain abnormalities in CLBP with comorbid depression by functional magnetic resonance imaging. Fourteen CLBP patients with depression, 25 CLBP patients without depression, and 24 matched controls were included. Alterations in spontaneous brain activity and connectivity were examined through regional homogeneity (ReHo) and functional connectivity (FC). Analysis of variance and post hoc analyses among groups were conducted. Correlational analyses were performed between neuroplasticity and clinical variables. Mediation analysis was conducted to elucidate the interrelationships among brain alterations, pain, and depression. Significant between-group differences in ReHo values were found across extensive brain regions, particularly the right dorsolateral prefrontal cortex (DLPFC). Altered FC between the DLPFC and cerebellum as well as the orbitofrontal cortex was noted. ReHo and FC were associated with depression, pain catastrophizing, and back pain-related disability. ReHo values of superior frontal gyrus and its FC to cerebellum mediated the correlation between BDI and variables such as pain intensity and pain catastrophizing. CLBP patients with comorbid depression exhibit abnormal regional homogeneity in regions involving the DLPFC, and altered functional networks are observed between the DLPFC and other areas. Central changes are correlated with back pain-related outcomes and mediate the relationship between pain and depression. Our findings contribute additional insights for identifying potential biomarkers of refractory CLBP with depression comorbidity, potentially aiding in pain phenotype stratification and optimizing pain management strategies.</div></div>","PeriodicalId":9302,"journal":{"name":"Brain Research Bulletin","volume":"229 ","pages":"Article 111408"},"PeriodicalIF":3.7000,"publicationDate":"2025-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The role of prefrontal cortex in chronic low back pain with comorbid depression: A resting-state fMRI study\",\"authors\":\"Yanqiao Zhao , Chen Gong , Pan Zhu , Suimin Guo , Yangyang Lin , Yafei Wang , Beibei Feng , Xiaochun Meng , Yuling Wang\",\"doi\":\"10.1016/j.brainresbull.2025.111408\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Patients with chronic low back pain (CLBP) experience comorbid depression. However, the central neural processing profile of CLBP with comorbid depression remains unclear. Therefore, this study aimed to investigate specific brain abnormalities in CLBP with comorbid depression by functional magnetic resonance imaging. Fourteen CLBP patients with depression, 25 CLBP patients without depression, and 24 matched controls were included. Alterations in spontaneous brain activity and connectivity were examined through regional homogeneity (ReHo) and functional connectivity (FC). Analysis of variance and post hoc analyses among groups were conducted. Correlational analyses were performed between neuroplasticity and clinical variables. Mediation analysis was conducted to elucidate the interrelationships among brain alterations, pain, and depression. Significant between-group differences in ReHo values were found across extensive brain regions, particularly the right dorsolateral prefrontal cortex (DLPFC). Altered FC between the DLPFC and cerebellum as well as the orbitofrontal cortex was noted. ReHo and FC were associated with depression, pain catastrophizing, and back pain-related disability. ReHo values of superior frontal gyrus and its FC to cerebellum mediated the correlation between BDI and variables such as pain intensity and pain catastrophizing. CLBP patients with comorbid depression exhibit abnormal regional homogeneity in regions involving the DLPFC, and altered functional networks are observed between the DLPFC and other areas. Central changes are correlated with back pain-related outcomes and mediate the relationship between pain and depression. Our findings contribute additional insights for identifying potential biomarkers of refractory CLBP with depression comorbidity, potentially aiding in pain phenotype stratification and optimizing pain management strategies.</div></div>\",\"PeriodicalId\":9302,\"journal\":{\"name\":\"Brain Research Bulletin\",\"volume\":\"229 \",\"pages\":\"Article 111408\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-06-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Brain Research Bulletin\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0361923025002205\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain Research Bulletin","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0361923025002205","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
The role of prefrontal cortex in chronic low back pain with comorbid depression: A resting-state fMRI study
Patients with chronic low back pain (CLBP) experience comorbid depression. However, the central neural processing profile of CLBP with comorbid depression remains unclear. Therefore, this study aimed to investigate specific brain abnormalities in CLBP with comorbid depression by functional magnetic resonance imaging. Fourteen CLBP patients with depression, 25 CLBP patients without depression, and 24 matched controls were included. Alterations in spontaneous brain activity and connectivity were examined through regional homogeneity (ReHo) and functional connectivity (FC). Analysis of variance and post hoc analyses among groups were conducted. Correlational analyses were performed between neuroplasticity and clinical variables. Mediation analysis was conducted to elucidate the interrelationships among brain alterations, pain, and depression. Significant between-group differences in ReHo values were found across extensive brain regions, particularly the right dorsolateral prefrontal cortex (DLPFC). Altered FC between the DLPFC and cerebellum as well as the orbitofrontal cortex was noted. ReHo and FC were associated with depression, pain catastrophizing, and back pain-related disability. ReHo values of superior frontal gyrus and its FC to cerebellum mediated the correlation between BDI and variables such as pain intensity and pain catastrophizing. CLBP patients with comorbid depression exhibit abnormal regional homogeneity in regions involving the DLPFC, and altered functional networks are observed between the DLPFC and other areas. Central changes are correlated with back pain-related outcomes and mediate the relationship between pain and depression. Our findings contribute additional insights for identifying potential biomarkers of refractory CLBP with depression comorbidity, potentially aiding in pain phenotype stratification and optimizing pain management strategies.
期刊介绍:
The Brain Research Bulletin (BRB) aims to publish novel work that advances our knowledge of molecular and cellular mechanisms that underlie neural network properties associated with behavior, cognition and other brain functions during neurodevelopment and in the adult. Although clinical research is out of the Journal''s scope, the BRB also aims to publish translation research that provides insight into biological mechanisms and processes associated with neurodegeneration mechanisms, neurological diseases and neuropsychiatric disorders. The Journal is especially interested in research using novel methodologies, such as optogenetics, multielectrode array recordings and life imaging in wild-type and genetically-modified animal models, with the goal to advance our understanding of how neurons, glia and networks function in vivo.