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首页> 外文期刊>Pancreatology: official journal of the International Association of Pancreatology (IAP) ... [et al.] >Pain-associated adaptive cortical reorganisation in chronic pancreatitis.
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Pain-associated adaptive cortical reorganisation in chronic pancreatitis.

机译:慢性胰腺炎中疼痛相关的适应性皮质重组。

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摘要

BACKGROUND/AIMS: In various chronic pain conditions cortical reorganisation seems to play a role in the symptomatology. The aims of this study were to investigate cortical reorganisation in patients with pain caused by chronic pancreatitis (CP) and to correlate putative cortical reorganisation to clinical pain scores. METHODS: 24 patients suffering from CP and 14 healthy volunteers were included. Patients' daily experience of pain was recorded in a pain diary. The sigmoid was stimulated electrically with simultaneous recording of evoked brain potentials (EPs). The brain source localisations reflecting direct neuronal activity were fitted by a five-dipole model projected to magnetic resonance imaging of the individual brains. RESULTS: Patients showed prolonged latencies of the EPs confined to the frontal region of the brain (p < 0.01). The corresponding brain sources were located in the bilateral insula, cingulate gyrus and bilateral secondary somatosensory area. The insular dipoles were localised more posterior in the patients than in healthy subjects (p < 0.01). The shift in insular dipole localisation was negatively correlated with the patients' clinical pain scores (p < 0.05). CONCLUSIONS: The findings indicate that sustained pain in CP leads to functional reorganisation of the insular cortex. We suggest its physiological correlate to be an adaptive response to chronic pain. and IAP.
机译:背景/目的:在各种慢性疼痛情况下,皮质重组似乎在症状学中起作用。这项研究的目的是调查慢性胰腺炎(CP)引起的疼痛患者的皮质重组,并将假定的皮质重组与临床疼痛评分相关联。方法:纳入24名患有CP的患者和14名健康志愿者。在疼痛日记中记录患者每天的疼痛经历。用电刺激乙状结肠,同时记录诱发的脑电势(EPs)。反映直接神经元活动的脑源定位由投影到各个大脑的磁共振成像的五偶极模型拟合。结果:患者表现出EP潜伏期延长,局限于大脑额叶区域(p <0.01)。相应的脑源位于双侧岛,扣带回和双侧次级体感区。患者的岛状偶极子比健康受试者更偏后(p <0.01)。岛状偶极子定位的变化与患者的临床疼痛评分呈负相关(p <0.05)。结论:研究结果表明,持续性CP疼痛导致岛状皮层功能重组。我们建议其生理相关性是对慢性疼痛的适应性反应。和IAP。

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