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Similarities and Differences in Resting‐State Brain Activity Changes of Distinct Chronic Pain Types

医学 脑岛 静息状态功能磁共振成像 额上回 舌回 眶额皮质 辅助电机区 功能磁共振成像 慢性疼痛 楔前 肠易激综合征 海马旁回 额内侧回 内科学 听力学 心脏病学 神经科学 前额叶皮质 精神科 心理学 认知 放射科 颞叶 癫痫
作者
Xiaofei Chen,Ruiyi Tang,Yihan Jin,Liqiang Wu,Yidan Liang,Kuanghui Xu,Ping He,Yun Guo,Jie Li
出处
期刊:Oral Diseases [Wiley]
标识
DOI:10.1111/odi.15271
摘要

ABSTRACT Objectives To explore neural similarities and differences between visceral and somatic pain by comparing spontaneous brain activity in patients with chronic temporomandibular disorder (TMD) and irritable bowel syndrome (IBS). Methods Twenty eight IBS patients, 21 TMD patients, and 28 healthy controls (HC) underwent resting‐state fMRI and behavioral assessments. The correlations between fMRI metrics such as the amplitude of low‐frequency fluctuations (ALFF), regional homogeneity (ReHo), functional connectivity (FC), and clinical manifestations were further analyzed. Results Compared with HC, both patient groups demonstrated increased ALFF in right parahippocampal gyrus (PHG), insula, medial superior frontal gyrus (SFGmed), precentral gyrus (PreCG), and increased ReHo in right SFGmed and left supplementary motor area (SMA). Compared with IBS patients, TMD patients exhibited reduced ALFF in right SFGmed and insula, increased ALFF in right PHG and PreCG, decreased ReHo in right SFGmed and left lingual gyrus, and increased ReHo in left SMA. Both patient groups exhibited enhanced right PHG‐related FC in left precuneus and right cingulate gyrus, and right insula‐related FC in left superior temporal gyrus and right paracentral lobule. Specifically, IBS patients showed higher FC between right PHG and orbitofrontal cortex than TMD patients, which was negatively correlated with mood and gastrointestinal symptoms. Mediation analysis revealed that pain in TMD and gastrointestinal symptoms in IBS mediated these relationships. Conclusion Visceral and somatic pain share abnormal activity in multiple brain networks. Abnormalities in affective region present potential neuroimaging markers for pain disorders, with depression in somatic pain linked to pain intensity and in visceral pain to gastrointestinal symptoms.

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