Sloan Gordon, Teh Kevin, Caunt Sharon, Wilkinson Iain, Selvarajah Dinesh, Tesfaye Solomon
Division of Clinical Medicine, University of Sheffield, Sheffield, U.K.
Diabetes Research Unit, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, U.K.
Diabetes. 2024 Sep 1;73(9):1486-1494. doi: 10.2337/db23-0931.
Altered functional connectivity has been demonstrated in key brain regions involved in pain processing in painful diabetic peripheral neuropathy. However, the impact of neuropathic pain treatment on functional connectivity does not appear to have been investigated. Sixteen participants underwent resting state functional MRI when optimally treated for neuropathic pain during their involvement in the Optimal Pathway for Treating Neuropathic Pain in Diabetes Mellitus trial and 1 week following withdrawal of treatment. On discontinuation of pain treatment, there was an increase in functional connectivity between the left thalamus and primary somatosensory cortex (S1) and the left thalamus and insular cortex, key brain regions that are involved in cerebral processing of pain. The changes in functional connectivity between scans also correlated with measures of pain (baseline pain severity and Neuropathic Pain Symptom Inventory). Moreover, when participants were stratified into higher- and lower-than-average baseline pain subgroups, the change in thalamic-S1 cortical functional connectivity between scans was significantly greater in those with high baseline pain compared with the lower-baseline-pain group. This study shows that thalamo-cortical functional connectivity has the potential to act as an objective biomarker for neuropathic pain in diabetes for use in clinical pain trials.
在糖尿病性周围神经病变的疼痛处理过程中,关键脑区的功能连接性已被证实发生了改变。然而,神经性疼痛治疗对功能连接性的影响似乎尚未得到研究。16名参与者在参与糖尿病性神经病变疼痛治疗的最佳途径试验中接受神经性疼痛最佳治疗时,以及在停止治疗1周后,进行了静息态功能磁共振成像。在停止疼痛治疗后,左丘脑与初级体感皮层(S1)以及左丘脑与岛叶皮层(参与疼痛大脑处理的关键脑区)之间的功能连接性增加。扫描之间功能连接性的变化也与疼痛指标(基线疼痛严重程度和神经性疼痛症状量表)相关。此外,当将参与者分为高于和低于平均基线疼痛的亚组时,与低基线疼痛组相比,高基线疼痛参与者扫描之间丘脑 - S1皮层功能连接性的变化明显更大。这项研究表明,丘脑 - 皮层功能连接性有可能作为糖尿病性神经病变疼痛的客观生物标志物,用于临床疼痛试验。