University of Barcelona, Barcelona, Spain.
Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Arthritis Rheumatol. 2024 Feb;76(2):293-303. doi: 10.1002/art.42691. Epub 2023 Dec 21.
Juvenile-onset fibromyalgia (JFM) is a paradigmatic chronic pain condition for which the underlying neurobiological substrates are poorly understood. This study examined, for the first time, data-driven resting-state functional connectivity (rsFC) alterations in 37 female adolescents with JFM compared with 43 healthy female adolescents and identified associations with bodily pain.
Whole-brain voxel-wise rsFC alterations were assessed using the intrinsic connectivity contrast, a measure of node centrality at each voxel, and seed-based analyses for interpretability. We studied the relationship between rsFC alterations in somatosensory systems and the location and extension of bodily pain.
Adolescents with JFM had voxel-wise rsFC reductions in the paracentral lobule (PCL)/primary somatosensory cortex (S1) (T = 4.89, family-wise error corrected p-value (pFWE) < 0.001) and left midcingulate cortex (T = 4.67, pFWE = 0.043). Post hoc analyses revealed reduced rsFC spanning major cortical sensory hubs (T > 4.4, pFWE < 0.030). Cortico-cortical rsFC reductions within PCL/S1 in JFM occurred in locations innervated by bodily areas where the pain was most frequent (F = 3.15; positive false discovery rate = 0.029) and predicted widespread pain (T > 4.4, pFWE < 0.045). Conversely, adolescents with JFM had increases in PCL/S1-thalamus (T = 4.75, pFWE = 0.046) and PCL/S1-anterior insula rsFC (T = 5.13, pFWE = 0.039).
Reduced cortico-cortical sensory integration involving PCL/S1 and spanning the sensory systems may underly critical pain sensory features in youth with JFM. Reduced sensory integration is paralleled by augmented cross-talk between sensory and affective/salience-processing regions, potentially indicating a shift toward more affectively colored sensory experiences to the detriment of specific sensory discrimination.
青少年纤维肌痛(JFM)是一种典型的慢性疼痛疾病,其潜在的神经生物学基础尚未完全了解。本研究首次在 37 名患有 JFM 的女性青少年与 43 名健康女性青少年中,通过数据驱动的静息状态功能连接(rsFC)变化来评估,同时识别了与躯体疼痛的关联。
使用内在连接对比评估全脑体素水平的 rsFC 变化,这是衡量每个体素节点中心度的一种方法,并进行基于种子点的分析以提高可解释性。我们研究了躯体感觉系统 rsFC 变化与躯体疼痛的位置和范围之间的关系。
与 JFM 相关的青少年存在中央旁小叶(PCL)/初级躯体感觉皮层(S1)的体素水平 rsFC 减少(T = 4.89,校正的家族-wise 错误率(pFWE)<0.001)和左中扣带皮层(T = 4.67,pFWE = 0.043)。事后分析显示,主要皮质感觉中枢的 rsFC 减少(T > 4.4,pFWE < 0.030)。JFM 中 PCL/S1 内的皮质间 rsFC 减少发生在受疼痛最频繁的躯体区域支配的位置(F = 3.15;阳性错误发现率 = 0.029),并预测广泛疼痛(T > 4.4,pFWE < 0.045)。相反,JFM 青少年 PCL/S1-丘脑(T = 4.75,pFWE = 0.046)和 PCL/S1-前岛叶 rsFC 增加(T = 5.13,pFWE = 0.039)。
涉及 PCL/S1 并跨越感觉系统的皮质间感觉整合减少可能是 JFM 青少年关键疼痛感觉特征的基础。感觉整合减少与感觉和情感/突显处理区域之间的交叉增强相平行,这可能表明更偏向情感色彩的感觉体验,而牺牲了特定的感觉辨别力。