Department of Physiology, Northwestern University, Feinberg School of Medicine, Chicago, IL, USA Department of Physical Medicine and Rehabilitation, Northwestern University, Feinberg School of Medicine, Chicago, IL, USA.
Pain. 2013 Oct;154(10):2160-2168. doi: 10.1016/j.pain.2013.06.044.
Neural mechanisms mediating the transition from acute to chronic pain remain largely unknown. In a longitudinal brain imaging study, we followed up patients with a single sub-acute back pain (SBP) episode for more than 1 year as their pain recovered (SBPr), or persisted (SBPp) representing a transition to chronic pain. We discovered brain white matter structural abnormalities (n=24 SBP patients; SBPp=12 and SBPr=12), as measured by diffusion tensor imaging (DTI), at entry into the study in SBPp in comparison to SBPr. These white matter fractional anisotropy (FA) differences accurately predicted pain persistence over the next year, which was validated in a second cohort (n=22 SBP patients; SBPp=11 and SBPr=11), and showed no further alterations over a 1-year period. Tractography analysis indicated that abnormal regional FA was linked to differential structural connectivity to medial vs lateral prefrontal cortex. Local FA was correlated with functional connectivity between medial prefrontal cortex and nucleus accumbens in SBPr. As we have earlier shown that the latter functional connectivity accurately predicts transition to chronic pain, we can conclude that brain structural differences, most likely existing before the back pain-inciting event and independent of the back pain, predispose subjects to pain chronification.
介导急性疼痛向慢性疼痛转变的神经机制在很大程度上尚不清楚。在一项纵向脑成像研究中,我们对经历单次亚急性背痛(SBP)发作的患者进行了 1 年以上的随访,他们的疼痛已经恢复(SBPr)或持续存在(SBPp),代表向慢性疼痛的转变。我们通过弥散张量成像(DTI)发现,与 SBPr 相比,在 SBPp 患者进入研究时存在脑白质结构异常(n=24 名 SBP 患者;SBPp=12,SBPr=12)。这些白质各向异性分数(FA)差异准确预测了未来 1 年的疼痛持续时间,在第二个队列(n=22 名 SBP 患者;SBPp=11,SBPr=11)中得到了验证,并且在 1 年内没有进一步的变化。轨迹分析表明,异常的区域 FA 与内侧前额叶皮质与外侧前额叶皮质的结构连接差异有关。在 SBPr 中,局部 FA 与内侧前额叶皮质与伏隔核之间的功能连接相关。正如我们之前所示,后者的功能连接准确地预测了向慢性疼痛的转变,因此我们可以得出结论,大脑结构差异很可能在引发背痛事件之前就存在,并且与背痛无关,使患者容易发生疼痛慢性化。