Neumann Nicola, Domin Martin, Schmidt Carsten-Oliver, Lotze Martin
Institute of Diagnostic Radiology and Neuroradiology, Functional Imaging Unit, University Medicine Greifswald, Greifswald, Germany.
Institute for Community Medicine- Department SHIP/KEF, University Medicine Greifswald, Greifswald, Germany.
Eur J Pain. 2023 Nov;27(10):1239-1248. doi: 10.1002/ejp.2153. Epub 2023 Jun 27.
Chronic pain of different aetiologies and localization has been associated with less grey matter volume (GMV) in several cortical and subcortical brain areas. Recent meta-analyses reported low reproducibility of GMV alterations between studies and pain syndromes.
To investigate GMV in common chronic pain conditions defined by body location (chronic back pain, n = 174; migraine, n = 92; craniomandibular disorder, n = 39) compared to controls (n = 296), we conducted voxel-based morphometry and determined GMV from high-resolution cranial MRIs obtained in an epidemiologic survey. Mediation analyses were performed between the presence of chronic pain and GMV testing the mediators stress and mild depression. The predictability of chronic pain was investigated with binomial logistic regression.
Whole-brain analyses yielded reduced GMV within the left anterior insula and the anterior cingulate cortex, for a ROI approach additionally the left posterior insula and left hippocampus showing less GMV across all patients with chronic pain. The relationship of pain with GMV in the left hippocampus was mediated by self-reported stressors in the last 12 months. Binomial logistic regression revealed a predictive effect for GMV in the left hippocampus and left anterior insula/temporal pole for the presence of chronic pain.
Chronic pain across three different pain conditions was characterized by less GMV in brain regions consistently described for different chronic pain conditions before. Less GMV in the left hippocampus mediated by experienced stress during the last year might be related to altered pain learning mechanisms in chronic pain patients.
Grey matter reorganization could serve as a diagnostic biomarker for chronic pain. In a large cohort, we here replicated findings of less grey matter volume across three pain conditions in the left anterior and posterior insula, anterior cingulate and left hippocampus. Less hippocampal grey matter was mediated by experienced stress.
不同病因和部位的慢性疼痛与多个皮质和皮质下脑区灰质体积(GMV)减少有关。最近的荟萃分析报告称,不同研究和疼痛综合征之间GMV改变的可重复性较低。
为了研究按身体部位定义的常见慢性疼痛状况(慢性背痛,n = 174;偏头痛,n = 92;颅下颌疾病,n = 39)与对照组(n = 296)相比的GMV,我们进行了基于体素的形态测量,并从一项流行病学调查中获得的高分辨率头颅磁共振成像(MRI)确定GMV。在慢性疼痛的存在与GMV之间进行中介分析,测试中介因素压力和轻度抑郁。用二项逻辑回归研究慢性疼痛的可预测性。
全脑分析显示,左侧前脑岛和前扣带回皮质内的GMV减少,对于感兴趣区(ROI)方法,所有慢性疼痛患者的左侧后脑岛和左侧海马体的GMV也较少。左侧海马体中疼痛与GMV的关系由过去12个月自我报告的应激源介导。二项逻辑回归显示,左侧海马体和左侧前脑岛/颞极的GMV对慢性疼痛的存在有预测作用。
三种不同疼痛状况下的慢性疼痛,其特征是在之前针对不同慢性疼痛状况一直描述的脑区中GMV较少。去年经历的压力介导的左侧海马体GMV减少可能与慢性疼痛患者疼痛学习机制改变有关。
灰质重组可作为慢性疼痛的诊断生物标志物。在一个大型队列中,我们在此重复了在左侧前后脑岛、前扣带回和左侧海马体中三种疼痛状况下灰质体积减少的发现。海马体灰质减少由经历的压力介导。