Bagarinao Epifanio, Johnson Kevin A, Martucci Katherine T, Ichesco Eric, Farmer Melissa A, Labus Jennifer, Ness Timothy J, Harris Richard, Deutsch Georg, Apkarian Vania A, Mayer Emeran A, Clauw Daniel J, Mackey Sean
Department of Anesthesiology, Perioperative and Pain Medicine, Division of Pain Medicine, Stanford University Medical Center, Stanford, CA, USA Department of Anesthesiology, Chronic Pain and Fatigue Research Center, University of Michigan, Ann Arbor, MI, USA Department of Physiology, Northwestern University, Feinberg School of Medicine, Chicago, IL, USA Gail and Gerald Oppenheimer Family Center for Neurobiology of Stress, Pain and Interoception Network (PAIN), David Geffen School of Medicine at UCLA, Los Angeles, CA, USA Department of Radiology, University of Alabama, Birmingham Medical Center, Birmingham, AL, USA Department of Anesthesiology, University of Alabama, Birmingham Medical Center, Birmingham, AL, USA.
Pain. 2014 Dec;155(12):2502-2509. doi: 10.1016/j.pain.2014.09.002. Epub 2014 Sep 19.
Neuroimaging studies have shown that changes in brain morphology often accompany chronic pain conditions. However, brain biomarkers that are sensitive and specific to chronic pelvic pain (CPP) have not yet been adequately identified. Using data from the Trans-MAPP Research Network, we examined the changes in brain morphology associated with CPP. We used a multivariate pattern classification approach to detect these changes and to identify patterns that could be used to distinguish participants with CPP from age-matched healthy controls. In particular, we used a linear support vector machine (SVM) algorithm to differentiate gray matter images from the 2 groups. Regions of positive SVM weight included several regions within the primary somatosensory cortex, pre-supplementary motor area, hippocampus, and amygdala were identified as important drivers of the classification with 73% overall accuracy. Thus, we have identified a preliminary classifier based on brain structure that is able to predict the presence of CPP with a good degree of predictive power. Our regional findings suggest that in individuals with CPP, greater gray matter density may be found in the identified distributed brain regions, which are consistent with some previous investigations in visceral pain syndromes. Future studies are needed to improve upon our identified preliminary classifier with integration of additional variables and to assess whether the observed differences in brain structure are unique to CPP or generalizable to other chronic pain conditions.
神经影像学研究表明,脑形态变化常伴随慢性疼痛状况。然而,对慢性盆腔疼痛(CPP)敏感且特异的脑生物标志物尚未得到充分识别。利用来自跨学科慢性盆腔疼痛研究网络(Trans-MAPP Research Network)的数据,我们研究了与CPP相关的脑形态变化。我们采用多变量模式分类方法来检测这些变化,并识别可用于区分CPP患者与年龄匹配的健康对照者的模式。具体而言,我们使用线性支持向量机(SVM)算法来区分两组的灰质图像。支持向量机权重为正的区域包括初级体感皮层、辅助运动前区、海马体和杏仁核内的几个区域,这些区域被确定为分类的重要驱动因素,总体准确率为73%。因此,我们基于脑结构确定了一个初步分类器,它能够以较高的预测能力预测CPP的存在。我们的区域研究结果表明,在CPP患者中,在所确定的分布性脑区可能发现更高的灰质密度,这与之前一些关于内脏疼痛综合征的研究一致。未来的研究需要通过整合更多变量来改进我们确定的初步分类器,并评估观察到的脑结构差异是否为CPP所特有,或者是否可推广到其他慢性疼痛状况。