Labus Jennifer S, Van Horn John D, Gupta Arpana, Alaverdyan Mher, Torgerson Carinna, Ashe-McNalley Cody, Irimia Andrei, Hong Jui-Yang, Naliboff Bruce, Tillisch Kirsten, Mayer Emeran A
Oppenheimer Family Center for the Neurobiology of Stress Departments of Departments of Medicine and Division of Digestive Diseases, UCLA, Los Angeles, CA, USA Physiology, UCLA, Los Angeles, CA, USA, and Psychiatry, UCLA, Los Angeles, CA, USA Pain and Interoception Network (PAIN), Los Angeles, CA, USA The Institute for Neuroimaging and Informatics (INI) and Laboratory of Neuro Imaging (LONI), Keck School of Medicine of USC, University of Southern California, Los Angeles, CA, USA Department of Biomedical Engineering, UCLA, Los Angeles, CA, USA VA Greater Los Angeles Healthcare System, Los Angeles, CA, USA.
Pain. 2015 Aug;156(8):1545-1554. doi: 10.1097/j.pain.0000000000000196.
Irritable bowel syndrome (IBS) is the most common chronic visceral pain disorder. The pathophysiology of IBS is incompletely understood; however, evidence strongly suggests dysregulation of the brain-gut axis. The aim of this study was to apply multivariate pattern analysis to identify an IBS-related morphometric brain signature that could serve as a central biological marker and provide new mechanistic insights into the pathophysiology of IBS. Parcellation of 165 cortical and subcortical regions was performed using FreeSurfer and the Destrieux and Harvard-Oxford atlases. Volume, mean curvature, surface area, and cortical thickness were calculated for each region. Sparse partial least squares discriminant analysis was applied to develop a diagnostic model using a training set of 160 females (80 healthy controls and 80 patients with IBS). Predictive accuracy was assessed in an age-matched holdout test set of 52 females (26 healthy controls and 26 patients with IBS). A 2-component classification algorithm comprising the morphometry of (1) primary somatosensory and motor regions and (2) multimodal network regions explained 36% of the variance. Overall predictive accuracy of the classification algorithm was 70%. Small effect size associations were observed between the somatosensory and motor signature and nongastrointestinal somatic symptoms. The findings demonstrate that the predictive accuracy of a classification algorithm based solely on regional brain morphometry is not sufficient, but they do provide support for the utility of multivariate pattern analysis for identifying meaningful neurobiological markers in IBS.
肠易激综合征(IBS)是最常见的慢性内脏疼痛疾病。IBS的病理生理学尚未完全明确;然而,有证据强烈表明脑-肠轴功能失调。本研究的目的是应用多变量模式分析来识别与IBS相关的脑形态学特征,该特征可作为核心生物学标志物,并为IBS的病理生理学提供新的机制性见解。使用FreeSurfer以及Destrieux和哈佛-牛津图谱对165个皮质和皮质下区域进行了分割。计算每个区域的体积、平均曲率、表面积和皮质厚度。应用稀疏偏最小二乘判别分析,使用160名女性(80名健康对照和80名IBS患者)的训练集建立诊断模型。在52名年龄匹配的保留测试集女性(26名健康对照和26名IBS患者)中评估预测准确性。一种由(1)主要躯体感觉和运动区域以及(2)多模态网络区域的形态测量组成的双成分分类算法解释了36%的方差。分类算法的总体预测准确性为70%。在躯体感觉和运动特征与非胃肠道躯体症状之间观察到小效应量关联。研究结果表明,仅基于区域脑形态测量的分类算法的预测准确性不足,但它们确实为多变量模式分析在识别IBS中有意义的神经生物学标志物方面的实用性提供了支持。