Altered white matter microstructure identified with tract-based spatial statistics in irritable bowel syndrome: a diffusion tensor imaging study

被引:0
作者
Jin Fang
Shumei Li
Meng Li
Queenie Chan
Xiaofen Ma
Huanhuan Su
Tianyue Wang
Wenfeng Zhan
Jianhao Yan
Ming Xu
Yaxi Zhang
Luxian Zeng
Junzhang Tian
Guihua Jiang
机构
[1] Guangdong No.2 Provincial People’s Hospital,Department of Medical Imaging
[2] Philips Healthcare,undefined
来源
Brain Imaging and Behavior | 2017年 / 11卷
关键词
Irritable bowel syndrome; Tract-based spatial statistics; Diffusion tensor imaging;
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学科分类号
摘要
The neural mechanisms underlying the pathophysiology of irritable bowel syndrome(IBS) are far from being completely understood. The purpose of the present study was to investigate potential white matter (WM) microstructural changes and underlying causes for WM impairment in IBS using diffusion tensor imaging. The present prospective study involved 19 patients with IBS and 20 healthy controls. Whole-brain voxel-wise analyses of fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD), and radial diffusivity (RD) were performed by tract-based spatial statistics (TBSS) to localize abnormal WM regions between the 2 groups. We found that IBS patients had significantly reduced FA (P < 0.05) in the splenium of the corpus callosum, the right retrolenticular area of the internal capsule and the right superior corona radiata. We also found increased MD (P < 0.05) in the splenium and body of the corpus callosum, the right retrolenticular area of the internal capsule, the right superior corona radiata and the right posterior limb of the internal capsule. In addition, IBS patients had significantly increased AD (P < 0.05) in the splenium of the corpus callosum, the bilateral retrolenticular area of the internal capsule and the left posterior limb of the internal capsule. We conclude that the WM microstructure is changed in IBS and the underlying pathological basis may be attributed to the axonal injury and loss. These results may lead to a better understanding of the pathophysiology of IBS.
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页码:1110 / 1116
页数:6
相关论文
共 99 条
[1]  
Berman SM(2008)Reduced brainstem inhibition during anticipated pelvic visceral pain correlates with enhanced brain response to the visceral stimulus in women with irritable bowel syndrome The Journal of Neuroscience 28 349-359
[2]  
Naliboff BD(2010)Altered brain structure in irritable bowel syndrome: potential contributions of pre-existing and disease-driven factors Gastroenterology 138 1783-1789
[3]  
Suyenobu B(2013)Diameter, length, speed, and conduction delay of callosal axons in macaque monkeys and humans: comparing data from histology and magnetic resonance imaging diffusion tractography The Journal of Neuroscience 33 14501-14511
[4]  
Labus JS(2003)Brain responses to visceral and somatic stimuli in patients with irritable bowel syndrome with and without fibromyalgia The American Journal of Gastroenterology 98 1354-1361
[5]  
Stains J(2008)Cortical thinning in IBS: implications for homeostatic, attention, and pain processing Neurology 70 153-154
[6]  
Ohning G(2006)The functional gastrointestinal disorders and the Rome III process Gastroenterology 130 1377-1390
[7]  
Mayer EA(2002)AGA technical review on irritable bowel syndrome Gastroenterology 123 2108-2131
[8]  
Blankstein U(2013)Diffusion tensor imaging detects microstructural reorganization in the brain associated with chronic irritable bowel syndrome Pain 154 1528-1541
[9]  
Chen J(2011)Altered brain microstructure assessed by diffusion tensor imaging in patients with chronic pancreatitis Gut 60 1554-1562
[10]  
Diamant NE(2013)Stress and visceral pain: focusing on irritable bowel syndrome Pain 154 S63-S70