Liu Jixin, Mu Junya, Liu Qianqian, Dun Wanghuan, Zhang Ming, Tian Jie
Center for Brain Imaging, School of Life Science and Technology, Xidian University, Xi'an, People's Republic of China.
Engineering Research Center of Molecular and Neuro Imaging, Ministry of Education, Xi'an, People's Republic of China.
Hum Brain Mapp. 2017 Sep;38(9):4386-4397. doi: 10.1002/hbm.23667. Epub 2017 Jun 13.
Neuroimaging studies described brain structural changes that comprise the mechanisms underlying individual differences in migraine development and maintenance. However, whether such interindividual variability in migraine was observed in a pretreatment scan is a predisposition for subsequent hypoalgesia to placebo treatment that remains largely unclear. Using T1-weighted imaging, we investigated this issue in 50 healthy controls (HC) and 196 patients with migraine without aura (MO). An 8-week double-blinded, randomized, placebo-controlled acupuncture was used, and we only focused on the data from the sham acupuncture group. Eighty patients participated in an 8-weeks sham acupuncture treatment, and were subdivided (50% change in migraine days from baseline) into recovering (MOr) and persisting (MOp) patients. Optimized voxel-based morphometry (VBM) and functional connectivity analysis were performed to evaluate brain structural and functional changes. At baseline, MOp and MOr had similar migraine activity, anxiety and depression; reduced migraine days were accompanied by decreased anxiety in MOr. In our findings, the MOr group showed a smaller volume in the left medial prefrontal cortex (mPFC), and decreased mPFC-related functional connectivity was found in the default mode network. Additionally, the reduction in migraine days after placebo treatment was significantly associated with the baseline gray matter volume of the mPFC which could also predict post-treatment groups with high accuracy. It indicated that individual differences for the brain structure in the pain modulatory system at baseline served as a substrate on how an individual facilitated or diminished hypoalgesia responses to placebo treatment in migraineurs. Hum Brain Mapp 38:4386-4397, 2017. © 2017 Wiley Periodicals, Inc.
神经影像学研究描述了大脑结构变化,这些变化构成了偏头痛发生和维持过程中个体差异的潜在机制。然而,偏头痛的这种个体间变异性在治疗前扫描中是否被观察到,是随后对安慰剂治疗产生痛觉减退的一个易患因素,这在很大程度上仍不清楚。我们使用T1加权成像,在50名健康对照者(HC)和196名无先兆偏头痛(MO)患者中研究了这个问题。采用了为期8周的双盲、随机、安慰剂对照针刺治疗,并且我们只关注假针刺组的数据。80名患者参与了为期8周的假针刺治疗,并根据偏头痛天数相对于基线的变化(50%)分为恢复组(MOr)和持续组(MOp)患者。进行了优化的基于体素的形态学测量(VBM)和功能连接分析,以评估大脑结构和功能变化。在基线时,MOp和MOr具有相似的偏头痛活动、焦虑和抑郁水平;MOr组偏头痛天数减少伴随着焦虑的减轻。在我们的研究结果中,MOr组左侧内侧前额叶皮质(mPFC)体积较小,并且在默认模式网络中发现与mPFC相关的功能连接减少。此外,安慰剂治疗后偏头痛天数的减少与mPFC的基线灰质体积显著相关,mPFC的基线灰质体积也能够高精度地预测治疗后分组。这表明,基线时疼痛调节系统中大脑结构的个体差异是个体促进或减弱偏头痛患者对安慰剂治疗痛觉减退反应的基础。《人类大脑图谱》38:4386 - 4397,2017年。© 2017威利期刊公司