Xu Jiayuan, Qin Wen, Liu Bing, Jiang Tianzi, Yu Chunshui
Department of Radiology and Tianjin Key Laboratory of Functional Imaging, Tianjin Medical University General Hospital, No. 154, Anshan Road, Heping District, Tianjin, 300052, China.
Brainnetome Center, Institute of Automation, Chinese Academy of Sciences, Beijing, 100190, China.
Brain Struct Funct. 2016 Nov;221(8):3891-3901. doi: 10.1007/s00429-015-1134-4. Epub 2015 Oct 25.
Different genotypic combinations of COMT and DRD2 can generate multiple subgroups with different levels of dopamine signaling. Its modulations on brain properties can be investigated by analyzing the combined gene effects of COMT and DRD2. However, the inherent association between modulation patterns of the dopamine system on structural and functional properties of the brain remains unknown. In 294 healthy young adults, we investigated both additive and non-additive interactions of COMT and DRD2 on gray matter volume (GMV) and resting-state functional connectivity (rsFC) using a voxel-based analysis. We found a significant non-additive COMT × DRD2 interaction in the right dorsal anterior cingulate cortex (dACC), exhibiting an inverted U-shape modulation by dopamine signaling. We also found a significant non-additive COMT × DRD2 interaction in the rsFC between the right dACC and precuneus, displaying a U-shape modulation by dopamine signaling. Moreover, this rsFC was negatively correlated with the GMV of the right dACC. Although the additive interaction did not pass corrections for multiple comparisons, we also found a trend towards an inverse modulation pattern and a negative correlation between the GMV and rsFC of the right inferior frontal gyrus. No genotypic differences were detected in any assessments of the cognition, mood and personality. These findings suggest that healthy young adults without optimal dopamine signaling may maintain their normal behavioral performance via a functional compensatory mechanism in response to structural deficit due to genetic variation.
儿茶酚-O-甲基转移酶(COMT)和多巴胺D2受体(DRD2)的不同基因型组合可产生具有不同多巴胺信号水平的多个亚组。通过分析COMT和DRD2的联合基因效应,可以研究其对大脑特性的调节作用。然而,多巴胺系统的调节模式与大脑结构和功能特性之间的内在关联仍不清楚。在294名健康的年轻成年人中,我们使用基于体素的分析方法,研究了COMT和DRD2对灰质体积(GMV)和静息态功能连接(rsFC)的加性和非加性相互作用。我们发现右侧背侧前扣带回皮质(dACC)存在显著的非加性COMT×DRD2相互作用,呈现出由多巴胺信号介导的倒U形调节。我们还发现右侧dACC与楔前叶之间的rsFC中存在显著的非加性COMT×DRD2相互作用,表现出由多巴胺信号介导的U形调节。此外,这种rsFC与右侧dACC的GMV呈负相关。尽管加性相互作用未通过多重比较校正,但我们还发现右侧额下回的GMV与rsFC之间存在反向调节模式和负相关的趋势。在认知、情绪和个性的任何评估中均未检测到基因型差异。这些发现表明,多巴胺信号未达到最佳水平的健康年轻成年人可能通过功能补偿机制来维持其正常的行为表现,以应对因基因变异导致的结构缺陷。