Department of Neurology and Neurosurgery, McGill University, 3081 University Street, Montréal, Quebec, Canada.
Cortex. 2010 Jun;46(6):750-60. doi: 10.1016/j.cortex.2009.06.008. Epub 2009 Jul 3.
Tourette syndrome (TS) implicates the disinhibition of the cortico-striatal-thalamic-cortical circuitry (CSTC). Previous studies used a volumetric approach to investigate this circuitry with inconsistent findings. Cortical thickness may represent a more reliable measure than volume due to the low variability in the cytoarchitectural structure of the grey matter.
66 magnetic resonance imaging scans were acquired from 34 TS subjects (age range 10-25, mean 17.19+/-4.1) and 32 normal controls (NC) (age range 10-20, mean 16.33+/-3.56). Brain morphology was assessed using the fully automated CIVET pipeline at the Montreal Neurological Institute.
We report (1) significant cortical thinning in the fronto-parietal and somatosensory-motor cortices in TS relative to NC (p<.05); (2) TS boys showed thinner cortex relative to TS girls in the fronto-parietal cortical regions (p<.05); (3) significant decrease in the fronto-parietal mean cortical thickness in TS subjects with age relative to NC and in the pre-central cortex in TS boys relative to TS girls; (4) significant negative correlations between tic severity and the somatosensory-motor cortical thickness.
TS revealed important thinning in brain regions particularly involved in the somatosensory/motor bodily representations which may play an important role in tics. Our findings are in agreement with Leckman et al. (1991) hypothesis stating that facial tics would be associated with dysfunction in an orofacial subset of the motor circuit, eye blinking with the occulo-motor circuit, whereas lack of inhibition to a dysfunction in the prefrontal cortex. Gender and age differences may reflect differential etiological factors, which have significant clinical relevance in TS and should be considered in developing and using diagnostic and therapeutic interventions.
妥瑞氏综合征(TS)涉及皮质-纹状体-丘脑-皮质回路(CSTC)的抑制失控。之前的研究使用容积法来研究该回路,但结果不一致。由于灰质的细胞结构变异较小,皮质厚度可能比体积更能代表可靠的测量指标。
从 34 名 TS 患者(年龄范围 10-25 岁,平均 17.19+/-4.1)和 32 名正常对照组(NC)(年龄范围 10-20 岁,平均 16.33+/-3.56)中获得 66 个磁共振成像扫描。使用蒙特利尔神经学研究所的全自动 CIVET 流水线评估脑形态。
我们报告了(1)与 NC 相比,TS 患者额顶和体感运动皮质变薄(p<.05);(2)TS 男孩额顶皮质区域的皮质厚度较 TS 女孩薄(p<.05);(3)与 NC 相比,TS 患者额顶皮质的平均皮质厚度随年龄降低,TS 男孩的中央前皮质的皮质厚度降低;(4)TS 患者的 tic 严重程度与体感运动皮质厚度呈显著负相关。
TS 患者大脑区域,特别是涉及体感/运动躯体表现的区域出现明显变薄,这可能在 tic 中起重要作用。我们的研究结果与 Leckman 等人(1991)的假说一致,即面部 tic 与运动回路的口面亚区功能障碍有关,眨眼与眼动回路有关,而抑制缺失则与前额叶皮质功能障碍有关。性别和年龄差异可能反映了不同的病因因素,这在 TS 中具有重要的临床意义,在开发和使用诊断和治疗干预措施时应予以考虑。