Liu C-Y, Yan S, Hou B, Li M-L, Gao S, Li A, Liu B, Xu W-H
Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Department of Radiology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China.
Eur J Neurol. 2020 Jun;27(6):1062-1065. doi: 10.1111/ene.14210. Epub 2020 Apr 3.
The role of intracranial steno-occlusive disease in cognitive impairment and dementia is unclear and has not been well studied.
A total of 32 consecutive patients (13 males, aged 54 ± 12 years) with asymptomatic steno-occlusive middle cerebral artery (MCA) disease, defined as >70% stenosis on maximum intensity projection images or a complete signal loss of MCA trunk on magnetic resonance angiography, and 20 age- and education-matched normal controls (12 males, 60 ± 8 years old) were compared for neuropsychological performance, gray matter volume and neural network analysis.
The patient group did not show a significant decrease in gray matter volume or cognitive tests except for their performance on the grooved pegboard test. However, graph analysis of resting-state functional magnetic resonance imaging showed significant decreases in network strength, global efficiency and the clustering coefficient, as well as a longer characteristic path length (P < 0.05). The diffusive decrease pattern was particularly located in interhemispheric connectivity and there was no compensatory hyperconnectivity in any brain regions.
In asymptomatic steno-occlusive MCA disease, cognition and neural network changes are mismatched and have underlying pathophysiological mechanisms that are different from those of neurodegenerative disease.
颅内狭窄闭塞性疾病在认知障碍和痴呆中的作用尚不清楚,且尚未得到充分研究。
共有32例连续患者(13例男性,年龄54±12岁)患有无症状性大脑中动脉(MCA)狭窄闭塞性疾病,定义为最大强度投影图像上狭窄>70%或磁共振血管造影显示MCA主干完全信号缺失,并与20例年龄和教育程度匹配的正常对照者(12例男性,60±8岁)进行神经心理学表现、灰质体积和神经网络分析比较。
除了沟槽插板测试表现外,患者组的灰质体积或认知测试未显示出显著下降。然而,静息态功能磁共振成像的图谱分析显示网络强度、全局效率和聚类系数显著降低,以及特征路径长度更长(P<0.05)。扩散性降低模式尤其位于半球间连接,且任何脑区均无代偿性高连接。
在无症状性MCA狭窄闭塞性疾病中,认知和神经网络变化不匹配,且具有与神经退行性疾病不同的潜在病理生理机制。