[前庭性偏头痛患者顶叶厣2的功能连接性改变:静息态fMRI研究]。

Z W Chen, C X Lin, Y J Liu, D Liu, L Q Rong, H Y Liu, X E Wei, L J Xiao
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引用次数: 0

摘要

研究目的研究前庭性偏头痛(VM)和无先兆偏头痛(MwoA)患者静息态功能连接(FC)的差异,以推断VM可能的神经影像学机制。研究方法选取徐州医科大学第二附属医院神经内科2019年12月至2022年12月收治的30例前庭性偏头痛患者为实验组(EG)(男6例,女24例,平均年龄38.3岁),26例无先兆偏头痛患者为对照组(男7例,女19例,平均年龄35.5岁)。研究人员收集了所有患者的一般人口统计学和临床数据,如性别、年龄、受教育年限、病程和发作频率,以及汉密尔顿焦虑量表(HAMA)、汉密尔顿抑郁量表(HAMD)、蒙特利尔认知评估(MoCA)、头痛视觉量表(VAS)、头痛影响测试 6(HIT-6)和偏头痛残疾评估问卷(MIDAS)的数据。头晕患者还接受了头晕障碍量表(DHI)、头晕视觉量表(VAS)和前庭障碍日常生活活动量表(VADL)的评估。所有患者都接受了静息态功能磁共振成像(fMRI)扫描。双侧顶叶厣皮层 2 (OP2) 和初级视觉皮层 (V1) 被用作感兴趣区 (ROI)。计算两组之间 ROI 和其他脑区的 FC 差异。针对差异显著的脑区,提取 EG 中每个受试者的 FC z 值,并对 FC z 值与患者临床特征进行皮尔逊偏相关分析:两组患者在性别、年龄、受教育年限、病程、发作频率以及 MoCA、HAMA 和 HAMD 评分方面均无明显差异(P>0.05)。VM患者的头痛VAS、HIT-6和MIDAS评分明显低于MwoA患者(PPP=0.007,r=0.480),右侧OP2和左侧丘脑之间的FC与VM患者的病程呈正相关(P=0.015,r=0.439)。结论VM的发病机制可能与前庭、疼痛和视觉运动网络的FC改变有关,这些神经通路的异常可能是VM发病机制的重要影像生物标志物。
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[Altered functional connectivity of parietal opercular 2 in patients with vestibular migraine: a resting-state fMRI study].

Objective: To investigate the differences in resting-state functional connectivity (FC) between patients with vestibular migraine (VM) and migraine without aura (MwoA) in order to infer the possible neuroimaging mechanisms of VM. Methods: Thirty VM patients admitted to the Department of Neurology of the Second Affiliated Hospital of Xuzhou Medical University from December 2019 to December 2022 were selected as the experimental group (EG) (6 males and 24 females, with mean age of 38.3 years) and 26 MwoA patients as the control group (7 males and 19 females, mean age 35.5 years). General demographic and clinical data such as gender, age, year of education, course of disease and frequency of attacks were collected for all the patients, as well as data of Hamilton Anxiety Scale (HAMA), Hamilton Depression Scale (HAMD), Montreal Cognitive Assessment (MoCA), headache Visual Arialogue Scale (VAS), Headache Impact Test 6 (HIT-6) and Migraine Disability Assessment Questionnaire (MIDAS). VM patients were also assessed by Dizziness Handicap Inventory (DHI), dizziness VAS and Vestibular Disorders Activities of Daily Living (VADL) scales. All patients underwent resting-sate functional Magnetic Resonance Imaging (fMRI) scans. Bilateral parietal opercular cortex 2 (OP2) and primary visual cortex (V1) were used as regions of interests (ROIs). Differences in FC between ROIs and other brain regions were calculated between the two groups. In view of the brain regions with significant differences, z-values of FC were extracted for each subject in the EG, and Pearson partial correlation analysis was conducted between z-values of FC and clinical characteristics of patients, P<0.05 was considered to have significant correlation. SPSS 22.0 was used for statistical analysis. Results: There was no significant difference in gender, age, years of education, course of disease, frequency of attack and scores of MoCA, HAMA and HAMD between the two groups (P>0.05). Headache VAS, HIT-6 and MIDAS scores in VM patients were significantly lower than those in MwoA patients (P<0.05). Compared with MwoA patients, the FC between left OP2 and bilateral precuneus and left thalamus was significantly increased in VM patients, and the FC between right OP2 and left thalamus and right anterior cingulate gyrus were significantly increased (P<0.05, False Discovery Rate correction). Correlation analysis showed that the FC between left OP2 and left precuneus was positively correlated with DHI score in VM patients (P=0.007, r=0.480), and the FC between right OP2 and left thalamus was positively correlated with the disease course in VM patients (P=0.015, r=0.439). Conclusions: The pathogenesis of VM may be related to the altered FC of vestibular, pain and visual-motor networks, abnormalities of these neural pathways may be important imaging biomarkers of VM pathogenesis.

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