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不同额区起源的额叶癫癎低代谢模式。

Patterns of hypometabolism in frontal lobe epilepsy originating in different frontal regions.

机构信息

Department of Neurology, Zhejiang Hospital, Hangzhou, Zhejiang, China.

Department of Radiology, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.

出版信息

Ann Clin Transl Neurol. 2022 Sep;9(9):1336-1344. doi: 10.1002/acn3.51630. Epub 2022 Jul 14.

DOI:10.1002/acn3.51630
PMID:35836348
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9463953/
Abstract

OBJECTIVES

Analysis of FDG-PET imaging commonly shows that hypometabolism extends into extra-epileptogenic zones (extra-EZ). This study investigates the distribution patterns of hypometabolism in frontal lobe epilepsy (FLE) originating in different frontal regions.

METHODS

Sixty-four patients with FLE were grouped by EZ localization according to Brodmann areas (BAs): Group 1 (the frontal motor and premotor area), BAs 4, 6, and 8; Group 2 (the inferior frontal gyrus and opercular area), BAs 44, 45, and 47; Group 3 (the dorsal prefrontal area), BAs 9, 10, 11, and 46; and Group 4 (the medial frontal and anterior cingulate gyrus), BAs 32 and 24. Regions of extra-EZ hypometabolism were statistically analyzed between FLE groups and healthy controls. Correlation analysis was performed to identify relationships between the intensity of hypometabolism and clinical characteristics.

RESULTS

Significant hypometabolism in the ipsilateral (Groups 1 and 4) or bilateral (Groups 2 and 3) anterior insulae was found. Groups 1 and 4 presented with limited distribution of extra-EZ hypometabolism, whereas Groups 2 and 3 showed widely distributed extra-EZ hypometabolism in the rectus gyrus, cingulate gyrus, and other regions. Additionally, the intensity of hypometabolism was correlated with epilepsy duration in Groups 2 and 3.

CONCLUSIONS

All FLE groups showed hypometabolism in the anterior insula. In addition, distinct patterns of extra-EZ hypometabolism were identified for each FLE group. This quantitative FDG-PET analysis expanded our understanding of the topography of epileptic networks and can guide EZ localization in the future.

摘要

目的

FDG-PET 成像分析通常显示,代谢低下延伸到癫痫外致痫区(extra-EZ)之外。本研究调查了起源于不同额叶区域的额叶癫痫(FLE)患者中代谢低下的分布模式。

方法

根据 Brodmann 区(BAs)将 64 例 FLE 患者分为 EZ 定位组:1 组(额叶运动和运动前区),BAs4、6 和 8;2 组(下额叶回和脑岛盖区),BAs44、45 和 47;3 组(背侧前额叶区),BAs9、10、11 和 46;4 组(内侧额叶和前扣带回),BAs32 和 24。对 FLE 组与健康对照组之间的 extra-EZ 代谢低下区域进行统计学分析。进行相关性分析以确定代谢低下强度与临床特征之间的关系。

结果

同侧(1 组和 4 组)或双侧(2 组和 3 组)前岛叶均存在明显的代谢低下。1 组和 4 组表现为 extra-EZ 代谢低下的局限性分布,而 2 组和 3 组则表现为直回、扣带回和其他区域广泛分布的 extra-EZ 代谢低下。此外,2 组和 3 组的代谢低下强度与癫痫持续时间相关。

结论

所有 FLE 组均在前岛叶表现出代谢低下。此外,还确定了每个 FLE 组的 extra-EZ 代谢低下的不同模式。这种定量 FDG-PET 分析扩展了我们对癫痫网络拓扑结构的理解,并可指导未来 EZ 的定位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b3/9463953/24e865fcebe9/ACN3-9-1336-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b3/9463953/7602d0fae4e0/ACN3-9-1336-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b3/9463953/7cac5f27fcc3/ACN3-9-1336-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b3/9463953/24e865fcebe9/ACN3-9-1336-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b3/9463953/7602d0fae4e0/ACN3-9-1336-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b3/9463953/7cac5f27fcc3/ACN3-9-1336-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9b3/9463953/24e865fcebe9/ACN3-9-1336-g001.jpg

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