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癫痫的影像遗传学:当前认知与新视角

Imaging Genetics in Epilepsy: Current Knowledge and New Perspectives.

作者信息

Wang Ge, Wu Wenyue, Xu Yuchen, Yang Zhuanyi, Xiao Bo, Long Lili

机构信息

Department of Neurology, Xiangya Hospital, Central South University, Changsha, China.

National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China.

出版信息

Front Mol Neurosci. 2022 May 30;15:891621. doi: 10.3389/fnmol.2022.891621. eCollection 2022.

DOI:10.3389/fnmol.2022.891621
PMID:35706428
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9189397/
Abstract

Epilepsy is a neurological network disease with genetics playing a much greater role than was previously appreciated. Unfortunately, the relationship between genetic basis and imaging phenotype is by no means simple. Imaging genetics integrates multidimensional datasets within a unified framework, providing a unique opportunity to pursue a global vision for epilepsy. This review delineates the current knowledge of underlying genetic mechanisms for brain networks in different epilepsy syndromes, particularly from a neural developmental perspective. Further, endophenotypes and their potential value are discussed. Finally, we highlight current challenges and provide perspectives for the future development of imaging genetics in epilepsy.

摘要

癫痫是一种神经网络疾病,遗传学所起的作用比之前认为的要大得多。不幸的是,遗传基础与影像学表型之间的关系绝非简单。影像遗传学在一个统一框架内整合多维数据集,为全面了解癫痫提供了独特契机。本综述阐述了不同癫痫综合征中脑网络潜在遗传机制的当前知识,特别是从神经发育的角度。此外,还讨论了内表型及其潜在价值。最后,我们强调了当前的挑战,并为癫痫影像遗传学的未来发展提供了展望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/496f/9189397/5064e4d5e701/fnmol-15-891621-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/496f/9189397/5064e4d5e701/fnmol-15-891621-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/496f/9189397/5064e4d5e701/fnmol-15-891621-g0001.jpg

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1
Imaging Genetics in Epilepsy: Current Knowledge and New Perspectives.癫痫的影像遗传学:当前认知与新视角
Front Mol Neurosci. 2022 May 30;15:891621. doi: 10.3389/fnmol.2022.891621. eCollection 2022.
2
Developmental psychopathology in an era of molecular genetics and neuroimaging: A developmental neurogenetics approach.发展神经遗传学视角下的分子遗传学与神经影像学时代的发展心理病理学。
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Idiopathic focal epilepsies: the "lost tribe".特发性局灶性癫痫:“失落的部落”。
Epileptic Disord. 2016 Sep 1;18(3):252-88. doi: 10.1684/epd.2016.0839.
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Quantitative magnetic resonance imaging traits as endophenotypes for genetic mapping in epilepsy.定量磁共振成像特征作为癫痫基因定位的内表型。
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Genetics of epilepsy syndromes starting in the first year of life.始于生命第一年的癫痫综合征的遗传学
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Epilepsy genetics in Africa: challenges and future perspectives.非洲的癫痫遗传学:挑战与未来展望。
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Revealing a brain network endophenotype in families with idiopathic generalised epilepsy.揭示特发性全身性癫痫家族中的脑网络内表型。
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Impaired cognitive function in idiopathic generalized epilepsy and unaffected family members: an epilepsy endophenotype.特发性全面性癫痫伴认知功能障碍患者及其未受影响的家庭成员:癫痫的内表型。
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The Genetics of Epilepsy.癫痫的遗传学
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本文引用的文献

1
Robust Multi-View Clustering With Incomplete Information.具有不完整信息的鲁棒多视图聚类
IEEE Trans Pattern Anal Mach Intell. 2023 Jan;45(1):1055-1069. doi: 10.1109/TPAMI.2022.3155499. Epub 2022 Dec 5.
2
Dual in Utero Electroporation in Mice to Manipulate Two Specific Neuronal Populations in the Developing Cortex.小鼠子宫内双电穿孔技术用于操纵发育中皮层的两个特定神经元群体
Front Bioeng Biotechnol. 2022 Jan 12;9:814638. doi: 10.3389/fbioe.2021.814638. eCollection 2021.
3
Expression of 4E-BP1 in juvenile mice alleviates mTOR-induced neuronal dysfunction and epilepsy.
4E-BP1 在幼年小鼠中的表达可减轻 mTOR 诱导的神经元功能障碍和癫痫。
Brain. 2022 May 24;145(4):1310-1325. doi: 10.1093/brain/awab390.
4
Neurobehavioural comorbidities of epilepsy: towards a network-based precision taxonomy.癫痫的神经行为共病:迈向基于网络的精准分类学。
Nat Rev Neurol. 2021 Dec;17(12):731-746. doi: 10.1038/s41582-021-00555-z. Epub 2021 Sep 22.
5
Where the genome meets the connectome: Understanding how genes shape human brain connectivity.从基因组到连接组:了解基因如何塑造人类大脑连接。
Neuroimage. 2021 Dec 1;244:118570. doi: 10.1016/j.neuroimage.2021.118570. Epub 2021 Sep 8.
6
Embedding Regularizer Learning for Multi-View Semi-Supervised Classification.用于多视图半监督分类的嵌入正则化学习
IEEE Trans Image Process. 2021;30:6997-7011. doi: 10.1109/TIP.2021.3101917.
7
Corrigendum: Convergent and Divergent Mechanisms of Epileptogenesis in mTORopathies.勘误:mTOR 病中癫痫发生的趋同和分歧机制
Front Neuroanat. 2021 Jul 6;15:715363. doi: 10.3389/fnana.2021.715363. eCollection 2021.
8
Integrating single-cell and spatial transcriptomics to elucidate intercellular tissue dynamics.整合单细胞和空间转录组学以阐明细胞间组织动力学。
Nat Rev Genet. 2021 Oct;22(10):627-644. doi: 10.1038/s41576-021-00370-8. Epub 2021 Jun 18.
9
Metabolic alterations of the dorsolateral prefrontal cortex in sleep-related hypermotor epilepsy: A proton magnetic resonance spectroscopy study.睡眠相关运动性癫痫患者背外侧前额叶皮质的代谢改变:质子磁共振波谱研究。
J Neurosci Res. 2021 Oct;99(10):2657-2668. doi: 10.1002/jnr.24866. Epub 2021 Jun 16.
10
Heritability of Magnetoencephalography Phenotypes Among Patients With Genetic Generalized Epilepsy and Their Siblings.遗传性全面性癫痫患者及其兄弟姐妹的脑磁图表型的遗传度。
Neurology. 2021 Jul 13;97(2):e166-e177. doi: 10.1212/WNL.0000000000012144. Epub 2021 May 27.