Pedersen Mangor, Kowalczyk Magdalena, Omidvarnia Amir, Perucca Piero, Gooley Samuel, Petrou Steven, Scheffer Ingrid E, Berkovic Samuel F, Jackson Graeme D
The Florey Institute of Neuroscience and Mental Health (M.P., M.K., A.O., S.P., I.E.S., G.D.J.), Parkville; Department of Neurology (I.E.S.), Royal Children's Hospital, Parkville; Department of Neuroscience (P.P.), Central Clinical School, Monash University; Department of Neurology (P.P.), The Royal Melbourne Hospital, Parkville; Department of Neurology (P.P.), Alfred Health, Melbourne; Department of Medicine (P.P., S.P.), The Royal Melbourne Hospital, The University of Melbourne, Parkville; Epilepsy Research Centre (S.G., I.E.S., S.F.B., G.D.J.), Department of Medicine, The University of Melbourne, Austin Health, Heidelberg; and Department of Pediatrics (I.E.S.), The University of Melbourne, Parkville, VIC, Australia.
Neurol Genet. 2019 Jun 7;5(4):e340. doi: 10.1212/NXG.0000000000000340. eCollection 2019 Aug.
To map functional MRI (fMRI) connectivity within and between the somatosensory cortex, putamen, and ventral thalamus in individuals from a family with a GABAergic deficit segregating with febrile seizures and genetic generalized epilepsy.
We studied 5 adults from a family with early-onset absence epilepsy and/or febrile seizures and a GABA receptor subunit gamma2 pathogenic variant () vs 5 age-matched controls. We infer differences between participants with the pathogenic variant and controls in resting-state fMRI connectivity within and between the somatosensory cortex, putamen, and ventral thalamus.
We observed increased fMRI connectivity within the somatosensory cortex and between the putamen and ventral thalamus in all individuals with the pathogenic variant compared with controls. Post hoc analysis showed less pronounced changes in fMRI connectivity within and between the primary visual cortex and precuneus.
Although our sample size was small, this preliminary study suggests that individuals with a pathogenic variant, raising risk of febrile seizures and generalized epilepsy, display underlying increased functional connectivity both within the somatosensory cortex and in striatothalamic networks. This human network model aligns with rodent research and should be further validated in larger cohorts, including other individuals with generalized epilepsy with and without known GABA pathogenic variants.
绘制一个家族中个体的功能磁共振成像(fMRI)连接图谱,该家族存在与热性惊厥和遗传性全身性癫痫相关的γ-氨基丁酸(GABA)能缺陷,图谱涉及躯体感觉皮层、壳核和腹侧丘脑内部及之间的连接情况。
我们研究了来自一个患有早发性失神癫痫和/或热性惊厥且存在GABA受体亚基γ2致病变异()的家族的5名成年人,并与5名年龄匹配的对照者进行比较。我们推断携带致病变异的参与者与对照者在静息态fMRI连接方面在躯体感觉皮层、壳核和腹侧丘脑内部及之间的差异。
与对照者相比,我们观察到所有携带致病变异的个体在躯体感觉皮层内部以及壳核与腹侧丘脑之间的fMRI连接增加。事后分析显示,初级视觉皮层和楔前叶内部及之间的fMRI连接变化不太明显。
尽管我们的样本量较小,但这项初步研究表明,携带致病变异的个体,其热性惊厥和全身性癫痫风险增加,在躯体感觉皮层内部以及纹状体丘脑网络中均显示出潜在的功能连接增加。这种人类网络模型与啮齿动物研究结果一致,应在更大的队列中进一步验证,包括其他患有全身性癫痫且有无已知GABA致病变异的个体。