Association Between Postsurgical Functional Connectivity and Seizure Outcome in Patients With Temporal Lobe Epilepsy.

IF 7.7 1区 医学 Q1 CLINICAL NEUROLOGY Neurology Pub Date : 2024-10-08 Epub Date: 2024-09-03 DOI:10.1212/WNL.0000000000209816
Behnaz Akbarian, Lucas E Sainburg, Andrew Janson, Graham Johnson, Derek J Doss, Baxter P Rogers, Dario J Englot, Victoria L Morgan
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Abstract

Background and objectives: Despite the success of presurgical network connectivity studies in predicting short-term (1-year) seizure outcomes, later seizure recurrence occurs in some patients with temporal lobe epilepsy (TLE). To uncover contributors to this recurrence, we investigated the relationship between functional connectivity and seizure outcomes at different time points after surgery in these patients.

Methods: Patients included were clinically diagnosed with unilateral mesial TLE after a standard clinical evaluation and underwent selective amygdalohippocampectomy. Healthy controls had no history of seizures or head injury. Using resting-state fMRI, we assessed the postsurgical functional connectivity node strength, computed as the node's total strength to all other nodes, between seizure-free (Engel Ia-Ib) and nonseizure-free (Engel Ic-IV) acquisitions. The change over time after surgery in different outcome groups in these nodes was also characterized.

Results: Patients with TLE (n = 32, mean age: 43.1 ± 11.9 years; 46.8% female) and 85 healthy controls (mean age: 37.7 ± 13.5 years; 48.2% female) were included. Resting fMRI was acquired before surgery and at least once after surgery in each patient (range 1-4 scans, 5-60 months). Differences between patients with (n = 30) and without (n = 18) seizure freedom were detected in the posterior insula ipsilateral to the resection (I-PIns: 95% CI -154.8 to -50.1, p = 2.8 × 10-4) and the bilateral central operculum (I-CO: 95% CI -163.2 to -65.1, p = 2.6 × 10-5, C-CO: 95% CI -172.7 to -55.8, p = 2.8 × 10-4). In these nodes, only those who were seizure-free had increased node strength after surgery that increased linearly over time (I-CO: 95% CI 1.0-5.2, p = 4.2 × 10-3, C-CO: 95% CI 1.0-5.2, p = 5.5 × 10-3, I-PIns: 95% CI 1.6-5.5, p = 0.9 × 10-3). Different outcome groups were not distinguished by node strength before surgery.

Discussion: The findings suggest that network evolution in the first 5 years after selective amygdalohippocampectomy surgery is related to seizure outcomes in TLE. This highlights the need to identify presurgical and surgical conditions that lead to disparate postsurgical trajectories between seizure-free and nonseizure-free patients to identify potential contributors to long-term seizure outcomes. However, the lack of including other surgical approaches may affect the generalizability of the results.

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颞叶癫痫患者术后功能连接性与癫痫发作结果之间的关系
背景和目的:尽管术前网络连通性研究在预测短期(1年)癫痫发作结果方面取得了成功,但一些颞叶癫痫(TLE)患者术后仍会复发。为了揭示导致这种复发的原因,我们研究了这些患者术后不同时间点的功能连接与癫痫发作结果之间的关系:纳入的患者都是经过标准临床评估后临床诊断为单侧中叶TLE,并接受了选择性杏仁海马切除术。健康对照组无癫痫发作或头部受伤史。通过静息态fMRI,我们评估了无癫痫发作(Engel Ia-Ib)和无癫痫发作(Engel Ic-IV)采集之间的术后功能连接节点强度,计算方法是节点与所有其他节点的总强度。这些节点在术后不同结果组别中的变化也具有特征性:研究对象包括32名TLE患者(平均年龄:43.1 ± 11.9岁;46.8%为女性)和85名健康对照组患者(平均年龄:37.7 ± 13.5岁;48.2%为女性)。每位患者在手术前和手术后至少进行一次静息 fMRI 扫描(扫描次数为 1-4 次,扫描时间为 5-60 个月)。在切除术同侧的后脑岛(I-PIns:95% CI -154.8至-50.1,p = 2.8 × 10-4)和双侧中央厣(I-CO:95% CI -163.2至-65.1,p = 2.6 × 10-5,C-CO:95% CI -172.7至-55.8,p = 2.8 × 10-4)发现了癫痫发作自由患者(n = 30)和无癫痫发作患者(n = 18)之间的差异。在这些结节中,只有那些无癫痫发作的患者术后结节强度增加,且随时间呈线性增长(I-CO:95% CI 1.0-5.2,p = 4.2 × 10-3;C-CO:95% CI 1.0-5.2,p = 5.5 × 10-3;I-PIns:95% CI 1.6-5.2,p = 5.5 × 10-3;I-PIns:95% CI 1.0-5.2,p = 5.5 × 10-3):95%CI:1.6-5.5,p = 0.9 × 10-3)。手术前的节点强度并不能区分不同的结果组:讨论:研究结果表明,选择性杏仁海马切除术后头5年的网络演变与TLE的发作结果有关。这突出表明,有必要识别导致无癫痫发作和无癫痫发作患者术后轨迹不同的手术前和手术条件,以确定导致长期癫痫发作结果的潜在因素。然而,由于没有纳入其他手术方法,可能会影响研究结果的普遍性。
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来源期刊
Neurology
Neurology 医学-临床神经学
CiteScore
12.20
自引率
4.00%
发文量
1973
审稿时长
2-3 weeks
期刊介绍: Neurology, the official journal of the American Academy of Neurology, aspires to be the premier peer-reviewed journal for clinical neurology research. Its mission is to publish exceptional peer-reviewed original research articles, editorials, and reviews to improve patient care, education, clinical research, and professionalism in neurology. As the leading clinical neurology journal worldwide, Neurology targets physicians specializing in nervous system diseases and conditions. It aims to advance the field by presenting new basic and clinical research that influences neurological practice. The journal is a leading source of cutting-edge, peer-reviewed information for the neurology community worldwide. Editorial content includes Research, Clinical/Scientific Notes, Views, Historical Neurology, NeuroImages, Humanities, Letters, and position papers from the American Academy of Neurology. The online version is considered the definitive version, encompassing all available content. Neurology is indexed in prestigious databases such as MEDLINE/PubMed, Embase, Scopus, Biological Abstracts®, PsycINFO®, Current Contents®, Web of Science®, CrossRef, and Google Scholar.
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