研究进展 情报发生 2026-10-31 · 发布于 2026-11-01

灰质改变的规范功能网络定位:特发性全面性癫痫的共同连接模式

来源:Front Neurol · PMID 42959045 · DOI 10.3389/fneur.2026.1957963 · 来源:IMA 知识库《文献层·文献监控卡片》2026-10-31 期 · 全文级(file_id dmlmcfQeUyzO,实际下载核验) · 全文已获取并通过归属校验

时间标签:数据日期 2026-10-31 · 生成时间 2026-11-01 05:30(Asia/Shanghai)| 检索窗口 PubMed edat 2026/10/28–2026/10/31 | 情报发生日期 2026-10-31

研究问题

However, the broader traditional perception of IGE as a benign disorder with limited long-term clinical impact has been challenged by accumulating evidence that individuals with IGE may experience persistent cognitive impairment (), psychiatric comorbidities (), and, in a substantial subset, inadequate seizure control or resistance to antiseizure medications ().;However, the direction and location of these findings have varied substantially across studies, with some reporting GM increases, others reporting decreases (), and several reporting no significant differences ().;In this context, functional connectivity network mapping (FCNM) provides a framework for testing whether spatially heterogeneous brain abnormalities are connected to a common functional network.

方法

Following the PRISMA guidelines, we conducted a comprehensive systematic search of the PubMed, Embase, and Web of Science databases to identify VBM studies on GM alterations in IGE, published up to 5 May 2026.;Studies were included according to the following criteria: (a) published in an English-language peer-reviewed journal as an original article; (b) investigated VBM-based differences in GM density or volume between IGE patients and HCs; and (c) reported whole-brain VBM findings with three-dimensional peak coordinates in Talairach or Montreal Neurological Institute (MNI) space.;Exclusion criteria were as follows: (a) non-original studies (e.g., review, meta-analysis, meeting abstract); (b) no coordinate system reported; (c) only reported regions of interest (ROI) results; (d) all reported coordinates outside the GM mask; (e) studies reporting results based on small-volume correction;

核心结论

After a systematic literature search and screening (), the 18 included studies yielded 18 independent contrasts and 111coordinates, including coordinates reflecting both decreased and increased GM.;Using the HCP normative connectome, FCNM revealed that anatomically heterogeneous GM alterations reported in IGE were associated with a common observed distributed normative connectivity pattern.;The principal nodes of this network were located in the bilateral middle temporal gyri (MTG), bilateral thalami, left superior frontal gyrus (SFG), and right putamen (voxel-wise FDR-corrected p < 0.05; network probability threshold ≥ 60%) (). ‖ 结论:However, because no coordinate-based null-model or permutation analysis was performed, these findings do not establish convergence beyond chance or disease-specific subcortical involvement.

局限

Importantly, because connectivity was derived from healthy participants, the identified network should be interpreted as the normative functional network connected to reported IGE-related GM alteration sites, rather than as direct evidence of abnormal functional connectivity in patients.;Studies using dynamic causal modeling and Granger causality analysis have additionally reported directional abnormalities in effective connectivity within the DMN (, ).;The thalamus is robustly engaged across the three principal seizure types associated with impaired consciousness—complex partial, generalized tonic–clonic, and absence seizures—and exhibits combined structural and functional connectivity abno

对本项目的价值

★☆☆☆☆ 脑老化是最大未满足需求,也是终点最难量化的领域;biomarker 与认知读数选择最敏感。最大样本量约 1,492。

全文来源

PMC JATS 全文(正文 37,363 字符,已过标题/DOI 逐字归属校验)

原文题录

  • 英文标题:Normative functional network localization of gray matter alterations in idiopathic generalized epilepsy.
  • 期刊与标识:Front Neurol · PMID 42959045 · DOI 10.3389/fneur.2026.1957963

A 级证据分级:A 级(同行评议人体研究)

本文属人体研究证据,但需注意:观察性或小样本干预的结论不等于已证实临床获益;效应量与长期安全性仍需更大规模、更长随访的试验验证。

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