The Spatial Divergence of Hypometabolism and Atrophy in Mesial Temporal Lobe Epilepsy: Combining 18F-FDG PET and Structural MRI for Predicting Postoperative Seizure Freedom.

IF 4 2区 医学 Q1 NEUROIMAGING
Yuming Li, Fanglan Li, Danyang Cao, Qiuxing Lin, Peiwen Liu, Wei Li, Yingying Zhang, Xiang Huang, Kailing Huang, Wenhao Li, Xiuli Li, Rang Li, Xiutian Sima, Qiyong Gong, Dong Zhou, Dongmei An
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引用次数: 0

Abstract

Surgical failure in temporal lobe epilepsy with hippocampal sclerosis (TLE-HS) may reflect insufficient disruption of epileptogenic networks. We investigated whether integrating quantitative spatial patterns of regional atrophy and hypometabolism, along with clinical features, could provide complementary prognostic information for postoperative seizure freedom. T1-weighted MRI, 18F-FDG-PET, and postoperative CT scans of patients with TLE-HS were retrospectively analyzed against a validated healthy control cohort to compute age- and gender-adjusted W-score maps. Regional relationships of atrophy and hypometabolism were assessed using bivariate correlations and multiple regression analyses. Machine learning models integrating laterality of seizure onset, preoperative (extra-)temporal atrophy/hypometabolism extent, seizure frequency, focal to bilateral tonic-clonic seizures during the preceding year, and resection volume were developed to predict seizure freedom 1 year after surgery. Model interpretability was assessed via permutation-based variable importance analysis. The cohort comprised 101 patients with TLE-HS (48 left, LHS; 53 right, RHS), including 72 patients who underwent anterior temporal lobectomy. Distinct modality-specific patterns emerged: hypometabolism was significantly greater than local atrophy in left temporo-limbic cortex in TLE-LHS, while atrophy exceeded hypometabolism in bilateral occipital regions in TLE-RHS. Positive correlations between local atrophy and hypometabolism were more robust in ipsilateral temporo-limbic cortex in TLE-LHS. The combined model integrating preoperative atrophy and hypometabolism features (AUC: 0.56-0.64) significantly outperformed single-modality models (pfdr < 0.05). Notably, incorporating clinical factors further enhanced predictive performance (AUC: 0.63-0.70) and model calibration. This comprehensive preoperative clinical-imaging model achieved robust prognostic efficacy that was not significantly improved by the addition of actual postoperative resection volumes. Structural MRI and 18F-FDG-PET reveal complementary facets of the epileptogenic network in TLE-HS. While integrating multimodal imaging with clinical metrics demonstrates significant synergistic potential for predicting surgical outcomes, our models remain exploratory. External validation in independent multi-center cohorts is required before translating these findings into precise clinical tools for surgical planning.

内侧颞叶癫痫低代谢和萎缩的空间散度:结合18F-FDG PET和结构MRI预测术后癫痫发作自由。
颞叶癫痫伴海马硬化(le - hs)的手术失败可能反映了致痫网络的破坏不足。我们研究了整合区域萎缩和低代谢的定量空间模式,以及临床特征,是否可以为术后癫痫发作自由提供补充的预后信息。回顾性分析经验证的健康对照队列的t1加权MRI、18F-FDG-PET和术后CT扫描的TLE-HS患者,以计算年龄和性别调整的w评分图。使用双变量相关和多元回归分析评估萎缩和低代谢的区域关系。机器学习模型整合了癫痫发作的偏侧性、术前颞叶萎缩/低代谢程度、癫痫发作频率、前一年的局灶性到双侧强直阵挛发作以及切除量,以预测手术后1年的癫痫发作自由。通过基于排列的变量重要性分析来评估模型的可解释性。该队列包括101例TLE-HS患者(左48例,左hs;右53例,右hs),其中72例患者接受了前颞叶切除术。出现了明显的模式特异性模式:在le - lhs中,左侧颞-边缘皮层的低代谢显著大于局部萎缩,而在le - rhs中,双侧枕区萎缩超过低代谢。TLE-LHS患者同侧颞边缘皮层局部萎缩与低代谢之间的正相关更为明显。综合术前萎缩和低代谢特征的联合模型(AUC: 0.56-0.64)明显优于单模态模型(pfdr 18F-FDG-PET),揭示了TLE-HS中癫痫发生网络的互补方面。虽然将多模态成像与临床指标相结合显示出预测手术结果的显著协同潜力,但我们的模型仍处于探索性阶段。在将这些发现转化为精确的临床手术计划工具之前,需要在独立的多中心队列中进行外部验证。
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来源期刊
Human Brain Mapping
Human Brain Mapping 医学-核医学
CiteScore
8.30
自引率
6.20%
发文量
401
审稿时长
3-6 weeks
期刊介绍: Human Brain Mapping publishes peer-reviewed basic, clinical, technical, and theoretical research in the interdisciplinary and rapidly expanding field of human brain mapping. The journal features research derived from non-invasive brain imaging modalities used to explore the spatial and temporal organization of the neural systems supporting human behavior. Imaging modalities of interest include positron emission tomography, event-related potentials, electro-and magnetoencephalography, magnetic resonance imaging, and single-photon emission tomography. Brain mapping research in both normal and clinical populations is encouraged. Article formats include Research Articles, Review Articles, Clinical Case Studies, and Technique, as well as Technological Developments, Theoretical Articles, and Synthetic Reviews. Technical advances, such as novel brain imaging methods, analyses for detecting or localizing neural activity, synergistic uses of multiple imaging modalities, and strategies for the design of behavioral paradigms and neural-systems modeling are of particular interest. The journal endorses the propagation of methodological standards and encourages database development in the field of human brain mapping.
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