てんかん発症に重要なキーとなる出血性病変の重要性

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2026-01-07 国立循環器病研究センター

国立循環器病研究センター(国循)の田中智貴医長、猪原匡史副院長らは、マサチューセッツ総合病院および香港大学との国際共同研究により、脳梗塞後てんかん(PSE)発症において出血性病変が重要な鍵となることを明らかにし、新たな予測モデルIsCHEMiAスコアを開発した。日本・米国・香港の計約4,000例の初回脳梗塞症例を解析した結果、梗塞サイズ5cm以上、出血性変化、早期発作、中大脳動脈領域病変、皮質病変、65歳未満の6因子がPSEリスクに強く関与することが判明した。本スコアは、既存のSeLECT/SeLECT2スコアを上回る高い予測精度を示し、国際的外的検証にも成功した。出血性病変による皮質過興奮性の関与が示唆され、PSE高リスク患者の早期同定や将来の予防的治療戦略の基盤となる成果である。研究成果は米国神経学会誌Neurologyに掲載された。


図1:他の既存のスコア(SeLECTスコア/SeLECT2スコア)との正確性の比較
AUC:Area under the curve、統計学的にモデルの正確性を示す指標。1が最高値、0が最低値
出典:本論文を改変

<関連情報>

脳卒中後てんかんの予測のための新しい画像ベースのリスクスコア(IsCHEMiA)の開発と国際的検証 Development and International Validation of a Novel Imaging-Based Risk Score (IsCHEMiA) for the Prediction of Poststroke Epilepsy

William C.Y. Leung, Tomotaka Tanaka, Rachel A. Donahue, Kandace Chi Wing Chan , Jianing Wang, Tommy Ho Fung Chung, Yuen Kwun Wong, …, and Aneesh B. Singhal
Neurology  Published:January 5, 2026
DOI:https://doi.org/10.1212/WNL.0000000000214486

Abstract

Background and Objectives

Stroke is one of the most common causes of adult-onset epilepsy. We aimed to develop a model to predict poststroke epilepsy (PSE) after a first-ever ischemic stroke, incorporating neuroimaging features of incident stroke.

Methods

We analyzed clinical and neuroimaging features of patients with first-ever acute ischemic stroke consecutively admitted to Massachusetts General Hospital, United States. We performed competing risk regression with all-cause mortality as a competing event and derived the final multivariable model using backward stepwise elimination by the Akaike Information Criterion. We externally validated the model in 3 international cohorts in Hong Kong (Queen Mary Hospital [HK-QMH], Ruttonjee Hospital [HK-RH]) and Japan (National Cerebral and Cardiovascular Center) by discrimination and calibration and compared its performance with the SeLECT and SeLECT2.0 scores.

Results

We included a final derivative cohort of 1,436 patients with a mean age of 67.4 years and a slight male predominance (54.7%), along with a total of 2,534 patients in the validation cohorts. PSE, defined as the occurrence or recurrence of unprovoked seizure >7 days after stroke, occurred in 5.5% of the overall study population. Six variables (infarct size [Is], cortical involvement [C], hemorrhagic transformation [H], early seizures [E], MCA involvement [Mi], and age younger than 65 [A]) were independent predictors included in the final model and formed the IsCHEMiA score. Model discrimination was consistent across all cohorts, with c-statistics of 0.870 (United States), 0.852 (HK-QMH), 0.857 (HK-RH), and 0.826 (Japan). The model was well calibrated at 1 and 3 years after stroke in the overall validation cohort. The IsCHEMiA score improved the prediction of PSE compared with SeLECT in all cohorts and the overall study population (c-statistic 0.848 vs 0.782, z = 5.170, p < 0.0001). For example, an IsCHEMiA score of 3 predicts a low risk of PSE at 1 year (2%) and 5 years (6%) while an IsCHEMiA score ≥8 predicts a high risk at 1 year (67%) and 5 years (78%).

Discussion

The IsCHEMiA score is an improved and readily applicable predictive model developed and validated using international stroke cohorts in the modern era of reperfusion therapies. It serves as a foundation for personalized management and may guide future clinical trials on antiepileptogenic therapies in acute ischemic stroke.

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