ABSTRACT NUMBER: ESOC2026LB58 PREDICTION OF ACUTE ISCHEMIC STROKE WITH LARGE VESSEL OCCLUSION WITH 5-HYDROXYMETHYLCYTOSINE BIOMARKERS

Abstract Background and aims Early identification of patients with acute ischemic stroke (AIS), especially AIS with large vessel occlusion (LVO-AIS), can assist with patient triage and implementation of reperfusion therapy. In this study, we investigated the potential of the 5-hydroxymethylcytosine (5hmC) modification of extracellular vesicle deoxyribonucleic acid (evDNA) to distinguish LVO-AIS from healthy controls (HC) and intracranial hemorrhage (ICH). Methods Early identification of patients with acute ischemic stroke (AIS), especially AIS with large vessel occlusion (LVO-AIS), can assist with patient triage and implementation of reperfusion therapy. In this study, we investigated the potential of the 5-hydroxymethylcytosine (5hmC) modification of extracellular vesicle deoxyribonucleic acid (evDNA) to distinguish LVO-AIS from healthy controls (HC) and intracranial hemorrhage (ICH). Results From May 2018 to December 2022, 113 LVO-AIS patients, 48 ICH patients, and 100 HC were enrolled. The prediction model effectively distinguished LVO-AIS patients from healthy controls using 5hmC markers (AUC = 0.975, 95% CI, 0.953-0.996), with a sensitivity of 94.4% and a specificity of 92.5%. Additionally, we found that 5hmC markers showed good performance for distinguishing LVO-AIS not only from healthy control (AUC = 0.913, 95%CI, 0.843-0.983), but from ICH patients (0.909, 95%CI, 0.853-0.965). Conclusions This study suggests that 5hmC markers derived from evDNA may serve as potential epigenetic biomarkers for diagnosing LVO-AIS in non-stroke individuals and, most importantly, hemorrhagic stroke. These findings require further confirmation, given the limited sample size and the wide time window. Conflict of interest Figure 1 - belongs to Methods Figure 2 - belongs to Results

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Journal
European Stroke Journal
Published
2026-05-01
DOI
https://doi.org/10.1093/esj/aakag023.1915
Primary Topic
Acute Ischemic Stroke Management
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article
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article

ABSTRACT NUMBER: ESOC2026LB58 PREDICTION OF ACUTE ISCHEMIC STROKE WITH LARGE VESSEL OCCLUSION WITH 5-HYDROXYMETHYLCYTOSINE BIOMARKERS

Shuang Song, Gaoting Ma, Shengcai Chen, Weizheng Xie et al.
European Stroke Journal
Acute Ischemic Stroke Management
article

ABSTRACT NUMBER: ESOC2026LB58 PREDICTION OF ACUTE ISCHEMIC STROKE WITH LARGE VESSEL OCCLUSION WITH 5-HYDROXYMETHYLCYTOSINE BIOMARKERS

Shuang Song, Gaoting Ma, Shengcai Chen, Weizheng Xie, L Zhang, Yuehua Chen, Jian Lin, Yifan Wu, Dapeng Mo, Junwei Hao, Tong Li
article en

Abstract

Abstract Background and aims Early identification of patients with acute ischemic stroke (AIS), especially AIS with large vessel occlusion (LVO-AIS), can assist with patient triage and implementation of reperfusion therapy. In this study, we investigated the potential of the 5-hydroxymethylcytosine (5hmC) modification of extracellular vesicle deoxyribonucleic acid (evDNA) to distinguish LVO-AIS from healthy controls (HC) and intracranial hemorrhage (ICH). Methods Early identification of patients with acute ischemic stroke (AIS), especially AIS with large vessel occlusion (LVO-AIS), can assist with patient triage and implementation of reperfusion therapy. In this study, we investigated the potential of the 5-hydroxymethylcytosine (5hmC) modification of extracellular vesicle deoxyribonucleic acid (evDNA) to distinguish LVO-AIS from healthy controls (HC) and intracranial hemorrhage (ICH). Results From May 2018 to December 2022, 113 LVO-AIS patients, 48 ICH patients, and 100 HC were enrolled. The prediction model effectively distinguished LVO-AIS patients from healthy controls using 5hmC markers (AUC = 0.975, 95% CI, 0.953-0.996), with a sensitivity of 94.4% and a specificity of 92.5%. Additionally, we found that 5hmC markers showed good performance for distinguishing LVO-AIS not only from healthy control (AUC = 0.913, 95%CI, 0.843-0.983), but from ICH patients (0.909, 95%CI, 0.853-0.965). Conclusions This study suggests that 5hmC markers derived from evDNA may serve as potential epigenetic biomarkers for diagnosing LVO-AIS in non-stroke individuals and, most importantly, hemorrhagic stroke. These findings require further confirmation, given the limited sample size and the wide time window. Conflict of interest Figure 1 - belongs to Methods Figure 2 - belongs to Results

European Stroke JournalVol. 11(Supplement_1)
Capital Medical University (CN), Peking University (CN), Beijing Tian Tan Hospital (CN), The Fifth People's Hospital of Anyang (CN), Beijing National Laboratory for Molecular Sciences (CN), The Second Nanning People's Hospital (CN), Peking University Third Hospital (CN), Huazhong University of Science and Technology (CN)
Good health and well-being
Openalex Percentile: Top 10%
Acute Ischemic Stroke Management
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