Evidence map›Paper›PMID 42179266›Full record

ArticleJournal of the American Heart Association2026

Neutrophil Extracellular Traps Are Associated With Early Neurological Deterioration in Patients With Acute Ischemic Stroke Receiving Intravenous Thrombolysis: A Prospective Cohort Study.

Lulu Pei, Wan Zhang, Ding Zhang, Zhaoyang Zhao, Yifang Zhou, Ce Zong, Jiaxin Wang, Zixin Chen, Hanbing Zhao, Yiwei Qian and 12 more

Abstract read
In one paragraph

Article in Journal of the American Heart Association, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors.

Lulu Pei *Department of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China.
Wan Zhang *Department of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China.
Ding ZhangDepartment of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China.
Zhaoyang ZhaoDepartment of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China.
Yifang ZhouDepartment of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China.
Ce ZongDepartment of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China.
Jiaxin WangDepartment of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China.
Zixin ChenDepartment of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China.
Hanbing ZhaoDepartment of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China.
Yiwei QianDepartment of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China.
Mengke TianDepartment of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China.ORCID 0000-0002-3055-7411
Xinjing LiuDepartment of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China.ORCID 0000-0002-6694-3138
Hui FangDepartment of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China.ORCID 0000-0003-4308-3793
Wenzheng RongDepartment of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China.
Kai LiuDepartment of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China.ORCID 0000-0003-3698-2707
Yapeng LiDepartment of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China.ORCID 0000-0003-3412-0652
Xiaohan XuDepartment of Clinical Sciences Liverpool School of Tropical Medicine Liverpool UK.ORCID 0000-0003-0950-9615
Xinyi LengDepartment of Medicine and Therapeutics The Chinese University of Hong Kong China.ORCID 0000-0001-7300-6647
Ming-Ming NingClinical Proteomics Research Center and Cardio-Neurology Clinic, Department of Neurology, Massachusetts General Hospital Harvard Medical School Boston MA USA.
Duolao WangDepartment of Clinical Sciences Liverpool School of Tropical Medicine Liverpool UK.ORCID 0000-0003-2788-2464
Yuming XuDepartment of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China.ORCID 0000-0003-2689-9897
Bo SongDepartment of Neurology The First Affiliated Hospital of Zhengzhou University Zhengzhou China.ORCID 0000-0002-4563-0781

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeutrophil extracellular traps contribute to thrombolytic resistance and the no-reflow phenomenon after acute ischemic stroke, thereby impairing microvascular reperfusion and leading to unfavorable clinical outcomes. This study investigated the association between prethrombolytic circulating neutrophil extracellular trap biomarkers, CitH3 (citrullinated histone 3) and MPO (myeloperoxidase)-DNA complexes, and early neurological deterioration (END) in patients with acute ischemic stroke treated with intravenous thrombolysis alone.

methodsWe prospectively enrolled patients with acute ischemic stroke who received standard-dose alteplase within 4.5 hours of symptom onset (January 2019-April 2023). Venous blood was drawn before intravenous thrombolysis to measure serum CitH3 and MPO-DNA. The primary outcome was END, defined as an increase of ≥4 points in NIHSS score at 24 hours versus baseline. Logistic regression with restricted cubic splines assessed associations between neutrophil extracellular trap biomarkers and END.

resultsAmong 287 patients (mean age 61.69±12.41 years, 70.4% male), 45 (15.7%) developed END. Serum CitH3 >17.67 ng/mL (odds ratio [OR], 3.81 [95% CI, 1.75-8.29]) and MPO-DNA >79.72 ng/mL (OR, 5.58 [95% CI, 2.36-13.21]) were independently associated with END. The associations remained significant when treated as continuous variables. Restricted cubic splines confirmed a linear dose-response relationship between higher CitH3 levels and END risk (

conclusionsSerum neutrophil extracellular traps may serve as promising biomarkers associated with END after intravenous thrombolysis in patients with acute ischemic stroke.

Indexed as

Brain IschemiaExtracellular TrapsFibrinolytic AgentsIschemic StrokeThrombolytic TherapyTissue Plasminogen ActivatorAgedBiomarkersFemaleHistonesHumansMaleMiddle AgedNeutrophilsPeroxidaseProspective StudiesBiomarkersFibrinolytic AgentsHistonesMPO protein, humanPeroxidaseTissue Plasminogen Activatoracute ischemic strokebiomarkerearly neurological deteriorationintravenous thrombolysisneutrophil extracellular traps

Identifiers

PMID42179266
PMCPMC13315136

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.