Evidence map›Paper›PMID 29201540›Full record

ArticleBrain and behavior2017

Erythropoietin regulates immune/inflammatory reaction and improves neurological function outcomes in traumatic brain injury.

Zi-Wei Zhou, Fei Li, Zhi-Tong Zheng, Ya-Dan Li, Tong-Heng Chen, Wei-Wei Gao, Jie-Li Chen, Jian-Ning Zhang

Open access · goldAbstract read
In one paragraph

Article in Brain and behavior, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 3 pooled it
3.1field-weighted citation impact, top 8% of its field
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

36 citing papers in PubMed, 3 syntheses or guidelines pooled it, 53 citations in OpenAlex.

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  13. Regulatory T lymphocytes in traumatic brain injury.Neurochemistry international · 2024
    Review
  14. Review
  15. Recombinant Erythropoietin Induces Oligodendrocyte Progenitor Cell Proliferation After Traumatic Brain Injury and Delayed Hypoxemia.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Article
  16. Tackling Neuroinflammation After Traumatic Brain Injury: Complement Inhibition as a Therapy for Secondary Injury.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Review
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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

8 authors at 5 institutions in 3 countries.

Zi-Wei ZhouDepartment of Neurosurgery Tianjin Medical University General Hospital Heping District Tianjin China.ORCID 0000-0002-5927-7835
Fei LiDepartment of Neurosurgery Tianjin Medical University General Hospital Heping District Tianjin China.
Zhi-Tong ZhengDepartment of Neurosurgery Tianjin Medical University General Hospital Heping District Tianjin China.
Ya-Dan LiIntensive Care Units Tianjin Huanhu Hospital Tianjin China.
Tong-Heng ChenDepartment of Neurosurgery The Second Hospital Tianjin Medical University Hexi District Tianjin China.
Wei-Wei GaoDepartment of Neurosurgery Tianjin Medical University General Hospital Heping District Tianjin China.
Jie-Li ChenDepartment of Neurology Henry Ford Hospital Detroit MI USA.
Jian-Ning ZhangDepartment of Neurosurgery Tianjin Medical University General Hospital Heping District Tianjin China.
Ministry of Education of the People's Republic of China · CNTianjin Medical University General Hospital · CNHenry Ford Hospital · USSecond Hospital of Tianjin Medical University · CNTianjin Huanhu Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Traumatic brain injury (TBI) remains a leading cause of disability and death among young people in China. Unfortunately, no specific pharmacological agents to block the progression of secondary brain injury have been approved for clinical treatment. Recently, neuroprotective effects of erythropoietin (EPO) have been demonstrated in addition to its principal function in erythropoiesis, and hence it is viewed as a potential drug for TBI. In this study, we have investigated the neuroprotective effects of EPO associated with immune/inflammatory modulation in a mouse experimental TBI model. Methods: EPO (5000 U/kg body weight, i.p.) was injected at 1 hr, 1, 2, and 3 days after TBI, and its effect on cognitive function, brain edema, immune/inflammatory cells including regulatory T cells (Tregs), neutrophils, CD3 Results: EPO treatment significantly decreased brain edema and improved cognitive function when compared to Saline-treated mice ( Conclusions: These findings suggest that EPO could improve neurological and cognitive functional outcomes as well as regulate immune/inflammatory reaction in TBI.

Indexed as

Brain Injuries, TraumaticAnimalsBrainBrain EdemaCognitionDisease Models, AnimalErythropoietinInflammationInterleukin-1betaMaleMiceNeuroprotective AgentsTreatment OutcomeTumor Necrosis Factor-alphaErythropoietinInterleukin-1betaNeuroprotective AgentsTumor Necrosis Factor-alphaerythropoietinneuroimmuneneuroinflammationregulatory T cell (Treg)traumatic brain injury

Identifiers

PMID29201540
PMCPMC5698857
OpenAlexW2762030602

What OpenQuestion holds

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Registered trials

None linked

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.