Evidence map›Paper›PMID 24724095›Full record

ReviewBioMed research international2014

Therapeutic implications of estrogen for cerebral vasospasm and delayed cerebral ischemia induced by aneurysmal subarachnoid hemorrhage.

Dale Ding, Robert M Starke, Aaron S Dumont, Gary K Owens, David M Hasan, Nohra Chalouhi, Ricky Medel, Chih-Lung Lin

Open access · hybridAbstract readReview
In one paragraph

Review in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 4% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

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  16. Neuroglobin, a Factor Playing for Nerve Cell Survival.International journal of molecular sciences · 2016
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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 2 countries.

Dale DingDepartment of Neurosurgery, University of Virginia, Charlottesville, VA 22908, USA.ORCID 0000-0002-2627-446X
Robert M StarkeDepartment of Neurosurgery, University of Virginia, Charlottesville, VA 22908, USA.
Aaron S DumontDepartment of Neurosurgery, Tulane University, New Orleans, LA 70112, USA.
Gary K OwensDepartment of Molecular Physiology and Biophysics, Robert M. Berne Cardiovascular Research Center, University of Virginia, Charlottesville, VA 22908, USA.
David M HasanDepartment of Neurosurgery, University of Iowa, Iowa City, IA 52242, USA.
Nohra ChalouhiDepartment of Neurological Surgery, Thomas Jefferson University, Philadelphia, PA 19106, USA.ORCID 0000-0002-2422-4346
Ricky MedelDepartment of Neurosurgery, Tulane University, New Orleans, LA 70112, USA.ORCID 0000-0003-3188-7823
Chih-Lung LinDepartment of Neurosurgery, Kaohsiung Medical University Hospital, No. 100, Tzyou 1st Road, Kaohsiung, Taiwan ; Faculty of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan.ORCID 0000-0002-6716-2771
University of Virginia · USTulane University · USKaohsiung Medical University · TWThomas Jefferson University · USUniversity of Iowa · US

Funding

Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Jay William FOX · 1987 to 2026
$72.1M
Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Jong Sung Kim · 1990 to 2026
$40.5M
TNF-a and vascular smooth muscle cell phenotypic modulation in cerebral aneurysmsK08NS067072 · NINDS · UNIVERSITY OF VIRGINIA · PI DUMONT, AARON S · 2009 to 2013
$886k
NCI NIH HHS P30 CA044579NIEHS NIH HHS P30 ES005605NINDS NIH HHS 1K08NS067072NINDS NIH HHS K08 NS067072
6 · The paper itself

Abstract

Cerebral vasospasm (CV) remains the leading cause of delayed morbidity and mortality following aneurysmal subarachnoid hemorrhage (SAH). However, increasing evidence supports etiologies of delayed cerebral ischemia (DCI) other than CV. Estrogen, specifically 17 β -estradiol (E2), has potential therapeutic implications for ameliorating the delayed neurological deterioration which follows aneurysmal SAH. We review the causes of CV and DCI and examine the evidence for E2-mediated vasodilation and neuroprotection. E2 potentiates vasodilation by activating endothelial nitric oxide synthase (eNOS), preventing increased inducible NOS (iNOS) activity caused by SAH, and decreasing endothelin-1 production. E2 provides neuroprotection by increasing thioredoxin expression, decreasing c-Jun N-terminal kinase activity, increasing neuroglobin levels, preventing SAH-induced suppression of the Akt signaling pathway, and upregulating the expression of adenosine A2a receptor. The net effect of E2 modulation of these various effectors is the promotion of neuronal survival, inhibition of apoptosis, and decreased oxidative damage and inflammation. E2 is a potentially potent therapeutic tool for improving outcomes related to post-SAH CV and DCI. However, clinical evidence supporting its benefits remains lacking. Given the promising preclinical data available, further studies utilizing E2 for the treatment of patients with ruptured intracranial aneurysms appear warranted.

Indexed as

AnimalsBrain IschemiaEstradiolEstrogensHumansNerve Tissue ProteinsNeuroprotective AgentsSubarachnoid HemorrhageVasodilationVasospasm, IntracranialEstradiolEstrogensNerve Tissue ProteinsNeuroprotective Agents

Identifiers

PMID24724095
PMCPMC3958795
OpenAlexW2078543429

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.