Evidence map›Paper›PMID 25957909›Full record

ArticleJournal of stroke and cerebrovascular diseases : the official journal of National Stroke Association2015

COX-2 rs20417 Polymorphism Is Associated with Stroke and White Matter Disease.

Jamary Oliveira-Filho, Ana C P Ornellas, Cathy R Zhang, Luciana M B Oliveira, Théo Araújo-Santos, Valeria M Borges, Laís M G B Ventura, Francisco J F B Reis, Roque Aras, André M Fernandes and 4 more

Open access · greenAbstract read
In one paragraph

Article in Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Association between IL-10 gene polymorphisms and the risk of ischemic stroke in a Chinese population.International journal of clinical and experimental pathology · 2015
    Article
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

14 authors at 5 institutions in 2 countries.

Jamary Oliveira-FilhoStroke and Cardiomyopathy Clinics, Federal University of Bahia, Salvador, Brazil; Instituto Nacional de Ciencia e Tecnologia em Doencas Tropicais (INCT-DT), Brazilian National Research Committee (CNPq), Salvador, Brazil. Electronic address: jamary@mail.harvard.edu.
Ana C P OrnellasStroke and Cardiomyopathy Clinics, Federal University of Bahia, Salvador, Brazil; Instituto Nacional de Ciencia e Tecnologia em Doencas Tropicais (INCT-DT), Brazilian National Research Committee (CNPq), Salvador, Brazil.
Cathy R ZhangStroke Division, Massachusetts General Hospital, Boston, USA.
Luciana M B OliveiraStroke and Cardiomyopathy Clinics, Federal University of Bahia, Salvador, Brazil; Instituto Nacional de Ciencia e Tecnologia em Doencas Tropicais (INCT-DT), Brazilian National Research Committee (CNPq), Salvador, Brazil.
Théo Araújo-SantosUniversidade Federal do Oeste da Bahia (UFOB), Barreiras, Brazil.
Valeria M BorgesCentro de Pesquisas Goncalo Moniz, Oswaldo Cruz Foundation-Bahia (CPqGM, FIOCRUZ-BA), Salvador, Brazil.
Laís M G B VenturaStroke and Cardiomyopathy Clinics, Federal University of Bahia, Salvador, Brazil; Instituto Nacional de Ciencia e Tecnologia em Doencas Tropicais (INCT-DT), Brazilian National Research Committee (CNPq), Salvador, Brazil.
Francisco J F B ReisStroke and Cardiomyopathy Clinics, Federal University of Bahia, Salvador, Brazil.
Roque ArasStroke and Cardiomyopathy Clinics, Federal University of Bahia, Salvador, Brazil.
André M FernandesStroke and Cardiomyopathy Clinics, Federal University of Bahia, Salvador, Brazil.
Jonathan RosandStroke Division, Massachusetts General Hospital, Boston, USA.
Steven M GreenbergStroke Division, Massachusetts General Hospital, Boston, USA.
Karen L FurieDepartment of Neurology, Brown University, Providence, USA.
Natalia S RostStroke Division, Massachusetts General Hospital, Boston, USA.
Universidade Federal da Bahia · BRMassachusetts General Hospital · USBrown University · USFundação Oswaldo Cruz · BRUniversidade Federal do Oeste da Bahia · BR

Funding

Sharing canonical human stroke dataR01NS063925 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI WU, ONA · 2009 to 2010
$1.4M
CHADSS: Chagas Disease Scan StudyR01NS064905 · NINDS · FEDERAL UNIVERSITY OF BAHIA · PI FURIE, KAREN L, OLIVEIRA-FILHO, JAMARY · 2011 to 2015
$1.3M
NINDS NIH HHS R01 NS063925NINDS NIH HHS R01NS063925NINDS NIH HHS R01 NS064905
6 · The paper itself

Abstract

backgroundTo investigate the effect of COX-2 polymorphism and its product, prostaglandin E2 (PGE2), on stroke risk in an endemic area for Chagas disease. In a separate cohort, to investigate the effect of COX-2 polymorphisms on the total burden of cerebral white matter disease.

methodsCases were outpatients with ischemic stroke; controls were stroke-free subjects from 2 outpatient clinics (heart failure and caregivers of a movement disorders clinic). We extracted DNA from total blood to investigate the rs20417 COX-2 polymorphism. Serologic tests (Enzime-linked immunosorbent assay) were performed to confirm Trypanosoma cruzi infection and to quantify PGE2 levels. In the Boston cohort, white matter hyperintensity volume (WMHv) was quantified on the admission brain magnetic resonance images of subjects with ischemic stroke, who also donated DNA for the COX-2 gene region analysis.

resultsWe studied 44 patients with stroke and 96 controls (46 with heart failure and 50 caregivers) in the Brazilian cohort; and 788 stroke patients (302 cardioembolic and 486 noncardioembolic) in the Boston cohort. In the Brazilian cohort, rs20417 polymorphism was associated with both stroke (P = 5 × 10(-6)) and decreased PGE2 levels (P = 4 × 10(-5)); similarly, Chagas was associated with stroke (P = 4 × 10(-3)) and decreased PGE2 levels (P = 7 × 10(-3)). In the Boston cohort, rs20417 polymorphism was associated with increased WMHv among noncardioembolic (P = .037), but not among cardioembolic stroke patients.

conclusionsVariation in COX-2 gene is associated with both symptomatic and silent brain cerebrovascular disease. This candidate gene region should be tested in population-based samples.

Indexed as

AgedCaregiversCohort StudiesCyclooxygenase 2DinoprostoneFemaleGenetic Association StudiesGenetic Predisposition to DiseaseGenotypeHumansLeukoencephalopathiesMagnetic Resonance ImagingMaleMiddle AgedPolymorphism, Single NucleotideStrokeCyclooxygenase 2DinoprostonePTGS2 protein, humanAcute cerebral infarctionChagas diseasecyclooxygenasegenetics of strokemagnetic resonance imagingprostaglandin E2

Identifiers

PMID25957909
PMCPMC4532599
OpenAlexW2147901121

What OpenQuestion holds

Textmetadata
LicenceTDM
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.