Evidence map›Paper›PMID 26648969›Full record

ArticleCerebrovascular diseases extra

The CXCR2 Gene Polymorphism Is Associated with Stroke in Patients with Essential Hypertension.

Yanina R Timasheva, Timur R Nasibullin, Olga E Mustafina

Open access · goldAbstract read
In one paragraph

Article in Cerebrovascular diseases extra. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Association between polymorphisms in CXCR2 gene and preeclampsia.Molecular genetics & genomic medicine · 2019
    Article
  7. Article
  8. Article
  9. 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

3 authors at 1 institution in 1 country.

Yanina R TimashevaInstitute of Biochemistry and Genetics, USC RAS, Ufa, Russia.
Timur R NasibullinInstitute of Biochemistry and Genetics, USC RAS, Ufa, Russia.
Olga E MustafinaInstitute of Biochemistry and Genetics, USC RAS, Ufa, Russia.
Institute of Biochemistry and Genetics of Ufa Scientific Centre · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypertension is the major risk factor for stroke, and genetic factors contribute to its development. Inflammation has been hypothesized to be the key link between blood pressure elevation and stroke. We performed an analysis of the association between inflammatory mediator gene polymorphisms and the incidence of stroke in patients with essential hypertension (EH). The study group consisted of 625 individuals (296 patients with noncomplicated EH, 71 hypertensive patients with ischemic stroke, and 258 control subjects). Both patients and controls were ethnic Tatars originating from the Republic of Bashkortostan (Russian Federation). The analysis has shown that the risk of ischemic stroke was associated with the CXCR2 rs1126579 polymorphism. Our results indicate that among patients with EH, the heterozygous genotype carriers had a higher risk of stroke (OR = 1.72, 95% CI 1.01-2.92), whereas the CXCR2*C/C genotype was protective against stroke (OR = 0.32, 95% CI 0.12-0.83). As shown by the gene-gene interaction analysis, the CXCR2 rs1126579 polymorphism was also present in all genotype/allele combinations associated with the risk of stroke. Genetic patterns associated with stroke also included polymorphisms in the CCL2, CCL18, CX3CR1, CCR5, and CXCL8 (IL8) genes, although no association between these loci and stroke was detected by individual analysis.

Indexed as

AdultAllelesAsian PeopleBashkiriaChemokinesEssential HypertensionGenotypeHumansHypertensionIncidenceInterleukin-8MaleMiddle AgedPolymorphism, GeneticReceptors, Interleukin-8BRisk FactorsChemokinesInterleukin-8Receptors, Interleukin-8BChemokinesCXCR2Essential hypertensionIschemic stroke

Identifiers

PMID26648969
PMCPMC4662298
OpenAlexW2221247037

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.