Evidence map›Paper›PMID 28351426›Full record

ArticleJournal of biomedical science2017

Associations of estradiol levels and genetic polymorphisms of inflammatory genes with the risk of ischemic stroke.

Yi-Chen Hsieh, Fang-I Hsieh, Yih-Ru Chen, Chaur-Jong Hu, Jiann-Shing Jeng, Sung-Chun Tang, Nai-Fang Chi, Huey-Juan Lin, Li-Ming Lien, Giia-Sheun Peng and 2 more

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Article in Journal of biomedical science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

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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

12 authors at 5 institutions in 1 country.

Yi-Chen HsiehProgram for Neural Regenerative Medicine, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan. ychsieh@tmu.edu.tw.
Fang-I HsiehSchool of Public Health, College of Public Health, Taipei Medical University, Taipei, Taiwan.
Yih-Ru ChenSchool of Public Health, College of Public Health, Taipei Medical University, Taipei, Taiwan.
Chaur-Jong HuDepartment of Neurology, Taipei Medical University Shuang Ho Hospital, New Taipei City, Taiwan.
Jiann-Shing JengStroke Center and Department of Neurology, National Taiwan University Hospital, Taipei, Taiwan.
Sung-Chun TangStroke Center and Department of Neurology, National Taiwan University Hospital, Taipei, Taiwan.
Nai-Fang ChiDepartment of Neurology, Taipei Medical University Shuang Ho Hospital, New Taipei City, Taiwan.
Huey-Juan LinDepartment of Emergency Medicine, Chi-Mei Medical Center, Tainan, Taiwan.
Li-Ming LienDepartment of Neurology, Shin Kong Wu Ho-Su Memorial Hospital, Taipei, Taiwan.
Giia-Sheun PengDivision of Neurology, Department of Internal Medicine, Taipei Veterans General Hospital, Hsinchu Branch, Hsinchu County, Taiwan.
Hung-Yi ChiouSchool of Public Health, College of Public Health, Taipei Medical University, Taipei, Taiwan. hychiou@tmu.edu.tw.
Formosa Stroke Genetic Consortium (FSGC)
Taipei Medical University · TWNational Taiwan University Hospital · TWTaipei Medical University-Shuang Ho Hospital · TWSouthern Taiwan University of Science and Technology · TWTaipei Veterans General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEstrogen plays an important role as an anti-inflammatory and neuroprotective agent in ischemic stroke. In this study, we analyzed the effect of a polygenic risk score (PRS) constructed using inflammatory genes and estradiol levels on the risk of ischemic stroke.

methodsThis case-control study was conducted with 624 ischemic stroke patients and 624 age- and gender-matched controls. The PRS estimated the polygenic contribution of inflammatory genes from ischemic stroke susceptibility loci. Estradiol levels were measured using a radioimmunoassay. High and low estradiol levels were defined according to the log-transformed median estradiol levels in female and male controls.

resultsSubjects in the fourth quartile of the PRS had a significant 1.57-fold risk of ischemic stroke (95% confidence interval [CI], 1.12 ~ 2.19), after adjusting for covariates compared to individuals in the lowest quartile. Compared to individuals with high estradiol levels and a low PRS as the reference group, those exposed to low estradiol levels and a high PRS had an increased risk of ischemic stroke (odds ratio, 3.35; 95% CI, 1.79 ~ 6.28). Similar results were also observed in males when the analysis was stratified by gender.

conclusionsOur data suggest that the PRS can be useful in evaluating a high risk of ischemic stroke among patients, especially those exposed to low estradiol levels.

Indexed as

Multifactorial InheritancePolymorphism, GeneticAgedBrain IschemiaCase-Control StudiesEstradiolEstrogensFemaleHumansMaleMiddle AgedRisk FactorsStrokeEstradiolEstrogensEstradiolInflammationIschemic strokePolygenic risk score

Identifiers

PMID28351426
PMCPMC5371181
OpenAlexW2602820169

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.