Evidence map›Paper›PMID 29235504›Full record

ArticleScientific reports2017

The β-fibrinogen gene 455G/A polymorphism associated with cardioembolic stroke in atrial fibrillation with low CHA

Xiaofeng Hu, Junjun Wang, Yaguo Li, Jiong Wu, Song Qiao, Shanhu Xu, Jun Huang, Linhui Chen

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. The Role of Major Inflammatory Biomarkers in the Pathogenesis of Atrial Fibrillation.The Journal of innovations in cardiac rhythm management · 2022
    Article
  9. Article
  10. Review
  11. Observational
  12. Brain sciences · 2020
    Article
  13. Article
  14. Article
  15. Review
  16. Lack of association betweenNeuropsychiatric disease and treatment · 2019
    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

8 authors at 2 institutions in 1 country.

Xiaofeng HuDepartment of Cardiology, Zhejiang Hospital, Hangzhou, 310013, Zhejiang Province, China.
Junjun WangDepartment of Neurology, Zhejiang Hospital, Hangzhou, 310013, Zhejiang Province, China.
Yaguo LiDepartment of Neurology, Zhejiang Hospital, Hangzhou, 310013, Zhejiang Province, China.
Jiong WuDepartment of Neurology, Zhejiang Hospital, Hangzhou, 310013, Zhejiang Province, China.
Song QiaoDepartment of Neurology, Zhejiang Hospital, Hangzhou, 310013, Zhejiang Province, China.
Shanhu XuDepartment of Neurology, Zhejiang Hospital, Hangzhou, 310013, Zhejiang Province, China.
Jun HuangInstitute of Biostatistics, School of Life Sciences Fudan University, Shanghai, 200082, China.
Linhui ChenDepartment of Neurology, Zhejiang Hospital, Hangzhou, 310013, Zhejiang Province, China. 465189964@qq.com.
Zhejiang Hospital · CNFudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous work has suggested that ischemic stroke (IS) may be more likely to occur in individuals with a genetic predisposition. In this study, we investigated the potential association of IS-relevant genetic risk factors with cardioembolic stroke (CES) in atrial fibrillation (AF) patients with low CHA2DS2-VaSc score. Genotyping was performed using the GenomeLab SNPstream genotyping platform for five IS-relevant SNPs (MMP-9 C1562T, ALOX5AP SG13S114A/T, MTHFR 677 C/T, FGB 455 G/A, and eNOS G298A) in 479 AF patients with CES and 580 age and sex-matched AF patients without CES. The multivariate analysis adjusted for potential confounders and demonstrated that FGB 455 G/A was independently associated with increased risk of CES in AF patients and the significance remained after Bonferroni correction in the additive, dominant, and recessive models with ORs of 1.548 (95% CI: 1.251-1.915, P = 0.001), 1.588 (95% CI: (1.226-2.057, P = 0.003), and 2.394 (95% CI: 1.357-4.223, P = 0.015), respectively. Plasma fibrinogen levels were significantly higher in patients with the A allele compared with patients with genotype of GG (3.29 ± 0.38 mg/dl vs. 2.87 ± 0.18 mg/dl, P < 0.001). We found for the first time that the A allele of FGB 455 G/A was a risk factor for CES in AF patients, probably by elevating the level of plasma fibrinogen.

Indexed as

5-Lipoxygenase-Activating ProteinsAgedAtrial FibrillationBiomarkersCase-Control StudiesCross-Sectional StudiesFemaleFibrinogenGenetic Association StudiesGenetic Predisposition to DiseaseHumansIntracranial EmbolismMaleMatrix Metalloproteinase 9Methylenetetrahydrofolate Reductase (NADPH2)Nitric Oxide Synthase Type III5-Lipoxygenase-Activating ProteinsALOX5AP protein, humanBiomarkersFGB protein, humanFibrinogenMatrix Metalloproteinase 9Methylenetetrahydrofolate Reductase (NADPH2)MMP9 protein, humanMTHFR protein, humanNitric Oxide Synthase Type IIINOS3 protein, human

Identifiers

PMID29235504
PMCPMC5727505
OpenAlexW2772055913

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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.