Evidence map›Paper›PMID 29936663›Full record

ArticleJournal of molecular neuroscience : MN2018

Associations of TF Gene Polymorphisms with the Risk of Ischemic Stroke.

Yi Cai, Shaofang Wu, Chaosheng Zeng, Qingjie Su, Jingxia Zhou, Pengxiang Li, Mingming Dai, Desheng Wang, Faqing Long

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular neuroscience : MN, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 93% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

9 authors at 1 institution in 1 country.

Yi CaiDepartment of Neurology, The Second Affiliated Hospital of Hainan Medical University, #48 Baishuitang Road, Xiuying District, Haikou, 570311, Hainan, China.
Shaofang WuDepartment of Breath Internal Medicine, The Second Affiliated Hospital of Hainan Medical University, Haikou, 570311, Hainan, China.
Chaosheng ZengDepartment of Neurology, The Second Affiliated Hospital of Hainan Medical University, #48 Baishuitang Road, Xiuying District, Haikou, 570311, Hainan, China.
Qingjie SuDepartment of Neurology, The Second Affiliated Hospital of Hainan Medical University, #48 Baishuitang Road, Xiuying District, Haikou, 570311, Hainan, China.
Jingxia ZhouDepartment of Neurology, The Second Affiliated Hospital of Hainan Medical University, #48 Baishuitang Road, Xiuying District, Haikou, 570311, Hainan, China.
Pengxiang LiDepartment of Neurology, The Second Affiliated Hospital of Hainan Medical University, #48 Baishuitang Road, Xiuying District, Haikou, 570311, Hainan, China.
Mingming DaiDepartment of Neurology, The Second Affiliated Hospital of Hainan Medical University, #48 Baishuitang Road, Xiuying District, Haikou, 570311, Hainan, China.
Desheng WangDepartment of Neurology, The Second Affiliated Hospital of Hainan Medical University, #48 Baishuitang Road, Xiuying District, Haikou, 570311, Hainan, China.
Faqing LongDepartment of Neurology, The Second Affiliated Hospital of Hainan Medical University, #48 Baishuitang Road, Xiuying District, Haikou, 570311, Hainan, China. qingfalong@sina.com.ORCID http://orcid.org/0000-0001-8617-0331
Hainan Medical University · CN

Funding

Natural Science Foundation of Hainan Province 817334
6 · The paper itself

Abstract

Ischemic stroke (IS) is the main cause of mortality and disability in China; thus, this study aimed to examine the association between six variants and their haplotypes within the transferrin (TF) gene and the risk of IS in the Southern Chinese Han population. Genotyping was performed using the Sequenom MassARRAY platform for 249 IS patients and 249 age- and sex-matched controls. The association between polymorphisms and IS risk was tested by Chi squared test and haplotype and stratification analysis. Odds ratios (ORs) and confidence intervals (CIs) were estimated by unconditional logistic regression analysis. The results of genetic model analyses indicated that the two SNPs (rs1880669 and rs2692695) were associated with decreased IS risk under the co-dominant, dominant, and additive models. Additionally, rs4525863 was also associated with decreased IS risk both under the dominant and additive models in males. Moreover, the CG haplotype of TF (rs1880669 and rs2692695) was significantly associated with a decreased risk of IS in the total population and males. Our findings suggested that polymorphisms (rs4525863, rs1880669, and rs2692695) of the TF gene might be a protective factor for IS in Southern Chinese Han population. Further large prospective studies are required to confirm these findings.

Indexed as

Polymorphism, Single NucleotideAgedBrain IschemiaCase-Control StudiesChinaFemaleHumansMaleMiddle AgedStrokeTransferrinTransferrinIschemic strokePolymorphismsSouthern Chinese Han populationTF

Identifiers

PMID29936663
OpenAlexW2810763469

What OpenQuestion holds

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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.