Evidence map›Paper›PMID 34239674›Full record

ArticleInternational journal of clinical and experimental pathology2021

Association of single-nucleotide polymorphism on chromosome 9 and ischemic stroke in Heilongjiang province in China.

Ming Jin, Hao Zhang, Qi Zhang, Xueyan Li, Nan Wu, Ying Hu, Changchun Qiu, Ningning Wang, Keyong Zhang

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2021. 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
0.1field-weighted citation impact, top 56% 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 2 institutions in 1 country.

Ming JinInstitute of Polygenic Disease, Qiqihar Medical University Qiqihar, Heilongjiang, China.
Hao ZhangInstitute of Polygenic Disease, Qiqihar Medical University Qiqihar, Heilongjiang, China.
Qi ZhangInstitute of Polygenic Disease, Qiqihar Medical University Qiqihar, Heilongjiang, China.
Xueyan LiInstitute of Polygenic Disease, Qiqihar Medical University Qiqihar, Heilongjiang, China.
Nan WuInstitute of Polygenic Disease, Qiqihar Medical University Qiqihar, Heilongjiang, China.
Ying HuInstitute of Polygenic Disease, Qiqihar Medical University Qiqihar, Heilongjiang, China.
Changchun QiuInstitute of Polygenic Disease, Qiqihar Medical University Qiqihar, Heilongjiang, China.
Ningning WangInstitute of Polygenic Disease, Qiqihar Medical University Qiqihar, Heilongjiang, China.
Keyong ZhangInstitute of Polygenic Disease, Qiqihar Medical University Qiqihar, Heilongjiang, China.
Qiqihar Medical University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a significant correlation between ischemic stroke (IS) and chromosome 9. However, its status was uncertain in China's cold regions. 1920 IS patients, and 1920 healthy individuals were included in the study. Blood samples were collected. The association of SNPs with IS was evaluated by Sequenom, and logistic regression models adjusted for known risk factors of IS were constructed to assess the SNPs' associations in cases and controls. We found rs1333040 and rs2383207 were associated with IS, compared with primitive genotypes. The genotype CT of rs7027526 has a protective role during IS development, while the effect of the genotype TT is still not clear. These results changed after stratification by age and sex. In conclusion, rs1333040 and rs2383207 SNPs in CDKN2BAS are associated with ischemic stroke in the Chinese Han population. This study confirms the association between 9p21.3 and IS.

Indexed as

associationCDKN2B-AS1ChineseFRMD3Ischemic stroke

Identifiers

PMID34239674
PMCPMC8255203
OpenAlexW3182312608

What OpenQuestion holds

Textmetadata
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.