Evidence map›Paper›PMID 27530126›Full record

Trial reportJournal of thrombosis and thrombolysis2016

An rs13293512 polymorphism in the promoter of let-7 is associated with a reduced risk of ischemic stroke.

Li Zhang, Junsu Yang, Qiang Xue, Dong Yang, Yibing Lu, Xuefeng Guang, Weihua Zhang, Ruiqiong Ba, Hongwen Zhu, Xiang Ma

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Journal of thrombosis and thrombolysis, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Consequences of genetic variants in miRNA genes.Computational and structural biotechnology journal · 2022
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Genetic Variants of RAMP2 and CLR are Associated with Stroke.Journal of atherosclerosis and thrombosis · 2017
    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

10 authors at 1 institution in 1 country.

Li ZhangDepartment of Neurology, The First People's Hospital of Qujing City, Qingjing, 655000, Yunnan, China.
Junsu YangDepartment of Neurology, The First People's Hospital of Qujing City, Qingjing, 655000, Yunnan, China.
Qiang XueDepartment of Cardiology, Yanan Hospital of Kunming, Kunming, 650051, Yunnan, China. xueqiang3513@126.com.
Dong YangDepartment of Cardiology, Yanan Hospital of Kunming, Kunming, 650051, Yunnan, China. yd707@163.com.
Yibing LuDepartment of Cardiology, Yanan Hospital of Kunming, Kunming, 650051, Yunnan, China.
Xuefeng GuangDepartment of Cardiology, Yanan Hospital of Kunming, Kunming, 650051, Yunnan, China.
Weihua ZhangDepartment of Cardiology, Yanan Hospital of Kunming, Kunming, 650051, Yunnan, China.
Ruiqiong BaDepartment of Neurology, The First People's Hospital of Qujing City, Qingjing, 655000, Yunnan, China.
Hongwen ZhuDepartment of Neurology, The First People's Hospital of Qujing City, Qingjing, 655000, Yunnan, China.
Xiang MaDepartment of Neurology, The First People's Hospital of Qujing City, Qingjing, 655000, Yunnan, China.
The First Hospital of Kunming · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The expression of let-7 family members was differentiated in ischemic stroke (IS), functioning as an important regulating molecular in the pathophysiology of stroke. We hypothesized that genetic polymorphism in the promoters of let-7 family may be associated with the risk of IS. To test this hypothesis, we investigated the association of the rs10877887 and rs13293512 in the promoters of let-7 family with the susceptibility to IS. A hospital-based case-control study was performed. The rs10877887 genotype was determined by using a polymerase chain reaction-restriction fragment length polymorphism assay, and the rs13293512 genotype was determined by using a TaqMan assay. We found that the rs13293512CC genotype was associated with a reduced risk of IS (CC vs. TT: adjusted OR = 0.43, 95 % CI 0.26-0.71; dominant model: adjusted OR = 0.70, 95 % CI 0.49-0.98; recessive model: adjusted OR = 0.45, 95 % CI, 0.28-0.73). Stratification analysis showed that the rs10877887TT carriers had a higher level of total cholesterol compared to rs10877887TC/CC carriers (P = 0.03). Combined analysis showed that the rs10877887TC/CC and rs13293512TC/CC genotypes had a reduced risk of IS risk (adjusted OR = 0.58, 95 % CI 0.36-0.95). Our findings suggest that the rs13293512 polymorphism may be a protective factor for the development of IS.

Indexed as

Promoter Regions, GeneticAgedBrain IschemiaCase-Control StudiesCholesterolFemaleHumansMaleMicroRNAsMiddle AgedPolymorphism, GeneticRisk FactorsStrokeCholesterolMicroRNAsmirnlet7 microRNA, humanIschemic strokeLet-7PolymorphismPromoter

Identifiers

PMID27530126
OpenAlexW2513378337

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.