Evidence map›Paper›PMID 23773531›Full record

ArticleCNS neuroscience & therapeutics2013

An association study on ADAM10 promoter polymorphisms and atherosclerotic cerebral infarction in a Chinese population.

You Li, Feng Liao, Xiao-Jian Yin, Li-Li Cui, Guo-Da Ma, Xiao-Xian Nong, Hai-Hong Zhou, Yan-Fang Chen, Bin Zhao, Ke-Shen Li

Open access · hybridAbstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.8field-weighted citation impact, top 18% 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

22 citing papers in PubMed, 33 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Genetic Variants ofBioMed research international · 2021
    Article
  11. Article
  12. Genetic variants ofAging · 2019
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Regulation of Alpha-Secretase ADAM10Frontiers in molecular neuroscience · 2017
    Review
  18. Changes of peripheral blood Vδ1 T cells in patients with atherosclerotic cerebral infarction.International journal of clinical and experimental pathology · 2017
    Article
  19. Review
  20. 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 2 institutions in 2 countries.

You LiGuangdong Key Laboratory of Age-Related Cardiac and Cerebral Diseases, Affiliated Hospital of Guangdong Medical College, Zhanjiang, China.
Feng Liao
Xiao-Jian Yin
Li-Li Cui
Guo-Da Ma
Xiao-Xian Nong
Hai-Hong Zhou
Yan-Fang Chen
Bin Zhao
Ke-Shen Li
Guangdong Medical College · CNAffiliated Hospital of Guangdong Medical College Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimDysregulation of the activity of the disintegrin/metalloproteinase ADAM10 could contribute to the development of atherosclerosis. Although a number of genetic studies have focused on the association of ADAM10 gene polymorphisms with susceptibility to diseases, no genetic association studies of ADAM10 gene variability with atherosclerotic cerebral infarction (ACI) have been conducted. The aim of this study was to analyze the potential association between ADAM10 promoter polymorphisms and ACI.

methodsThe associations between rs653765 and rs514049 polymorphisms of the ADAM10 promoter and the possible risk of ACI were assessed among 347 patients with ACI and 299 matched healthy individuals in a case-control study.

resultsOverall, there was a significant difference in the genotypes frequencies of rs653765 (P = 0.04) between the ACI and control subjects. In addition, the rs653765 mutated allele of ADAM10 was significantly associated with increased ADAM10 expression in patients with ACI (P = 0.032). In contrast, the allele frequency of rs514049 was not statistically associated with ACI, and the rs514049 variant A > C did not affect the expression of ADAM10 either.

conclusionOur findings indicate a positive association between the rs653765 polymorphism of ADAM10 and ACI, as well as a negative result for rs514049. In addition, a significant increase in ADAM10 expression was observed in patients with ACI carrying the rs653765 C > T mutation. This new knowledge about ADAM10 might be clinically important and confirm a role for ADAM10 in the pathophysiology of ACI, with potentially important therapeutic implications.

Indexed as

ADAM10 ProteinADAM ProteinsAgedAged, 80 and overAmyloid Precursor Protein SecretasesAsian PeopleAtherosclerosisCase-Control StudiesCerebral InfarctionFemaleGenetic Association StudiesHumansMaleMembrane ProteinsMiddle AgedPromoter Regions, GeneticADAM10 ProteinADAM10 protein, humanADAM ProteinsAmyloid Precursor Protein SecretasesMembrane ProteinsADAM10Atherosclerotic cerebral infarctionPolymorphism

Identifiers

PMID23773531
PMCPMC4233972
OpenAlexW1982469029

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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.