Evidence map›Paper›PMID 26828698›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2016

Effect of MTHFR Gene Polymorphism Impact on Atherosclerosis via Genome-Wide Methylation.

Xuefeng Lin, Wei Zhang, Qun Lu, Xinjun Lei, Tingzhong Wang, Xuanmao Han, Aiqun Ma

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 24% 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

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

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Review
  6. Genetic Risk Factors of Intracranial Atherosclerosis.Current atherosclerosis reports · 2020
    Review
  7. Review
  8. Genetic and Epigenetic Regulation of Aortic Aneurysms.BioMed research international · 2017
    Review
  9. Review
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

7 authors at 2 institutions in 1 country.

Xuefeng LinDepartment of Cardiovascular Medicine, First Affiliated Hospital of Xi'an Jiaotong University; Key Laboratory of Molecular Cardiology, Shanxi Province; Institute of Cardiovascular Channelopathy; Key Laboratory of Environment & Genes Related to Diseases (Xi'an Jiaotong University), Ministry, Xi'an, Shaanxi, China (mainland).
Wei ZhangDepartment of Cardiovascular Medicine, First Affiliated Hospital of Xi'an Jiaotong University; Key Laboratory of Molecular Cardiology, Shanxi Province; Institute of Cardiovascular Channelopathy; Key Laboratory of Environment & Genes Related to Diseases (Xi'an Jiaotong University), Ministry, Xi'an, Shaanxi, China (mainland).
Qun LuDepartment of Cardiovascular Medicine, First Affiliated Hospital of Xi'an Jiaotong University; Key Laboratory of Molecular Cardiology, Shanxi Province; Institute of Cardiovascular Channelopathy; Key Laboratory of Environment & Genes Related to Diseases (Xi'an Jiaotong University), Ministry, Xi'an, Shaanxi, China (mainland).
Xinjun LeiDepartment of Cardiovascular Medicine, First Affiliated Hospital of Xi'an Jiaotong University; Key Laboratory of Molecular Cardiology, Shanxi Province; Institute of Cardiovascular Channelopathy; Key Laboratory of Environment & Genes Related to Diseases (Xi'an Jiaotong University), Ministry, Xi'an, Shaanxi, China (mainland).
Tingzhong WangDepartment of Cardiovascular Medicine, First Affiliated Hospital of Xi'an Jiaotong University; Key Laboratory of Molecular Cardiology, Shanxi Province; Institute of Cardiovascular Channelopathy; Key Laboratory of Environment & Genes Related to Diseases (Xi'an Jiaotong University), Ministry, Xi'an, Shaanxi, China (mainland).
Xuanmao HanDepartment of Cardiovascular Medicine, First Affiliated Hospital of Baotou Medical College, Baotou, Inner Mongolia, China (mainland).
Aiqun MaDepartment of Cardiovascular Medicine, First Affiliated Hospital of Xi'an Jiaotong University; Key Laboratory of Molecular Cardiology, Shanxi Province; Institute of Cardiovascular Channelopathy; Key Laboratory of Environment & Genes Related to Diseases (Xi'an Jiaotong University), Ministry, Xi'an, Shaanxi, China (mainland).
First Affiliated Hospital of Xi'an Jiaotong University · CNBaotou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAtherosclerosis seriously threats human health. Homocysteine is an independent risk factor closely related to DNA methylation. MTHFR C667T loci polymorphism is closely associated with homocysteine level. This study aimed to investigate the relationship among MTHFR C667T loci polymorphism, genome-wide methylation, and atherosclerosis. MATERIAL/

methodsBlood sample was collected from 105 patients with coronary atherosclerosis and 105 healthy controls. Pyrosequencing methylation was used to detect LINE-1 methylation level. Polymerase chain reaction-restriction enzyme fragment length polymorphism (PCR-RFLP) was used to test MTHFR.

resultsLINE-1 methylation level in the patient group was significantly lower than in the controls (t=5.007, P<0.001). MTHFR C667T genotype distribution presented marked differences in the 2 groups. TT genotype carriers had significantly increased risk of atherosclerosis (OR=3.56, P=0.009). Three different genotypes of MTHFR C667T loci showed different LINE-1 methylation level between the 2 groups (P<0.01). LINE-1 methylation level in TT and CT genotype carriers was obviously lower than in CC genotype carriers (P<0.05).

conclusionsMTHFR C667T loci polymorphism may affect atherosclerosis by regulating genome methylation level.

Indexed as

Genetic Predisposition to DiseaseGenome, HumanAtherosclerosisDNA MethylationElectrophoresis, Agar GelFemaleGenetic LociHumansLinkage DisequilibriumLong Interspersed Nucleotide ElementsMaleMethylenetetrahydrofolate Reductase (NADPH2)Middle AgedPolymorphism, Single NucleotideMethylenetetrahydrofolate Reductase (NADPH2)MTHFR protein, human

Identifiers

PMID26828698
PMCPMC4743680
OpenAlexW2263526750

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.