Evidence map›Paper›PMID 28444966›Full record

ArticleClinical cardiology2017

Correlation between genetic polymorphisms within the MAPK1/HIF-1/HO-1 signaling pathway and risk or prognosis of perimenopausal coronary artery disease.

Nan Guo, Nan Zhang, Liqiu Yan, Xufen Cao, Jiawang Wang, Yunfei Wang

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cardiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 27% 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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 17 citations in OpenAlex.

  1. Pooled it
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  5. Review
  6. The Modulation of Nrf-2/HO-1 Signaling Axis byPlants (Basel, Switzerland) · 2021
    Article
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  9. Aging · 2019
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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

6 authors at 1 institution in 1 country.

Nan GuoDepartment of Cardiology, Cangzhou Central Hospital, Hebei Medical University, Cangzhou, P. R. China.
Nan ZhangDepartment of Cardiothoracic Surgery, Cangzhou Central Hospital, Hebei Medical University, Cangzhou, P. R. China.ORCID http://orcid.org/0000-0002-4713-0908
Liqiu YanDepartment of Cardiology, Cangzhou Central Hospital, Hebei Medical University, Cangzhou, P. R. China.
Xufen CaoDepartment of Cardiology, Cangzhou Central Hospital, Hebei Medical University, Cangzhou, P. R. China.
Jiawang WangDepartment of Cardiology, Cangzhou Central Hospital, Hebei Medical University, Cangzhou, P. R. China.
Yunfei WangDepartment of Cardiology, Cangzhou Central Hospital, Hebei Medical University, Cangzhou, P. R. China.
Hebei Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMitogen-activated protein kinase-1 (MAPK1), as well as its downstream factors of hypoxia-inducible factor-1 (HIF-1) and heme oxygenase-1 (HO-1), have been documented to be involved in modulating development of coronary artery disease (CAD). HYPOTHESIS: Genetic mutations within the MAPK1/HIF-1/HO-1 signaling pathway could alter the risk of perimenopausal CAD in Chinese patients.

methodsPeripheral blood samples were gathered from 589 CAD patients and 860 healthy controls, and 12 potential single-nucleotide polymorphisms (SNPs) were obtained from HapMap database and previously published studies. Genotyping of SNPs was implemented with the TaqMan SNP Genotyping Assays. Odds ratios (OR) and 95% confidence intervals (CI) were utilized to evaluate the correlations between SNPs and CAD risk.

resultsRegarding MAPK1 , rs6928 (OR: 1.71, 95% CI: 1.47-1.98, P < 0.05), rs9340 (OR: 0.85, 95% CI: 0.73-0.99, P < 0.05), and rs11913721 (OR: 0.70, 95% CI: 0.52-0.95, P < 0.05) were remarkably associated with susceptibility to perimenopausal CAD. Of these, rs9340 and rs11913721 were also regarded as protective factors for perimenopausal CAD patients. Moreover, results of HIF-1 indicated noticeable correlations between combined SNPs of rs1087314 and rs2057482 and risk of perimenopausal CAD (OR: 1.24, 95% CI: 1.01-1.53, P < 0.05; and OR: 0.71, 95% CI: 0.55-0.91, P < 0.05, respectively). Nonetheless, rs2071746 in HO-1 was found to be only associated with perimenopausal CAD risk (OR: 0.67, 95% CI: 0.58-0.78, P < 0.05).

conclusionsThe genetic mutations within MAPK1 (rs6928, rs9340, rs11913721), HIF-1 (rs1087314, rs2057482), and HO-1 (rs2071746) could alter susceptibility to perimenopausal CAD in this Chinese population.

Indexed as

PerimenopausePolymorphism, Single NucleotideChinaChi-Square DistributionCoronary AngiographyCoronary Artery DiseaseCoronary StenosisFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseHeme Oxygenase-1HumansHypoxia-Inducible Factor 1Mitogen-Activated Protein Kinase 1Odds RatioHeme Oxygenase-1HMOX1 protein, humanHypoxia-Inducible Factor 1MAPK1 protein, humanMitogen-Activated Protein Kinase 1Gene-Gene InteractionMAPK1/HIF-1/HO-1 SignalingPerimenopausal CADSingle-Nucleotide PolymorphismSusceptibility

Identifiers

PMID28444966
PMCPMC6490459
OpenAlexW2610135500

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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.