Evidence map›Paper›PMID 30181378›Full record

ArticleBioscience reports2018

Investigation of Renalase gene rs2576178 polymorphism in patients with coronary artery disease.

Ning Hu, Jun Wang, Pengfei Hu, Zhongmei Li

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Renalase stimulates aldosterone production via PMCA4b/cAMP in NCI-H295R cells.Journal of enzyme inhibition and medicinal chemistry · 2026
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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

4 authors at 2 institutions in 1 country.

Ning HuDepartment of Cardiology, Ningbo Municipal Hospital of Traditional Chinese Medicine, 819 Guang'an Road, Ningbo, Zhejiang, China.
Jun WangBinjiang Clinic, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
Pengfei HuDepartment of Cardiology, the Second Affiliated Hospital of Zhejiang Chinese Medical University, 318 Chaowang Road, Hangzhou, Zhejiang, China.
Zhongmei LiDepartment of Intensive Care Unit, Ningbo Municipal Hospital of Traditional Chinese Medicine, 819 Guang'an Road, Ningbo, Zhejiang, China lizhongmei1980@163.com.
Ningbo Municipal People's Government · CNZhejiang Chinese Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renalase gene rs2576178 polymorphism has been demonstrated to be a risk factor of ischemic stroke, essential hypertension, and end-stage renal disease, but the association Renalase with risk of coronary artery disease (CAD) has been less reported. Therefore, we detected Renalase rs2576178 polymorphism in 449 CAD patients and 507 healthy controls using matrix-assisted laser-desorption ionization (MALDI)/time of flight (TOF)-mass spectrometry (MS). It was found that GG genotype or G allele of rs2576178 polymorphism was associated with the risk of CAD. Stratified analysis indicated that Renalase polymorphism significantly increased the risk of CAD in females, smokers, and alcoholics. However, there was no significant association between different genotypes of rs2576178 polymorphism and clinical parameters. In summary, Renalase rs2576178 polymorphism is associated with increased risk of CAD, but this finding should be confirmed by larger studies with more diverse ethnic populations.

Indexed as

Genetic Predisposition to DiseaseAllelesAsian PeopleCoronary Artery DiseaseFemaleGenetic Association StudiesGenotypeHumansKidney Failure, ChronicMaleMiddle AgedMonoamine OxidasePolymorphism, Single NucleotideRisk FactorsStrokeMonoamine Oxidaserenalasecoronary heart diseasemolecular epidemiologyRenalasers2576178 polymorphism

Identifiers

PMID30181378
PMCPMC6137248
OpenAlexW2889748519

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.