Evidence map›Paper›PMID 32150081›Full record

ArticleMedicine2020

Association of polymorphisms of preptin, irisin and adropin genes with susceptibility to coronary artery disease and hypertension.

Haidong Wang, Xiaojing Wang, Yuan Cao, Wenxiu Han, Yujin Guo, Guangsheng Yang, Jun Zhang, Pei Jiang

Open access · goldAbstract read
In one paragraph

Article in Medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 31% 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

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

  1. Pooled it
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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

8 authors at 5 institutions in 1 country.

Haidong WangPhase I Clinical Trial Centre, The Affiliated Lianyungang Hospital of Xuzhou Medical University/The First People's Hospital of Lianyungang.
Xiaojing WangAffiliated Jining First People's Hospital of Jining Medical University, Jining Medical University.
Yuan CaoPediatric surgery, The Affiliated Lianyungang Hospital of Xuzhou Medical, University/The First People's Hospital of Lianyungang.
Wenxiu HanAffiliated Jining First People's Hospital of Jining Medical University, Jining Medical University.
Yujin GuoAffiliated Jining First People's Hospital of Jining Medical University, Jining Medical University.
Guangsheng YangPhase I Clinical Trial Centre, The Affiliated Lianyungang Hospital of Xuzhou Medical University/The First People's Hospital of Lianyungang.
Jun ZhangDepartment of Pharmacy, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Pei JiangAffiliated Jining First People's Hospital of Jining Medical University, Jining Medical University.
Affiliated Hospital of Jining Medical University · CNXuzhou Medical College · CNFirst Affiliated Hospital of Zhengzhou University · CNJining First People's Hospital · CNThe First People’s Hospital of Lianyungang · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesPreptin, irisin and adropin are 3 new players in energy regulation that are related body mass index, lipids, glucose and insulin levels which may affect incidence of cardiovascular diseases. The aim of the present study was to evaluate eight single nucleotide polymorphisms (SNPs) of preptin genes (rs1003483, rs1004446, rs2239681, rs680, and rs3741204), irisin (rs16835198 and rs3480) and adropin (rs2281997) gene in patients with coronary artery disease (CAD) and hypertension.

methodsThis case-control study was carried out on 372 volunteers, which were divided into 3 subgroups including: CAD patients with hypertension (CAD+H+), CAD patients with no hypertension (CAD+H-), and non-hypertensive non-CAD subjects as control group (CAD-H-) as health control. Genomic DNA from whole blood was extracted and eight SNPs were assessed using polymerase chain reaction- ligase detection reaction method.

resultsA significant difference was found in the genotype and allele frequency of preptin rs1003483 gene in CAD+H+ compared to CAD+H- groups (P = .019 and P = .018, respectively). Allele frequency of rs1003483 was significantly different between CAD+H- groups and healthy control groups (P = .043). There also existed a significant difference the genotype frequency of rs1004446 gene in CAD+H+ compared to CAD+H- groups (P = .027).

conclusionsThe findings of present study revealed that the preptin rs1003483 and rs1004446 gene polymorphism might serve as predisposing factor in CAD and hypertension.

Indexed as

AdultCase-Control StudiesChinaCoronary Artery DiseaseFemaleFibronectinsHumansHypertensionInsulin-Like Growth Factor IIIntercellular Signaling Peptides and ProteinsMaleMiddle AgedPeptide FragmentsPolymorphism, GeneticRisk FactorsEnho protein, humanFibronectinsFNDC5 protein, humanInsulin-Like Growth Factor IIIntercellular Signaling Peptides and ProteinsPeptide Fragmentspreptin

Identifiers

PMID32150081
PMCPMC7478509
OpenAlexW3011720984

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Registered trials

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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.