Evidence map›Paper›PMID 31275446›Full record

ArticleDisease markers2019

The Relationship between Plasma Soluble Receptor for Advanced Glycation End Products and Coronary Artery Disease.

Xiangming Wang, Tingting Xu, Deeraj Mungun, Chuanwei Zhou, Zhimin Zha, Miao Lu, Chuyan Fen, Yan Guo

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 20% 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, 19 citations in OpenAlex.

  1. Review
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  11. AGE-RAGE Stress and Coronary Artery Disease.The International journal of angiology : official publication of the International College of Angiology, Inc · 2021
    Review
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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 1 institution in 1 country.

Xiangming WangDepartment of Geriatric Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.ORCID 0000-0002-3751-3868
Tingting XuDepartment of Geriatric Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Deeraj MungunDepartment of Geriatric Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Chuanwei ZhouDepartment of Geriatric Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Zhimin ZhaDepartment of Geriatric Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Miao LuDepartment of Geriatric Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Chuyan FenDepartment of Geriatric Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Yan GuoDepartment of Geriatric Cardiology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.ORCID 0000-0002-8067-5475
Jiangsu Province Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInflammation is involved in the development and progression of coronary artery disease (CAD). The role of the receptor for advanced glycation end products (RAGE) in the development of CAD has been recognized. The expression of sRAGE and S100A12 in patients with coronary artery disease from different studies was inconsistent. We attempted to determine the expression of sRAGE and S100A12 and their relationship in the subjects with different severity levels of CAD.

methodsA total of 259 patients undergoing coronary angiography were enrolled from the Department of Geriatric Cardiology in the First Affiliated Hospital of Nanjing Medical University from January 2014 to December 2016. Groups were divided as follows: normal coronary artery (control group), nonobstructive coronary atherosclerosis (<50% stenosis in all coronary vessels, NOCA group), stable angina (SAP group), and acute coronary syndrome (ACS group). During CAG or PCI, peripheral arterial blood was collected from all the patients. Plasma sRAGE and S100A12 levels were measured by ELISA. We calculated the SYNTAX score of each patient with CAD according to the result of CAG.

resultsThe levels of sRAGE were significantly elevated in the ACS group compared with those in the control group, the NOCA group, and the SAP group. sRAGE levels were similar among the control group, the NOCA group, and the SAP group. Plasma S100A12 levels were significantly higher in the ACS group than in the control group and the NOCA group. Baseline correlations between plasma levels of sRAGE and plasma S100A12 in the ACS group were significant. Plasma sRAGE concentration was increasing in patients with ACS and was significantly positively correlated with the increasing SYNTAX score. ROC curve analysis revealed that the combination of sRAGE and S100A12 had a good performance in the prediction of high-risk CAD patients.

conclusionThe plasma levels of sRAGE and S100A12 can be increased in patients with ACS. The elevated sRAGE concentration may be independently associated with the severity of CAD and the inflammatory process. sRAGE combined with S100A12 may be used as a predictor of severe coronary heart disease.

Indexed as

AgedAged, 80 and overBiomarkersCoronary Artery DiseaseFemaleHumansMaleMiddle AgedReceptor for Advanced Glycation End ProductsS100A12 ProteinAGER protein, humanBiomarkersReceptor for Advanced Glycation End ProductsS100A12 ProteinS100A12 protein, human

Identifiers

PMID31275446
PMCPMC6589321
OpenAlexW2946948136

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.