Evidence map›Paper›PMID 27300745›Full record

Trial reportGlycoconjugate journal2016

Correlation among soluble receptors for advanced glycation end-products, soluble vascular adhesion protein-1/semicarbazide-sensitive amine oxidase (sVAP-1) and cardiometabolic risk markers in apparently healthy adolescents: a cross-sectional study.

Radana Gurecká, Ivana Koborová, Melinda Csongová, Jozef Šebek, Katarína Šebeková

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Glycoconjugate journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Radana GureckáFaculty of Medicine, Institute of Molecular BioMedicine, Comenius University, Sasinkova 4, 811 08, Bratislava, Slovakia.
Ivana KoborováFaculty of Medicine, Institute of Molecular BioMedicine, Comenius University, Sasinkova 4, 811 08, Bratislava, Slovakia.
Melinda CsongováFaculty of Medicine, Institute of Molecular BioMedicine, Comenius University, Sasinkova 4, 811 08, Bratislava, Slovakia.
Jozef ŠebekSlovak Academy of Sciences, Institute of Materials & Machine Mechanics, Bratislava, Slovakia.
Katarína ŠebekováFaculty of Medicine, Institute of Molecular BioMedicine, Comenius University, Sasinkova 4, 811 08, Bratislava, Slovakia. kata.sebekova@gmail.com.
Comenius University Bratislava · SKSlovak Academy of Sciences · SK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In non-diabetics, low levels of soluble receptor for advanced glycations end products (sRAGE) associate with an increased risk of development of diabetes, cardiovascular afflictions, or death. The majority of studies in non-diabetics report an inverse relationship between measures of obesity, cardiometabolic risk factors and sRAGE and/or endogenous secretory RAGE (esRAGE) levels. To elucidate whether this inconsistency is related to the metabolically healthy obese phenotype, or a different impact of the risk factors in presence and absence of obesity, we analyzed data from 2206 apparently healthy adolescents (51 % girls) aged 15-to-19 years. The association of sRAGE levels with soluble vascular adhesion protein-1/semicarbazide sensitive amine oxidase (sVAP-1/SSAO) was also investigated. Centrally obese, including metabolically healthy, adolescents present significantly lower sRAGE and esRAGE, but not sVAP-1, levels in comparison with their lean counterparts. An increasing number of cardiometabolic risk factors did not associate with significant changes in sRAGE, esRAGE or sVAP-1 levels either in lean or in obese subjects. In multivariate analyses, WHtR, hsCRP, markers of glucose homeostasis, renal function, adiponectin, and sVAP-1 associated significantly with sRAGE and esRAGE. SVAP-1 correlated significantly with glycemia, adiponectin, hsCRP, and sRAGE. Thus, in adolescents, a decline in sRAGE and esRAGE precedes the development of metabolic syndrome. When combined, standard and non-standard cardiometabolic risk factors explain only minor proportion in a variability of sRAGE and esRAGE (8 %-11 %); or sVAP-1 (12 %-20 %). Elucidation of pathogenetic mechanisms underlying early decline in sRAGE and esRAGE levels in obese adolescents and their clinical impact with regard to future cardiometabolic health requires further studies.

Indexed as

AdolescentAmine Oxidase (Copper-Containing)BiomarkersCell Adhesion MoleculesFemaleHeart DiseasesHumansMaleObesityReceptor for Advanced Glycation End ProductsRisk FactorsAGER protein, humanAmine Oxidase (Copper-Containing)AOC3 protein, humanBiomarkersCell Adhesion MoleculesReceptor for Advanced Glycation End ProductsAdolescentsCardiometabolic risk factorsesRAGEMicroinflammationObesitysRAGEsVAP-1

Identifiers

PMID27300745
OpenAlexW2420959467

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.