Evidence map›Paper›PMID 30409203›Full record

Observational studyRespiratory research2018

Serum AGE/RAGEs as potential biomarker in idiopathic pulmonary fibrosis.

Carlos Machahua, Ana Montes-Worboys, Lurdes Planas-Cerezales, Raquel Buendia-Flores, Maria Molina-Molina, Vanesa Vicens-Zygmunt

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Respiratory research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

28 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
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  11. Review
  12. An explainable machine learning-driven proposal of pulmonary fibrosis biomarkers.Computational and structural biotechnology journal · 2023
    Article
  13. Article
  14. Idiopathic pulmonary fibrosis: Current and future treatment.The clinical respiratory journal · 2022
    Review
  15. Article
  16. Article
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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 3 institutions in 1 country.

Carlos MachahuaPneumology Research Group, IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain.
Ana Montes-WorboysPneumology Research Group, IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain.
Lurdes Planas-CerezalesPneumology Research Group, IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain.
Raquel Buendia-FloresPneumology Research Group, IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain.
Maria Molina-MolinaPneumology Research Group, IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain. mariamolinamolina@hotmail.com.
Vanesa Vicens-ZygmuntPneumology Research Group, IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain.
Institut d'Investigació Biomédica de Bellvitge · ESCentre for Biomedical Network Research on Rare Diseases · ESBellvitge University Hospital · ES

Funding

Instituto de Salud Carlos III PI15/00710
6 · The paper itself

Abstract

backgroundThe soluble receptor for advanced glycation end-products (sRAGE) has been suggested that it acts as a decoy for capturing advanced glycation end-products (AGEs) and inhibits the activation of the oxidative stress and apoptotic pathways. Lung AGEs/sRAGE is increased in idiopathic pulmonary fibrosis (IPF). The objective of the study was to evaluate the AGEs and sRAGE levels in serum as a potential biomarker in IPF.

methodsSerum samples were collected from adult patients: 62 IPF, 22 chronic hypersensitivity pneumonitis (cHP), 20 fibrotic non-specific interstitial pneumonia (fNSIP); and 12 healthy controls. In addition, 23 IPF patients were re-evaluated after 3-year follow-up period. Epidemiological and clinical features were recorded: age, sex, smoking habits, and lung function. AGEs and sRAGE were evaluated by ELISA, and the results were correlated with pulmonary functional test values.

resultsIPF and cHP groups presented a significant increase of AGE/sRAGE serum concentration compared with fNSIP patients. Moreover, an inverse correlation between AGEs and sRAGE levels were found in IPF, and serum sRAGE at diagnosis correlated with FVC and DLCO values. Additionally, changes in serum AGEs and sRAGE correlated with % change of FVC, DLCO and TLC during the follow-up. sRAGE levels below 428.25 pg/ml evolved poor survival rates.

conclusionsThese findings demonstrate that the increase of AGE/sRAGE ratio is higher in IPF, although the levels were close to cHP. AGE/sRAGE increase correlates with respiratory functional progression. Furthermore, the concentration of sRAGE in blood stream at diagnosis and follow-up could be considered as a potential prognostic biomarker.

Indexed as

AgedAlveolitis, Extrinsic AllergicBiomarkersFemaleGlycation End Products, AdvancedHumansIdiopathic Pulmonary FibrosisMaleMiddle AgedProspective StudiesReceptor for Advanced Glycation End ProductsAGER protein, humanBiomarkersGlycation End Products, AdvancedReceptor for Advanced Glycation End ProductsAGEsBiomarkerIPFRAGEs

Identifiers

PMID30409203
PMCPMC6225674
OpenAlexW2900128226

What OpenQuestion holds

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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.