Evidence map›Paper›PMID 30568439›Full record

ArticleInternational journal of chronic obstructive pulmonary disease2018

The usefulness of soluble receptor for advanced glycation end-products in the identification of COPD frequent exacerbator phenotype.

Joanna Miłkowska-Dymanowska, Adam J Białas, Karolina Szewczyk, Zofia Kurmanowska, Paweł Górski, Wojciech J Piotrowski

Abstract read
In one paragraph

Article in International journal of chronic obstructive pulmonary disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

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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.

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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.

Joanna Miłkowska-DymanowskaDepartment of Pneumology and Allergy, Medical University of Łódź, Łódź, Poland, joanna.milkowska-dymanowska@umed.lodz.pl.
Adam J BiałasDepartment of Pneumology and Allergy, Medical University of Łódź, Łódź, Poland, joanna.milkowska-dymanowska@umed.lodz.pl.
Karolina SzewczykDepartment of Pneumology and Allergy, Medical University of Łódź, Łódź, Poland, joanna.milkowska-dymanowska@umed.lodz.pl.
Zofia KurmanowskaDepartment of Pneumology and Allergy, Medical University of Łódź, Łódź, Poland, joanna.milkowska-dymanowska@umed.lodz.pl.
Paweł GórskiDepartment of Pneumology and Allergy, Medical University of Łódź, Łódź, Poland, joanna.milkowska-dymanowska@umed.lodz.pl.
Wojciech J PiotrowskiDepartment of Pneumology and Allergy, Medical University of Łódź, Łódź, Poland, joanna.milkowska-dymanowska@umed.lodz.pl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Exacerbations of COPD (ECOPDs) are important events in the course of COPD, accelerating the rate of decline in lung function and increasing the mortality risk. A growing body of evidence suggests the significance of the "frequent exacerbator" phenotype. This phenotype seems to be associated with a more severe airflow limitation, symptoms, health-related quality of life impairment, and higher mortality. However, there is no described biomarker that would help to identify this group of patients. Patients and methods: Patients with COPD in "D" GOLD category were monitored for 3 years according to events of ECOPD. Serum samples were collected from the patients. Circulating level of plasma soluble receptor for advanced glycation end-products (sRAGE) was measured using commercially available high sensitivity kits. The receiver operating characteristic (ROC) curve analysis was used to assess the usefulness of sRAGE to identify frequent exacerbator phenotype. Log-rank test was used in the analysis of time to the subsequent exacerbation. Pearson ( Results: Nineteen patients were enrolled. The area under the ROC curve (AUROC) for sRAGE for the identification of frequent exacerbator phenotype was 0.81. Analysis identified the cutoff point as 850.407 pg/mL, characterized by a sensitivity of 0.80 (95% CI: 0.28-1.0) and specificity of 0.93 (95% CI: 0.66-1.0). Additionally, in the group with sRAGE ≤850.407 pg/mL, we observed significantly shorter time to the subsequent exacerbation: median of 32 vs 105.5 days ( Conclusion: sRAGE seems to be useful in the identification of frequent exacerbator phenotype. This parameter may also be used in the prediction of time to ECOPD. Our findings should be confirmed in a sufficiently powered larger sample.

Indexed as

AgedBiomarkersDisease ProgressionFemaleHumansLungMaleMiddle AgedPhenotypePilot ProjectsPredictive Value of TestsPrognosisPulmonary Disease, Chronic ObstructiveReceptor for Advanced Glycation End ProductsReproducibility of ResultsSpirometryAGER protein, humanBiomarkersReceptor for Advanced Glycation End ProductsCOPDexacerbations of COPDfrequent exacerbator phenotype of COPDprediction of AECOPDsRAGE

Identifiers

PMID30568439
PMCPMC6276626

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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.