Evidence map›Paper›PMID 33762606›Full record

ArticleScientific reports2021

Potential novel biomarkers for chronic lung allograft dysfunction and azithromycin responsive allograft dysfunction.

Cecilia Veraar, Jonathan Kliman, Alberto Benazzo, Felicitas Oberndorfer, Maria Laggner, Philipp Hacker, Thomas Raunegger, Stefan Janik, Peter Jaksch, Walter Klepetko and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

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  10. Genetic Deletion ofInternational journal of molecular sciences · 2022
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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

12 authors at 1 institution in 1 country.

Cecilia Veraar *Division of Cardiac Thoracic Vascular Anaesthesia and Intensive Care Medicine, Department of Anaesthesiology, General Intensive Care and Pain Medicine, Medical University of Vienna, Vienna, Austria.
Jonathan Kliman *Division of Surgery, Department of Thoracic Surgery, Medical University of Vienna, Vienna, Austria.
Alberto BenazzoDivision of Surgery, Department of Thoracic Surgery, Medical University of Vienna, Vienna, Austria.
Felicitas OberndorferClinical Institute of Pathology, Medical University of Vienna, Vienna, Austria.
Maria LaggnerDivision of Surgery, Department of Thoracic Surgery, Medical University of Vienna, Vienna, Austria.
Philipp HackerDivision of Surgery, Department of Thoracic Surgery, Medical University of Vienna, Vienna, Austria.
Thomas RauneggerDivision of Surgery, Department of Thoracic Surgery, Medical University of Vienna, Vienna, Austria.
Stefan JanikDepartment of Otorhinolaryngology, Head and Neck Surgery, Medical University of Vienna, Vienna, Austria.
Peter JakschDivision of Surgery, Department of Thoracic Surgery, Medical University of Vienna, Vienna, Austria.
Walter KlepetkoDivision of Surgery, Department of Thoracic Surgery, Medical University of Vienna, Vienna, Austria.
Hendrik J AnkersmitDivision of Surgery, Department of Thoracic Surgery, Medical University of Vienna, Vienna, Austria.
Bernhard MoserDivision of Surgery, Department of Thoracic Surgery, Medical University of Vienna, Vienna, Austria. bernhard.moser@meduniwien.ac.at.
Medical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic Lung Allograft Dysfunction (CLAD), manifesting as Bronchiolitis Obliterans Syndrome (BOS) or Restrictive Allograft Syndrome (RAS), is the main reason for adverse long-term outcome after Lung Transplantation (LTX). Until now, no specific biomarkers exist to differentiate between CLAD phenotypes. Therefore, we sought to find suitable cytokines to distinguish between BOS, RAS and Azithromycin Responsive Allograft Dysfunction (ARAD); and reveal potential similarities or differences to end-stage fibrotic diseases. We observed significantly increased Lipocalin-2 serum concentrations in RAS compared to BOS patients. In addition, in RAS patients immunohistochemistry revealed Lipocalin-2 expression in bronchial epithelium and alveolar walls. Patients with ARAD showed significantly lower Activin-A serum concentrations compared to Stable-LTX and BOS patients. Further, increased serum concentrations of Lipocalin-2 and Activin-A were predictors of worse freedom-from-CLAD in Stable-LTX patients. These biomarkers serve as promising serum biomarkers for CLAD prediction and seem suitable for implementation in clinical practice.

Indexed as

ActivinsAdultAgedAzithromycinBiomarkersBronchiBronchiolitis ObliteransCytokinesFemaleHumansLipocalin-2Lung TransplantationMaleMatrix Metalloproteinase 9Middle AgedPhenotypeactivin AActivinsAzithromycinBiomarkersCytokinesLipocalin-2Matrix Metalloproteinase 9

Identifiers

PMID33762606
PMCPMC7990920
OpenAlexW3137488545

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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.