Evidence map›Paper›PMID 35887906›Full record

ArticleJournal of clinical medicine2022

Chronic Lung Allograft Dysfunction Is Associated with Increased Levels of Cell-Free Mitochondrial DNA in Bronchoalveolar Lavage Fluid of Lung Transplant Recipients.

Emmanuel Schneck, Ingolf Askevold, Ramona Rath, Andreas Hecker, Martin Reichert, Stefan Guth, Christian Koch, Michael Sander, Werner Seeger, Konstantin Mayer and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 47% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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

14 authors at 2 institutions in 1 country.

Emmanuel SchneckDepartment of Anesthesiology, Operative Intensive Care Medicine and Pain Therapy, Justus Liebig University of Giessen, 35392 Giessen, Germany.ORCID 0000-0003-0565-1550
Ingolf AskevoldDepartment of General and Thoracic Surgery, University Hospital Giessen, Justus Liebig University of Giessen, 35392 Giessen, Germany.
Ramona RathDepartment of Internal Medicine II, Universities of Giessen and Marburg Lung Center (UGMLC), Member of the German Center for Lung Research (DZL), Justus-Liebig University of Giessen, 35392 Giessen, Germany.
Andreas HeckerDepartment of General and Thoracic Surgery, University Hospital Giessen, Justus Liebig University of Giessen, 35392 Giessen, Germany.
Martin ReichertDepartment of General and Thoracic Surgery, University Hospital Giessen, Justus Liebig University of Giessen, 35392 Giessen, Germany.ORCID 0000-0003-0795-0941
Stefan GuthDepartment of Thoracic Surgery, Kerckhoff Heart and Lung Center, 61231 Bad Nauheim, Germany.ORCID 0000-0003-2238-9574
Christian KochDepartment of Anesthesiology, Operative Intensive Care Medicine and Pain Therapy, Justus Liebig University of Giessen, 35392 Giessen, Germany.ORCID 0000-0002-2655-7363
Michael SanderDepartment of Anesthesiology, Operative Intensive Care Medicine and Pain Therapy, Justus Liebig University of Giessen, 35392 Giessen, Germany.ORCID 0000-0003-1677-3609
Werner SeegerDepartment of Internal Medicine II, Universities of Giessen and Marburg Lung Center (UGMLC), Member of the German Center for Lung Research (DZL), Justus-Liebig University of Giessen, 35392 Giessen, Germany.
Konstantin MayerDepartment of Internal Medicine II, Universities of Giessen and Marburg Lung Center (UGMLC), Member of the German Center for Lung Research (DZL), Justus-Liebig University of Giessen, 35392 Giessen, Germany.
Winfried PadbergDepartment of General and Thoracic Surgery, University Hospital Giessen, Justus Liebig University of Giessen, 35392 Giessen, Germany.
Natascha SommerDepartment of Internal Medicine II, Universities of Giessen and Marburg Lung Center (UGMLC), Member of the German Center for Lung Research (DZL), Justus-Liebig University of Giessen, 35392 Giessen, Germany.
Stefan KuhnertDepartment of Internal Medicine II, Universities of Giessen and Marburg Lung Center (UGMLC), Member of the German Center for Lung Research (DZL), Justus-Liebig University of Giessen, 35392 Giessen, Germany.ORCID 0000-0002-1698-2155
Matthias HeckerDepartment of Internal Medicine II, Universities of Giessen and Marburg Lung Center (UGMLC), Member of the German Center for Lung Research (DZL), Justus-Liebig University of Giessen, 35392 Giessen, Germany.
Justus-Liebig-Universität Gießen · DEKerckhoff Klinik · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic Lung Allograft Dysfunction (CLAD) is a life-threatening complication that limits the long-term survival of lung transplantation patients. Early diagnosis remains the basis of efficient management of CLAD, making the need for distinctive biomarkers critical. This explorative study aimed to investigate the predictive power of mitochondrial DNA (mtDNA) derived from bronchoalveolar lavages (BAL) to detect CLAD. The study included 106 lung transplant recipients and analyzed 286 BAL samples for cell count, cell differentiation, and inflammatory and mitochondrial biomarkers, including mtDNA. A receiver operating curve analysis of mtDNA levels was used to assess its ability to detect CLAD. The results revealed a discriminatory pro-inflammatory cytokine profile in the BAL fluid of CLAD patients. The concentration of mtDNA increased in step with each CLAD stage, reaching its highest concentration in stage 4, and correlated significantly with decreasing FEV1. The receiver operating curve analysis of mtDNA in BAL revealed a moderate prediction of CLAD when all stages were grouped together (AUROC 0.75, p-value < 0.0001). This study has found the concentration mtDNA in BAL to be a potential predictor for the early detection of CLAD and the differentiation of different CLAD stages, independent of the underlying pathology.

Indexed as

BOSCLADinflammationmitochondriatransplantation

Identifiers

PMID35887906
PMCPMC9322792
OpenAlexW4285732731

What OpenQuestion holds

Textmetadata
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.