Evidence map›Paper›PMID 38834656›Full record

ArticleScientific reports2024

Parallel detection of multiple biomarkers in a point-of-care-competent device for the prediction of exacerbations in chronic inflammatory lung disease.

Niels Röckendorf, Katrin Ramaker, Karoline Gaede, Kristof Tappertzhofen, Lars Lunding, Michael Wegmann, Peter Horbert, Karina Weber, Andreas Frey

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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

2 citing papers in PubMed.

  1. Cellular Metabolic Signatures of Long COVID-19.Infectious disease reports · 2026
    Article
  2. 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

9 authors.

Niels Röckendorf *Division of Mucosal Immunology and Diagnostics, Priority Area Chronic Lung Diseases, Research Center Borstel - Leibniz Lung Center, Member of Leibniz Health Technologies, Parkallee 1-40, Borstel, Germany.
Katrin Ramaker *Division of Mucosal Immunology and Diagnostics, Priority Area Chronic Lung Diseases, Research Center Borstel - Leibniz Lung Center, Member of Leibniz Health Technologies, Parkallee 1-40, Borstel, Germany.
Karoline GaedeBioMaterialBank-North, Department of Medicine, Research Center Borstel - Leibniz Lung Center, Parkallee 1-40, Borstel, Germany.
Kristof TappertzhofenDivision of Mucosal Immunology and Diagnostics, Priority Area Chronic Lung Diseases, Research Center Borstel - Leibniz Lung Center, Member of Leibniz Health Technologies, Parkallee 1-40, Borstel, Germany.
Lars LundingDivision of Lung Immunology, Priority Area Chronic Lung Diseases, Research Center Borstel - Leibniz Lung Center, Member of Leibniz Health Technologies, Parkallee 1-40, Borstel, Germany.
Michael WegmannDivision of Lung Immunology, Priority Area Chronic Lung Diseases, Research Center Borstel - Leibniz Lung Center, Member of Leibniz Health Technologies, Parkallee 1-40, Borstel, Germany.
Peter HorbertDepartment of Spectroscopy and Imaging, Leibniz Institute of Photonic Technology, Member of Leibniz Health Technologies, Member of the Leibniz Centre for Photonics in Infection Research (LPI), Albert-Einstein-Straße 9, Jena, Germany.
Karina WeberDepartment of Spectroscopy and Imaging, Leibniz Institute of Photonic Technology, Member of Leibniz Health Technologies, Member of the Leibniz Centre for Photonics in Infection Research (LPI), Albert-Einstein-Straße 9, Jena, Germany.
Andreas FreyDivision of Mucosal Immunology and Diagnostics, Priority Area Chronic Lung Diseases, Research Center Borstel - Leibniz Lung Center, Member of Leibniz Health Technologies, Parkallee 1-40, Borstel, Germany. afrey@fz-borstel.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sudden aggravations of chronic inflammatory airway diseases are difficult-to-foresee life-threatening episodes for which advanced prognosis-systems are highly desirable. Here we present an experimental chip-based fluidic system designed for the rapid and sensitive measurement of biomarkers prognostic for potentially imminent asthma or COPD exacerbations. As model biomarkers we chose three cytokines (interleukin-6, interleukin-8, tumor necrosis factor alpha), the bacterial infection marker C-reactive protein and the bacterial pathogen Streptococcus pneumoniae-all relevant factors in exacerbation episodes. Assay protocols established in laboratory environments were adapted to 3D-printed fluidic devices with emphasis on short processing times, low reagent consumption and a low limit of detection in order to enable the fluidic system to be used in point-of-care settings. The final device demonstrator was validated with patient sample material for its capability to detect endogenous as well as exogenous biomarkers in parallel.

Indexed as

BiomarkersPoint-of-Care SystemsPulmonary Disease, Chronic ObstructiveStreptococcus pneumoniaeAsthmaC-Reactive ProteinCytokinesHumansInterleukin-6Lab-On-A-Chip DevicesPrognosisTumor Necrosis Factor-alphaBiomarkersC-Reactive ProteinCytokinesInterleukin-6Tumor Necrosis Factor-alpha

Identifiers

PMID38834656
PMCPMC11150478

What OpenQuestion holds

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LicenceCC BY
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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.