Evidence map›Paper›PMID 27799756›Full record

Trial reportInternational journal of chronic obstructive pulmonary disease2016

Reduction of neutrophilic lung inflammation by inhalation of the compatible solute ectoine: a randomized trial with elderly individuals.

Klaus Unfried, Ursula Krämer, Ulrich Sydlik, Andrea Autengruber, Andreas Bilstein, Sabine Stolz, Alessandra Marini, Tamara Schikowski, Stefanie Keymel, Jean Krutmann

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in International journal of chronic obstructive pulmonary disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Pooled it
  2. Review
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  4. Article
  5. Article
  6. Article
  7. Fullerenol CInternational journal of nanomedicine · 2024
    Article
  8. Article
  9. Article
  10. Targeting the EGFR-ERK axis using the compatible solute ectoine to stabilize CFTR mutant F508del.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  11. Review
  12. Metabolic Engineering ofFrontiers in bioengineering and biotechnology · 2022
    Article
  13. Article
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  15. Review
  16. Review
  17. Article
  18. Article
  19. Innate immunity in ischemia-reperfusion injury and graft rejection.Current opinion in organ transplantation · 2019
    Review
  20. 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

10 authors at 2 institutions in 2 countries.

Klaus UnfriedIUF Leibniz Research Institute of Environmental Medicine.
Ursula KrämerIUF Leibniz Research Institute of Environmental Medicine.
Ulrich SydlikIUF Leibniz Research Institute of Environmental Medicine.
Andrea AutengruberIUF Leibniz Research Institute of Environmental Medicine.
Andreas Bilsteinbitop AG, Witten.
Sabine StolzIUF Leibniz Research Institute of Environmental Medicine.
Alessandra MariniIUF Leibniz Research Institute of Environmental Medicine.
Tamara SchikowskiIUF Leibniz Research Institute of Environmental Medicine.
Stefanie KeymelDepartment of Cardiology, Pneumology and Angiology, Medical Faculty, Heinrich-Heine-University, Düsseldorf, Germany.
Jean KrutmannIUF Leibniz Research Institute of Environmental Medicine.
Leibniz Institute of Environmental Medicine · DEHeinrich Heine University Düsseldorf · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCompatible solutes are natural substances that are known to stabilize cellular functions. Preliminary ex vivo and in vivo studies demonstrated that the compatible solute ectoine restores natural apoptosis rates of lung neutrophils and contributes to the resolution of lung inflammation. Due to the low toxicity and known compatibility of the substance, an inhalative application as an intervention strategy for humans suffering from diseases caused by neutrophilic inflammation, like COPD, had been suggested. As a first approach to test the feasibility and efficacy of such a treatment, we performed a population-based randomized trial.

objectiveThe objective of the study was to test whether the daily inhalation of the registered ectoine-containing medical device (Ectoin

methodsA double-blinded placebo-controlled trial was performed to study the efficacy and safety of an ectoine-containing therapeutic. Prior to and after both inhalation periods, lung function, inflammatory parameters in sputum, serum markers, and quality-of-life parameters were determined.

resultsWhile the other outcomes revealed no significant effects, sputum parameters were changed by the intervention. Nitrogen oxides (nitrate and nitrite) were significantly reduced after ectoine inhalation with a mean quotient of 0.65 (95% confidence interval 0.45-0.93). Extended analyses considering period effects revealed that the percentage of neutrophils in sputum was significantly lower after ectoine inhalation than in the placebo group (

conclusionThe current study is the first human trial in which the effects of inhaled ectoine on neutrophilic lung inflammation were investigated. Besides demonstrating beneficial effects on inflammatory sputum parameters, the study proves the feasibility of the therapeutic approach in an aged study group.

Indexed as

Administration, InhalationAgedAged, 80 and overAge FactorsAmino Acids, DiaminoAnti-Inflammatory AgentsApoptosisCross-Over StudiesDouble-Blind MethodFeasibility StudiesFemaleGermanyHumansInflammation MediatorsLungMaleAmino Acids, DiaminoAnti-Inflammatory AgentsectoineInflammation MediatorsNitratesNitritesair pollutionextremolytesmolecular preventionneutrophil apoptosisosmolytesSALIA cohort

Identifiers

PMID27799756
PMCPMC5076798
OpenAlexW2536698174

What OpenQuestion holds

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LicenceCC BY-NC
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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.