Evidence map›Paper›PMID 41013424›Full record

Observational studyRespiratory research2025

Acute COPD exacerbation despite triple inhaled therapy: a molecular insight - TripleEx study.

Noriane A Sievi, Felix Schmidt, Kai Fricke, Diego M Baur, Sarah Basler, Jonas Herth, Malcolm Kohler

Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in Respiratory research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04638920 (Molecular Breath Print of COPD Patients With Exacerbations Despite Triple Inhalational Therapy), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

NCT04638920 completednot on this map

Molecular Breath Print of COPD Patients With Exacerbations Despite Triple Inhalational Therapy (TripleEX)

TypeobservationalSponsorMalcolm KohlerRan2020 to 2024Enrolled35ConditionsCOPD ExacerbationArmsNo intervention
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  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

7 authors.

Noriane A SieviDepartment of Pulmonology, University Hospital Zurich, Raemistrasse 100, Zurich, 8091, Switzerland. noriane.sievi@usz.ch.
Felix SchmidtDepartment of Pulmonology, University Hospital Zurich, Raemistrasse 100, Zurich, 8091, Switzerland.
Kai FrickeDepartment of Pulmonology, University Hospital Zurich, Raemistrasse 100, Zurich, 8091, Switzerland.
Diego M BaurDepartment of Pulmonology, University Hospital Zurich, Raemistrasse 100, Zurich, 8091, Switzerland.
Sarah BaslerDepartment of Pulmonology, University Hospital Zurich, Raemistrasse 100, Zurich, 8091, Switzerland.
Jonas HerthDepartment of Pulmonology, University Hospital Zurich, Raemistrasse 100, Zurich, 8091, Switzerland.
Malcolm KohlerDepartment of Pulmonology, University Hospital Zurich, Raemistrasse 100, Zurich, 8091, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic obstructive pulmonary disease (COPD) is a progressive respiratory disorder characterized by persistent airflow limitation and acute exacerbations (AECOPD), which accelerate disease progression. Although triple inhaled therapy is recommended for patients with severe COPD and frequent AECOPD, some patients continue to experience exacerbations. The mechanisms behind this remain unclear. Exhaled breath analysis has the potential to unravel molecular changes during AECOPD, thereby adding to the understanding of molecular drivers for AECOPD. This study aimed to investigate metabolic changes in exhaled breath during AECOPD compared to stable state.

methodsIn COPD patients treated with triple inhaled therapy we conducted real time breath analysis during AECOPD and subsequent stable state. Molecular breath patterns were compared between AECOPD and stable state by pathway enrichment analysis. Minimum description length model was used to build a feature based prediction model differentiating AECOPD from stable state.

results28 patients (61% male) with a mean (SD) age of 65 (10.2) years with severe AECOPD were included. Metabolic alterations were predominantly detected in aminosugar, linoleate, and butanoate pathways. AECOPD could be discriminated from stable state with high power (AUC = 0.84), and balanced good sensitivity and specificity (86% each).

conclusionMetabolic analysis of AECOPD revealed disturbances in aminosugar metabolism as a potential driver mechanism and thus may be a therapeutic target for patients with exacerbations despite triple inhaled therapy. Moreover, real-time breath analysis could enable rapid detection of AECOPD, improving diagnostic accuracy and treatment efficiency.

trial registrationClinicalTrials.gov (NCT04638920), registered on 20.11.2020.

Indexed as

Bronchodilator AgentsDisease ProgressionPulmonary Disease, Chronic ObstructiveAdministration, InhalationAgedBreath TestsDrug Therapy, CombinationFemaleHumansMaleMiddle AgedBronchodilator AgentsBiomarkersBreath researchCOPDExacerbationSESI-HRMSTriple inhaled therapy

Identifiers

PMID41013424
PMCPMC12465680

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Registered trials

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.