Evidence map›Paper›PMID 41158484›Full record

ArticleERJ open research2025

Comorbidity profiles in chronic obstructive pulmonary disease: a multicohort study.

Line Egerod, Else A M D Ter Haar, Morten A Karsdal, Diana J Leeming, Carmel B Nanthakumar, Julie C Yates, Dirk-Jan Slebos, Simon D Pouwels, Jorine E Hartman, Jannie M B Sand

Abstract read
In one paragraph

Article in ERJ open research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. 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.

Line EgerodDepartment of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.ORCID https://orcid.org/0009-0009-7057-4222
Else A M D Ter HaarUniversity of Groningen, University Medical Center Groningen, Groningen Research Institute for Asthma and COPD, Groningen, The Netherlands.ORCID https://orcid.org/0000-0002-5895-0725
Morten A KarsdalNordic Bioscience, Herlev, Denmark.
Diana J LeemingNordic Bioscience, Herlev, Denmark.
Carmel B NanthakumarRespiratory Biology, GSK-HQ, London, UK.
Julie C YatesGSK R&D, Durham, NC, USA.
Dirk-Jan SlebosUniversity of Groningen, University Medical Center Groningen, Groningen Research Institute for Asthma and COPD, Groningen, The Netherlands.ORCID https://orcid.org/0000-0001-9555-3422
Simon D PouwelsUniversity of Groningen, University Medical Center Groningen, Groningen Research Institute for Asthma and COPD, Groningen, The Netherlands.ORCID https://orcid.org/0000-0001-7345-8061
Jorine E HartmanUniversity of Groningen, University Medical Center Groningen, Groningen Research Institute for Asthma and COPD, Groningen, The Netherlands.ORCID https://orcid.org/0000-0001-8765-9673
Jannie M B SandNordic Bioscience, Herlev, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Comorbidities are common in COPD, adversely affecting patients' health. Cluster analysis has been proposed to study phenotypic variability, but inconsistent results have raised concerns. This study uses uniform machine learning techniques across large COPD cohorts to identify comorbidity clusters. Methods: Cluster analysis was conducted using data from COPD patients from the ECLIPSE study. 13 comorbidities were grouped using hierarchical clustering on self-organising maps to identify dominant subgroups. The analysis was replicated in COPD patients from the Groningen Severe COPD Cohort (GSCC). Results: 2054 of 2164 ECLIPSE participants (1337 (65%) men; mean±sd age 63.3±7.1 years; 22.0% Global Initiative for Chronic Obstructive Lung Disease (GOLD) stage E) with sufficient data were included in the analysis. Four clusters were identified: Musculoskeletal (C1: more females, lower nutritional status), Mental (C2: younger females, highest comorbidity count), Circulatory (C3: more males, older) and Metabolic (C4: older males, high nutritional status). The replication analysis (776 of 1030 GSCC participants; 266 (34.3%) men; mean±sd age 61.4±6.9 years; 58.9% GOLD stage E) confirmed three clusters. Two clusters (C1, C2) showed similar phenotypic signatures to those in ECLIPSE, while the third combined features of C3 and C4. In ECLIPSE, C1 was associated with increased mortality (HR 2.30, 95% CI 1.26-4.13, p=0.006), which was not replicated in GSSC. Conclusion: Comorbidity clusters exist in COPD and are linked to different patient subgroups with varying symptom burden. While cohort-specific variations in disease outcomes were observed, overall, the study's findings support the presence of comorbidity profiles with potential to improve disease management.

Identifiers

PMID41158484
PMCPMC12557400

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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.