Evidence map›Paper›PMID 39411574›Full record

ReviewInternational journal of chronic obstructive pulmonary disease2024

Temporal Dynamics of Cardiovascular Risk in Patients with Chronic Obstructive Pulmonary Disease During Stable Disease and Exacerbations: Review of the Mechanisms and Implications.

Sami O Simons, Amy B Heptinstall, Zoe Marjenberg, Jonathan Marshall, Hana Mullerova, Paola Rogliani, Clementine Nordon, Nathaniel M Hawkins

Abstract readReview
In one paragraph

Review in International journal of chronic obstructive pulmonary disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
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  11. Review
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  15. Review
  16. Article
  17. Proactive Strategies for Mitigating Cardiopulmonary Risk in COPD.Federal practitioner : for the health care professionals of the VA, DoD, and PHS · 2025
    Article
  18. Article
  19. 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

8 authors.

Sami O SimonsDepartment of Respiratory Medicine, NUTRIM Institute for Nutrition and Translational Research in Metabolism, Maastricht University, Maastricht, The Netherlands.ORCID 0000-0002-4296-5076
Amy B HeptinstallMaverex Ltd, Newcastle Upon Tyne, UK.
Zoe MarjenbergMaverex Ltd, Newcastle Upon Tyne, UK.
Jonathan MarshallBioPharmaceuticals Medical, Respiratory and Immunology, AstraZeneca, Cambridge, UK.
Hana MullerovaBioPharmaceuticals Medical, Respiratory and Immunology, AstraZeneca, Cambridge, UK.ORCID 0000-0002-0949-0101
Paola RoglianiDepartment of Experimental Medicine, Unit of Respiratory Medicine, University of Rome 'Tor Vergata', Rome, Italy.ORCID 0000-0001-7801-5040
Clementine NordonBioPharmaceuticals Medical, Respiratory and Immunology, AstraZeneca, Cambridge, UK.
Nathaniel M HawkinsCardiology, University of British Columbia, Vancouver, Canada.ORCID 0000-0003-1286-2014

Funding

AstraZeneca, Boehringer Ingelheim, Chiesi Farmaceutici, GlaxoSmithKline and Roche GRANTS OR CONTRACTSNovartis
6 · The paper itself

Abstract

Introduction: Exacerbations of chronic obstructive pulmonary disease (COPD) are risk factors for severe cardiovascular (CV) events, with the risk remaining significantly elevated long after the symptomatic phase of the exacerbation. The pathophysiology underpinning the relationship between acute events of both COPD and CV diseases has been understudied. Our objectives were to review the mechanisms by which COPD exacerbations increase the risk of CV events and understand the temporality of this risk. Methods: A pragmatic and targeted literature review was conducted with a focus on identifying recent, high-impact papers up to June 2023, guided by insights from subject matter experts including pulmonologists and cardiologists. Results: A substantial number of inter-related mechanisms underpin the spiral of anatomical and functional deterioration of lung and heart affecting COPD patients during stable state. In turn, an exacerbation of COPD may trigger a CV event, during and beyond the symptomatic phase, due to ventilation/perfusion mismatch, oxygen supply-demand imbalance, oxidative stress, systemic inflammation, hypercoagulable state, dynamic hyperinflation, pulmonary hypertension, and sympathetic activation. However, no study was identified that explored the mechanisms by which an exacerbation confers a sustained risk of CV event. Conclusion: While our review identified multiple dynamic and interacting pathophysiological mechanisms during and after an exacerbation of COPD that contribute to increasing the risk of a wide range of cardiac events, little is known regarding the precise long-term mechanisms after acute exacerbation to explain the persistent increased CV event risk beyond the symptomatic phase. The temporal changes in static and dynamic substrates need further characterization to better understand the different risk factors and risk periods for a CV event following the onset of an exacerbation. Moreover, guideline-directed cardiopulmonary therapies should be implemented at every opportunity; preventing exacerbations and intensively treating traditional CV risk factors should be a focus in COPD management.

Indexed as

Cardiovascular DiseasesDisease ProgressionHeart Disease Risk FactorsPulmonary Disease, Chronic ObstructiveHumansLungPrognosisRisk AssessmentRisk FactorsTime Factorsacute eventscardiopulmonarycardiovascular diseasecardiovascular events

Identifiers

PMID39411574
PMCPMC11474009

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.