Evidence map›Paper›PMID 33372069›Full record

Observational studyBMJ open2020

Cardiovascular risk prediction using physical performance measures in COPD: results from a multicentre observational study.

Jilles M Fermont, Marie Fisk, Charlotte E Bolton, William MacNee, John R Cockcroft, Jonathan Fuld, Joseph Cheriyan, Divya Mohan, Kaisa M Mäki-Petäjä, Ali B Al-Hadithi and 7 more

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in BMJ open, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
1.0field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 2 syntheses or guidelines pooled it, 12 citations in OpenAlex.

  1. Methods to assess atherosclerotic cardiovascular risk in chronic respiratory diseases: a systematic review.European respiratory review : an official journal of the European Respiratory Society · 2025
    Pooled it
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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

17 authors at 6 institutions in 2 countries.

Jilles M FermontDivision of Experimental Medicine and Immunotherapeutics, Department of Medicine, University of Cambridge, Cambridge, UK jmf88@medschl.cam.ac.uk.ORCID 0000-0001-5042-5785
Marie FiskDivision of Experimental Medicine and Immunotherapeutics, Department of Medicine, University of Cambridge, Cambridge, UK.ORCID 0000-0002-1292-7642
Charlotte E BoltonDivision of Respiratory Medicine and NIHR Nottingham BRC respiratory theme, University of Nottingham, Nottingham, UK.ORCID 0000-0002-9578-2249
William MacNeeCentre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, UK.
John R CockcroftDepartment of Cardiology, Columbia University Medical Center, New York City, New York, USA.
Jonathan FuldDepartment of Respiratory Medicine, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Joseph CheriyanDivision of Experimental Medicine and Immunotherapeutics, Department of Medicine, University of Cambridge, Cambridge, UK.ORCID 0000-0001-6921-1592
Divya MohanMedical Innovation, Value Evidence Outcomes, GSK R&D, Philadelphia, Pennsylvania, USA.
Kaisa M Mäki-PetäjäDivision of Experimental Medicine and Immunotherapeutics, Department of Medicine, University of Cambridge, Cambridge, UK.ORCID 0000-0001-7312-6200
Ali B Al-HadithiDivision of Experimental Medicine and Immunotherapeutics, Department of Medicine, University of Cambridge, Cambridge, UK.ORCID 0000-0003-0417-9653
Ruth Tal-SingerMedical Innovation, Value Evidence Outcomes, GSK R&D, Philadelphia, Pennsylvania, USA.ORCID 0000-0002-5275-8062
Hana MüllerovaGSK R&D, Uxbridge, UK.
Michael I PolkeyDepartment of Respiratory Medicine, Royal Brompton Hospital, London, UK.ORCID 0000-0003-1243-8571
Angela M WoodBritish Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.ORCID 0000-0002-7937-304X
Carmel M McEnieryDivision of Experimental Medicine and Immunotherapeutics, Department of Medicine, University of Cambridge, Cambridge, UK.
Ian B WilkinsonDivision of Experimental Medicine and Immunotherapeutics, Department of Medicine, University of Cambridge, Cambridge, UK.
ERICA consortium
University of Cambridge · GBCambridge University Hospitals NHS Foundation Trust · GBColumbia University Irving Medical Center · USQueen's Medical Centre · GBRoyal Brompton Hospital · GBUniversity of Nottingham · GB

Funding

British Heart Foundation RG/13/13/30194British Heart Foundation RG/18/13/33946Chief Scientist Office [UK]Department of Health [UK]Medical Research Council MR/L003120/1Wellcome Trust
6 · The paper itself

Abstract

objectivesAlthough cardiovascular disease (CVD) is a common comorbidity associated with chronic obstructive pulmonary disease (COPD), it is unknown how to improve prediction of cardiovascular (CV) risk in individuals with COPD. Traditional CV risk scores have been tested in different populations but not uniquely in COPD. The potential of alternative markers to improve CV risk prediction in individuals with COPD is unknown. We aimed to determine the predictive value of conventional CVD risk factors in COPD and to determine if additional markers improve prediction beyond conventional factors.

designData from the Evaluation of the Role of Inflammation in Chronic Airways disease cohort, which enrolled 729 individuals with Global Initiative for Chronic Obstructive Lung Disease (GOLD) stage II-IV COPD were used. Linked hospital episode statistics and survival data were prospectively collected for a median 4.6 years of follow-up.

settingFive UK centres interested in COPD.

participantsPopulation-based sample including 714 individuals with spirometry-defined COPD, smoked at least 10 pack years and who were clinically stable for >4 weeks.

interventionsBaseline measurements included aortic pulse wave velocity (aPWV), carotid intima-media thickness (CIMT), C reactive protein (CRP), fibrinogen, spirometry and Body mass index, airflow Obstruction, Dyspnoea and Exercise capacity (BODE) Index, 6 min walk test (6MWT) and 4 m gait speed (4MGS) test. PRIMARY AND SECONDARY OUTCOME MEASURES: New occurrence (first event) of fatal or non-fatal hospitalised CVD, and all-cause and cause-specific mortality.

resultsOut of 714 participants, 192 (27%) had CV hospitalisation and 6 died due to CVD. The overall CV risk model C-statistic was 0.689 (95% CI 0.688 to 0.691). aPWV and CIMT neither had an association with study outcome nor improved model prediction. CRP, fibrinogen, GOLD stage, BODE Index, 4MGS and 6MWT were associated with the outcome, independently of conventional risk factors (p<0.05 for all). However, only 6MWT improved model discrimination (C=0.727, 95% CI 0.726 to 0.728).

conclusionPoor physical performance defined by the 6MWT improves prediction of CV hospitalisation in individuals with COPD. TRIAL REGISTRATION NUMBER: ID 11101.

Indexed as

Cardiovascular DiseasesPulmonary Disease, Chronic ObstructiveCarotid Intima-Media ThicknessHeart Disease Risk FactorsHumansPhysical Functional PerformancePulse Wave AnalysisRisk Factorscardiac epidemiologychronic airways diseaseepidemiologyprimary carerespiratory medicine (see thoracic medicine)

Identifiers

PMID33372069
PMCPMC7772292
OpenAlexW3117992160

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.