Evidence map›Paper›PMID 36299367›Full record

ArticleERJ open research2022

Mortality associated with metabolic syndrome in people with COPD managed in primary care.

Urvee Karsanji, Rachael A Evans, Jennifer K Quint, Kamlesh Khunti, Claire A Lawson, Emily Petherick, Neil J Greening, Sally J Singh, Matthew Richardson, Michael C Steiner

Abstract read
In one paragraph

Article in ERJ open research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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

  1. Pooled it
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  3. Article
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  5. 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.

Urvee KarsanjiNIHR Leicester Biomedical Research Centre - Respiratory, Dept of Respiratory Sciences, College of Life Sciences, University of Leicester, Leicester, UK.ORCID https://orcid.org/0000-0002-2376-5028
Rachael A EvansNIHR Leicester Biomedical Research Centre - Respiratory, Dept of Respiratory Sciences, College of Life Sciences, University of Leicester, Leicester, UK.ORCID https://orcid.org/0000-0002-1667-868X
Jennifer K QuintNational Heart and Lung Institute, Imperial College London, London, UK.ORCID https://orcid.org/0000-0003-0149-4869
Kamlesh KhuntiNIHR Applied Research Collaboration East Midlands, Diabetes Research Centre, University of Leicester, Leicester, UK.
Claire A LawsonNIHR Applied Research Collaboration East Midlands, Diabetes Research Centre, University of Leicester, Leicester, UK.
Emily PetherickSchool of Sport, Exercise and Health Sciences, Loughborough University, Loughborough, UK.
Neil J GreeningNIHR Leicester Biomedical Research Centre - Respiratory, Dept of Respiratory Sciences, College of Life Sciences, University of Leicester, Leicester, UK.
Sally J SinghNIHR Leicester Biomedical Research Centre - Respiratory, Dept of Respiratory Sciences, College of Life Sciences, University of Leicester, Leicester, UK.
Matthew RichardsonNIHR Leicester Biomedical Research Centre - Respiratory, Dept of Respiratory Sciences, College of Life Sciences, University of Leicester, Leicester, UK.
Michael C SteinerNIHR Leicester Biomedical Research Centre - Respiratory, Dept of Respiratory Sciences, College of Life Sciences, University of Leicester, Leicester, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: The prevalence of metabolic syndrome (MetS) has been reported to be higher in selected populations of people with COPD. The impact of MetS on mortality in COPD is unknown. We used routinely collected healthcare data to estimate the prevalence of MetS in people with COPD managed in primary care and determine its impact on 5-year mortality. Methods: Records from 103 955 patients with COPD from the Clinical Practice Research Datalink (CPRD-GOLD) between 2009 to 2017 were scrutinised. MetS was defined as the presence of three or more of: obesity, hypertension, lowered high-density lipoprotein cholesterol, elevated triglycerides or type 2 diabetes mellitus (T2DM). Univariate and multivariable Cox regression models were constructed to determine the prognostic impact of MetS on 5-year mortality. Similar univariate models were constructed for individual components of the definition of MetS. Results: The prevalence of MetS in the COPD cohort was 10.1%. Univariate analyses showed the presence of MetS increased mortality (hazard ratio (HR) 1.19, 95% CI: 1.12-1.27, p<0.001), but this risk was substantially attenuated in the multivariable analysis (HR 1.06, 95% CI: 0.99-1.13, p Conclusion: MetS in patients with COPD is associated with higher 5-year mortality, but this impact was minimal when adjusted for indices of COPD disease severity and other comorbidities. Individual components of the MetS definition exerted differential impacts on mortality suggesting limitation to the use of MetS as a multicomponent condition in predicting outcome in COPD.

Identifiers

PMID36299367
PMCPMC9589337

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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.