Mortality associated with Metabolic Syndrome in people with COPD managed in primary care
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 HDL 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 (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=0.085). The presence of hypertension (HR 1.70, 95% CI:1.63–1.77, p<0.001) and T2DM (HR 1.41, 95% CI:1.34–1.48, p<0.001) increased and obesity (HR 0.74, 95% CI:0.71–0.78, p<0.001) reduced mortality risk.
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.
Funding
K. Khunti is supported by the National Institute for Health Research (NIHR) Applied Research Collaboration East Midlands and the NIHR Leicester Biomedical Research Centre (BRC). R.A. Evans awarded a NIHR Clinician Scientist Fellowship (CS-2016-16-020). N.J. Greening is funded by a NIHR Post-Doctoral Fellowship (pdf-2017-10-052). E. Petherick acknowledges support from the NIHR Leicester BRC, which is a partnership between University Hospitals of Leicester NHS Trust, Loughborough University and the University of Leicester.
History
Citation
ERJ Open Res, 2022; 8: 00211-2022Author affiliation
NIHR Leicester Biomedical Research CentreVersion
- VoR (Version of Record)