Stable-State Midrange Proadrenomedullin Is Associated With Severe Exacerbations in COPD

Emanuel Citgez* (Corresponding Author), Maaike Zuur-Telgen, Job van der Palen, Paul van der Valk, Daiana Stolz, Marjolein G.J. Brusse-Keizer

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Background: Elevated levels of midrange proadrenomedullin (MR-proADM) are associated with worse outcome in different diseases, including COPD. The association of stable-state MR-proADM with severe acute exacerbations of COPD (AECOPDs) requiring hospitalization, or with community-acquired pneumonia (CAP) in patients with COPD, has not been studied yet. The aim of this study was to evaluate the association of stable-state MR-proADM with severe AECOPD and CAP in patients with COPD.

Methods: This study pooled data of 1,285 patients from the Cohort of Mortality and Inflammation in COPD (COMIC) and PRedicting Outcome using systemic Markers In Severe Exacerbations of Chronic Obstructive Pulmonary Disease (PROMISE-COPD) cohort studies. Time until first severe AECOPD was compared between patients with high (≥ 0.87 nmol/L) or low (< 0.87 nmol/L) levels of plasma MR-proADM in stable state as previously defined. For time until first CAP, only COMIC data (n = 795) were available.

Results: Patients with COPD with high-level stable-state MR-proADM have a significantly higher risk for severe AECOPD compared with those with low-level MR-proADM with a corrected hazard ratio (HR) of 1.30 (95% CI, 1.01-1.68). Patients with high-level stable-state MR-proADM had a significantly higher risk for CAP compared with patients with COPD with low-level MR-proADM in univariate analysis (HR, 1.93; 95% CI, 1.24-3.01), but after correction for age, lung function, and previous AECOPD, the association was no longer significant (corrected HR, 1.10; 95% CI, 0.68-1.80).

Conclusions: Stable-state high-level MR-proADM in patients with COPD is associated with severe AECOPD but not with CAP.

Original languageEnglish
Pages (from-to)51-57
Number of pages7
Issue number1
Publication statusPublished - 1 Jul 2018


  • biomarkers
  • COPD
  • pneumonia


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