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High suPAR and Low Blood Eosinophil Count are Risk Factors for Hospital Readmission and Mortality in Patients with COPD

Authors Håkansson KEJ, Ulrik CS, Godtfredsen NS, Kallemose T, Andersen O, Eugen-Olsen J, Marsaa K, Rasmussen LJH

Received 4 September 2019

Accepted for publication 21 February 2020

Published 5 April 2020 Volume 2020:15 Pages 733—743


Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 4

Editor who approved publication: Dr Richard Russell

Kjell E J Håkansson,1 Charlotte S Ulrik,1,2 Nina S Godtfredsen,1,2 Thomas Kallemose,3 Ove Andersen,2– 4 Jesper Eugen-Olsen,3 Kristoffer Marsaa,5 Line JH Rasmussen3,6

1Department of Respiratory Medicine, Copenhagen University Hospital Amager and Hvidovre, Hvidovre, Denmark; 2Institute of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark; 3Clinical Research Centre, Copenhagen University Hospital Amager and Hvidovre, Hvidovre, Denmark; 4Emergency Department, Copenhagen University Hospital Amager and Hvidovre, Hvidovre, Denmark; 5Palliative Unit, Copenhagen University Hospital Herlev and Gentofte, Herlev, Denmark; 6Department of Psychology and Neuroscience, Duke University, Durham, NC, USA

Correspondence: Kjell E J Håkansson
Department of Respiratory Medicine, Copenhagen University Hospital Amager and Hvidovre, Kettegård Allé 30 2650, Hvidovre, Denmark
Tel +45 21438688

Introduction: The biomarker soluble urokinase plasminogen activator receptor (suPAR) has been associated with increased mortality in chronic obstructive pulmonary disease (COPD), while elevated blood eosinophils have been associated with better survival. We hypothesized that suPAR and blood eosinophil count are independent risk factors for readmission and mortality after an acute admission in patients with COPD.
Methods: This retrospective cohort study comprised 4022 patients with prevalent COPD acutely admitted to Hvidovre Hospital, Denmark. Irrespective of cause of admission, suPAR and blood eosinophils were measured, and patients were followed up to 365 days. Associations with 365-day respiratory readmission, all-cause readmission and all-cause mortality were investigated by Cox regression analyses adjusted for age, sex, Charlson score and C-reactive protein.
Results: suPAR was significantly elevated in patients who later experienced readmission or died. At 365 days, hazard ratios (HRs) for all-cause readmission and mortality reached 1.61 (95% CI 1.40– 1.85; p< 0.0001) and 3.40 (95% CI 2.64– 4.39; p< 0.0001), respectively, for COPD patients in the fourth suPAR quartile compared to patients in the first suPAR quartile. High blood eosinophils (> 300 cells/μL) were associated with lower risk of mortality (HR 0.49, 95% CI 0.39– 0.62; p< 0.0001) compared with patients with < 150 cells/μL. When stratifying patients by suPAR quartiles and blood eosinophil counts, the highest relative mortality rate was found in patients belonging to both the fourth suPAR quartile and the low blood eosinophil (< 150 cells/μL) group.
Conclusion: In this cohort of COPD patients acutely admitted to a hospital, elevated suPAR concentrations were associated with both higher risk of all-cause readmission and mortality, whereas higher blood eosinophil count was associated with lower risk of mortality.

Keywords: acute admission, biomarker, hospitalization, prognosis, retrospective cohort, inflammation


Chronic obstructive pulmonary disease (COPD) is one of the world’s most common chronic diseases, posing a considerable economic and social burden worldwide.1 COPD is characterized by a decline in lung function and overall health status as well as acute exacerbations of COPD (AECOPD). As COPD progresses, patients often experience repeated hospitalizations due to exacerbations and comorbidities. Besides major impacts on quality of life and healthcare-associated costs,2 all-cause readmissions have been shown to be an independent risk factor of COPD mortality.3,4 This highlights the need for novel risk prediction tools to help identifying hospitalized COPD patients at high risk of future readmission and mortality.

Several prognostic markers for hospitalization and/or COPD-related mortality have been suggested, such as presence of emphysema and severity of airflow limitation,5,6 but reliable biomarkers for COPD readmission and mortality risk are yet to be found. suPAR is the soluble form of the urokinase plasminogen activator receptor (uPAR), a membrane receptor consisting of three domains (DI, DII and DIII). uPAR is expressed on a range of cells such as lymphocytes, monocytes, endothelial and smooth muscle cells, where uPAR and its soluble form are a central part of the plasmin/plasminogen pathway and are involved in chemotaxis, immune system activation and tissue remodeling. As such, suPAR is considered a broadly applicable inflammatory marker in both acute and chronic disease with associations ranging from diabetes and arrhythmias to acute all-cause mortality.79

In COPD, suPAR is associated with small airway fibrosis and emphysema through complex molecular and genetic pathways,10 and neutrophils are thought to be a central source of circulating suPAR.11,12 Furthermore, studies have shown that suPAR is elevated in patients with stable COPD compared to healthy controls,13 as well as being a biomarker of poor prognosis and increased 90-day mortality in COPD patients in an emergency department (ED) setting.14

Another area of interest in COPD biomarkers are eosinophils, neutrophils and their resulting inflammatory profiles. Both types of inflammation have been associated to adverse outcomes in (AE)COPD.1517 In eosinophilic inflammation, higher and, in particular, fluctuating blood eosinophil counts have been suggested as risk markers for unstable disease and exacerbations.18 The GOLD 2019 guidelines have introduced blood eosinophil count as a possible biomarker to identify at-risk patients and candidates for inhaled corticosteroid treatment.1 Despite the recent surge in inflammatory profile research and the roles of eosinophils and other inflammation markers in COPD, our knowledge of their roles in clinical outcomes is still limited. Furthermore, little is known about the relationship between suPAR and blood eosinophils, but with suPAR being thought to stem from activated neutrophils,11 we hypothesize that they may reflect separate inflammatory mechanisms and as such provide distinct clinical information about adverse outcomes in COPD when measured in combination.

We have previously shown that suPAR is associated with 30- and 90-day mortality in acutely admitted patients with COPD.14 Here, we hypothesize that plasma suPAR and blood eosinophil count are independently associated with both long-term (365-days) readmission and mortality in patients acutely admitted with COPD as either primary or secondary diagnosis.

Materials and Methods


The study was approved by the Danish Health and Medicines Authority (ref. 3-3013-1061/2) and the Danish Data Protection Agency (ref. HVH-2014-018, 02767).

Study Subjects and Study Design

This study is based on a retrospective, registry-based cohort study of 29,088 medical patients who were acutely admitted to the ED, Copenhagen University Hospital Amager and Hvidovre, Hvidovre, Denmark, from November 18, 2013, to March 17, 2017. The follow-up period ended June 17, 2017, ensuring follow-up of minimum 90 days for all patients. The ED receives unselected, adult internal medicine patients of all specialties except patients suspected of gastroenterological diseases, as previously described.14 In this study, we included all patients who 1) were admitted to the ED during the study period, 2) had a diagnosis of COPD (ICD-10: J440, J441, J449) registered before (within the past 2 years) or during the admission, and 3) had suPAR concentrations measured as part of the standard admission blood tests. suPAR and mortality data on a subgroup (n=2838) of this COPD cohort has previously been published.14

The index admission was defined as the first admission where a patient had suPAR measured. Data on suPAR and blood eosinophil count were obtained via the electronic hospital database LABKA. All data on diagnoses and admissions were obtained from the Danish National Patient Registry. Vital status was obtained from the Danish Civil Registration System.19 Follow-up was at 30, 90 or 365 days. The Charlson comorbidity index (Charlson score) was used to create a compound score of disease burden due to comorbidities, based on concurrent ICD-10 diagnoses on a per-patient basis. The score was used to correct for co/multimorbidity in our multivariate analyses and was calculated using a SAS macro20 with updated weights as defined by Quan et al.21 All primary and secondary diagnoses registered in the National Patient Registry for the past 2 years before the index admission were used to calculate the score. The 17 original Charlson groups were collapsed into 9 major comorbidity groups (the Charlson group “Chronic Pulmonary Disease” was omitted): Cardiovascular disease (comprised of the Charlson groups “Myocardial Infarction”, “Congestive Heart Failure”, “Peripheral Vascular Disease”, and “Cerebrovascular Disease”), “Dementia”, “Peptic Ulcer Disease”, Liver Disease (“Mild Liver Disease” and “Moderate or Severe Liver Disease”), Diabetes ("Diabetes without Chronic Complications", "Diabetes with Chronic Complications"), “Renal Disease”, Cancer (“Cancer”, “Metastatic Carcinoma”), and Other (“Connective Tissue Disease-Rheumatic Disease”, “Hemiplegia and Paraplegia”, “AIDS/HIV”). In addition, we registered whether patients had a history of acute exacerbations (ICD-10: J441) in the past 2 years before the index admission, and whether the following specific comorbidities were present in the past 2 years before or during the index admission: Hypertension (ICD-10: I10-I15), Myocardial Infarction (ICD-10: I21, I22, I252), Stroke (ICD-10: I61, I63, I649), Type 2 Diabetes (ICD-10: E11), and Lung Cancer (ICD-10: C34). We identified causes of admissions as A-diagnoses (primary diagnoses) registered for the index admission or readmissions, based on ICD-10 chapters, as shown in Table 2. In addition, we identified the following specific respiratory diagnoses as causes of admissions/readmissions: acute upper respiratory infections (ICD-10: J00–06), influenza or pneumonia (ICD-10: J09–18), other acute lower respiratory infections (ICD-10: J20–22), chronic lower respiratory diseases (ICD-10: J40–47), acute respiratory distress syndrome or pulmonary edema (ICD-10: J80–81), other interstitial pulmonary diseases (ICD-10: J84), pleural effusion (ICD-10: J90–91), pneumothorax (ICD-10: J93), and respiratory failure (ICD-10: J96). It should be noted that a patient can have more than one cause of admission/readmission, e.g., if a patient was transferred between wards during the admission.

Table 1 Baseline Characteristics of Patients Acutely Hospitalized with Prevalent COPD

Table 2 Causes of Index Admission and 365-Day Readmission in 4022 Patients with Prevalent COPD


Admission blood tests were analyzed at the Department of Clinical Biochemistry, Hvidovre Hospital. Plasma suPAR concentrations were measured using the suPARnostic AUTO Flex ELISA kit (ViroGates A/S, Birkerød, Denmark).7 The suPARnostic® ELISA measures the full length (DI-DIII) and the cleaved (DIIDIII) suPAR molecules. Blood eosinophil counts were measured using Sysmex XE5000 (Sysmex Corporation, Kobe, Japan; until February 2015) and Sysmex XN9000 (from February 2015) analyzers. C-reactive Protein (CRP) was measured using a COBAS 6000 analyzer (Roche Diagnostics, Mannheim, Germany).

Statistical Analyses

Primary outcomes were acute (unplanned) readmission and all-cause mortality within 365 days from the index admission. Secondary outcomes were identical outcomes within 30 or 90 days. Data on secondary outcomes are presented in the Supplementary Material. For readmissions, we examined all-cause readmissions and respiratory readmissions (i.e., the first readmission for any of the following respiratory ICD-10 diagnoses, regardless of whether another non-respiratory readmission had transpired before: J00–06, J09–18, J20–22, J40–47, J80–81, J84, J90–91, J93, J96).

Continuous variables are presented as median and interquartile range (IQR), and categorical variables are presented as number (n) and percentages (%).

Population-specific suPAR quartiles were generated. To create categorical blood eosinophils groups, cut-offs were defined as low eosinophils (<150 cells/μL), intermediate eosinophils (150–300 cells/μL) and high eosinophils (>300 cells/μL).1,22,23 Results from blood eosinophil analyses were available for 97.5% of the patients.

Unadjusted and multivariable adjusted Cox regression analyses were used to estimate the association of suPAR, continuous (log2-transformed) and categorical (quartiles), with risk of readmission and mortality in separate models. Similar models were fitted for eosinophils (log2-transformed or low/intermediate/high blood eosinophil count). Results are presented as hazard ratios (HRs) with 95% confidence intervals (CIs). The adjusted models include the following variables: age, sex, Charlson score, CRP, suPAR and eosinophils. In the Cox regression analyses of readmission, death before readmission was considered a competing endpoint. The HR for readmission is therefore calculated for the cause-specific hazard of readmission, with censoring at the time of death. The proportional hazards assumption was evaluated by the Schoenfeld residuals; if fits violated the assumption, modifications were made to the model by stratifying the hazard by the adjusted variables. The discriminative ability of suPAR and blood eosinophil count to predict 365-day readmission and mortality was analyzed using area under the curve (AUC) for receiver operating characteristics (ROC) curves. We calculated sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) at cut-off values determined using Youden’s index24 or the cut-off for the highest suPAR quartile or 150 cells/μL for blood eosinophil count.

Cumulative incidence plots for survival and readmission stratified by suPAR quartiles are presented to illustrate the outcome distribution of COPD patients over time.

SAS Enterprise Guide 7.11 (SAS Institute Inc, Cary, NC) and R 3.60 (R Foundation for Statistical Computing, Vienna, Austria) were used for statistical analysis. R 3.60 was used to create the figures. A P-value <0.05 was considered statistically significant.


A total of 29,088 patients were admitted to the ED and had suPAR analyzed during the study period. Of these patients, 4022 (55.5% women, median age 73.1 years) had a prevalent COPD diagnosis and were included in the present study. The median length of stay was 2.1 days (Table 1).

The most common comorbidities were cardiovascular diseases (25.1%) and diabetes (13.4%). Of all patients, 19.5% had a history of at least one acute exacerbation within the past two years (Table 1). For half of the patients, the primary cause of index admission was respiratory disease (n=1982, 49.3%), with the most common diagnosis being chronic lower respiratory disease (n=941) (Table 2).

At the index admission, COPD patients had a median suPAR of 3.9 ng/mL and a median blood eosinophil count of 100 cells/μL (Table 1). The mean follow-up time was 297.8 days (SD 125.6). During this period, 2326 patients (57.8%) were readmitted for any cause (of which 938 (40.3%) were due to respiratory diagnoses), and 1268 patients (31.5%) had a respiratory readmission (Table 2). Of the patients, 26.1% died within 365 days (Table 3).

Table 3 Rates of Readmission and Mortality Within 365 Days in 4022 Patients with COPD Following Hospitalization Stratified by suPAR Quartiles or Blood Eosinophil Counts


COPD patients who were readmitted due to respiratory diagnoses had significantly higher median suPAR at the time of index admission compared to event-free patients (4.0 (2.9–5.5) vs 3.3 (2.6–4.4) ng/mL, p<0.0001). Similarly for all-cause readmissions, patients who were later readmitted had significantly higher median suPAR at the time of index admission compared to event-free patients (4.1 (IQR 3.0–5.7) vs 3.3 (IQR 2.6–4.4) ng/mL, p<0.0001) (Table 3). When stratified into suPAR quartiles, higher readmission rates were observed with increasing suPAR quartiles (Figure 1).

Figure 1 Cumulative incidence plot of mortality (top) and readmission (bottom) within 365 days, stratified by quartiles of suPAR, for 4022 patients acutely admitted with chronic obstructive pulmonary disease.

In univariate Cox regression analyses, elevated suPAR was associated with increased risk of both respiratory and all-cause readmission in COPD patients (Table 4). When adjusting for age, sex, Charlson score, CRP and blood eosinophils, only all-cause readmission remained associated with suPAR (365 days HR for fourth vs first suPAR quartile: 1.61, 95% CI 1.40–1.85) (Table 4).

Table 4 HRs for Readmission and Mortality Within 365 Days Following Hospitalization in Patients with COPD (n=4022), for Continuous suPAR (Log2-Transformed) or Stratified by suPAR Quartiles

COPD patients who died during follow-up had significantly higher median suPAR at the time of index admission compared to event-free patients (5.3 (IQR 3.8–7.1) vs 3.3 ng/mL (IQR 2.6–4.4) ng/mL, p<0.0001) (Table 3). All-cause mortality increased with increasing suPAR quartiles (Figure 1), reaching an HR of 3.40 (95% CI 2.64–4.39) in the fourth quartile vs the first quartile at 365 days after adjusting for age, sex, Charlson score, CRP and blood eosinophils (Table 4).

In ROC curve analyses, the AUCs for suPAR were 0.53 (95% CI 0.51–0.55) for predicting all-cause readmission (Supplementary Figure 1) and 0.71 (95% CI 0.69–0.72) for predicting mortality (Supplementary Figure 2).

The clinical performance of suPAR was evaluated using sensitivity/specificity analyses for cut-offs determined by 1) Youden’s index (YI) and 2) the fourth suPAR quartile cut-off. For predicting 365-day all-cause readmission, a sensitivity of 54.3% and a specificity of 54.5% (PPV 62.2%, NPV 46.4%) were achieved using the YI optimal cut-off of 3.9 ng/mL. Using the fourth quartile cut-off (5.6 ng/mL) yielded a sensitivity of 26.7% and specificity 76.2% (PPV 60.8%, NPV 43.0%).

For 365-day mortality, a sensitivity of 63.6% and a specificity of 68.8% (PPV 41.9%, NPV 84.2%) were achieved using the YI calculated optimal cut-off of 4.5 ng/mL. Corresponding results using the fourth quartile cutoff (5.6 ng/mL) were sensitivity 45.7% and specificity 81.7% (PPV 46.8%, NPV 80.9%).

Blood Eosinophil Count in COPD

For patients with COPD, median blood eosinophil count was significantly lower for patients who were readmitted compared to patients without events (Table 3), and a trend towards a lower risk of all-cause readmission was seen in patients with high blood eosinophil counts (>300 cells/μL) in the adjusted Cox regression analysis (HR 0.90 (95% CI 0.80–1.02); p=0.09) (Table 5).

Table 5 HRs for Readmission and Mortality Within 365 Days Following Hospitalization in Patients with COPD (n=3849), for Continuous Blood Eosinophil Count (Log2-Transformed) or Stratified by Low, Intermediate, and High Blood Eosinophil Count

COPD patients who died during follow-up had significantly lower median blood eosinophil count at the time of index admission compared to event-free patients (Table 3). Of all deaths within 365 days, 71.0% (n=746) were observed in patients with blood eosinophil counts <150 cells/µL (Table 3). In patients with high blood eosinophil counts (>300 cells/μL), the HR reached 0.49 (95% CI 0.39–0.62) for 365-day mortality in the adjusted model (Table 5).

In ROC curve analyses, the AUC for blood eosinophil count was 0.56 (95% CI 0.54–0.58) for predicting all-cause readmission (Supplementary Figure 1) and 0.63 (95% CI 0.61–0.65) for predicting mortality (Supplementary Figure 2).

For predicting 365-day all-cause readmission, a cut-off for blood eosinophil count determined by YI of 5 cells/µL yielded a sensitivity of 88.5% and a specificity of 16.7% (PPV 59.8%, NPV 51.0%). Using the cut-off of 150 cells/µL yielded a sensitivity of 39.0% and specificity of 62.0% (PPV 59.0%, NPV 42.1%) for predicting 365-day readmission.

For predicting 365-day mortality, a cut-off for blood eosinophil count determined by YI of 85 cells/µL yielded a sensitivity of 62.5% and a specificity of 58.5% (PPV 34.6%, NPV 81.6%). Using the cut-off of 150 cells/µL yielded a sensitivity of 75.8% and specificity of 40.5% (PPV 30.9%, NPV 82.7%) for predicting 365-day mortality.

When 365-day event rates were stratified by both suPAR quartiles and blood eosinophil groups (low/intermediate/high), all-cause readmission events were evenly distributed amongst both suPAR quartiles and blood eosinophil counts (Figure 2A). In contrast, mortality events were increasing in frequency with both increasing suPAR quartiles and decreasing blood eosinophil counts, with the group of patients belonging to the fourth suPAR quartile in combination with low blood eosinophil counts showing the highest relative mortality rate (53.0% group mortality) (Figure 2B).

Figure 2 Heatmap of 365-days all-cause readmission (A) and mortality (B) events in 3849 patients with chronic obstructive pulmonary disease acutely admitted to a hospital, stratified by suPAR and blood eosinophil count on admission. Colors in the figure represent the percentage of patients with an event and the numbers represent the total number of patients in strata. P-values represent Chi2-tests by suPAR quartile after stratification for blood eosinophil count, versus event-free patients. Abbreviation: suPAR, soluble urokinase plasminogen activator receptor.


In this study, suPAR was associated with hospital readmission and all-cause mortality in acutely admitted COPD patients. Median suPAR concentrations were consistently higher at the time of admission in patients who were either readmitted or died, and the risk of readmission and mortality was particularly high for those with the highest suPAR level. Furthermore, high blood eosinophil counts were associated with lower risk of all-cause mortality.

suPAR has previously been shown to be elevated in a wide range of patients with chronic diseases such as diabetes and cardiovascular disease.7 Beyond stable, chronic diseases, we have previously shown elevated suPAR to be a reliable marker for readmission and mortality in unselected, acutely admitted medical patients in an ED setting.7,20 In our previous study on a sub-set of the present study population, we showed that suPAR was strongly associated with 30- and 90-day mortality in COPD patients.14 These findings are replicated in the current, extended cohort and are also supported by our findings of an association between suPAR and 365-day mortality. When compared to healthy controls, several studies have found elevated suPAR concentrations in (AE)COPD patients.13,25,26 In contrast, a smaller study failed to find elevated suPAR concentrations in patients with stable COPD, perhaps due to the relatively mild disease severity in patients enrolled, or due to differences in the assays used to measure suPAR.27 A recent study has shown that suPAR concentrations in COPD patients correlate with forced expiratory volume in 1 second (FEV1), Tiffeneau Index as well as Medical Research Council Dyspnea Score.28 Of note, suPAR was further elevated in patients with more than two exacerbations per year.28

Several intrinsic risk factors for COPD readmission are known, including low FEV1, hypoxia and comorbidities.29 Indeed, comorbidity is likely an important factor in readmission risk as approximately 40% of the initial readmissions in the present study were due to respiratory disease, and more than 30% of the cohort had a readmission caused be respiratory disease during the follow-up. This is a marked increase from previous research estimating respiratory readmissions to account for 27% of readmissions after AECOPD,30 perhaps due to the present cohort including all-cause index admissions. These findings combined with the high comorbidity burden in COPD patients highlight the need for a relatively nonspecific disease marker, when searching for a prognostic biomarker of readmission.31 However, suPAR was not independently associated with respiratory readmissions, and based on ROC curve analyses, the suPAR AUC for all-cause readmissions was poor. In contrast, suPAR demonstrated an AUC of 0.71 (95% CI 0.69–0.72) for mortality in our cohort and a negative predictive value of 84.2% for a suPAR concentration above 4.45 ng/mL, suggesting that measurement of suPAR on admission is an acceptable marker for mortality risk assessment in clinical usage. A recent study showed that suPAR outperformed standard emergency triage in predicting mortality in ED patients, and the combination of triage and suPAR >5.7 ng/L (equivalent to the fourth suPAR quartile in the present study) yielded an AUC of 0.87 (0.82–0.93).32 This suggests that suPAR indeed is a viable clinical marker for all-cause mortality in acutely admitted patients with COPD.

Blood Eosinophil Count, Readmission and Mortality in COPD

We observed a trend towards lower risk of all-cause readmission in patients with blood eosinophil counts above 300 cells/μL. With respiratory readmissions in the present study being dominated by exacerbations, our results stand in contrast to the Copenhagen General Population Cohort, as well as the COPDGene and ECLIPSE cohorts, where increasing blood eosinophil count was reported to associate with increased risk of recurrent exacerbations in stable COPD.18,23 However, there is conflicting evidence with analyses of the BODE, CHAIN and SPIROMICS cohorts showing no association between blood eosinophils and increased exacerbation risk.33,34 Furthermore, and perhaps more relevant to the setting of the present study, a recent study on AECOPD also showed an increased risk of (re)exacerbation in patients with elevated blood eosinophils.35

Despite the conflicting findings on readmission, our findings on lower risk of mortality in patients with blood eosinophil counts above 300 cells/μL are seemingly well supported in the literature with regard to AECOPD.33,35 While the overall role and mechanisms of eosinophils in COPD are still debated, post hoc analyses of the WISDOM and FLAME trials, as well as a study by Pascoe and colleagues, have found that patients with elevated blood eosinophil count respond well to corticosteroids during AECOPD.22,36,37 This might in part explain the relative increase in mortality in patients with lower blood eosinophil counts who could be considered to have a more neutrophilic inflammatory profile, representing a COPD phenotype with poorer bronchodilator and steroid therapy response, and thus a relatively high short-term mortality due to low treatment efficacy. Indeed, two smaller studies have previously associated low eosinophil counts to increased mortality in AECOPD.38,39 Eosinopenia (defined as <40 cells/μL) was associated with readmission within 30 days and has been proposed as a part of an AECOPD mortality prediction score.38,40 A plethora of biomarkers for readmission and mortality in (AE)COPD have been suggested.41,42 Common themes include either a panel of biomarkers or demographical data to calculate risk, but there is little coherence between studies regarding which parameters to include.

In terms of clinical performance, a cut-off of 150 cells/µL reached a similar negative predictive value (82.7%) for 365-day mortality prediction as suPAR. Interestingly, our study found that high suPAR concentrations (>3.5 ng/mL) were associated to higher mortality, with a majority (53.0%) of mortality events occurring in patients with low blood eosinophil counts and high suPAR concentrations. This suggests that concurrent measurement of blood eosinophils and suPAR could hold clinical value in improving risk assessment in COPD patients in comparison to suPAR or blood eosinophils alone.


A limitation of the present study is the lack of information on patient smoking status, as smoking has been shown to affect suPAR concentrations and isoform expression.43,44 suPAR concentrations decrease with smoking cessation, but those with the highest suPAR concentrations while smoking also have the highest suPAR concentrations after cessation,45 and as such, we believe this possible bias to be non-differential. Furthermore, the present trial is a single-center trial, which could mean that the results are less representative for other hospitals. Confounding due to the lack of information on other clinical risk factors for readmission and mortality, such as FEV1 and dyspnea grade cannot be dismissed. The Danish patient registries used are validated, but some misdiagnoses are inevitable. All analyses were based on a single measurement at the time of index admission and thus any changes due to treatment or simple disease progression during in-hospital stay were not assessed.

In contrast to other cohorts of COPD patients, most of the patients (55%) were women which could suggest a selection bias in our cohort. However, this could also be due to the relatively high prevalence of smoking women in Denmark,46 giving rise to a significant number of Danish women with COPD,47 along with a general tendency for men with COPD in being less inclined to contact healthcare modalities overall.48 Moreover, there is evidence suggesting that women are prone to frequent, as well as more severe, exacerbations.49,50


To conclude, elevated suPAR was associated with increased readmission and mortality risk in COPD patients, while high blood eosinophil count was associated with lower mortality risk in COPD patients, suggesting that both biomarkers are useful in COPD. Interestingly, elevated suPAR is associated with higher mortality even in patients with low and normal blood eosinophil counts.


AECOPD, Acute Exacerbation of Chronic Obstructive Pulmonary Disease; AUC, Area Under the Curve; CI, Confidence Interval; COPD, Chronic Obstructive Pulmonary Disease; CRP, C-Reactive Protein; ED, Emergency Department; FEV1, Forced Expiratory Volume, 1 second; HR, Hazard Ratio; IQR, Interquartile Range; ROC, Receiver Operating Characteristics; suPAR, Soluble Urokinase Plasminogen Activator Receptor; YI, Youden’s Index.

Author Contributions

KH is the guarantor of this study. All authors contributed to data analysis, drafting and revising the article, gave final approval of the version to be published, and agree to be accountable for all aspects of the work.


OA and JEO report patents related to suPAR (methods of selecting and treating subjects with low-grade inflammation and metabolic disorders; patent number: 9645157 with royalties paid to Copenhagen University Hospital Amager and Hvidovre). JEO and LJHR report personal fees or grants, respectively, from ViroGates A/S. JEO is a CSO (current) of ViroGates A/S. LJHR was supported by a postdoctoral fellowship from the Lundbeck Foundation (grant #R288-2018-380). JEO reports personal fees from ViroGates A/S Denmark, outside the submitted work. KM reports personal fees from Norgine, Kyowa Kirin, Chiesi Pharma, GlaxoSmithKline, Boehringer Ingelheim, Novartis, outside the submitted work. The authors report no other conflicts of interest in this work.


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