Abstract
Purpose
Peripheral blood eosinophilic counts are susceptible to many factors and have variability over time. There are limited studies on association of blood eosinophilia with long-term mortality of chronic obstructive pulmonary disease (COPD) patients and these results remain controversial. Our aims were to explore the association of blood eosinophilia at index hospitalization and stability of blood eosinophilia stability over 5 years with all-cause mortality of patients hospitalized for acute exacerbation of COPD (AECOPD).
Patients and Methods
Eight hundred twenty-nine patients hospitalized for AECOPD between 2013 and 2014 were included in this study and grouped into two groups according to blood eosinophil with 150 cells/μL used as the cutoff value to form eosinophilic and non-eosinophilic groups. Two hundred forty-one COPD inpatients with at least three blood eosinophils measured from different hospitalizations were used for analysis of longitudinally eosinophilic stability and divided into three groups according to the same cutoff value: predominantly (PE), intermittently (IE) and rarely (RE) eosinophilic groups. Cox regression analysis was used to determine the association of blood eosinophilia and all-cause mortality.
Results
In patients hospitalized for AECOPD, 261 (31.5%) at baseline and 41 (17%) based on at least three measurements of blood eosinophils had increased blood eosinophils. For all-cause mortality, eosinophilic COPD patients at index hospitalization had a lower all-cause mortality compared with non-eosinophilic COPD patients (hazard ratio 0.77, 95% confidence interval 0.6–0.99, P=0.04). In patients readmitted for AECOPD by longitudinal eosinophil stability, with the RE group used as reference, the PE group was associated with a lower all-cause mortality of AECOPD patients (hazard ratio 0.43, 95% confidence interval 0.22–0.85, P=0.016), compared to the IE group (hazard ratio 0.72, 95% confidence interval 0.47–1.11, P=0.133).
Conclusion
Patients with increased eosinophils (using eosinophil 150 cells/μL as a cutoff value), especially predominantly increased eosinophil levels based on multiple measurements, had a lower risk of all-cause mortality. Blood eosinophilia can be used as a biomarker in hospitalized COPD exacerbations for predicting the risk of all-cause mortality.
Keywords: acute exacerbation, chronic obstructive pulmonary disease, blood eosinophilia, mortality
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Introduction
Acute exacerbations of chronic obstructive pulmonary disease (AECOPD) are associated with high mortality and hospital readmission,1 and are heterogeneous with respect to etiology, response to therapy, and prognosis. Identification of special phenotypes in patients with AECOPD is necessary to establish personalized management for COPD patients.
Increased blood eosinophilic inflammation has been found in some stable and acute exacerbation COPD patients.2–7 Eosinophilic COPD patients appear to be a subgroup of patients with specific clinical phenotype who present with better responsiveness to corticosteroid in preventing lung function decline and reducing the failure of COPD exacerbation treatment.8–10 These findings may suggest blood eosinophilia can be used as a potential prognostic marker for predicting the risk of mortality of COPD patients.
At present, the relationship between blood eosinophilia at index hospitalization and mortality of COPD patients is controversial.11–14 Further studies showed blood eosinophil counts were susceptible to many factors and had variability throughout the course of COPD15–20 and using only one measurement of blood eosinophil count may not be a reliable predictor of COPD clinical outcome. Presently, there is no general consensus on the cutoff value for categorizing blood eosinophils to guide management of COPD patients. Therefore, it is important to explore studies on the association of the stability of blood eosinophil counts over time and mortality of COPD patients. Some previous studies revealed that persistently increased blood eosinophil counts were associated with better survival of COPD patients, but study subjects were mainly concentrated in stable COPD patients.15,18,19 To date, there are very limited studies on the stability of increased blood eosinophils over time and its association with mortality of patients hospitalized for AECOPD.
Therefore, our aim was to assess the association of increased blood eosinophil counts at index hospitalization with all-cause mortality of patients hospitalized for AECOPD. Specifically, our aim was to explore the stability of blood eosinophil counts based on at least three measurements over 5 years and its association with all-cause mortality of AECOPD inpatients.
Methods
Study Subjects
The patients first admitted for AECOPD at Beijing Chao-Yang Hospital, in Beijing, People's Republic of China at the index hospitalization date from January 1, 2013, to December 31, 2014, were initially included in this study. The subject enrollment flow diagram is shown in Figure 1. COPD was diagnosed according to the Global Initiative for Chronic Obstructive Pulmonary Disease (GOLD)21 and specific inclusion criteria were as follows: all study subjects were 40 years of age or older; smoking history ≥10 pack-year or/and biomass history ≥10 years and post bronchodilator forced expiratory volume in 1 second (FEV1)/forced vital capacity (FVC)% <70%; discharged alive; the blood eosinophil counts taken within 24 hours after the index hospitalization (including emergency room). The exclusion criteria were defined as follows: 1) active tumor; 2) asthma-COPD overlap as discharged diagnosis, however patients with a history of asthma were not excluded; 3) other clinically relevant lung disease; and 4) patients lost to follow up. Since AECOPD is mainly triggered by respiratory tract infections, we included patients with pneumonia. Therefore, 829 inpatients with primary discharged diagnosis of AECOPD were used for analysis of the association of blood eosinophils at baseline with all-cause mortality. In order to analyze the association of longitudinal stability of blood eosinophils and all-cause mortality, 241 inpatients who underwent at least three hospitalizations for AECOPD over 5 years and had available blood eosinophilic counts measured within 24 hours after each admission were selected. All data was collected from an inpatient electronic management system. This study was conducted in accordance with the Declaration of Helsinki. The research scheme was approved by the ethics committee of Beijing Chao-Yang Hospital (IRB No.2017–23). Informed consent from patients was waived because this study was observational, non-interventional and had no risk or harm to COPD patients. We declared that the patients’ data were confidential and did not compromise the patients’ interest.
Figure 1.
The subject enrollment flow diagram.
Definitions of Blood Eosinophils
A pre-specified eosinophil cutoff value of 150 cells/μL was used to characterize the study cohort and determine associations with clinical outcomes.19 The study subjects using 150 cells/μL as the cutoff value of blood eosinophil counts were categorized as eosinophilic (≥150 cells/μL) and non-eosinophilic (<150 cells/μL) groups.
In order to investigate the fluctuation of blood eosinophils, 241 COPD patients underwent three to six blood eosinophil measurements over 5 years. A total of 165 patients had three available blood eosinophil results, 66 patients had four available blood eosinophils, nine patients had five available blood eosinophils and one patient had six available blood eosinophils. All the results of blood eosinophils were measured within 24 hours at each hospital admission. Each result of blood eosinophil counts came from different hospitalizations for AECOPD. For patients who had more than one hospitalization for AECOPD in 1 year, if the interval between hospitalizations was within 30 days, it was counted as one hospitalization and the first measured blood eosinophil count was used for analysis. COPD patients were divided into three groups according to 150 cells/μL as the cutoff value of blood eosinophils: predominantly (PE), intermittently (IE) and rarely (RE) eosinophilic groups.22 The PE group was defined as blood eosinophil counts ≥150 cells/μL measured within 24 hours at each hospitalization for AECOPD or the presence of blood eosinophil counts <150 cells/μL occurred only once during multiple hospitalizations; the RE group was defined as blood eosinophil counts <150 cells/μL measured within 24 hours at each hospitalization for AECOPD or the presence of blood eosinophil counts ≥150 cells/μL occurred only once during multiple hospitalizations; the IE group was defined when none of the above-mentioned criteria were met. However, the patients who had only three available blood eosinophil results were defined as the PE group if each blood eosinophil count was ≥150 cells/μL or as the RE group if each blood eosinophil count was <150 cells/μL, and the other patients were defined as the IE group.
Study Variables and Outcomes
All subjects’ demographic characteristics (age, gender, height, weight, and smoking history), clinical symptoms (sputum, dyspnea), laboratory test (blood routine test, biochemistry), drug treatment during admission (antibiotic, inhaled corticosteroid (ICS) and intravenous corticosteroid administrations; intravenous corticosteroid was expressed as equivalent dose of oral prednisone), history of asthma and hospitalization for AECOPD in the previous year were collected. Comorbidity was quantified according to the Charlson Comorbidity Index.23
In addition, the primary outcome was all-cause mortality which was investigated by telephone contact and/or checking electronic medical record from January 1, 2013 to March 19, 2018. The telephone follow-up of all patients was completed from January 1, 2018 to March 19, 2018. The date of the last telephone contact for survival status was defined as the final date of outcome follow-up, which was March 19, 2018.
Data Analysis
Continuous variables were summarized as mean and standard deviation (SD), and categorical variables were summarized as absolute numbers and percentages. Comparison of categorical variables were performed using the chi-square test or Fisher’s exact test. For continuous variables, Student's t-test or analysis of variance was done for data with normal distribution and the nonparametric test was done for data not showing normal distribution. The Kaplan–Meier analysis was performed to compare all-cause mortality of patients with different blood eosinophilic levels. The Cox proportional hazards regression models were conducted to evaluate the association of blood eosinophil counts at baseline and longitudinal stability of blood eosinophil counts with the risk of all-cause mortality, respectively. In the Cox proportional hazards regression models, potential confounding factors were adjusted such as age (using ≥60 years as cutoff value), hospitalization for AECOPD in the previous year, Charlson Comorbidity Index. A two-sided P-value <0.05 was considered statistically significant. All data were analyzed using IBM SPSS Statistics for Window, version 23.0 (SPSS, IBM Corporation, Armonk, NY, USA) and the R software (Version 3.6.1).
We also performed repeatedly the association analysis of baseline blood eosinophil and all-cause mortality of patients with at least three blood eosinophil counts measured at admission for AECOPD, as sensitivity analysis.
Results
The Clinical Characteristics of Patients Hospitalized for AECOPD at Baseline
We identified 829 AECOPD patients with blood eosinophil counts at baseline. These COPD patients were stratified into non-eosinophilic (n=568) and eosinophilic (n=261) groups according to 150 cells/μL used as cutoff value of blood eosinophil counts. The baseline characteristics of 829 patients hospitalized for AECOPD are shown in Table 1. Compared with the non-eosinophilic group, the eosinophilic group tended to have a lower Charlson Comorbidity Index (P<0.001), a shorter time since onset of symptoms (P=0.021), a lower neutrophil fraction (P<0.001), a lower proportion of intravenous corticosteroids treatments (P<0.001), a lower proportion of dual antibiotics treatments (P=0.027) and a shorter length of stay (P=0.002). In intravenous corticosteroid-treated patients, the eosinophilic group tended to have shorter days of intravenous corticosteroid treatment (P=0.01) and lower total amount of intravenous corticosteroids treatment (P=0.008) than the non-eosinophil group. For the usage of ICS during index hospitalization, there was no statistical difference between groups (P=0.965). There were no significant differences in other variables.
Table 1.
Baseline Characteristics and Outcomes of Patients Hospitalized for AECOPD According to Blood Eosinophil ≥150 Cells/μL as the Cutoff Value
| Variables | Eosinophils ≥150 Cells/μL (N=261) | Eosinophils <150 Cells/μL (N=568) | P-value |
|---|---|---|---|
| Male | 197 (75.5) | 391 (68.8) | 0.051 |
| Age ≥60 years | 235 (90.0) | 507 (89.3) | 0.734 |
| Smoking history | 199 (76.2) | 423 (74.5) | 0.584 |
| Pack-years | 41.25±26.36 | 41.27±36.43 | 0.363 |
| BMId, kg/m2 | 23.12±4.49 | 23.45±4.48 | 0.200 |
| History of asthma | 20 (7.7) | 49 (8.6) | 0.641 |
| Comorbidities | |||
| Systemic hypertension | 116 (44.4) | 276 (48.6) | 0.267 |
| Cardiac artery disease | 53 (20.3) | 138 (24.3) | 0.205 |
| Atrial fibrillation | 15 (5.7) | 51 (9.0) | 0.110 |
| Congestive heart failure | 9 (3.4) | 26 (4.6) | 0.453 |
| Diabetes | 48 (18.4) | 122 (21.5) | 0.306 |
| Cerebrovascular disease | 22 (8.4) | 53 (9.3) | 0.674 |
| Connective tissue disease | 1 (0.4) | 7 (1.2) | 0.245 |
| Liver disease | 2 (0.8) | 5 (0.9) | 0.868 |
| Charlson Comorbidity Index | 1.61±0.85 | 1.86±0.93 | <0.001 |
| Hospitalization for COPD in the previous year | 92 (35.2) | 207 (36.4) | 0.739 |
| Time since onset of symptoms, years | 16.31±14.92 | 17.95±14.00 | 0.021 |
| Sputum During Admission | 0.150 | ||
| None | 23 (8.8) | 30 (5.3) | |
| White | 161 (61.7) | 369 (65) | |
| Purulent | 77 (29.5) | 169 (29.8) | |
| Dyspnea during admission | 254 (97.3) | 559 (98.4) | 0.286 |
| Laboratory | |||
| WBC,109/L | 7.40±2.34 | 8.09±3.60 | 0.110 |
| Neutrophil, % | 64.53±10.48 | 76.32±36.28 | <0.001 |
| Hemoglobin, g/L | 134.91±21.88 | 132.28±20.45 | 0.057 |
| Albumin, g/L | 33.25±4.1 | 32.81±4.51 | 0.113 |
| Drug Treatment During Admission | |||
| ICS | 194 (74.3) | 423 (74.5) | 0.965 |
| IVS, | 60 (23) | 204 (35.9) | <0.001 |
| Duration of IVS, days | 3.97±2.66 | 5.04±3.31 | 0.01 |
| Total amount of IVS, mg | 204.17±154.4 | 261.13±180.49 | 0.008 |
| Antibiotics | 0.027 | ||
| None | 10 (3.8) | 20 (3.5) | 0.886a |
| Single antibiotic | 181 (69.3) | 342 (60.2) | 0.007b |
| Dual antibiotics | 70 (26.8) | 206 (36.3) | 0.345c |
| Length of stay, days | 9 [2–42] | 10 [1–78] | 0.002 |
Notes: Data are presented as no. (%), mean±SD, or median [range]. aComparison between none and single antibiotic groups. cComparison between none and dual antibiotics groups. bComparison between single and dual antibiotics groups. dBMI has 146 missing values. There are 26 (10%) and 120 (21.1%) missing values in the eosinophils ≥150 cells/μL group and eosinophils <150 cells/μL group, respectively.
Abbreviations: AECOPD, acute exacerbation of chronic obstructive pulmonary disease; BMI, body mass index; COPD, chronic obstructive pulmonary disease; WBC, white blood cell; ICS, inhaled corticosteroid; IVS, intravenous corticosteroid.
Survival Analyses for Patients Hospitalized for AECOPD at Baseline
The median follow-up (interquartile range) was 46 months (33–54). Overall, 312 (37.6%) COPD patients died during the follow up. There was no statistical difference in specific cause of death between the two groups at baseline (P=0.794) (Table 2).
Table 2.
Comparisons of Overall and Specific Cause of Death Among Patients Hospitalized for AECOPD According to Blood Eosinophil ≥150 Cells/μL as the Cutoff Value
| Cause of Death | Eosinophils ≥150 Cells/μL (N=84) | Eosinophils <150 Cells/μL (N=228) | P-value |
|---|---|---|---|
| All causes | 84 (32.2) | 228 (40.1) | 0.028 |
| Major Causes | 0.794 | ||
| Respiratory disease | 54 (64.3) | 153 (67.1) | |
| Cardiovascular disease | 8 (9.5) | 24 (10.5) | |
| Cancer | 8 (9.5) | 23 (10.1) | |
| Other diseases | 14 (16.7) | 28 (12.3) |
Note: Data are presented as no. (%).
Abbreviation: AECOPD, acute exacerbation of chronic obstructive pulmonary disease.
The Kaplan–Meier survival curves between non-eosinophilic and eosinophilic groups are shown in Figure 2. The eosinophilic group tended to have a lower risk of all-cause mortality compared with the non-eosinophilic group (P=0.023).
Figure 2.
Kaplan–Maier survival curves for the groups, blood eosinophil (Eos) ≥150 cells/μL and blood eosinophil (Eos) <150 cells/μL (P=0.023).
Table 3 shows Cox regression analysis for the association of increased eosinophils measured at index hospitalization with the risk of all-cause death among patients hospitalized for AECOPD. The unadjusted Cox regression analysis showed blood eosinophil ≥150 cells/μL was associated with lower risk of all-cause mortality (Hazard Ratio [HR]= 0.75, 95% Confidence Interval [CI], 0.58–0.96, P=0.025). The multi-adjusted Cox regression analysis showed the association remained unchanged after adjusting for age ≥ 60 years, Charlson Comorbidity Index and hospitalization for COPD in the previous year (HR=0.77, 95% CI, 0.60–0.99, P=0.040). When the association analysis was repeatedly performed using 200 cells/μL as the cutoff value in the same model, blood eosinophils ≥ 200 cells/μL were associated with lower risk of all-cause mortality with borderline statistical significance (HR=0.76, 95% CI, 0.58–1.01, P=0.055) (Supplementary Table A1).Once the cutoff value of blood eosinophil counts was raised to 300 cells/μL, the association did not reach statistical significance due to the relatively low number of patients above the cutoff value limiting the statistical power (HR=0.78, 95% CI, 0.55–1.10, P=0.153) (Supplementary Table A2).
Table 3.
The Association of Increased Eosinophils Measured at Index Hospitalization with the Risk of All-Cause Death Among Patients Hospitalized for AECOPD According to Cox Regression Analysis (N=829)
| Variables | Unadjusted HR (95% CI) | P-value | Multi-Adjusted HR (95% CI) | P-value |
|---|---|---|---|---|
| Age ≥60 years | 2.15 (1.33–3.46) | 0.002 | 2.15 (1.34–3.47) | 0.002 |
| Eosinophils (≥150 cells/μL) | 0.75 (0.58–0.96) | 0.025 | 0.77 (0.60–0.99) | 0.040 |
| Charlson Comorbidity Index | 1.19 (1.06–1.33) | 0.003 | 1.14 (1.02–1.28) | 0.024 |
| Hospitalization for COPD in the previous year | 1.39 (1.11–1.74) | 0.004 | 1.39 (1.11–1.74) | 0.004 |
Abbreviations: AECOPD, acute exacerbation of chronic obstructive pulmonary disease; COPD, chronic obstructive pulmonary disease.
To control a selection bias from the missing data due to unavailability to follow up in the Cox regression analysis, 200 patients who were lost to follow up were defined as censoring data which were included in the same Cox regression model, as a sensitivity analysis. Supplementary Table A3 showed the association still remained statistically significant (HR=0.75, 95% CI, 0.59–0.97, P=0.025).
Baseline Characteristics of Patients with Readmission by Longitudinal Eosinophil Stability
We identified 241 AECOPD patients with at least three blood eosinophil counts. These COPD patients were stratified into rarely eosinophilic (RE, n=103), intermittently eosinophilic (IE, n=97), predominantly eosinophilic (PE, n=41) groups according to 150 cells/μL of blood eosinophil counts as the cutoff value (Table 4). Compared with other two groups, the PE group tended to have a higher proportion of male patients (P=0.042) and a lower neutrophil fraction (P=0.011). In intravenous corticosteroid-treated patients, the PE group tended to have shorter days of intravenous corticosteroid treatment (P=0.014) and lower total amount of intravenous corticosteroid treatment (P=0.023). For the usage of ICS at index hospitalization, there was no statistical significance among the three groups (P=0.797). There was no significant difference in other variables.
Table 4.
Baseline Characteristics and Outcomes at the Index Hospitalization of Patients with Readmission by Longitudinal Eosinophil Stabilitya (N=241)
| Variables | Rare Eosinophil ≥150 Cells/μL (N=103) | Intermittent Eosinophil ≥150 Cells/μL (N=97) | Predominant Eosinophil ≥150 Cells/μL (N=41) | P-value |
|---|---|---|---|---|
| Male | 61 (59.2) | 67 (69.1) | 33 (80.5) | 0.042 |
| Age ≥ 60 years | 91 (88.3) | 90 (92.8) | 38 (92.7) | 0.502 |
| Smoking history | 71 (68.9) | 75 (77.3) | 35 (85.4) | 0.097 |
| Pack-years | 40.21±29.73 | 39.51±29.25 | 42.04±22.86 | 0.909 |
| BMIb, kg/m2 | 23.05±5.1 | 22.60±5.21 | 22.86±5.60 | 0.733 |
| History of asthma | 9 (8.7) | 9 (9.3) | 5 (12.2) | 0.811 |
| Comorbidities | ||||
| Systemic hypertension | 50 (48.5) | 47 (48.5) | 17 (41.5) | 0.713 |
| Cardiac artery disease | 28 (27.2) | 24 (24.7) | 6 (14.6) | 0.277 |
| Atrial fibrillation | 5 (4.9) | 5 (5.2) | 5 (12.2) | 0.22 |
| Congestive heart failure | 7 (6.8) | 4 (4.1) | 1 (2.4) | 0.490 |
| Diabetes | 21 (20.4) | 17 (17.5) | 9 (22.0) | 0.799 |
| Cerebrovascular disease | 12 (11.7) | 6 (6.2) | 2 (4.9) | 0.257 |
| Connective tissue disease | 2 (1.9) | 2 (2.1) | 0 (0) | 0.658 |
| Liver disease | 2 (1.9) | 1 (1.0) | 1 (2.4) | 0.803 |
| Charlson Comorbidity Index | 1.98±1.08 | 1.7±0.93 | 1.73±0.92 | 0.127 |
| Hospitalization for COPD in the previous year | 55 (53.4) | 52 (53.6) | 21 (51.2) | 0.965 |
| Time since onset of symptoms, years | 18.56±14.9 | 18.24±13.69 | 18.76±13.30 | 0.925 |
| Sputum During Admission | 0.945 | |||
| None | 4 (3.9) | 5 (5.2) | 1 (2.4) | |
| White | 64 (62.1) | 57 (58.8) | 26 (63.4) | |
| Purulent | 35 (34) | 35 (36.1) | 14 (34.1) | |
| Dyspnea during admission | 103 (100) | 96 (99) | 40 (97.6) | 0.333 |
| Laboratory | ||||
| WBC x109/L | 8.12±3.6 | 7.59±2.98 | 7.5±2.49 | 0.591 |
| Neutrophil, % | 73.78±11.86 | 72.15±11.44 | 67.82±10.28 | 0.011 |
| Hemoglobin, g/L | 136.4±21.77 | 131.18±20.45 | 133.06±15.34 | 0.207 |
| Albumin, g/L | 33.57±4.26 | 32.86±4.29 | 32.43±3.52 | 0.314 |
| Drug Treatment During Admission | ||||
| ICS | 80 (77.7) | 78 (80.4) | 31 (75.6) | 0.797 |
| IVS | 44 (42.7) | 33 (34) | 11 (26.8) | 0.163 |
| Duration of IVS, days | 4.73±3.25 | 5.49±3.02 | 2.82±2.04 | 0.014 |
| Total amount of IVS, mg | 254.55±204.55 | 290.3±195.44 | 145.46±105.96 | 0.023 |
| Antibiotics | 0.079 | |||
| None | 0 (0) | 0 (0) | 1 (2.4) | |
| Single antibiotic | 58 (56.3) | 65 (67) | 28 (68.3) | |
| Dual antibiotics | 45 (43.7) | 32 (33) | 12 (29.3) | |
| Length of stay, days | 10 [4–78] | 9 [4–34] | 8 [5–42] | 0.055 |
Notes: Data are presented as no. (%), mean ±SD, or median [range]. aLongitudinal eosinophil stability denotes prevalence of increased and low blood eosinophils over time. bBMI has 13 missing values. There are 4 (3.9%), 7 (7.2%) and 2 (4.9%) missing values in rare eosinophil ≥150 cells/μL group, intermittent eosinophil ≥ 150 cells/μL group and predominant eosinophil ≥150 cells/μL group, respectively.
Abbreviations: BMI, body mass index; WBC, white blood cell; COPD, chronic obstructive pulmonary disease; WBC, white blood cell; ICS, inhaled corticosteroid; IVS, intravenous corticosteroid.
Survival Analysis of Patients Readmitted for AECOPD by Longitudinal Eosinophil Stability
The median follow-up (interquartile range) was 48 months (35–56), and 96 (39.8%) COPD patients died during the follow up. There was no significant difference in specific cause of death among the three groups (P=0.088) (Table 5).
Table 5.
Comparison of Overall and Specific Cause of Death Among Patients Readmitted for AECOPD by Longitudinal Eosinophil Stabilitya
| Cause of Death | Rare Eosinophil ≥150 Cells/μL (N=49) | Intermittent Eosinophil ≥150 Cells/μL (N=37) | Predominant Eosinophil ≥150 Cells/μL (N=10) | P-value |
|---|---|---|---|---|
| All causes | 49 (47.6) | 37 (38.1) | 10 (24.4) | 0.034 |
| Major Causes | 0.088 | |||
| Respiratory disease | 35 (71.4) | 30 (81.1) | 4 (40) | |
| Cardiovascular disease | 5 (10.2) | 5 (13.5) | 2 (20) | |
| Cancer | 7 (14.3) | 1 (2.7) | 2 (20) | |
| Other diseases | 2 (4.1) | 1 (2.7) | 2 (20) |
Notes: Data are presented as no. (%). aLongitudinal eosinophil stability denotes that prevalence of increased and low blood eosinophils over time.
Abbreviation: AECOPD, acute exacerbation of chronic obstructive pulmonary disease.
The Kaplan–Meier survival curves showed the PE group tended to have a lower risk of all-cause mortality compared with the IE and RE groups (P=0.035) (Figure 3).
Figure 3.
Kaplan–Maier survival curves for the groups, rare eosinophilic (RE), intermittently eosinophilic (IE) and predominantly eosinophilic (PE) (P=0.035).
Table 6 shows the Cox regression analysis for the association of predominantly high eosinophils with the risk of all-cause death among patients readmitted for AECOPD. Utilizing the RE group as a reference point, the unadjusted Cox regression analysis revealed predominant eosinophils ≥150 cells/μL were associated with lower risk of all-cause mortality of COPD patients (HR=0.44, 95% CI, 0.22–0.86, P=0.017) compared to intermittent eosinophils ≥150 cells/μL (HR=0.73, 95% CI, 0.48–1.12, P=0.147). The multi-adjusted Cox regression analysis revealed predominant eosinophils ≥150 cells/μL were still associated with lower risk of all-cause mortality of COPD patients (multi-adjusted HR 0.43, 95% CI 0.22–0.85, P=0.016) compared to intermittent eosinophils ≥150 cells/μL (HR=0.72, 95% CI, 0.47–1.11, P=0.133) after adjusting for other variables. We repeatedly performed the analysis using 200 cells/μL and 300 cells/μL as the cutoff values in the same Cox regression model. However, it was no longer significant (Supplementary Tables A4, A5).
Table 6.
The Association of Predominant Eosinophilia with the Risk of All-Cause Death Among Patients Readmitted for AECOPD According to Cox Regression Analysis
| Variables | Unadjusted HR (95% CI) | P-value | Multi-Adjusted HR (95% CI) | P-value |
|---|---|---|---|---|
| Age≥60 years | 2.70 (0.99–7.34) | 0.052 | 2.92 (1.07–7.98) | 0.036 |
| Eosinophils ≥150 cells/μL | ||||
| Rare eosinophilia | Reference | Reference | ||
| Intermittent eosinophilia | 0.73 (0.48–1.12) | 0.147 | 0.72 (0.47–1.11) | 0.133 |
| Predominant eosinophilia | 0.44 (0.22–0.86) | 0.017 | 0.43 (0.22–0.85) | 0.016 |
| P trend | 0.040 | 0.037 | ||
| Charlson Comorbidity Index | 1.17 (0.99–1.39) | 0.072 | 1.13 (0.95–1.35) | 0.174 |
| Hospitalization for COPD in the previous year | 1.60 (1.05–2.43) | 0.028 | 1.53 (1.01–2.33) | 0.047 |
Abbreviations: AECOPD, acute exacerbation of chronic obstructive pulmonary disease; COPD, chronic obstructive pulmonary disease.
In order to control selective bias, nine missing patients who had three or more blood eosinophils were included in the same Cox regression model as a sensitivity analysis, Supplementary Table A6 showed predominantly high eosinophils ≥ 150 cells/μL was still independently associated with lower risk of all-cause death among patients readmitted for AECOPD (HR=0.43, 95% CI, 0.22–0.85, P=0.016).
Sensitivity Analysis on the Association of Increased Eosinophils (≥150 cells/μL) Measured at Baseline with the Risk of All-Cause Death Among Patients Readmitted for AECOPD
When Cox regression analysis was used for the association of blood eosinophil measured at index admission for AECOPD and all-cause mortality of patients with at least three blood eosinophil counts, increased blood eosinophil ≥150 cells/μL was no longer associated with lower risk of all-cause mortality (Supplementary Table A7).
Discussion
Our study subjects were based on inpatients with COPD exacerbation, which was different from the previous studies from stable COPD patients. Our findings predicted that when using 150 cells/μL of blood eosinophil counts as cutoff value, increased blood eosinophils measured at index hospitalization was associated with lower risk of all-cause mortality in patients hospitalized for AECOPD. More importantly, predominantly increased eosinophils based on three or more measurements were still associated with lower all-cause mortality among patients readmitted for AECOPD by longitudinal eosinophil stability.
Eosinophilic inflammation was thought to be a characteristic of asthma and has been found to be present in some COPD patients. Up to now, there is still no clear agreement as to the most appropriate cutoff value used for categorizing blood eosinophils. In some previous studies of COPD patients, a 2% cutoff value of blood eosinophil counts is generally used.4,5,24 Using 150 cells/μL as a cutoff value showed a similar pattern of differences to 2% of blood eosinophils as a cutoff value. The correlation strength reached 0.88 between samples classification using 2% and 150 cells/μL as cutoff values (P<0.001).2 Therefore, it is reasonable to use absolute numbers ≥150 cells/μL as an alternative measure to the 2% eosinophil cutoff. Furthermore, a relative percentage of total leukocyte count as a cutoff value of blood eosinophils was thought to be less reliable compared with using absolute blood eosinophil count.25 The Global Initiative for Obstructive Lung Disease (GOLD) 2020 recommends a cutoff of 300 cells/μL for the escalation and de-escalation of inhaled corticosteroids among patients with COPD. The previous study showed the prevalence of increased blood eosinophil counts may be lower in COPD exacerbations than in stable periods.20 We also found only 13.9% patients hospitalized for AECOPD in this study had blood eosinophil counts above 300 cells/μL at index hospitalization. Thomas et al26 also proposed that using lower eosinophilic cutoff values (100 or 150 cells/μL) was more beneficial for investigation of the stability of blood eosinophil counts over time. Therefore, 150 cells/μL was selected as the cutoff value of blood eosinophils in our study.
In our study, 31.5% patients hospitalized for AECOPD had increased blood eosinophilic counts ≥150 cells/μL at index hospitalization. These patients presented with fewer comorbidities, lower neutrophil fraction, shorter time since onset of symptoms and length of stay, which was similar to some previous studies.4,7,27 The corticosteroids and antibiotics are two classes of medications commonly used for COPD exacerbations, AECOPD patients are heterogeneous with respect to response to pharmacologic therapies. In the present study, any case decision to treatment of intravenous corticosteroids was based on clinical practice methods other than blood eosinophil status. This study revealed eosinophilic COPD patients had a lower proportion of intravenous corticosteroids administration. For those patients administered intravenous corticosteroids, eosinophilic COPD patients had a significantly shorter course and lower consumption of intravenous corticosteroid relative to non-eosinophilic COPD patients. These results in our study showed COPD inpatients with high eosinophils presented with a better response to intravenous corticosteroids treatment, which were consistent with some previous studies.4,7,9,10 However, there was no significant difference between groups in inhaled corticosteroids during index admission. COPD exacerbations are mainly triggered by respiratory tract infection. Our study showed eosinophilic COPD patients had a lower proportion of dual antibiotic treatment compared with non-eosinophilic COPD patients, which may further suggest eosinophilic COPD patients may have mild bacterial infection. These data may predict a lower risk of all-cause mortality among eosinophilic COPD patients.
During the median follow-up of 46 months, 312 patients hospitalized for COPD died in the period of follow-up. Blood eosinophils ≥150 cells/μL measured at baseline were associated with lower risk of all-cause mortality among patients hospitalized for COPD exacerbations (this trend persisted after excluding patients with a history of asthma, see Supplementary Table A8). We also repeated these analyses using 200 cells/μL and 300 cells/μL as cutoff values of blood eosinophils. Blood eosinophils ≥200 cells/μL were associated with lower risk of all-cause death with borderline statistical significance (P=0.055), while it was no longer significant when 300 cells/μL was used as the cutoff value of blood eosinophil. It may be related to a relatively low percentage of higher blood eosinophil counts in this study. Otherwise, we compute interquartile levels of blood eosinophil counts and put the variables of interquartile levels of blood eosinophil counts into the same Cox regression model. We repeated the association analysis and observed that with the 1st interquartile level as reference group, the risk of death at the 2nd, 3rd, and 4th interquartile levels gradually decreased and the linear trend reached to statistical significance (Supplementary Table A9). The sensitivity analysis indicated that the higher the blood eosinophil counts, the lower the risk of all-cause death. Some previous studies also showed similar results.5,11-13 However, another study from France revealed there was no association of increased blood eosinophils and mortality of COPD patients regardless of the cutoff values.14 There might be some reasons which can explain these discrepancies: most importantly, blood eosinophils naturally fluctuate over time and are affected by many factors. Furthermore, selective differences in the cutoff values of blood eosinophils may affect the final results. Another point to consider is the difference of recruited study subjects’ illness severity. The study subjects from our study and Li et al13 were patients hospitalized for AECOPD, Salturk et al5 study subjects were patients who were admitted to ICU with acute respiratory failure, while other studies' subjects were from stable COPD patients.11,12,14 In addition, whether patients suffering with asthma were included or not may affect study results.
Considering that blood eosinophil counts are significantly variable over time, a single measurement may not be a reliable predictor for mortality of COPD patients. Some studies have shown the association of stability of blood eosinophils over time with mortality of COPD patients.15,18,19 However, these study subjects were mainly concentrated on stable COPD patients. There are limited studies on the association of longitudinally eosinophilic stability with all-cause mortality of patients frequently hospitalized for AECOPD. In our study of hospitalized patients with COPD, 17% had predominantly high eosinophils and had lower all-cause mortality compared to those with rare blood eosinophils ≥150 cells/μL (the result remained unchanged after excluding patients with a history of asthma, see Supplementary Table A10). This finding was consistent with those from previous studies from stable COPD patients.15,18,19 However, no statistically significant association was observed when using 200 cells/μL or 300 cells/μL as the cutoff values of blood eosinophils. This was due to the few number of patients with blood eosinophils ≥200 cells/μL and even fewer patients with blood eosinophils ≥300 cells/μL which limited the statistical power. This needs to be further confirmed by a large scale cohort study.
Our study suggested patients with increased eosinophils had a lower risk of all-cause mortality. It is well known that COPD patients with increased eosinophils present with better responsiveness to ICS. Therefore, this reduction in all-cause mortality among patients with increased blood eosinophil counts may be as a result of exposure to inhaled corticosteroids. Accordingly, we made further analysis adjusting for inhaled corticosteroids usage during index hospitalization in a Cox regression model, and the association analysis remained significant (Supplementary Table A11, A12). However, since we did not collect medication after index hospitalization, it is unknown what impact inhaled corticosteroids have on long-term mortality of stable COPD patients. Further studies are needed to confirm it.
In our study, we also performed repeated analysis for an association of baseline blood eosinophil ≥150 cells/μL and all-cause mortality of patients with at least three blood eosinophil counts measured at admission for AECOPD. There was no statistical difference in mortality of COPD between the non-eosinophilic and eosinophilic groups, which may be related to a change in the sample size of the database. For this small database, longitudinal stability of blood eosinophils used to predict all-cause mortality of COPD patients was superior to a single measurement of baseline blood eosinophils.
There were some strengths. COPD exacerbations are heterogeneous and blood eosinophils have variability, we chose patients hospitalized for AECOPD as the study subjects and analyzed blood eosinophil levels from subjects’ subsequent hospitalizations. To our surprise, increased eosinophils (using lower eosinophils 150 cells/μL as cutoff value) at index hospitalization or blood eosinophil longitudinal pattern over 5 years were associated with lower risk of all-cause mortality of patients hospitalized for AECOPD, which was different from those studies from stable COPD patients. Moreover, this study was from “real life” nature and not any intervention, therefore, it was more beneficial to clinical management of COPD patients. However, there were some limitations. Because pre-hospitalization medication use was unavailable, it was difficult to rule out the impact of pre-hospitalization corticosteroid administration on blood eosinophil counts, which may be the result of the relatively lower prevalence of increased blood eosinophil counts. Secondly, due to the nature of retrospective studies, some confounding variables such as pulmonary function test, MRC dyspnea score, medication treatment after index discharge were also unavailable and thus were not analyzed in our study, which might bias our results to some extent. Another study limitation is that it was a single-center study of patients hospitalized for AECOPD in the People's Republic of China, therefore, the results may not be generalizable to the entire Chinese COPD population. Further multicenter studies of the Chinese population are very necessary to confirm these results.
Conclusion
These data suggested that patients with increased eosinophils (using lower eosinophil 150 cells/μL as the cutoff value), especially predominantly increased eosinophil levels based on multiple measurements, had a lower risk of all-cause mortality. Blood eosinophilia can be used as a biomarker in hospitalized COPD exacerbations for predicting all-cause mortality.
Funding Statement
This work was supported by the National Key R&D Program of China (2016YFC1303900), the Beijing Municipal Administration of Hospitals’ Mission Plan, the People's Republic of China (No. SML20150301), Capital’s Funds for Health Improvement and Research (No. CFH2016-4-1062) and Chinese Medical Association Chronic Respiratory Disease Fund (No. CRD 08020440122).
Disclosure
Ying Zhang’s present address: Department of Respiratory and Critical Care Medicine, Cangzhou Central Hospital, Cangzhou, Hebei 061000, China. Ying Zhang and Li-Rong are co-first authors. The authors report no conflicts of interest in this work.
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