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Original Research

Increased serum IL-17 and decreased serum IL-10 and IL-35 levels correlate with the progression of COPD

, , , &
Pages 2483-2494 | Published online: 20 Aug 2018

Figures & data

Table 1 Clinical data of included patients (75 cases)

Table 2 Correlations between clinical features and the serum levels of IL-17, IL-10, and IL-35 in patients with stable COPD (N=75)

Figure 1 Correlation between clinical factors and the serum level of IL-17 in patients with stable COPD.

Notes: (A) The expression of serum IL-17 was upregulated in patients with stable COPD compared with those in the control group (P<0.001). (B) Increased serum IL-17 level positively correlated with the age of patients (P=0.039). (C) Serum IL-17 expression did not correlate with the smoking status of patients (P=0.096). (D) The serum level of IL-17 in patients with GOLD-3 and -4 was higher than that in patients with GOLD-1 and -2 (*P<0.001). (E) Patients with mMRC scores of 3 and 4 showed higher serum levels of IL-17 compared with those with mMRC score of 2 (*P<0.001). (F) Patients with a long clinical history displayed a higher expression of serum IL-17 than those with a short history (*P<0.001).
Abbreviations: COPD, chronic obstructive pulmonary disease; GOLD, Global initiative for chronic obstructive Lung Disease; IL, interleukin; mMRC, modified British Medical Research Council.
Figure 1 Correlation between clinical factors and the serum level of IL-17 in patients with stable COPD.

Figure 2 Correlation between clinical factors and the serum level of IL-10 in patients with stable COPD.

Notes: (A) Patients with stable COPD showed lower levels of serum IL-10 than those in the control group (P<0.001). (B) Decreased IL-10 negatively correlated with the age of patients (P=0.001). (C) Decreased IL-10 negatively correlated with the smoking status of patients (P=0.001). (D) Patients with GOLD-3 and -4 showed lower levels of serum IL-10 than those with GOLD-1 and -2 (*P<0.001). (E) Serum level of IL-10 in patients with mMRC score of 4 was lower than in those with mMRC scores of 2 and 3 (*P<0.001). (F) Patients with longer clinical history displayed a lower expression of serum IL-10 than those with a short history (*P<0.001).
Abbreviations: COPD, chronic obstructive pulmonary disease; GOLD, Global initiative for chronic Obstructive Lung Disease; IL, interleukin; mMRC, modified British Medical Research Council.
Figure 2 Correlation between clinical factors and the serum level of IL-10 in patients with stable COPD.

Figure 3 Correlation between clinical factors and the serum level of IL-35 in patients with stable COPD.

Notes: (A) A lower level of serum IL-35 was observed in patients with stable COPD compared with those in the control group (P<0.001). (B) The upregulation of serum IL-35 negatively correlated with the age of patients (P<0.001). (C) The upregulation of serum IL-35 negatively correlated with the smoking status of patients (P=0.027). (D) Patients with GOLD-3 and -4 showed lower levels of serum IL-35 than those with GOLD-1 and -2 (*P<0.001). (E) Patients with mMRC scores of 3 and 4 showed lower levels of serum IL-35 than those with mMRC score of 2 (*P<0.001). (F) Patients with a long clinical history displayed a lower expression of serum IL-35 than those with a short history (*P<0.001).
Abbreviations: COPD, chronic obstructive pulmonary disease; GOLD, Global initiative for chronic Obstructive Lung Disease; IL, interleukin; mMRC, modified British Medical Research Council.
Figure 3 Correlation between clinical factors and the serum level of IL-35 in patients with stable COPD.

Table 3 Linear correlation analysis of important indicators (N=75)

Figure 4 Correlation between the serum levels of IL-17, IL-10, and IL-35 in patients with stable COPD.

Notes: (A) Histogram of serum IL-17 and IL-10 shows that the normalized residuals belonged to normal distribution (P>0.05). (B) The P–P plot suggests that scatter points derived from IL-17 and IL-10 had normal distribution (P<0.05). (C) The dependent variable is approximately linear with the standardized predictive value, which indicates that IL-17 and IL-10 had a negative linear correlation (P<0.001). (D) The vast majority of normalized residuals did not exceed 3, suggesting no abnormal values of IL-17 and IL-10 were found. (E) Histogram of IL-17 and IL-35 shows that the normalized residuals belonged to normal distribution (P>0.05). (F) The P–P plot suggests that scatter points derived from IL-17 and IL-35 showed a normal distribution (P<0.05). (G) The dependent variable is approximately linear with the standardized predictive value, which indicates that IL-17 and IL-35 had a negative linear correlation (P<0.001). (H) The vast majority of normalized residuals did not exceed 3, suggesting no abnormal values of IL-17 and IL-35 were found. (I) Histogram of IL-10 and IL-35 shows that the normalized residuals had normal distribution (P>0.05). (J) The P–P plot suggests that scatter points derived from IL-10 and IL-35 had normal distribution (P<0.05). (K) The dependent variable is approximately linear with the standardized predictive value, which indicates that IL-10 and IL-35 had a positive linear correlation (P<0.001). (L) The vast majority of normalized residuals did not exceed 3, suggesting no abnormal values of IL-10 and IL-35 were found.
Abbreviations: COPD, chronic obstructive pulmonary disease; IL, interleukin.
Figure 4 Correlation between the serum levels of IL-17, IL-10, and IL-35 in patients with stable COPD.

Figure 5 Correlation between the serum levels of IL-17, IL-10, and IL-35 and pulmonary function in patients with stable COPD.

Notes: (A) Histogram of serum IL-17 and FEV1/FVC suggests that these variables had a characteristic of normal distribution (P>0.05). (B) The dependent variable is approximately linear with the standardized predictive value, which indicates that serum IL-17 and FEV1/FVC of patients had a negative linear correlation (P<0.001). (C) Histogram of serum IL-17 and FEV1% predicted suggests that these variables had a characteristic of normal distribution (P>0.05). (D) The dependent variable is approximately linear with the standardized predictive value, which indicates that serum IL-17 and FEV1% predicted of patients had a negative linear correlation (P<0.001). (E) Histogram of serum IL-10 and FEV1/FVC suggests that these variables had a characteristic of normal distribution (P>0.05). (F) The dependent variable is approximately linear with the standardized predictive value, which indicates that serum IL-10 and FEV1/FVC of patients had a negative linear correlation (P<0.001). (G) Histogram of serum IL-10 and FEV1% predicted suggests that these variables had a characteristic of normal distribution (P>0.05). (H) The dependent variable is approximately linear with the standardized predictive value, which indicates that serum IL-10 and FEV1% predicted of patients had a negative linear correlation (P<0.001). (I) Histogram of serum IL-35 and FEV1/FVC suggests that these variables had a characteristic of normal distribution (P>0.05). (J) The dependent variable is approximately linear with the standardized predictive value, which indicates that serum IL-35 and FEV1/FVC of patients had a negative linear correlation (P<0.001). (K) Histogram of serum IL-35 and FEV1% predicted suggests that these variables had a characteristic of normal distribution (P>0.05). (L) The dependent variable is approximately linear with the standardized predictive value, which indicates that serum IL-35 and FEV1% predicted of patients had a negative linear correlation (P<0.001).
Abbreviations: COPD, chronic obstructive pulmonary disease; FEV1, forced expiratory volume in 1 second; FVC, forced vital capacity; IL, interleukin.
Figure 5 Correlation between the serum levels of IL-17, IL-10, and IL-35 and pulmonary function in patients with stable COPD.