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Table 1 Profiles of the four participant groups

From: Positive association between the plasma levels of 5-hydroxyindoleacetic acid and the severity of depression in patients with chronic obstructive pulmonary disease

Parameter

Control subjects

COPD patients

Nonsmokers

Smokers

Non-depressed

Depressed

Number of subjects

23

13

50

20

Age (yr)

66.7 ± 9.0

66.5 ± 11.6

68.5 ± 7.2

68.2 ± 7.8

Gendera (no. of males; %)

15 (65.2)

12 (92.3)

47 (94.0)

14 (70.0)

Body mass index (kg/m2)

22.1 ± 2.4

23.0 ± 2.8

21.9 ± 3.1

19.8 ± 3.8†

Smoking statusa

    

Non / Ex / Cu (no.)

23 / 0 / 0

0 / 4 / 9

0 / 33 / 17

0 / 14 / 6

Smoke index (pack-yrs)

0

40.0 ± 18.2***

59.3 ± 30.3***

52.2 ± 27.0***

Comorbiditiesa

    

Hypertension (no; %)

7 (30.4)

4 (30.8)

13 (26.0)

4 (20.0)

Diabetes (no; %)

5 (21.7)

1 (7.7)

11 (22.0)

6 (30.0)

Duration of COPD (yr)

N/A

N/A

5.3 ± 3.9

5.5 ± 4.4

GOLD stagea

    

I / II / III / IV (no.)

N/A

N/A

7 / 22 / 17 / 4

2 / 4 / 8 / 6

Lung function parameters

    

Before bronchodilator

    

FVC (L)

3.5 ± 0.9

3.6 ± 0.7

3.4 ± 0.8

2.7 ± 0.9*†‡

%FVC

108.5 ± 17.0

105.6 ± 19.3

98.8 ± 18.3

86.4 ± 22.2**†

FEV1 (L)

2.6 ± 0.6

2.6 ± 0.5

1.5 ± 0.6***†††

1.1 ± 0.7***†††

%FEV1

100.8 ± 14.3

94.9 ± 20.1

54.9 ± 20.8***†††

44.8 ± 24.9***†††

FEV1/FVC (%)

77.2 ± 6.9

73.8 ± 5.2

44.4 ± 12.7***†††

41.0 ± 16.2***†††

After bronchodilator

    

FVC (L)

3.4 ± 0.9

3.5 ± 0.7

3.4 ± 0.8

2.6 ± 1.0*†‡

%FVC

108.0 ± 17.4

104.3 ± 18.0

99.3 ± 18.5

84.9 ± 23.5**†‡

FEV1 (L)

2.7 ± 0.6

2.7 ± 0.4

1.6 ± 0.6***†††

1.2 ± 0.7***†††

%FEV1

103.0 ± 15.5

96.5 ± 19.9

56.4 ± 20.8***†††

45.3 ± 25.0***†††

FEV1 / FVC (%)

79.2 ± 6.5

76.0 ± 5.9

45.6 ± 13.4***†††

42.3 ± 15.9***†††

Reversibility of FEV1 (%)

2.2 ± 4.5

1.8 ± 3.8

3.3 ± 5.3

1.0 ± 5.2

Arterial blood gases

    

PaO2 (Torr)

90.3 ± 7.5

92.9 ± 5.9

76.6 ± 9.5***†††

71.9 ± 13.9***†††

PaCO2 (Torr)

41.4 ± 3.2

41.7 ± 3.5

40.0 ± 4.0

44.6 ± 7.1‡

mMRC dyspnea scale

0.0 ± 0.0

0.2 ± 0.6

1.0 ± 1.1***†††

2.1 ± 1.6***†††§

SGRQ

    

Total score (units)

8.4 ± 8.3

15.7 ± 12.0

32.6 ± 15.9***††

57.8 ± 20.8***†††¶

Symptom score (units)

19.6 ± 13.4

30.9 ± 18.9

40.8 ± 21.3**††

66.2 ± 16.7***†††¶

Activity score (units)

6.0 ± 7.1

20.9 ± 17.2

42.9 ± 24.1***†††

68.2 ± 29.7***†††§

Impact score (units)

6.2 ± 10.0

8.0 ± 9.9

21.3 ± 13.9**††

52.0 ± 23.2***†††¶

CES-D scale

1.7 ± 2.9

2.5 ± 3.1

8.5 ± 5.2***†††

24.5 ± 6.0***†††¶

Treatments for COPDb

    

LAMA (no; %)

0

0

33 (66.0)

16 (80.0)

LABA (no; %)

0

0

21 (42.0)

10 (50.0)

ICS (no; %)

0

0

15 (30.0)

11 (55.5)

SRT (no; %)

0

0

7 (14.0)

4 (20.0)

  1. All data were expressed as mean ± SD and compared by one-way ANOVA and Tukey-Kramer test for multiple comparisons among the four groups.
  2. a Data were compared among groups by chi-squared test for trend.
  3. b Data were compared between depressed and non-depressed COPD patients by Fisher’s exact test. Numbers of non-depressive and depressive COPD patients who used salmeterol and fluticasone devices in combination were 13 and 10, respectively. Some patients were taking multiple medications.
  4. * p<0.05, ** p<0.01, and *** p<0.001 vs. nonsmokers.
  5. † p<0.05, †† p<0.01, and ††† p<0.001 vs. smokers.
  6. ‡ p<0.05, § p<0.01, and ¶ p<0.001 vs. non-depressed COPD patients.
  7. Non, non-smokers; Ex, ex-smokers; Cu, current smokers; GOLD, Global Initiative for Chronic Obstructive Lung Disease; FVC, forced expiratory capacity; FEV1, forced expiratory volume in 1 second; PaO2, partial pressure of arterial oxygen; PaCO2, partial pressure of arterial carbon dioxide; mMRC, modified Medical Research Council; SGRQ, St George’s respiratory questionnaire; CES-D, Center for Epidemiological Studies depression scale; LAMA, long-acting muscarinic receptor antagonist; LABA, long-acting β2 agonist; ICS, inhaled corticosteroid; SRT, slow-release theophylline; N/A, not available.