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Table 3 Incidences and hazard ratios for COPD hospitalisation by intron-8 polythymidine tract and F508del genotype during 24 years follow-up

From: Asthma and COPD in cystic fibrosis intron-8 5T carriers. A population-based study

Poly-T

Expected exon-9 skipping, %

F508del heterozygosity

n

Incidence n/10000 person-years

P-value*

Unadjusted HR (95%CI)

Adjusted HR (95%CI)

90% power HR

9T/9T

7

 

83

40

0.10

1.8 (0.89–3.6)

1.7 (0.85–3.5)

2.3

7T/9T

13

 

1540

21

0.70

0.95 (0.75–1.2)

0.99 (0.78–1.3)

1.3

7T/7T

18

 

6905

22

-

1.0

1.0

-

6T/7T

≥18

 

4

105

0.08

4.9 (0.69–35)

7.6 (1.0–55)

11

5T/9T

43

 

40

21

0.90

0.92 (0.23–3.7)

0.75 (0.19–3.0)

3.0

5T/7T

48

 

308

11

0.03

0.47 (0.23–0.95)

0.49 (0.23–1.0)

1.6

5T/5T

78

 

2

0

0.73

-

-

19

9T/9T

-

yes

23

0

0.25

-

-

3.8

7T/9T

-

yes

217

25

0.73

1.1 (0.63–1.9)

1.1 (0.62–1.9)

1.7

7T/7T

-

yes

5

0

0.59

 

-

9.7

5T/9T

-

yes

4

0

0.63

-

-

11

  1. *P-values are for the comparison with 7T/7T individuals without the F508del deletion by log-rank test. Cox regression adjusted for gender, age at study entry, tobacco use during follow-up, and FEV1 % predicted at study entry. 90% power to detect a hazard ratio (HR) of COPD at 2-sided P < 0.05. 95%CI = 95% confidence interval. Hospitalizations from COPD (ICD8: 491–492; ICD10: J41–44) were drawn from the Danish National Discharge Register from 1976 through 2000.