Increased risk of both ulcerative colitis and Crohn's disease in a population suffering from COPD
(2008) In Lung 186(3). p.167-172- Abstract
- Chronic obstructive pulmonary disease (COPD) is characterized by chronic inflammation of the airways. In the majority of cases, the inflammation is triggered by tobacco smoke. Smoking also affects the pathogenesis of inflammatory bowel disease (IBD), protecting against ulcerative colitis (UC) and promoting development of Crohn's disease (CD). The present study was undertaken to investigate occurrence of IBD among COPD patients, indicating common inflammatory pathways and shared vulnerability on a genetic basis. The study was designed as a population-based cohort study. All individuals discharged with a diagnosis of COPD from 1987 to 2002 were identified in the Swedish Inpatient Register (n = 180,239). Controls and first-degree relatives of... (More)
- Chronic obstructive pulmonary disease (COPD) is characterized by chronic inflammation of the airways. In the majority of cases, the inflammation is triggered by tobacco smoke. Smoking also affects the pathogenesis of inflammatory bowel disease (IBD), protecting against ulcerative colitis (UC) and promoting development of Crohn's disease (CD). The present study was undertaken to investigate occurrence of IBD among COPD patients, indicating common inflammatory pathways and shared vulnerability on a genetic basis. The study was designed as a population-based cohort study. All individuals discharged with a diagnosis of COPD from 1987 to 2002 were identified in the Swedish Inpatient Register (n = 180,239). Controls and first-degree relatives of both cases and controls were identified using the Multi-Generation Register. Finally, all individuals (n = 1,174,557) were compared with the Inpatient Register, identifying discharges with a diagnosis of UC or CD. Hazard ratios (HR) for IBD were determined by Cox proportional hazards regression analysis. COPD patients had a significantly higher risk of both UC (HR 1.83; 95% CI 1.61-2.09) and CD (HR 2.72; 95% CI 2.33-3.18). Among first-degree relatives of COPD patients, there was also an overall increased risk of CD (HR 1.25; 95% CI 1.09-1.43) but not of UC (HR 1.09; 95% CI 0.96-1.23). The kinship of first-degree relatives displayed an increased risk of both UC and CD among siblings (HR 1.49; 95% CI 1.15-1.91 and HR 1.46; 95% CI 1.12-1.89, respectively). The results suggest that COPD and IBD may have inflammatory pathways in common, including genetic variants of genes predisposing for disease. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1201727
- author
- Ekbom, Anders ; Brandt, Lena ; Granath, Fredrik ; Löfdahl, Claes-Göran LU and Egesten, Arne LU
- organization
- publishing date
- 2008
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- genetics, inflammation, mucosa, COPD, ulcerative colitis, Crohn's disease
- in
- Lung
- volume
- 186
- issue
- 3
- pages
- 167 - 172
- publisher
- Springer
- external identifiers
-
- wos:000256324400005
- scopus:44449179986
- pmid:18330638
- ISSN
- 1432-1750
- DOI
- 10.1007/s00408-008-9080-z
- language
- English
- LU publication?
- yes
- id
- 01e512e4-f77b-42e0-8b8d-98f4297662fa (old id 1201727)
- date added to LUP
- 2016-04-01 13:19:32
- date last changed
- 2022-03-29 06:52:03
@article{01e512e4-f77b-42e0-8b8d-98f4297662fa, abstract = {{Chronic obstructive pulmonary disease (COPD) is characterized by chronic inflammation of the airways. In the majority of cases, the inflammation is triggered by tobacco smoke. Smoking also affects the pathogenesis of inflammatory bowel disease (IBD), protecting against ulcerative colitis (UC) and promoting development of Crohn's disease (CD). The present study was undertaken to investigate occurrence of IBD among COPD patients, indicating common inflammatory pathways and shared vulnerability on a genetic basis. The study was designed as a population-based cohort study. All individuals discharged with a diagnosis of COPD from 1987 to 2002 were identified in the Swedish Inpatient Register (n = 180,239). Controls and first-degree relatives of both cases and controls were identified using the Multi-Generation Register. Finally, all individuals (n = 1,174,557) were compared with the Inpatient Register, identifying discharges with a diagnosis of UC or CD. Hazard ratios (HR) for IBD were determined by Cox proportional hazards regression analysis. COPD patients had a significantly higher risk of both UC (HR 1.83; 95% CI 1.61-2.09) and CD (HR 2.72; 95% CI 2.33-3.18). Among first-degree relatives of COPD patients, there was also an overall increased risk of CD (HR 1.25; 95% CI 1.09-1.43) but not of UC (HR 1.09; 95% CI 0.96-1.23). The kinship of first-degree relatives displayed an increased risk of both UC and CD among siblings (HR 1.49; 95% CI 1.15-1.91 and HR 1.46; 95% CI 1.12-1.89, respectively). The results suggest that COPD and IBD may have inflammatory pathways in common, including genetic variants of genes predisposing for disease.}}, author = {{Ekbom, Anders and Brandt, Lena and Granath, Fredrik and Löfdahl, Claes-Göran and Egesten, Arne}}, issn = {{1432-1750}}, keywords = {{genetics; inflammation; mucosa; COPD; ulcerative colitis; Crohn's disease}}, language = {{eng}}, number = {{3}}, pages = {{167--172}}, publisher = {{Springer}}, series = {{Lung}}, title = {{Increased risk of both ulcerative colitis and Crohn's disease in a population suffering from COPD}}, url = {{http://dx.doi.org/10.1007/s00408-008-9080-z}}, doi = {{10.1007/s00408-008-9080-z}}, volume = {{186}}, year = {{2008}}, }