Responses Induced by Smoking in Individuals Being Susceptible and Non-Susceptible for Development of COPD
NCT ID: NCT00807469
Last Updated: 2008-12-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
120 participants
OBSERVATIONAL
2009-01-31
2015-01-31
Brief Summary
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Objective:
* To define mediators involved in the early induction of COPD in susceptible smokers (and so to define new drug targets)
* To develop new biological and clinical markers for the early diagnosis and monitoring of COPD
* To compare between susceptible and non-susceptible individuals the corticosteroid responsiveness of bronchial epithelial cells in vitro, and to study the mechanisms of smoking-induced corticosteroid unresponsiveness.
* To study the role of candidate genes that may play a role in the development of fixed airway obstruction, and to identify clues for patient's responsiveness to specific drugs.
Detailed Description
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* Local inflammation before and after cigarette smoking assessed by exhaled breath condensate, microprobe sampling and bronchial biopsies.
* Systemic inflammation before and after cigarette smoking assessed by the expression of established and newly developed markers on innate immune cells associated with pre-activation.
* Extensive clinical characterisation including life style factors, lung function, CT scanning of the lung.
* Corticosteroid responsiveness of epithelial cells in vitro.
* Distribution of candidate genes (SNPs) for COPD between the 5 different groups ( see description below) and associations with the inflammatory responses on acute smoking.
Conditions
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Keywords
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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1
20 healthy individuals not susceptible for COPD (age 18-40 years, \>0\>10 packyears, FEV1/VC \>70%, FEV1 \>85% predicted)
No interventions assigned to this group
2
20 healthy individuals susceptible for COPD (age 18-40 years \>20 packyears, FEV1/VC \>70%, FEV1 \>85% predicted) and high prevalence of COPD in smoking family members older than 45 years
No interventions assigned to this group
3
20 healthy individuals very susceptible for COPD (age 18-40 years, \> 0 \> 10 packyears, FEV1/VC \>70%, FEV1 \>85% predicted), and one of the smoking family members has severe early onset COPD or mild COPD with very low smoke exposure
No interventions assigned to this group
4
30 healthy individuals not susceptible for COPD (age 40-75 years, \>20 packyears, FEV1/VC \>70%, FEV1 \>85% predicted)
No interventions assigned to this group
5
30 COPD patients with GOLD stage II (age 40-75 years, \>10 packyears, FEV1/VC \<\_70%, FEV1 50-80% predicted)
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Age, pack years, FEV1/FVC and FEV1% predicted must fit in one of the 5 groups described above.
* Able to stop smoking for 10 days and start smoking 3-4 cigarettes within 1 hour
* Physically and mentally able to undergo the total study protocol
* Written informed consent
Exclusion Criteria
* Alpha-1-antitrypsin deficiency
* Selected grade 1-3 co-morbidity listed in the ACE-27
* Active pulmonary infection like tuberculosis, pneumonia, flue, tracheobronchitis
* Active extra-pulmonary infection like hepatitis A-C, cystitis, gastro-enteritis etc
* Pulmonary diseases like sarcoidosis, IPF, silicosis, hypersensitivity pneumonitis
* Life threatening diseases like carcinoma, AIDS (including HIV+), acute leukaemia etc
* Medication that may affect the results of the study: NSAID's, immunosuppressive agents like prednisolon, metotrexate, azathioprine,Acenocoumarol
18 Years
75 Years
ALL
Yes
Sponsors
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University Medical Center Groningen
OTHER
UMC Utrecht
OTHER
GlaxoSmithKline
INDUSTRY
Nycomed
INDUSTRY
Top Institute Pharma
OTHER
Responsible Party
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Pulmonary Department UMCG Groningen, Postbus 9700 RB Groningen
Principal Investigators
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Dirkje Postma, Dr. Prof. MD
Role: PRINCIPAL_INVESTIGATOR
UMCG
Locations
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Universitair Medisch Centrum Groningen
Groningen, Provincie Groningen, Netherlands
Countries
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Central Contacts
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Facility Contacts
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Nick ten Hacken, MD
Role: primary
References
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Boudewijn IM, Faiz A, Steiling K, van der Wiel E, Telenga ED, Hoonhorst SJM, Ten Hacken NHT, Brandsma CA, Kerstjens HAM, Timens W, Heijink IH, Jonker MR, de Bruin HG, Sebastiaan Vroegop J, Pasma HR, Boersma WG, Wielders P, van den Elshout F, Mansour K, Spira A, Lenburg ME, Guryev V, Postma DS, van den Berge M. Nasal gene expression differentiates COPD from controls and overlaps bronchial gene expression. Respir Res. 2017 Dec 21;18(1):213. doi: 10.1186/s12931-017-0696-5.
Loi ALT, Hoonhorst S, van Aalst C, Langereis J, Kamp V, Sluis-Eising S, Ten Hacken N, Lammers JW, Koenderman L. Proteomic profiling of peripheral blood neutrophils identifies two inflammatory phenotypes in stable COPD patients. Respir Res. 2017 May 22;18(1):100. doi: 10.1186/s12931-017-0586-x.
Hoonhorst SJ, Lo Tam Loi AT, Pouwels SD, Faiz A, Telenga ED, van den Berge M, Koenderman L, Lammers JW, Boezen HM, van Oosterhout AJ, Lodewijk ME, Timens W, Postma DS, Ten Hacken NH. Advanced glycation endproducts and their receptor in different body compartments in COPD. Respir Res. 2016 Apr 26;17:46. doi: 10.1186/s12931-016-0363-2.
Hoonhorst SJ, Timens W, Koenderman L, Lo Tam Loi AT, Lammers JW, Boezen HM, van Oosterhout AJ, Postma DS, Ten Hacken NH. Increased activation of blood neutrophils after cigarette smoking in young individuals susceptible to COPD. Respir Res. 2014 Oct 10;15(1):121. doi: 10.1186/s12931-014-0121-2.
Hoonhorst SJ, ten Hacken NH, Lo Tam Loi AT, Koenderman L, Lammers JW, Telenga ED, Boezen HM, van den Berge M, Postma DS. Lower corticosteroid skin blanching response is associated with severe COPD. PLoS One. 2014 Mar 12;9(3):e91788. doi: 10.1371/journal.pone.0091788. eCollection 2014.
Lo Tam Loi AT, Hoonhorst SJ, Franciosi L, Bischoff R, Hoffmann RF, Heijink I, van Oosterhout AJ, Boezen HM, Timens W, Postma DS, Lammers JW, Koenderman L, Ten Hacken NH. Acute and chronic inflammatory responses induced by smoking in individuals susceptible and non-susceptible to development of COPD: from specific disease phenotyping towards novel therapy. Protocol of a cross-sectional study. BMJ Open. 2013 Feb 1;3(2):e002178. doi: 10.1136/bmjopen-2012-002178. Print 2013.
Other Identifiers
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23440
Identifier Type: -
Identifier Source: org_study_id