Mendelian Randomization Study of Interleukin-6 in Chronic Obstructive Pulmonary Disease

YMTA van Durme, Lies Lahousse, Katia Verhamme, Lisette Stolk, Mark Eijgelsheim, Daan Loth, André Uitterlinden, Monique Breteler, GF Joos, Bert Hofman, Bruno Stricker, Guy Brusselle

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Abstract

Background: Cross-sectional studies have demonstrated that increased levels of interleukin-6 (IL6) are present in the airways and blood samples of patients with chronic obstructive pulmonary disease (COPD). Objectives: To investigate the association between IL6 and the risk of COPD using a Mendelian randomization approach. Methods: Eight common single-nucleotide polymorphisms (SNPs) in the region of the IL6 gene were genotyped using both TaqMan and Illumina in the Rotterdam Study, a prospective population-based cohort study consisting of 7,983 participants aged 55 years or older, including 928 COPD patients. At baseline, blood was drawn in a random sample of 714 subjects to measure the IL6 plasma level. Analysis of variance, logistic regression, and Cox proportional hazard models - adjusted for age, gender, pack years, and BMI - were used for analyses. Results: High levels of IL6 (>2.4 pg/ml, the highest tertile) were associated with a three-fold increased risk of developing COPD, in comparison to low levels (<1.4 pg/ml, the lowest tertile). The rs2056576 SNP was associated with a 10% increase in the risk of COPD per additional T allele. However, the association was no longer significant after adjustment. No association was found with other common SNPs in the IL6 gene and COPD. Conclusions: Although increased IL6 plasma levels at baseline are associated with the risk of developing COPD during follow-up, there was no strong evidence for an association between common variation in the IL6 gene and the risk of COPD. Copyright (C) 2011 S. Karger AG, Basel
Original languageUndefined/Unknown
Pages (from-to)530-538
Number of pages9
JournalRespiration
Volume82
Issue number6
DOIs
Publication statusPublished - 2011

Research programs

  • EMC MM-01-39-09-A
  • EMC NIHES-01-64-01
  • EMC NIHES-01-64-03
  • EMC NIHES-03-77-02

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