1. Association of IL-6 gene polymorphisms and COPD in a Spanish population.
- Author
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Córdoba-Lanús E, de-Torres JP, López-Aguilar C, Rodríguez-Pérez MC, Maca-Meyer N, Montejo-de-Garcini A, Aguirre-Jaime A, Pérez-Méndez L, and Casanova C
- Subjects
- Adult, Aged, Case-Control Studies, Female, Genetic Markers, Genetic Predisposition to Disease, Genotype, Haplotypes, Humans, Male, Middle Aged, Promoter Regions, Genetic genetics, Smoking genetics, Interleukin-6 genetics, Polymorphism, Single Nucleotide, Pulmonary Disease, Chronic Obstructive genetics
- Abstract
Interleukin-6 (IL-6) is a potential mediator of systemic effects of Chronic Obstructive Pulmonary Disease (COPD). In the present case-control study we investigated the association of promoter polymorphisms of this gene and COPD in a cohort of 191 patients, smokers without COPD (n=75) and a healthy control population (n=296). Besides spirometry, exercise capacity (6MWD, 6 min walking distance) and body mass index (BMI) were measured in COPD patients. Genotyping of the IL-6 polymorphisms at positions -174, -572 and -597 was performed. The -597G/A and -174G/C polymorphisms were not associated with the disease. However, the -572G/C polymorphism was significantly associated with COPD susceptibility under a dominant model of inheritance. The frequency of the genotypes containing the C allele was significantly lower in the COPD cases (9.9%) compared with the healthy control group (16.9%) and smokers (23.1%), (OR=0.46, p=0.032 and OR=0.28, p=0.012, respectively). The GCG (-597/-572/-174) haplotype was significantly associated with the disease (OR=0.37, p=0.022, COPD cases vs. healthy subjects and OR=0.17, p=0.011, COPD cases vs. smokers). Moreover, a borderline association was also found for the -572G allele and hypoxemia (PaO(2)<60 mmHg) (p=0.05). Our data suggest that the IL-6 -572C allele may confer a diminished risk of developing COPD.
- Published
- 2008
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