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Clinical Chemistry 0: clinchem.2007.092692v1, 2007; 10.1373/clinchem.2007.092692
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Received on May 29, 2007
Accepted on October 2, 2007

Molecular Diagnostics and Genetics

IL18 Haplotypes Are Associated with Serum IL-18 Concentrations in a Population-Based Study and a Cohort of Individuals with Premature Coronary Heart Disease

Simon R. Thompson 1, Pamela A. McCaskie 2, John P. Beilby 3, Joseph Hung 4, Michelle Jennens 3, Caroline Chapman 3, Peter Thompson 5, Steve E. Humphries 1*

1 Department of Cardiovascular Genetics, University College London, 5 University Street, London, United Kingdom
2 Laboratory for Genetic Epidemiology, Western Australian Institute for Medical Research, University of Western Australia, Perth, Australia
3 Clinical Biochemistry, Western Australia Centre for Pathology and Medical Research, University of Western Australia, Perth, Australia
4 Sir Charles Gairdner Hospital Campus, Heart Research Institute of Western Australia, Perth, Australia, and School of Medicine and Pharmacology, University of Western Australia, Perth, Australia
5 Sir Charles Gairdner Hospital Campus, Heart Research Institute of Western Australia, Perth, Australia

* To whom correspondence should be addressed. E-mail: rmhaseh{at}ucl.ac.uk.

Background: Interleukin (IL)-18 is a proinflammatory cytokine that has been implicated in several diseases, including atherosclerosis, and increased circulating IL-18 concentrations increase risk of future coronary heart disease (CHD). We evaluated the effect of common variation within the IL18 gene on concentrations of circulating IL-18.

Methods: We measured IL-18, by ELISA, in the population-based study group [Carotid Ultrasound Disease Assessment Study (CUDAS)] and a predominantly male cohort with premature cardiovascular disease [Carotid Ultrasound in Patients with Ischaemic Heart Disease (CUPID)]. Using a tagging single-nucleotide polymorphism (SNP) approach that captured >90% of genetic variation, we identified 4 common (>10%) haplotypes.

Results: A common SNP was associated with differences in IL-18 concentrations; in CUDAS individuals carrying 2 copies of the rare allele, concentrations were 13% higher than in those with no copies (P = 0.002). Haplotypes were also associated with significant differences in IL-18 concentrations in CUDAS and CUPID. Haplotype GTATA (frequency 23%) was associated with significantly lower IL-18 than others. In CUDAS, those carrying 2 copies had IL-18 concentrations 15% lower than those carrying no copies (P = 0.002); in CUPID, the difference was 22% (P = 0.004). These associations remained significant after adjustment for age, sex, hypertension, HDL cholesterol, waist-to-hip ratio, and alcohol consumption. Despite being associated with differences in IL-18 concentrations, the haplotypes did not occur at different frequencies in those with or without carotid atherosclerotic plaques.

Conclusions: Variation within IL18 affects IL-18 concentrations in healthy and diseased individuals and thus may influence the pathophysiology of plaques at all stages of CHD progression.







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