AI Article Synopsis

  • The study aimed to investigate the relationship between IL-18 gene polymorphism and early signs of atherosclerosis, specifically looking at intima-media thickness, coronary artery compliance, and flow-mediated dilatation in young healthy Caucasians.
  • The research involved 2,260 participants with a mean age of 31.7 years and analyzed various haplotypes of the IL-18 gene.
  • The findings indicated no overall association between IL-18 gene polymorphism and atherosclerosis, but a specific haplotype in men was linked to significantly lower intima-media thickness, highlighting a gender-based difference in genetic impact.

Article Abstract

Background And Aim: Interleukin-18 (IL-18) is a pro-atherosclerotic cytokine. We wanted to evaluate whether IL-18 gene polymorphism associates independently of risk factors, with early subclinical markers of atherosclerosis (intima-media thickness (IMT), coronary artery compliance (CAC), and flow-mediated dilatation (FMD)) in a population of young healthy Caucasian adults.

Methods: This study was based on the on-going Cardiovascular Risk in Young Finns Study consisting of 2260 young adults, mean age being 31.7 (range 24-39 years) (1247 women and 1013 men).

Results: Five studied tagSNPs formed six major haplotypes, which accounted for 99.9% of all variation of the IL-18 gene. According to adjusted analysis of variance, the IL-18 gene polymorphism did not associate with subclinical atherosclerosis in the whole study population. However, one major haplotype associated differently among men and women with IMT (P = 0.011). Male carriers of a major CCTgT haplotype (n = 441) seemed to have a lower IMT when compared to the non-carriers (-0.016 mm, 95% confidence interval (CI) -0.028 to -0.004, P = 0.014). Among women no significant associations were observed.

Conclusions: Among all study subjects, the polymorphism of the IL-18 gene is not associated with subclinical markers of atherosclerosis. However, among men one major IL-18 haplotype seemed to associate with substantially lower IMT values.

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Source
http://dx.doi.org/10.3109/07853891003769940DOI Listing

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