-174G>C interleukin-6 gene polymorphism in Tunisian patients with coronary artery disease
2011

IL-6 Gene Polymorphism and Coronary Artery Disease in Tunisians

Sample size: 824 publication 10 minutes Evidence: moderate

Author Information

Author(s): Ghazouani Lakhdar, Abboud Nesrine, Khalifa Sonia Ben Hadj, Added Faouzi, Khalfallah Ali Ben, Nsiri Brahim, Mediouni Mounira, Mahjoub Touhami

Primary Institution: Research Unit of Biology and Genetics of Cancer, Haematological and Autoimmune Diseases, Faculty of Pharmacy of Monastir, Monastir, Tunisia

Hypothesis

The -174G>C IL-6 promoter variant contributes to the risk of coronary artery disease (CAD) among Tunisians.

Conclusion

The -174G>C IL-6 promoter variant is not associated with an increased risk of CAD among Tunisians.

Supporting Evidence

  • The frequency of the -174C allele was lower in Tunisians than in Europeans.
  • The distribution of -174 G>C genotypes was similar between CAD patients and control subjects.
  • -174C allele carriage did not increase the CAD relative risk.
  • The study was the first to examine the association of IL-6 promoter variants with CAD in Tunisians.
  • Regression analysis confirmed the lack of association of -174G/C genotypes with CAD.

Takeaway

This study looked at a gene variant to see if it affects heart disease risk in Tunisians, and found it doesn't seem to make a difference.

Methodology

A case-control study involving 418 CAD patients and 406 matched controls, with IL-6 genotyping performed by PCR-restriction fragment length polymorphism.

Potential Biases

The study's focus on a single ethnic group may limit the generalizability of the findings.

Limitations

The study was limited to a specific ethnic group and did not measure plasma IL-6 concentrations.

Participant Demographics

418 CAD patients (87 females, 331 males) and 406 controls (107 females, 299 males), matched for age and sex.

Statistical Information

P-Value

p=0.55

Confidence Interval

1.09 (0.80-1.49)

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.4103/0256-4947.75777

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