Investigation of 89 candidate gene variants for effects on all-cause mortality following acute coronary syndrome
2008

Genetic Variants and Mortality After Acute Coronary Syndrome

Sample size: 811 publication 10 minutes Evidence: moderate

Author Information

Author(s): Morgan Thomas M, Xiao Lan, Lyons Patrick, Kassebaum Bethany, Krumholz Harlan M, Spertus John A

Primary Institution: Vanderbilt University School of Medicine

Hypothesis

Do candidate gene variants affect all-cause mortality following acute coronary syndrome?

Conclusion

The study found that most candidate genes were not associated with post-ACS mortality, except for the IRS1 variant which showed borderline significance.

Supporting Evidence

  • 16 out of 89 genetic variants were potentially associated with mortality.
  • 6 variants were significantly associated with mortality at p<0.05.
  • The IRS1 Gly972Arg variant showed a strong association with mortality.

Takeaway

The researchers looked at genes to see if they could predict who might die after a heart problem, but they mostly found that these genes didn't help much.

Methodology

The study genotyped 89 genetic variants in 811 ACS survivors and performed survival analyses and Cox regression.

Potential Biases

Potential bias from focusing on a single racial group and the small sample size may limit generalizability.

Limitations

The study had limited power due to a small number of deaths and focused only on white patients.

Participant Demographics

811 self-reported white patients of European ancestry with acute coronary syndrome.

Statistical Information

P-Value

P = 0.001 for IRS1 variant

Confidence Interval

0.02, 0.84 for A/G and 0.05, 0.99 for G/G genotypes of IRS1

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1186/1471-2350-9-66

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