Lack of association of two common polymorphisms on 9p21 with risk of coronary heart disease and myocardial infarction; results from a prospective cohort study
2008

Study on Genetic Variants and Heart Disease Risk

Sample size: 7983 publication Evidence: moderate

Author Information

Author(s): Abbas Dehghan, Mandy van Hoek, Eric JG Sijbrands, Ben A Oostra, Albert Hofman, Cornelia M van Duijn, Jacqueline CM Witteman

Primary Institution: Erasmus Medical Center, Rotterdam, the Netherlands

Hypothesis

Are the SNPs rs10757278 and rs10757274 associated with the risk of coronary heart disease and myocardial infarction in an elderly population?

Conclusion

The study found no significant association between the SNPs and the risks of coronary heart disease and myocardial infarction.

Supporting Evidence

  • The study included 7983 participants aged 55 years and older.
  • No significant association was found between the SNPs and the risks of coronary heart disease or myocardial infarction.
  • The study had sufficient power to detect effect sizes as shown in published studies.

Takeaway

The researchers looked at two genetic changes to see if they could cause heart problems in older people, but they found that they didn't.

Methodology

The study used a population-based, prospective cohort design with Cox proportional hazards analyses to assess associations.

Limitations

The study may be underpowered to detect the effect of age on the association and participants were not fully followed.

Participant Demographics

Participants were elderly individuals aged 55 years and older from the Rotterdam Study.

Statistical Information

Confidence Interval

95% confidence interval for CHD and MI were 1.03 (0.90, 1.18) and 0.94 (0.82, 1.08) respectively.

Digital Object Identifier (DOI)

10.1186/1741-7015-6-30

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