Validation of the association between AGTRL1 polymorphism and coronary artery disease in the Japanese and Korean populations

J Hum Genet. 2009 Sep;54(9):554-6. doi: 10.1038/jhg.2009.78. Epub 2009 Aug 14.


Coronary artery disease (CAD) and stroke are the major health problems in many countries because of their increasing prevalence and high mortality. It is well known that CAD and stroke are based on atherosclerosis and shared environmental and genetic risk factors. Recently, an association of a functional sequence variation -154G>A in the angiotensin receptor-like 1 (AGTRL1) with a susceptibility to stroke was reported. In this study, we investigated a total of 1479 CAD cases and 2062 controls from the Japanese and Korean populations to validate the association of AGTRL1 with CAD. However, we obtained no evidence of the association in both the Japanese (odds ratio (OR)=0.95, 95% confidence interval (CI); 0.82-1.10, P=0.47, allele count model) and Korean (OR=0.90, 95% CI; 0.77-1.05, P=0.18, allele count model) populations. In addition, there was no trend of association between the risk allele and severity of coronary atherosclerosis. These data suggested that AGTRL1 did not contribute much to the atherosclerosis of the coronary artery.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Apelin Receptors
  • Asians / genetics*
  • Case-Control Studies
  • Coronary Artery Disease / genetics*
  • Female
  • Humans
  • Korea
  • Male
  • Middle Aged
  • Polymorphism, Genetic / genetics*
  • Receptors, G-Protein-Coupled / genetics*


  • APLNR protein, human
  • Apelin Receptors
  • Receptors, G-Protein-Coupled