Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2011 Jun;13(3):225-32.
doi: 10.1007/s11883-011-0173-4.

Genome-wide association studies in atherosclerosis

Affiliations
Review

Genome-wide association studies in atherosclerosis

S Sivapalaratnam et al. Curr Atheroscler Rep. 2011 Jun.

Abstract

Cardiovascular disease remains the major cause of worldwide morbidity and mortality. Its pathophysiology is complex and multifactorial. Because the phenotype of cardiovascular disease often shows a marked heritable pattern, it is likely that genetic factors play an important role. In recent years, large genome-wide association studies have been conducted to decipher the molecular mechanisms underlying this heritable and prevalent phenotype. The emphasis of this review is on the recently identified 17 susceptibility loci for coronary artery disease. Implications of their discovery for biology and clinical medicine are discussed. A description of the landscape of human genetics in the near future in the context of next-generation sequence technologies is provided at the conclusion of this review.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Proposed sites of action for the proteins involved in the pathogenesis of atherosclerosis: liver, vessel wall, plaque and thrombus

References

    1. Berenson GS, Srinivasan SR, Bao W, et al. Association between multiple cardiovascular risk factors and atherosclerosis in children and young adults. The Bogalusa heart study. N Engl J Med. 1998;338:1650–6. doi: 10.1056/NEJM199806043382302. - DOI - PubMed
    1. Marenberg ME, Risch N, Berkman LF, et al. Genetic susceptibility to death from coronary heart disease in a study of twins. N Engl J Med. 1994;330:1041–6. doi: 10.1056/NEJM199404143301503. - DOI - PubMed
    1. Sivapalaratnam S, Boekholdt SM, Trip MD et al. Family history of premature coronary heart disease and risk prediction in the EPIC-Norfolk prospective population study. Heart 2010 - PMC - PubMed
    1. Aouizerat BE, Allayee H, Cantor RM, et al. A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11. Am J Hum Genet. 1999;65:397–412. doi: 10.1086/302490. - DOI - PMC - PubMed
    1. Wang L, Fan C, Topol SE, et al. Mutation of MEF2A in an inherited disorder with features of coronary artery disease. Science. 2003;302:1578–81. doi: 10.1126/science.1088477. - DOI - PMC - PubMed

Publication types