Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation: Cardiovascular Genetics
Search: search_blue_button Advanced Search
Circulation: Cardiovascular Genetics. 2008;1:39-42
doi: 10.1161/CIRCGENETICS.108.789727
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bown, M. J.
Right arrow Articles by Sayers, R. D.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Bown, M. J.
Right arrow Articles by Sayers, R. D.
Related Collections
Right arrow CV surgery: aortic and vascular disease
Right arrow Genetics of cardiovascular disease

Original Articles

Association Between the Coronary Artery Disease Risk Locus on Chromosome 9p21.3 and Abdominal Aortic Aneurysm

Matthew J. Bown, MD, FRCS; Peter S. Braund, BSc, PhD; John Thompson, MSc, PhD; Nicholas J.M. London, MD, FRCS, MRCP; Nilesh J. Samani, MD, FRCP, FMedSci and Robert D. Sayers, MD, FRCS

From the Departments of Cardiovascular Sciences (M.J.B., P.S.B., N.J.M.L., N.J.S., R.D.S.) and Health Sciences (J.T.), University of Leicester, Leicester, UK.

Correspondence to Mr Matthew Bown, Department of Cardiovascular Sciences, Vascular Surgery Group, Clinical Sciences Building, Leicester Royal Infirmary, Leicester, LE2 7LX, UK. E-mail m.bown{at}le.ac.uk

Received May 2, 2008; accepted July 25, 2008.

Background— Recent genome-wide studies have shown a significant association of a locus on chromosome 9p21.3 and coronary artery disease. We performed a case-control study to investigate the association between this locus and abdominal aortic aneurysm (AAA).

Methods and Results— A total of 1714 patients (899 patients with AAA and 815 controls) were genotyped for the lead single-nucleotide polymorphism, rs1333049, on chromosome 9p21. The frequency of the C (risk) allele of rs1333049 in the control group was 0.471. There was a significant association between the C allele and AAA (odds ratio, 1.22; 95% confidence interval, 1.06 to 1.39; P=0.004). The genotypic-specific odds ratios (compared with the GG genotype) were 1.17 (95% confidence interval, 0.93 to 1.47; P=0.191) for the GC genotype and 1.50 (95% confidence interval, 1.14 to 1.97; P=0.004) for the CC genotype. In logistic regression modeling, the association of the CC genotype with AAA was independent of the presence of clinical coronary artery disease (odds ratio, 1.46; 95% confidence interval, 1.11 to 1.94; P=0.008).

Conclusions— Our study shows that the recently identified chromosome 9 variant that increases risk of coronary artery disease is also associated with the presence of AAA. The findings suggest that the effect of this locus on risk of cardiovascular disease extends beyond the coronary circulation.

Key Words: aneurysm • aorta • cardiovascular diseases • genetics


 

CLINICAL PERSPECTIVE




This article has been cited by other articles:


Home page
CirculationHome page
C. Newton-Cheh, N. R. Cook, M. VanDenburgh, E. B. Rimm, P. M. Ridker, and C. M. Albert
A Common Variant at 9p21 Is Associated With Sudden and Arrhythmic Cardiac Death
Circulation, November 24, 2009; 120(21): 2062 - 2068.
[Abstract] [Full Text] [PDF]


Home page
Circ Cardiovasc GenetHome page
N. J. Samani and H. Schunkert
Chromosome 9p21 and Cardiovascular Disease: The Story Unfolds
Circ Cardiovasc Genet, December 1, 2008; 1(2): 81 - 84.
[Full Text] [PDF]