Genetics 100 for Cardiologists: Basics of Genome-Wide Association Studies

被引:25
作者
Dube, Joseph B.
Hegele, Robert A.
机构
[1] Univ Western Ontario, Schulich Sch Med & Dent, Dept Med, London, ON N6A 5K8, Canada
[2] Univ Western Ontario, Schulich Sch Med & Dent, Dept Biochem, London, ON N6A 5K8, Canada
基金
加拿大健康研究院;
关键词
CORONARY-ARTERY-DISEASE; CARDIOVASCULAR-DISEASE; RISK SCORE; SUSCEPTIBILITY LOCI; CHROMOSOME; 9P21.3; ATHEROSCLEROSIS; CHOLESTEROL; VARIANTS; ARTICLE; WOMEN;
D O I
10.1016/j.cjca.2012.10.011
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The spring of 2012 marked the fifth anniversary of the widespread appearance in the biomedical literature of genome-wide association studies (GWAS) of diseases of adulthood. Articles reporting GWAS results now regularly appear in dozens of general medicine and cardiology journals. As of August 2012, more than 1700 published GWAS have reported findings across a range of human diseases. Many of these reported new genetic determinants of cardiovascular disease, including coronary artery disease and its risk factors such as diabetes, dyslipidemia, and hypertension. Though GWAS reports follow a standard format, superficially they can appear intimidating to most non-geneticists, whom we suspect often skip over them. Considering the importance of GWAS in cardiovascular science and medicine, and because they show no signs of fading, it is important for cardiovascular medical personnel and scientists to understand GWAS fundamentals. In this article, we provide a roadmap for the nonexpert reader to navigate through GWAS of cardiovascular disease. We cover the basic essentials needed to understand GWAS: underlying theory, mechanics, analysis and display, interpretation, and relevance. Areas covered include the relationship between GWAS and standard epidemiologic study design, the concepts of DNA sequence variation and linkage disequilibrium, the particular statistical considerations in studies involving many independent variables and large sample sizes, the meaning and interpretation of Manhattan plots, and the biologic and clinical significance of GWAS-based discoveries. We conclude with comments about the limitations of GWAS and about what to look for in the "post-GWAS era."
引用
收藏
页码:10 / 17
页数:8
相关论文
共 46 条
[1]
Genetic Mapping in Human Disease [J].
Altshuler, David ;
Daly, Mark J. ;
Lander, Eric S. .
SCIENCE, 2008, 322 (5903) :881-888
[2]
How to Use an Article About Genetic Association A: Background Concepts [J].
Attia, John ;
Ioannidis, John P. A. ;
Thakkinstian, Ammarin ;
McEvoy, Mark ;
Scott, Rodney J. ;
Minelli, Cosetta ;
Thompson, John ;
Infante-Rivard, Claire ;
Guyatt, Gordon .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2009, 301 (01) :74-81
[3]
How to Use an Article About Genetic Association B: Are the Results of the Study Valid? [J].
Attia, John ;
Ioannidis, John P. A. ;
Thakkinstian, Ammarin ;
McEvoy, Mark ;
Scott, Rodney J. ;
Minelli, Cosetta ;
Thompson, John ;
Infante-Rivard, Claire ;
Guyatt, Gordon .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2009, 301 (02) :191-197
[4]
BOTSTEIN D, 1980, AM J HUM GENET, V32, P314
[5]
A genetic risk score based on direct associations with coronary heart disease improves coronary heart disease risk prediction in the Atherosclerosis Risk in Communities (ARIC), but not in the Rotterdam and Framingham Offspring, Studies [J].
Brautbar, Ariel ;
Pompeii, Lisa A. ;
Dehghan, Abbas ;
Ngwa, Julius S. ;
Nambi, Vijay ;
Virani, Salim S. ;
Rivadeneira, Fernando ;
Uitterlinden, Andre G. ;
Hofman, Albert ;
Witteman, Jacqueline C. M. ;
Pencina, Michael J. ;
Folsom, Aaron R. ;
Cupples, L. Adrienne ;
Ballantyne, Christie M. ;
Boerwinkle, Eric .
ATHEROSCLEROSIS, 2012, 223 (02) :421-426
[6]
Genetic Loci Associated With Plasma Concentration of Low-Density Lipoprotein Cholesterol, High-Density Lipoprotein Cholesterol, Triglycerides, Apolipoprotein A1, and Apolipoprotein B Among 6382 White Women in Genome-Wide Analysis With Replication [J].
Chasman, Daniel I. ;
Pare, Guillaume ;
Zee, Robert Y. L. ;
Parker, Alex N. ;
Cook, Nancy R. ;
Buring, Julie E. ;
Kwiatkowski, David J. ;
Rose, Lynda M. ;
Smith, Joshua D. ;
Williams, Paul T. ;
Rieder, Mark J. ;
Rotter, Jerome I. ;
Nickerson, Deborah A. ;
Krauss, Ronald M. ;
Miletich, Joseph P. ;
Ridker, Paul M. .
CIRCULATION-CARDIOVASCULAR GENETICS, 2008, 1 (01) :21-U115
[7]
Promise and pitfalls of the Immunochip [J].
Cortes, Adrian ;
Brown, Matthew A. .
ARTHRITIS RESEARCH & THERAPY, 2011, 13 (01)
[8]
General cardiovascular risk profile for use in primary care - The Framingham Heart Study [J].
D'Agostino, Ralph B. ;
Vasan, Ramachandran S. ;
Pencina, Michael J. ;
Wolf, Philip A. ;
Cobain, Mark ;
Massaro, Joseph M. ;
Kannel, William B. .
CIRCULATION, 2008, 117 (06) :743-753
[9]
A Genome-Wide Association Study for Coronary Artery Disease Identifies a Novel Susceptibility Locus in the Major Histocompatibility Complex [J].
Davies, Robert W. ;
Wells, George A. ;
Stewart, Alexandre F. R. ;
Erdmann, Jeanette ;
Shah, Svati H. ;
Ferguson, Jane F. ;
Hall, Alistair S. ;
Anand, Sonia S. ;
Burnett, Mary S. ;
Epstein, Stephen E. ;
Dandona, Sonny ;
Chen, Li ;
Nahrstaedt, Janja ;
Loley, Christina ;
Koenig, Inke R. ;
Kraus, William E. ;
Granger, Christopher B. ;
Engert, James C. ;
Hengstenberg, Christian ;
Wichmann, H. -Erich ;
Schreiber, Stefan ;
Tang, W. H. Wilson ;
Ellis, Stephen G. ;
Rader, Daniel J. ;
Hazen, Stanley L. ;
Reilly, Muredach P. ;
Samani, Nilesh J. ;
Schunkert, Heribert ;
Roberts, Robert ;
McPherson, Ruth .
CIRCULATION-CARDIOVASCULAR GENETICS, 2012, 5 (02) :217-225
[10]
Rare Variants Create Synthetic Genome-Wide Associations [J].
Dickson, Samuel P. ;
Wang, Kai ;
Krantz, Ian ;
Hakonarson, Hakon ;
Goldstein, David B. .
PLOS BIOLOGY, 2010, 8 (01)