The Genetic Basis of Coronary Artery Disease: From Candidate Genes to Whole Genome Analysis

被引:29
作者
Franchini, Massimo [4 ]
Peyvandi, Flora [1 ,2 ,3 ]
Mannucci, Pier Mannuccio [1 ,2 ,3 ]
机构
[1] Univ Milan, Angelo Bianchi Bonomi Hemophilia & Thrombosis Ctr, I-20122 Milan, Italy
[2] Univ Milan, Dept Med & Med Specialties, Luigi Villa Fdn, I-20122 Milan, Italy
[3] Maggiore Hosp, IRCCS, Mangiagalli & Regina Elena Fdn, Milan, Italy
[4] Univ Hosp Parma, Immunohematol & Transfus Ctr, Parma, Italy
关键词
D O I
10.1016/j.tcm.2008.04.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Coronary artery disease is a major socioeconomic problem in industrialized as well as in developing countries. Thus, many research efforts continue to address the identification of acquired and inherited risk factors of this complex disease. Recent advances in genotyping technology have made available newer and more powerful tools I-or the identification of susceptibility genes that in turn may provide new opportunities to evaluate the individual cardiovascular risk profile, detect novel disease pathways, and develop innovative therapeutic approaches. Replication of results is essential to establish unequivocally the impact of genetic variants in complex diseases. At the moment, only distinct but tightly linked single nucleotide polymorphisms on chromosome 9 have been consistently shown to be associated with different clinical phenotypes of coronary artery disease. (Trends Cardiovasc Med 2 008; IS: 157-162) (C) 2008, Elsevier Inc.
引用
收藏
页码:157 / 162
页数:6
相关论文
共 51 条
  • [41] The effect of HapMap on cardiovascular research and clinical practice
    Skelding, Kimberly A.
    Gerhard, Glenn S.
    Simari, Robert D.
    Holmes, David R., Jr.
    [J]. NATURE CLINICAL PRACTICE CARDIOVASCULAR MEDICINE, 2007, 4 (03): : 136 - 142
  • [42] Meta-analysis: Apolipoprotein E genotypes and risk for coronary heart disease
    Song, YQ
    Stampfer, MJ
    Liu, SM
    [J]. ANNALS OF INTERNAL MEDICINE, 2004, 141 (02) : 137 - 147
  • [43] Heart disease and stroke statistics - 2006 update - A report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee
    Thom, T
    Haase, N
    Rosamond, W
    Howard, VJ
    Rumsfeld, J
    Manolio, T
    Zheng, ZJ
    Flegal, K
    O'Donnell, C
    Kittner, S
    Lloyd-Jones, D
    Goff, DC
    Hong, YL
    Adams, R
    Friday, G
    Furie, K
    Gorelick, P
    Kissela, B
    Marler, J
    Meigs, J
    Roger, V
    Sidney, S
    Sorlie, P
    Steinberger, J
    Wasserthiel-Smoller, S
    Wilson, M
    Wolf, P
    [J]. CIRCULATION, 2006, 113 (06) : E85 - E151
  • [44] Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction
    Topol, EJ
    McCarthy, J
    Gabriel, S
    Moliterno, DJ
    Rogers, WJ
    Newby, LK
    Freedman, M
    Metivier, J
    Cannata, R
    O'Donnell, CJ
    Kottke-Marchant, K
    Murugesan, G
    Plow, EF
    Stenina, O
    Daley, GQ
    [J]. CIRCULATION, 2001, 104 (22) : 2641 - 2644
  • [45] Genetic determinants of arterial thrombosis
    Voetsch, B
    Loscalzo, J
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2004, 24 (02) : 216 - 229
  • [46] Mutation of MEF2A in an inherited disorder with features of coronary artery disease
    Wang, LJ
    Fan, C
    Topol, SE
    Topol, EJ
    Wang, Q
    [J]. SCIENCE, 2003, 302 (5650) : 1578 - 1581
  • [47] Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis
    Wang, Q
    Rao, SQ
    Shen, GQ
    Li, L
    Moliterno, DJ
    Newby, LK
    Rogers, WJ
    Cannata, R
    Zirzow, E
    Elston, RC
    Topol, EJ
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (02) : 262 - 271
  • [48] Lack of association of polymorphisms of the lymphotoxin α gene with myocardial infarction in Japanese
    Yamada, A
    Ichihara, S
    Murase, Y
    Kato, T
    Izawa, H
    Nagata, K
    Murohara, T
    Yamada, Y
    Yokota, M
    [J]. JOURNAL OF MOLECULAR MEDICINE-JMM, 2004, 82 (07): : 477 - 483
  • [49] Prediction of the risk of myocardial infarction from polymorphisms in candidate genes
    Yamada, Y
    Izawa, H
    Ichihara, S
    Takatsu, F
    Ishihara, H
    Hirayama, H
    Sone, T
    Tanaka, M
    Yokota, M
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (24) : 1916 - 1923
  • [50] Seven haemostatic gene polymorphisms in coronary disease: meta-analysis of 66 155 cases and 91 307 controls
    Ye, Z
    Liu, EHC
    Higgins, JPT
    Keavney, BD
    Lowe, GDO
    Collins, R
    Danesh, J
    [J]. LANCET, 2006, 367 (9511) : 651 - 658