메뉴 건너뛰기




Volumn 58, Issue 4, 2011, Pages 426-434

Influence of 9p21.3 Genetic Variants on Clinical and Angiographic Outcomes in Early-Onset Myocardial Infarction

(28)  Ardissino, Diego a   Berzuini, Carlo b   Merlini, Piera Angelica c   Mannuccio Mannucci, Pier d   Surti, Aarti e   Burtt, Noel e   Voight, Benjamin e,f   Tubaro, Marco g   Peyvandi, Flora d   Spreafico, Marta d   Celli, Patrizia h   Lina, Daniela a   Notarangelo, Maria Francesca a   Ferrario, Maurizio i   Fetiveau, Raffaela i   Casari, Giorgio j   Galli, Michele k   Ribichini, Flavio l   Rossi, Marco L m   Bernardi, Francesco n   more..


Author keywords

9p21.3 genetic variants; early onset myocardial infarction; outcomes; rs1333040

Indexed keywords

ADULT; ARTICLE; CARDIOVASCULAR DISEASE; CARDIOVASCULAR MORTALITY; CHROMOSOME 9P; CHROMOSOME 9P21.3; CONTROLLED STUDY; CORONARY ANGIOGRAPHY; CORONARY ARTERY ATHEROSCLEROSIS; CORONARY ARTERY DISEASE; CORONARY ARTERY RECANALIZATION; FEMALE; FOLLOW UP; GENETIC VARIABILITY; HEART INFARCTION; HEART REINFARCTION; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; ITALY; MAJOR CLINICAL STUDY; MALE; ONSET AGE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; ANGIOCARDIOGRAPHY; CASE CONTROL STUDY; CHROMOSOME 9; DISEASE COURSE; GENETIC PREDISPOSITION; GENETICS; MIDDLE AGED;

EID: 80053316001     PISSN: 07351097     EISSN: 15583597     Source Type: Journal    
DOI: 10.1016/j.jacc.2010.11.075     Document Type: Article
Times cited : (61)

References (22)
  • 1
    • 0028330005 scopus 로고
    • Genetic susceptibility to death from coronary heart disease in a study of twins
    • Marenberg, M.E., Risch, N., Berkman, L.F., Floderus, B., de Faire, U., Genetic susceptibility to death from coronary heart disease in a study of twins. N Engl J Med 330 (1994), 1041–1046.
    • (1994) N Engl J Med , vol.330 , pp. 1041-1046
    • Marenberg, M.E.1    Risch, N.2    Berkman, L.F.3    Floderus, B.4    de Faire, U.5
  • 2
    • 0036378360 scopus 로고    scopus 로고
    • Heritability of death from coronary heart disease: a 36-year follow-up of 20 966 Swedish twins
    • Zdravkovic, S., Wienke, A., Pedersen, N.L., Marenberg, M.E., Yashin, A.I., De Faire, U., Heritability of death from coronary heart disease: a 36-year follow-up of 20 966 Swedish twins. J Intern Med 252 (2002), 247–254.
    • (2002) J Intern Med , vol.252 , pp. 247-254
    • Zdravkovic, S.1    Wienke, A.2    Pedersen, N.L.3    Marenberg, M.E.4    Yashin, A.I.5    De Faire, U.6
  • 3
    • 84969213492 scopus 로고    scopus 로고
    • Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
    • Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 447 (2007), 661–678.
    • (2007) Nature , vol.447 , pp. 661-678
  • 4
    • 34250010480 scopus 로고    scopus 로고
    • A common variant on chromosome 9p21 affects the risk of myocardial infarction
    • Helgadottir, A., Thorleifsson, G., Manolescu, A., et al. A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science 316 (2007), 1491–1493.
    • (2007) Science , vol.316 , pp. 1491-1493
    • Helgadottir, A.1    Thorleifsson, G.2    Manolescu, A.3
  • 5
    • 34249996115 scopus 로고    scopus 로고
    • A common allele on chromosome 9 associated with coronary heart disease
    • McPherson, R., Pertsemlidis, A., Kavaslar, N., et al. A common allele on chromosome 9 associated with coronary heart disease. Science 316 (2007), 1488–1491.
    • (2007) Science , vol.316 , pp. 1488-1491
    • McPherson, R.1    Pertsemlidis, A.2    Kavaslar, N.3
  • 6
    • 34547623750 scopus 로고    scopus 로고
    • Genomewide association analysis of coronary artery disease
    • Samani, N.J., Erdmann, J., Hall, A.S., et al. Genomewide association analysis of coronary artery disease. N Engl J Med 357 (2007), 443–453.
    • (2007) N Engl J Med , vol.357 , pp. 443-453
    • Samani, N.J.1    Erdmann, J.2    Hall, A.S.3
  • 7
    • 85038613029 scopus 로고    scopus 로고
    • Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
    • Myocardial Infarction Genetics Consortium. Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet, 2009, 41334–41341.
    • (2009) Nat Genet , pp. 41334-41341
  • 8
    • 38949209549 scopus 로고    scopus 로고
    • Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population
    • Shen, G.Q., Rao, S., Martinelli, N., et al. Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population. J Hum Genet 53 (2008), 144–150.
    • (2008) J Hum Genet , vol.53 , pp. 144-150
    • Shen, G.Q.1    Rao, S.2    Martinelli, N.3
  • 9
    • 38649091662 scopus 로고    scopus 로고
    • The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm
    • Helgadottir, A., Thorleifsson, G., Magnusson, K.P., et al. The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. Nat Genet 40 (2008), 217–224.
    • (2008) Nat Genet , vol.40 , pp. 217-224
    • Helgadottir, A.1    Thorleifsson, G.2    Magnusson, K.P.3
  • 10
    • 38549092257 scopus 로고    scopus 로고
    • Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease
    • Shen, G.Q., Li, L., Rao, S., et al. Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease. Arterioscler Thromb Vasc Biol 28 (2008), 360–365.
    • (2008) Arterioscler Thromb Vasc Biol , vol.28 , pp. 360-365
    • Shen, G.Q.1    Li, L.2    Rao, S.3
  • 11
    • 41649085340 scopus 로고    scopus 로고
    • Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease
    • Schunkert, H., Gotz, A., Braund, P., et al. Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease. Circulation 117 (2008), 1675–1684.
    • (2008) Circulation , vol.117 , pp. 1675-1684
    • Schunkert, H.1    Gotz, A.2    Braund, P.3
  • 12
    • 40549109924 scopus 로고    scopus 로고
    • Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p
    • Broadbent, H.M., Peden, J.F., Lorkowski, S., et al., PROCARDIS Consortium. Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p. Hum Mol Genet 17 (2008), 806–814.
    • (2008) Hum Mol Genet , vol.17 , pp. 806-814
    • Broadbent, H.M.1    Peden, J.F.2    Lorkowski, S.3
  • 13
    • 41649091577 scopus 로고    scopus 로고
    • Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations
    • Hinohara, K., Nakajima, T., Takahashi, M., et al. Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations. J Hum Genet 53 (2008), 357–359.
    • (2008) J Hum Genet , vol.53 , pp. 357-359
    • Hinohara, K.1    Nakajima, T.2    Takahashi, M.3
  • 14
    • 48049115182 scopus 로고    scopus 로고
    • Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study
    • Assimes, T.L., Knowles, J.W., Basu, A., et al. Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study. Hum Mol Genet 17 (2008), 2320–2328.
    • (2008) Hum Mol Genet , vol.17 , pp. 2320-2328
    • Assimes, T.L.1    Knowles, J.W.2    Basu, A.3
  • 15
    • 58749087343 scopus 로고    scopus 로고
    • Cardiovascular disease risk prediction with and without knowledge of genetic variation at chromosome 9p21.3
    • Paynter, N.P., Chasman, D.I., Buring, J.E., Shiffman, D., Cook, N.R., Ridker, P.M., Cardiovascular disease risk prediction with and without knowledge of genetic variation at chromosome 9p21.3. Ann Intern Med 150 (2009), 65–72.
    • (2009) Ann Intern Med , vol.150 , pp. 65-72
    • Paynter, N.P.1    Chasman, D.I.2    Buring, J.E.3    Shiffman, D.4    Cook, N.R.5    Ridker, P.M.6
  • 16
    • 77149160077 scopus 로고    scopus 로고
    • Association between 9p21 genomic markers and heart disease: a meta-analysis
    • Palomaki, G.E., Melillo, S., Bradley, L.A., Association between 9p21 genomic markers and heart disease: a meta-analysis. JAMA 303 (2010), 648–656.
    • (2010) JAMA , vol.303 , pp. 648-656
    • Palomaki, G.E.1    Melillo, S.2    Bradley, L.A.3
  • 17
    • 63149194355 scopus 로고    scopus 로고
    • Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease
    • Horne, B.D., Carllquist, J.F., Muhlestein, J.B., Bair, T.L., Anderson, J.L., Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease. Circ Cardiovasc Genet 1 (2008), 85–92.
    • (2008) Circ Cardiovasc Genet , vol.1 , pp. 85-92
    • Horne, B.D.1    Carllquist, J.F.2    Muhlestein, J.B.3    Bair, T.L.4    Anderson, J.L.5
  • 18
    • 56349096706 scopus 로고    scopus 로고
    • Genetic variation at the 9p21 locus predicts angiographic coronary artery disease prevalence but not extent and has clinical utility
    • Anderson, J.L., Horne, B.D., Kolek, M.J., et al. Genetic variation at the 9p21 locus predicts angiographic coronary artery disease prevalence but not extent and has clinical utility. Am Heart J 156 (2008), 1155–1162.
    • (2008) Am Heart J , vol.156 , pp. 1155-1162
    • Anderson, J.L.1    Horne, B.D.2    Kolek, M.J.3
  • 19
    • 47349129207 scopus 로고    scopus 로고
    • Association of genetic variation on chromosome 9p21 with susceptibility and progression of atherosclerosis: a population-based, prospective study
    • Ye, S., Willeit, J., Kronenberg, F., Xu, Q., Kiechl, S., Association of genetic variation on chromosome 9p21 with susceptibility and progression of atherosclerosis: a population-based, prospective study. J Am Coll Cardiol 52 (2008), 378–384.
    • (2008) J Am Coll Cardiol , vol.52 , pp. 378-384
    • Ye, S.1    Willeit, J.2    Kronenberg, F.3    Xu, Q.4    Kiechl, S.5
  • 20
    • 0028206843 scopus 로고
    • Continuing evolution of therapy for coronary artery disease: Initial results from the era of coronary angioplasty
    • Mark, D.B., Nelson, C.L., Califf, R.M., et al. Continuing evolution of therapy for coronary artery disease: Initial results from the era of coronary angioplasty. Circulation 89 (1994), 2015–2025.
    • (1994) Circulation , vol.89 , pp. 2015-2025
    • Mark, D.B.1    Nelson, C.L.2    Califf, R.M.3
  • 21
    • 18444369013 scopus 로고    scopus 로고
    • The structure of haplotype blocks in the human genome
    • Gabriel, S.B., Schaffner, S.F., Nguyen, H., et al. The structure of haplotype blocks in the human genome. Science 296 (2002), 2225–2229.
    • (2002) Science , vol.296 , pp. 2225-2229
    • Gabriel, S.B.1    Schaffner, S.F.2    Nguyen, H.3
  • 22
    • 67449103171 scopus 로고    scopus 로고
    • Evaluation of the association of genetic variants on the chromosomal loci 9p21.3, 6q25.1, and 2q36.3 with angiographically characterized coronary artery disease
    • Muendlein, A., Saely, C.H., Rhomberg, S., et al. Evaluation of the association of genetic variants on the chromosomal loci 9p21.3, 6q25.1, and 2q36.3 with angiographically characterized coronary artery disease. Atherosclerosis 205 (2009), 174–180.
    • (2009) Atherosclerosis , vol.205 , pp. 174-180
    • Muendlein, A.1    Saely, C.H.2    Rhomberg, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.