Association between gene polymorphisms and myocardial infarction in Han Chinese of Yunnan province

Chinese Journal of Medical Genetics

Volumn 29, Issue 4, 2012, Pages 413-419

  Qi, Lin ^a,b   Li, Jian Mei ^c   Sun, Hao ^a   Huang, Xiao Qin ^a   Lin, Ke Qin ^a   Chu, Jia You ^a   Yang, Zhao Qing ^a  

^a INSTITUTE OF MEDICAL BIOLOGY   (China)

^b KUNMING MEDICAL UNIVERSITY   (China)

^c Second People's Hospital of Yunnan Province   (China)

Author keywords

Gene; Genetic association; Myocardial infarction; Polymorphism

Indexed keywords

BLOOD CLOTTING FACTOR 12; BLOOD CLOTTING FACTOR 7; FIBRINOGEN;

ARTICLE; CHINA; CHROMOSOME 9P; CONTROLLED STUDY; DISEASE ASSOCIATION; DNA POLYMORPHISM; GENE FREQUENCY; GENOTYPE; HEART INFARCTION; HUMAN; MAJOR CLINICAL STUDY; POLYMERASE CHAIN REACTION; PYROSEQUENCING; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

ADULT; AGED; AGED, 80 AND OVER; CHINA; FACTOR VII; FACTOR XII; FEMALE; FIBRINOGEN; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; MYOCARDIAL INFARCTION; POLYMORPHISM, GENETIC;

EID: 84866752697     PISSN: 10039406     EISSN: None     Source Type: Journal    
DOI: 10.3760/cma.j.issn.1003-9406.2012.04.008     Document Type: Article

References (24)

1. Iacoviello L, Di Castelnuovo A, De Knijff P, et al. Polymorphisms in the coagulation factor VII gene and the risk of myocardial infarction. N Engl J Med, 1998,338:79-85. (Pubitemid 28042270)
2. Ogawa M, Abe S, Biro S, et al. R353Q polymorphism, activated factor VII, and risk of premature myocardial infarction in Japanese men. Circ J, 2004,68:520-525. (Pubitemid 38856024)
3. Di Castelnuovo A, D'Orazio A, Amore C, et al. The decanucleotide insertion/deletion polymorphism in the promoter region of the coagulation factor VII gene and the risk of familial myocardial infarction. Thromb Res, 2000,98:9-17. (Pubitemid 30114256)
4. Feng Y, Ye X, Pang Y. A novel mutation in a patient with congenital coagulation factor XII deficiency. Chin Med J, 2008, 121:1241-1244.
5. Chang DY, OU-Yang J, Shao XY, et al. Analysis of the coagulation factor XII 46C/T polymorphism in a pedigree and related literature review. Chin J Thromb Hemost, 2009,15:154-157.
6. Helgadottir A, Thorleifsson G, Manolescu A, et al. A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science, 2007,316:1491-1493. (Pubitemid 46906618)
7. Green F, Kelleher C, Wilkes H, et al. A common genetic polymorphism associated with lower coagulation factor VII levels in healthy individuals. Arterioscler Thromb, 1991,11:540-546.
8. Lindman AS, Pedersen JI, Arnesen H, et al. Coagulation factor VII R353Q polymorphism, and serum choline-containing phospholipids in males at high risk for coronary heart disease. Thromb Res, 2004,113,57-65. (Pubitemid 38481672)
9. Song J, Yoon YM, Jung HJ, et al. Plasminogen activator inhibitor-1 4G/5G promoter polymorphism and coagulation factor VII Arg353Gln polymorphism in Korean patients with coronary artery disease. J Korean Med Sci, 2000,15:146-152.
10. Huang ZJ, Wang SY, Gan ML, et al. Association of coagulation factor VII gene polymorphisms with myocardial infarction patients of Han nationlity in south of China. Chin J Mod Med, 2009,19:1575-1577.
11. Zhao LS, Jin HZ, Yu H, et al. Distribution of R353Q polymorphism of coagulation factor VII gene in coronary heart disease patients. J Zhenzhou Univ (Med Sci), 2007,42:655-656.
12. Marchetti G, Patracchini P, Papacchini M, et al. A polymorphism in the 5′region of coagulation factor VII gene (F7) caused by an inserted decanucleotide. Hum Genet, 1993,90:575-576. (Pubitemid 23072852)
13. Tao R, Yu JD, Lu L, et al. Analysis of the relationship between F VII activity and polymorphism. Chin J Cardiol, 2000,28:27-29.
14. Zhao LS, Yang W, Xue GH, et al. Association of polymorphisms of coagulation factor VII gene with coronary heart disease in Henan Han population. Chin Circulation J, 2008,23:86-89.
15. Taymaz H, Erarslan S, Oner ET, et al. Sequence variations within the genes related to hemostatic imbalance and their impact on coronary artery disease in Turkish population. Thrombosis Research, 2007,119:55-62. (Pubitemid 44716207)
16. Halbmayer WM, Haushofer A, Radek J, et al. Prevalence of factor XII (Hageman factor) deficiency among 426 patients with coronary heart disease awaiting cardiac surgery. Coron Artery Dis, 1994,5:451454.
17. Kohler HP, Futers TS, Grant PJ. F XII (46C→T) polymorphism and in vivo generation of F XII activity-gene frequencies and relationship in patients with coronary artery disease. Thromb Haemost, 1999,81:745-747. (Pubitemid 29216561)
18. Chen XC, Xu MT, Jin LZ, et al. Association of - 148C/T, - 455G/A gene polymorphisms of FBG with coronary heart disease in Henan Han Population. Sci China 4eries C Life Sci, 2008,38:687-693.
19. Ma HL, Chen JL, Feng J, et al. G - 455-A polymorphism of β-fibrinogen gene in yong patients with myocardial infarction. Chin J Cardiol, 2002,30:74-77.
20. Reilly MP, Li M, He J, et al. Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardil infarction in the presence of coronary atherosclerosis, two genome-wide association studies. Lancet, 2011,377:383-392.
21. Hiura Y, Fukushima Y, Yuno M, et al. Validation of the association of genetic variants on chromosome 9p21 and 1q41 with myocardial infarction in a Japanese population. Circ J, 2008,72:1213-1217.
22. The Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature, 2007,447:661-678.
23. Samani NJ, Erdmann J, Hall AS, et al. Genomewide association analysis of coronary artery disease. N Engl J Med, 2007, 357: 443-453. (Pubitemid 47204873)
24. Kim WY, Sharpless NE. The regulation of 1NK4/ARF in cancer and aging. Cell,2006,127:265-275.