Association of single nucleotide polymorphism rs2076185 in chromosome 6P24.1 with premature coronary artery diseases in Chinese Han population

Journal of Geriatric Cardiology

Volumn 13, Issue 2, 2016, Pages 138-144

  Liu, Xin ^a   Zhang, Min ^a   Shan, Hong Wei ^a   Song, Xian Tao ^a   Lyu, Shu Zheng ^a  

^a CAPITAL MEDICAL UNIVERSITY   (China)

Author keywords

Chinese Han population; Gene; Premature coronary artery disease; Single nucleotide polymorphism

Indexed keywords

ADULT; ALLELE; ANGIOCARDIOGRAPHY; ARTICLE; CHINESE; CHROMOSOME 6P; CONTROLLED STUDY; CORONARY ARTERY DISEASE; FEMALE; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MASS SPECTROMETRY; PREMATURE CORONARY ARTERY DISEASE; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84960889624     PISSN: 16715411     EISSN: None     Source Type: Journal    
DOI: 10.11909/j.issn.1671-5411.2016.02.008     Document Type: Article

References (21)

1. Mathers CD, Loncar D. Projections of global mortality and burden of disease from 2002 to 2030. PLoS Med 2006; 3: e442.
2. Wang W, Hu SS, Kong LZ, et al. Summary of report on cardiovascular diseases in China, 2012. Biomed Environ Sci 2014; 27: 552-558.
3. Wang F, Xu CQ, He Q, et al. Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han population. Nat Genet 2011: 43: 345-349.
4. Lu X, Wang L, Chen S, et al. Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease. Nat Genet 2012: 44: 890-894.
5. Tayebi N, Ke T, Foo JN, et al. Association of single nucleo-tide polymorphism rs6903956 on chromosome 6p24.1 with coronary artery disease and lipid levels in different ethnic groups of the Singaporean population. Clin Biochem 2013; 46: 755-759.
6. Dechamethakun S, Ikeda S, Arai T, et al. Associations between the CDKN2A/B, ADTRP and PDGFD polymorphisms and the development of coronary atherosclerosis in Japanese patients. J Atheroscler Thromb 2014; 21: 680-690.
7. National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III). Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) final report. Circulation. 2002; 106: 3143-3421.
8. Lupu C, Zhu H, Popescu NI, et al. Novel protein ADTRP regulates TFPI expression and function in human endothelial cells in normal conditions and in response to androgen. Blood 2011; 118: 4463-4471.
9. Park JW, Cai J, McIntosh I, et al. High throughput SNP and expression analyses of candidate genes for non-syndromic oral clefts. J Med Genet 2006; 43: 598-608.
10. Chinetti-Gbaguidi G, Copin C, Derudas B, et al. The coronary artery disease-associated gene C6ORF105 is expressed in human macrophages under the transcriptional control of PPARγ. FEBS Lett 2015; 589: 461-466.
11. Van Ginderachter JA, Movahedi K, Hassanzadeh Ghassabeh G, et al. Classical and alternative activation of mononuclear phagocytes: picking the best of both worlds for tumor promotion. Immunobiology 2006; 211: 487-501.
12. Gordon S, Taylor PR. Monocyte and macrophage heterogeneity. Nat Rev Immunol 2005; 5: 953-964.
13. Golledge J, Mangan S, Clancy P. Effects of peroxisome pro-liferator-activated receptor ligands in modulating tissue factor and tissue factor pathway inhibitor in acutely symptomatic carotid atheromas. Stroke 2007; 38: 1501-1508.
14. Labounty TM, Gomez MJ, Achenbach S, et al. Body mass index and the prevalence, severity, and risk of coronary artery disease: an international multicentre study of 13, 874 patients. Eur Heart J Cardiovasc Imaging 2013; 14: 456-463.
15. Chaudru.V, Laud K, Avril MF, et al. Melanocortin-1 receptor (MCIR) gene Variants and dysplastic nevi modify penetranc of CDKN2A mutations in French melanoma-prone pedigress. Cancer Epidemiol Biomarkers Prev 2005; 14: 2384-2390.
16. Mendonça MI, Dos Reis RP, Freitas AI, et al. Gene-gene interaction affects coronary artery disease risk. Rev Port Car-dio 2009; 28: 397-415.
17. Sing CF, Stengard JH, Kardia SL, et al. Genes, environment, and cardiovascular disease. Arterioscler Thromb Vasc Biol 2003; 23: 1190-1196.
18. Engelman CD, Baurley JW, Chiu YF, et al. Detecting gene-environment interactions in genome-wide association data. Genet Epidemiol 2009; 33 (Suppl 1): S68-S73.
19. Claramunt R, Pedrola L, Sevilla T, et al. Genetics of Char-cot-Marie-Tooth disease type 4A: mutations, inheritance, phenotypic variability, and founder effect. J Med Genet 2005; 42: 358-365.
20. Li JZ, Absher DM, Tang H, et al. Worldwide human relationships inferred from genome-wide patterns of variation. Science 2008; 319: 1100-1104.
21. Chen WW, Gao RL, Liu LS, et al. Report on Cardiovascular Diseases in China (2013). Chinese Circulation Journal 2014; 29: 487-491. [Article in Chinese]