Associations of the ATP-binding cassette transporter A1 R219K polymorphism with HDL-C level and coronary artery disease risk: A meta-analysis

Atherosclerosis

Volumn 215, Issue 2, 2011, Pages 428-434

  Ma, Xiang yu ^a   Liu, Jian ping ^a   Song, Zhi yuan ^a  

^a THIRD MILITARY MEDICAL UNIVERSITY   (China)

Author keywords

ATP binding cassette transporter A1; Coronary artery disease; HDL C; Meta analysis

Indexed keywords

ABC TRANSPORTER A1; HIGH DENSITY LIPOPROTEIN CHOLESTEROL;

ALLELE; ARTICLE; ASIAN; CHOLESTEROL BLOOD LEVEL; CORONARY ARTERY DISEASE; DISEASE ASSOCIATION; EPIDEMIOLOGICAL DATA; ETHNICITY; GENETIC ASSOCIATION; GENETIC RISK; GENOTYPE; HETEROZYGOTE; HUMAN; MEDLINE; POPULATION RISK; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SYSTEMATIC REVIEW;

ASIAN CONTINENTAL ANCESTRY GROUP; ATP-BINDING CASSETTE TRANSPORTERS; CHOLESTEROL, HDL; CORONARY ARTERY DISEASE; EUROPEAN CONTINENTAL ANCESTRY GROUP; HUMANS; POLYMORPHISM, GENETIC;

EID: 79953032939     PISSN: 00219150     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.atherosclerosis.2011.01.008     Document Type: Article

References (48)

1. Subcommittee S. Heart disease and stroke statistics-2008 update: a report from the American heart association statistics committee and stroke statistics subcommittee. Circulation 2008, 117:e25.
2. Schmitz G., Buechler C. ABCA1: regulation, trafficking and association with heteromeric proteins. Ann Med 2002, 34:334-347.
3. Remaley A.T., Rust S., Rosier M., et al. Human ATP-binding cassette transporter 1 (ABC1): genomic organization and identification of the genetic defect in the original Tangier disease kindred. Proc Natl Acad Sci USA 1999, 96:12685-12690.
4. Brooks-Wilson A., Marcil M., Clee S.M., et al. Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. Nat Genet 1999, 22:336-345.
5. Clee S., Zwinderman A., Engert J., et al. Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease. Circulation 2001, 13r.
6. Stroup D.F., Berlin J.A., Morton S.C., et al. Meta-analysis of observational studies in epidemiology: a proposal for reporting. Meta-analysis Of Observational Studies in Epidemiology (MOOSE) group. JAMA 2000, 283:2008-2012.
7. Tunstall-Pedoe H., Kuulasmaa K., Amouyel P., et al. Myocardial infarction and coronary deaths in the World Health Organization MONICA Project. Registration procedures, event rates, and case-fatality rates in 38 populations from 21 countries in four continents. Circulation 1994, 90:583-612.
8. Little J., Bradley L., Bray M.S., et al. Reporting, appraising, and integrating data on genotype prevalence and gene-disease associations. Am J Epidemiol 2002, 56:300-310.
9. Mantel N., Haenszel W. Statistical aspects of the analysis of data from retrospective studies of disease. J Natl Cancer Inst 1959, 22:719-748.
10. Dersimonian R., Kacker R. Random-effects model for meta-analysis of clinical trials: an update. Contemp Clin Trials 2007, 28:105-114.
11. Dersimonian R., Laird N. Meta-analysis in clinical trials. Control Clin Trials 1986, 7:177-188.
12. Doosti M., Najafi M., Reza J.Z., et al. The role of ATP-binding-cassette-transporter-A1 (ABCA1) gene polymorphism on coronary artery disease risk. Transl Res 2010, 155:185-190.
13. Wang Y., Zhang X. Association between R219K polymorphism of ATP-binding cassette transporter 1 gene in Xinjiang Uygur population and coronary heart disease. Chin J Cardiovas Rehabil Med 2009, 18:35-39.
14. Porchay-Balderelli I., An F., Emery N., et al. Relationships between common polymorphisms of adenosine triphosphate-binding cassette transporter A1 and high-density lipoprotein cholesterol and coronary heart disease in a population with type 2 diabetes mellitus. Metabolism 2009, 8:74-79.
15. Li J., Wang L.F., Li Z.Q., et al. Effect of R219K polymorphism of the ABCA1 gene on the lipid-lowering effect of pravastatin in Chinese patients with coronary heart disease. Clin Exp Pharmacol Physiol 2009, 6:567-570.
16. Zhang X., Xu L., Zhang H. The Association between ABCA1 Gene R219K PolymorphISM and Coronary Heart Disease. Prev Treat Cardio-Cerebral-Vascular Dis 2008, 8:304-307.
17. Yu B., Deng B. Correlation of polymorphism of R219K in ABCAl with lipid metabolism and the risk Of AM I. J Tongji Univ 2008, 29:64-67.
18. Liu J., Gao G., Gao J. Study of correlations of ABCA1 R219K gene polymorphism with coronary heart disease in subjects with type 2 diabetes. Chin J Diabetes 2008, 16:104-107.
19. Frikke-Schmidt R., Nordestgaard B.G., Jensen G.B., et al. Genetic variation in ABCA1 predicts ischemic heart disease in the general population. Arterioscler Thromb Vasc Biol 2008, 28:180-186.
20. Balcerzyk A., Zak I., Krauze J. Protective effect of R allele of PON1 gene on the coronary artery disease in the presence of specific genetic background. Dis Markers 2008, 24:81-88.
21. Nebel A., Croucher P.J., El Mokhtari N.E., et al. Common coding polymorphisms in the ABCA1 gene and risk of early-onset coronary heart disease in northern Germany. Atherosclerosis 2007, 193:458-460.
22. Wang X., Qi X., Li R. Assiciation between ABCA1 R219K polymorphism and coronary artery disease in north China. Shandong Med 2006, 46:46-47.
23. Martin M., Gonzalez P., Reguero J.J., et al. ABCA1 polymorphisms and prognosis after myocardial infarction in young patients. Int J Cardiol 2006, 110:267-268.
24. Andrikovics H., Pongracz E., Kalina E., et al. Decreased frequencies of ABCA1 polymorphisms R219K and V771M in Hungarian patients with cerebrovascular and cardiovascular diseases. Cerebrovasc Dis 2006, 21:254-259.
25. Sun P., Bo X.P., Guo D.P., et al. Study on the association of ABCA1 gene common variants with the risk of coronary atherosclerotic heart disease. Chin J Cardiol 2005, 33:627-630.
26. Li Y., Zhang S.Z., Ma Y.X., et al. Relationship between the R219K polymorphism of ATP-binding cassette transporter 1 gene and coronary heart disease. Yi Chuan 2005, 27:549-552.
27. Zhao S., Xiao Z. The study on ABCA1 R219K genetic variation in patients with coronary heart disease. Chin J Cardiol 2004, 32:712-716.
28. Wang X., Fu Y., Jiang H. Polymorphism of R219K of ABCA1 gene in patients with coronary artery disease. J Clin Cardiol 2004, 20:215-219.
29. Bertolini S., Pisciotta L., Di Scala L., et al. Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia. Atherosclerosis 2004, 174:57-65.
30. Harada T., Imai Y., Nojiri T., et al. A common Ile 823 Met variant of ATP-binding cassette transporter A1 gene (ABCA1) alters high density lipoprotein cholesterol level in Japanese population. Atherosclerosis 2003, 169:105-112.
31. Evans D., Beil F.U. The association of the R219K polymorphism in the ATP-binding cassette transporter 1 (ABCA1) gene with coronary heart disease and hyperlipidaemia. J Mol Med 2003, 81:264-270.
32. Cenarro A., Artieda M., Castillo S., et al. A common variant in the ABCA1 gene is associated with a lower risk for premature coronary heart disease in familial hypercholesterolaemia. J Med Genet 2003, 40:163.
33. Sandhofer A., Iglseder B., Kaser S., et al. The influence of two variants in the adenosine triphosphate C binding cassette transporter 1 gene on plasma lipids and carotid atherosclerosis. Metabolism 2008, 57:1398-1404.
34. Benton J., Jingzhong D., Tsai M., et al. Associations between two common polymorphisms in the ABCA1 gene and subclinical atherosclerosis: Multi-Ethnic Study of Atherosclerosis (MESA). Atherosclerosis 2007, 193:352-360.
35. Wu Y., Bai H. Analysis of ATP binding cassette A1 gene R219K polymorphism in patient with hypertriglyceridemia in chinses population. China J Med Genet 2007, 24:177-181.
36. Boekholdt S., Souverein O., Tanck M., et al. Common variants of multiple genes that control reverse cholesterol transport together explain only a minor part of the variation of HDL cholesterol levels. Clin Genet 2006, 69:263-270.
37. Hodoglugil U., Williamson D., Huang Y., et al. Common polymorphisms of ATP binding cassette transporter A1, including a functional promoter polymorphism, associated with plasma high density lipoprotein cholesterol levels in Turks. Atherosclerosis 2005, 183:199-212.
38. Zhao S., Xiao Z, Li Q Relationship between ATP-binding cassette transportter 1 R219K genetic variation and blood lipids. Chin Med J 2004, 84:1421-1425.
39. Bressler J., Folsom A., Couper D., et al. Genetic variants identified in a European genome-wide association study that were found to predict incident coronary heart disease in the Atherosclerosis Risk in Communities Study. Am J Epidemiol 2009.
40. Burton P.R., Clayton D.G., Cardon L.R., et al. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 2007, 447:661-678.
41. Erdmann J., Grosshennig A., Braund P.S., et al. New susceptibility locus for coronary artery disease on chromosome 3q22.3. Nat Genet 2009, 41:280-282.
42. 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.
43. Kathiresan S., Voight B.F., Purcell S., et al. Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet 2009, 41:334-341.
44. Mcpherson R., Pertsemlidis A., Kavaslar N., et al. A common allele on chromosome 9 associated with coronary heart disease. Science 2007, 316:1488-1491.
45. Qasim A., Matthews L., Qu L., et al. Association of genome wide loci for CAD with distribution of coronary disease. J Am Coll Cardiol 2010, 55:A124.
46. Samani N.J., Erdmann J., Hall A.S., et al. Genomewide association analysis of coronary artery disease. N Engl J Med 2007, 57:443-453.
47. Tregouet D., Konig I., Erdmann J., et al. Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. Nat Genet 2009, 41:283-285.
48. Galbraith R. Graphical display of estimates having differing standard errors. Technometrics 1988, 271-281.