The rs5888 single nucleotide polymorphism in scavenger receptor class B type 1 (SCARB1) gene and the risk of premature coronary artery disease: A case-control study

Lipids in Health and Disease

Volumn 15, Issue 1, 2016, Pages

  Goodarzynejad, Hamidreza ^a   Boroumand, Mohammadali ^a   Behmanesh, Mehrdad ^b   Ziaee, Shayan ^a   Jalali, Arash ^a  

^a TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b TARBIAT MODARES UNIVERSITY   (Iran)

Author keywords

Coronary angiography; Coronary artery disease; Premature atherosclerosis; rs5888 polymorphism; Scavenger receptor class B type I

Indexed keywords

SCAVENGER RECEPTOR BI; LIPID; SCARB1 PROTEIN, HUMAN; SCAVENGER RECEPTOR B;

ADULT; ANGIOCARDIOGRAPHY; ARTICLE; CASE CONTROL STUDY; CONTROLLED STUDY; CORONARY ARTERY DISEASE; CORONARY ARTERY OBSTRUCTION; DISEASE SEVERITY; FEMALE; GENETIC RISK; GENSINI SCORE; HIGH RESOLUTION MELTING ANALYSIS; HUMAN; IRANIAN PEOPLE; MAJOR CLINICAL STUDY; MALE; REAL TIME POLYMERASE CHAIN REACTION; SCAVENGER RECEPTOR CLASS B TYPE 1 GENE; SEX DIFFERENCE; SINGLE NUCLEOTIDE POLYMORPHISM; AGAR GEL ELECTROPHORESIS; BLOOD; GENE FREQUENCY; GENETIC PREDISPOSITION; GENETICS; MIDDLE AGED; ODDS RATIO; RISK FACTOR;

ADULT; CASE-CONTROL STUDIES; CORONARY ARTERY DISEASE; ELECTROPHORESIS, AGAR GEL; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LIPIDS; MALE; MIDDLE AGED; ODDS RATIO; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS; SCAVENGER RECEPTORS, CLASS B;

EID: 84954088122     PISSN: None     EISSN: 1476511X     Source Type: Journal    
DOI: 10.1186/s12944-016-0176-9     Document Type: Article

References (37)

1. Celik T, Iyisoy A. Premature coronary artery disease in young patients: an uncommon but growing entity. Int J Cardiol. 2010;144(1):131-2. doi: 10.1016/j.ijcard.2008.12.150. Epub 2009 Jan 26.
2. De Sutter J, De Bacquer D, Kotseva K, Sans S, Pyörälä K, Wood D, et al. Screening of family members of patients with premature coronary heart disease Results from the EUROASPIRE II family survey. Eur Heart J. 2003;24(3):249-57.
3. Vaisi-Raygani A, Ghaneialvar H, Rahimi Z, Nomani H, Saidi M, Bahrehmand F, et al. The angiotensin converting enzyme D allele is an independent risk factor for early onset coronary artery disease. Clin Biochem. 2010;43(15):1189-94. doi: 10.1016/j.clinbiochem.2010.07.010.
4. Cengel A, Tanindi A. Myocardial infarction in the young. J Postgrad Med. 2009;55(4):305-13. doi: 10.4103/0022-3859.58944.
5. Kay A, Marz W, Hoffmann MM, Zhang Q, Masana L, Cavanna J, et al. Coronary artery disease and dyslipidemia within Europe: genetic variants in lipid transport gene loci in German subjects with premature coronary artery disease. Atheroscler Suppl. 2002;3(1):27-33.
6. Kumar P, Luthra K, Dwivedi M, Behl VK, Pandey RM, Misra A. Apolipoprotein E gene polymorphisms in patients with premature myocardial infarction: a case-controlled study in Asian Indians in North India. Ann Clin Biochem. 2003;40(Pt 4):382-7. doi: 10.1258/000456303766477020.
7. Almeida KA, Strunz CM, Maranhao RC, Mansur AP. The S447X polymorphism of lipoprotein lipase: effect on the incidence of premature coronary disease and on plasma lipids. Arq Bras Cardiol. 2007;88(3):297-303.
8. Ji J, Herbison CE, Mamotte CD, Burke V, Taylor RR, van Bockxmeer FM. Hepatic lipase gene -514 C/T polymorphism and premature coronary heart disease. J Cardiovasc Risk. 2002;9(2):105-13.
9. Abd El-Aziz TA, Mohamed RH, Hagrass HA. Increased risk of premature coronary artery disease in Egyptians with ABCA1 (R219K), CETP (TaqIB), and LCAT (4886C/T) genes polymorphism. J Clin Lipidol. 2014;8(4):381-9. doi: 10.1016/j.jacl.2014.06.001.
10. Van Eck M, Pennings M, Hoekstra M, Out R, Van Berkel TJ. Scavenger receptor BI and ATP-binding cassette transporter A1 in reverse cholesterol transport and atherosclerosis. Curr Opin Lipidol. 2005;16(3):307-15.
11. Mineo C, Shaul PW. Functions of scavenger receptor class B, type I in atherosclerosis. Curr Opin Lipidol. 2012;23(5):487-93. doi: 10.1097/MOL.0b013e328357ba61.
12. Constantineau J, Greason E, West M, Filbin M, Kieft JS, Carletti MZ, et al. A synonymous variant in scavenger receptor, class B, type I gene is associated with lower SR-BI protein expression and function. Atherosclerosis. 2010;210(1):177-82. doi: 10.1016/j.atherosclerosis.2009.11.029.
13. Acton S, Osgood D, Donoghue M, Corella D, Pocovi M, Cenarro A, et al. Association of polymorphisms at the SR-BI gene locus with plasma lipid levels and body mass index in a white population. Arterioscler Thromb Vasc Biol. 1999;19(7):1734-43.
14. Wu DF, Yin RX, Cao XL, Chen WX, Aung LH, Wang W, et al. Scavenger receptor class B type 1 gene rs5888 single nucleotide polymorphism and the risk of coronary artery disease and ischemic stroke: a case-control study. Int J Med Sci. 2013;10(12):1771-7. doi: 10.7150/ijms.7044.
15. Rodriguez-Esparragon F, Rodriguez-Perez JC, Hernandez-Trujillo Y, Macias-Reyes A, Medina A, Caballero A, et al. Allelic variants of the human scavenger receptor class B type 1 and paraoxonase 1 on coronary heart disease: genotype-phenotype correlations. Arterioscler Thromb Vasc Biol. 2005;25(4):854-60. doi: 10.1161/01.atv.0000157581.88838.03.
16. Hong SH, Kim YR, Yoon YM, Min WK, Chun SI, Kim JQ. Association between HaeIII polymorphism of scavenger receptor class B type I gene and plasma HDL-cholesterol concentration. Ann Clin Biochem. 2002;39(Pt 5):478-81. doi: 10.1258/000456302320314485.
17. Rejeb J, Omezzine A, Boumaiza I, Rebhi L, Kacem S, Rejeb NB, et al. Association of three polymorphisms of scavenger receptor class BI gene (exon8, exon1, intron5) with coronary stenosis in a coronary Tunisian population. Gene. 2012;511(2):383-8. doi: 10.1016/j.gene.2012.09.070.
18. Stanislovaitiene D, Lesauskaite V, Zaliuniene D, Smalinskiene A, Gustiene O, Zaliaduonyte-Peksiene D, et al. SCARB1 single nucleotide polymorphism (rs5888) is associated with serum lipid profile and myocardial infarction in an age- and gender-dependent manner. Lipids Health Dis. 2013;12:24. doi: 10.1186/1476-511x-12-24.
19. Gensini GG. A more meaningful scoring system for determining the severity of coronary heart disease. Am J Cardiol. 1983;51(3):606.
20. Boroumand M, Ghaedi M, Mohammadtaghvaei N, Pourgholi L, Anvari MS, Davoodi G, et al. Association of estrogen receptor alpha gene polymorphism with the presence of coronary artery disease documented by coronary angiography. Clin Biochem. 2009;42(9):835-9. doi: 10.1016/j.clinbiochem.2009.01.005.
21. Boroumand M, Pourgholi L, Ziaee S, Anvari MS, Jalali A, Goodarzynejad H. The association between Factor V Leiden with the presence and severity of coronary artery disease. Clin Biochem. 2014;47(6):356-60.
22. Wu DF, Yin RX, Yan TT, Aung LH, Cao XL, Miao L, et al. The SCARB1 rs5888 SNP and serum lipid levels in the Guangxi Mulao and Han populations. Int J Med Sci. 2012;9(8):715-24. doi: 10.7150/ijms.4815.
23. Roberts CG, Shen H, Mitchell BD, Damcott CM, Shuldiner AR, Rodriguez A. Variants in scavenger receptor class B type I gene are associated with HDL cholesterol levels in younger women. Hum Hered. 2007;64(2):107-13. doi: 10.1159/000101962.
24. Richard E, von Muhlen D, Barrett-Connor E, Alcaraz J, Davis R, McCarthy JJ. Modification of the effects of estrogen therapy on HDL cholesterol levels by polymorphisms of the HDL-C receptor, SR-BI: the Rancho Bernardo Study. Atherosclerosis. 2005;180(2):255-62. doi: 10.1016/j.atherosclerosis.2004.12.013.
25. Shen WJ, Hu J, Hu Z, Kraemer FB, Azhar S. Scavenger receptor class B type I (SR-BI): a versatile receptor with multiple functions and actions. Metabolism. 2014;63(7):875-86. doi: 10.1016/j.metabol.2014.03.011.
26. Morabia A, Ross BM, Costanza MC, Cayanis E, Flaherty MS, Alvin GB, et al. Population-based study of SR-BI genetic variation and lipid profile. Atherosclerosis. 2004;175(1):159-68. doi: 10.1016/j.atherosclerosis.2004.03.014.
27. McCarthy JJ, Lewitzky S, Reeves C, Permutt A, Glaser B, Groop LC, et al. Polymorphisms of the HDL receptor gene associated with HDL cholesterol levels in diabetic kindred from three populations. Hum Hered. 2003;55(4):163-70.
28. Osgood D, Corella D, Demissie S, Cupples LA, Wilson PW, Meigs JB, et al. Genetic variation at the scavenger receptor class B type I gene locus determines plasma lipoprotein concentrations and particle size and interacts with type 2 diabetes: the framingham study. J Clin Endocrinol Metab. 2003;88(6):2869-79.
29. Wu DF, Yin RX, Hu XJ, Aung LH, Cao XL, Miao L, et al. Association of rs5888 SNP in the scavenger receptor class B type 1 gene and serum lipid levels. Lipids Health Dis. 2012;11:50. doi: 10.1186/1476-511x-11-50.
30. den Hoed M, Strawbridge RJ, Almgren P, Gustafsson S, Axelsson T, Engstrom G, et al. GWAS-identified loci for coronary heart disease are associated with intima-media thickness and plaque presence at the carotid artery bulb. Atherosclerosis. 2015;239(2):304-10. doi: 10.1016/j.atherosclerosis.2015.01.032.
31. Deloukas P, Kanoni S, Willenborg C, Farrall M, Assimes TL, Thompson JR, et al. Large-scale association analysis identifies new risk loci for coronary artery disease. Nat Genet. 2013;45(1):25-33. doi: 10.1038/ng.2480.
32. Ritsch A, Sonderegger G, Sandhofer A, Stanzl U, Tancevski I, Eller P, et al. Scavenger receptor class B type I polymorphisms and peripheral arterial disease. Metabolism. 2007;56(8):1135-41. doi: 10.1016/j.metabol.2007.04.009.
33. Komar AA. Genetics. SNPs, silent but not invisible. Science. 2007;315(5811):466-7. doi: 10.1126/science.1138239.
34. Kimchi-Sarfaty C, Oh JM, Kim IW, Sauna ZE, Calcagno AM, Ambudkar SV, et al. A "silent" polymorphism in the MDR1 gene changes substrate specificity. Science. 2007;315(5811):525-8. doi: 10.1126/science.1135308.
35. Komar AA. Silent SNPs: impact on gene function and phenotype. Pharmacogenomics. 2007;8(8):1075-80. doi: 10.2217/14622416.8.8.1075.
36. Cartegni L, Chew SL, Krainer AR. Listening to silence and understanding nonsense: exonic mutations that affect splicing. Nat Rev Genet. 2002;3(4):285-98. doi: 10.1038/nrg775.
37. McCarthy JJ, Lehner T, Reeves C, Moliterno DJ, Newby LK, Rogers WJ, et al. Association of genetic variants in the HDL receptor, SR-B1, with abnormal lipids in women with coronary artery disease. J Med Genet. 2003;40(6):453-8.