Low-density lipoprotein receptor-related protein-associated protein (LRPAP1) gene IVS5 insertion/deletion polymorphism is not a risk factor for gallstone disease in a Polish population

Digestive and Liver Disease

Volumn 40, Issue 2, 2008, Pages 122-125

  Juzyszyn, Z ^a   Kurzawski, M ^a   Modrzejewski, A ^a   Sulikowski, T ^a   Pawlik, A ^a   Czerny, B ^a   Drozdzik M ^a  

^a POMERANIAN MEDICAL UNIVERSITY   (Poland)

Author keywords

Gallstone disease; Genetic polymorphism; LRPAP1

Indexed keywords

LOW DENSITY LIPOPROTEIN RECEPTOR RELATED PROTEIN ASSOCIATED PROTEIN;

ADULT; AGED; ALLELE; ARTICLE; CAUCASIAN; CHOLELITHIASIS; CONTROLLED STUDY; FEMALE; GENE DELETION; GENE FREQUENCY; GENE INSERTION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; HUMAN; INTRON; MAJOR CLINICAL STUDY; MALE; POLAND; POLYMERASE CHAIN REACTION; POPULATION RESEARCH; RISK FACTOR;

ADULT; AGED; AGED, 80 AND OVER; FEMALE; GALLSTONES; GENETICS, POPULATION; HUMANS; LDL-RECEPTOR RELATED PROTEIN-ASSOCIATED PROTEIN; MALE; MIDDLE AGED; POLAND; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; RISK FACTORS;

EID: 38049020536     PISSN: 15908658     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dld.2007.08.009     Document Type: Article

References (24)

1. Kratzer W., Kachele V., Mason R.A., Hill V., Hay B., Haug C., et al. Gallstone prevalence in Germany: the Ulm gallbladder stone study. Dig Dis Sci 43 (1998) 1285-1291
2. Tsai C.J., Leitzmann M.F., Willett W.C., and Giovannucci E.L. Glycemic load, glycemic index, and carbohydrate intake in relation to risk of cholecystectomy in women. Gastroenterology 129 (2005) 105-112
3. Leitzmann M.F., Rimm E.B., Willett W.C., Spiegelman D., Grodstein F., Stampfer M.J., et al. Recreational physical activity and the risk of cholecystectomy in women. N Engl J Med 341 (1999) 777-784
4. Lammert F., and Sauerbruch T. Mechanisms of disease: the genetic epidemiology of gallbladder stones. Nat Clin Pract Gastroenterol Hepatol 2 (2005) 423-433
5. Kesaniemi Y.A., Koskenvuo M., Vuoristo M., and Miettinen T.A. Biliary lipid composition in monozygotic and dizygotic pairs of twins. Gut 30 (1989) 1750-1756
6. Katsika D., Grjibovski A., Einarsson C., Lammert F., Lichtenstein P., and Marschall H.U. Genetic and environmental influences on symptomatic gallstone disease: a Swedish study of 43,141 twin pairs. Hepatology 41 (2005) 1138-1143
7. Rosmorduc O., Hermelin B., Boelle P.Y., Parc R., Taboury J., and Poupon R. ABCB4 gene mutation-associated cholelithiasis in adults. Gastroenterology 125 (2003) 452-459
8. van Mil S.W., van der Woerd W.L., van der Brugge G., Sturm E., Jansen P.L., Bull L.N., et al. Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11. Gastroenterology 127 (2004) 379-384
9. Pullinger C.R., Eng C., Salen G., Shefer S., Batta A.K., Erickson S.K., et al. Human cholesterol 7alpha-hydroxylase (CYP7A1) deficiency has a hypercholesterolemic phenotype. J Clin Invest 110 (2002) 109-117
10. Petitti D.B., Friedman G.D., and Klatsky A.L. Association of a history of gallbladder disease with a reduced concentration of high-density-lipoprotein cholesterol. N Engl J Med 304 (1981) 1396-1398
11. Mohr G.C., Kritz-Silverstein D., and Barrett-Connor E. Plasma lipids and gallbladder disease. Am J Epidemiol 134 (1991) 78-85
12. Thijs C., Knipschild P., and Brombacher P. Serum lipids and gallstones: a case-control study. Gastroenterology 99 (1990) 843-849
13. Ashcom J.D., Tiller S.E., Dickerson K., Cravens J.L., Argraves W.S., and Strickland D.K. The human alpha 2-macroglobulin receptor: identification of a 420-kD cell surface glycoprotein specific for the activated conformation of alpha 2-macroglobulin. J Cell Biol 110 (1990) 1041-1048
14. Herz J. The switch on the RAPper's necklace. Mol Cell 23 (2006) 451-455
15. Willnow T.E., Sheng Z., Ishibashi S., and Herz J. Inhibition of hepatic chylomicron remnant uptake by gene transfer of a receptor antagonist. Science 264 (1994) 1471-1474
16. Willnow T.E., Rohlmann A., Horton J., Otani H., Braun J.R., Hammer R.E., et al. RAP, a specialized chaperone, prevents ligand-induced ER retention and degradation of LDL receptor-related endocytic receptors. EMBO J 15 (1996) 2632-2639
17. Benes P., Muzik J., Benedik J., Elbl L., Znojil V., and Vacha J. Relation between the insertion/deletion polymorphism in the gene coding for receptor associated protein (RAP) and plasma apolipoprotein AI (apoAI) and high-density lipoprotein cholesterol (HDL) levels. Clin Genet 57 (2000) 309-310
18. Dixit M., Choudhuri G., Keshri L.J., and Mittal B. Association of low density lipoprotein receptor related protein-associated protein (LRPAP1) gene insertion/deletion polymorphism with gallstone disease. J Gastroenterol Hepatol 21 (2006) 847-849
19. Dixit M., Choudhuri G., and Mittal B. Association of lipoprotein receptor, receptor-associated protein, and metabolizing enzyme gene polymorphisms with gallstone disease: A case-control study. Hepatol Res 36 (2006) 61-69
20. Gustincich S., Manfioletti G., Del Sal G., Schneider C., and Carninci P. A fast method for high-quality genomic DNA extraction from whole human blood. Biotechniques 11 (1991) 298-300 302
21. McCarthy J.J., Meyer J., Moliterno D.J., Newby L.K., Rogers W.J., Topol E.J., et al. Evidence for substantial effect modification by gender in a large-scale genetic association study of the metabolic syndrome among coronary heart disease patients. Hum Genet 114 (2003) 87-98
22. Sanchez L., Alvarez V., Gonzalez P., Gonzalez I., Alvarez R., and Coto E. Variation in the LRP-associated protein gene (LRPAP1) is associated with late-onset Alzheimer disease. Am J Med Genet 105 (2001) 76-78
23. Viturro E., de Oya M., Lasuncion M.A., Gorgojo L., Moreno J.M., Benavente M., et al. Cholesterol and saturated fat intake determine the effect of polymorphisms at ABCG5/ABCG8 genes on lipid levels in children. Genet Med 8 (2006) 594-599
24. Herron K.L., McGrane M.M., Waters D., Lofgren I.E., Clark R.M., Ordovas J.M., et al. The ABCG5 polymorphism contributes to individual responses to dietary cholesterol and carotenoids in eggs. J Nutr 136 (2006) 1161-1165