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Published in: BMC Medical Genetics 1/2010

Open Access 01-12-2010 | Research article

Genetic variants associated with fasting blood lipids in the U.S. population: Third National Health and Nutrition Examination Survey

Authors: Man-huei Chang, Ajay Yesupriya, Renée M Ned, Patricia W Mueller, Nicole F Dowling

Published in: BMC Medical Genetics | Issue 1/2010

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Abstract

Background

The identification of genetic variants related to blood lipid levels within a large, population-based and nationally representative study might lead to a better understanding of the genetic contribution to serum lipid levels in the major race/ethnic groups in the U.S. population.

Methods

Using data from the second phase (1991-1994) of the Third National Health and Nutrition Examination Survey (NHANES III), we examined associations between 22 polymorphisms in 13 candidate genes and four serum lipids: high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), total cholesterol (TC), and triglycerides (TG). Univariate and multivariable linear regression and within-gene haplotype trend regression were used to test for genetic associations assuming an additive mode of inheritance for each of the three major race/ethnic groups in the United States (non-Hispanic white, non-Hispanic black, and Mexican American).

Results

Variants within APOE (rs7412, rs429358), PON1 (rs854560), ITGB3 (rs5918), and NOS3 (rs2070744) were found to be associated with one or more blood lipids in at least one race/ethnic group in crude and adjusted analyses. In non-Hispanic whites, no individual polymorphisms were associated with any lipid trait. However, the PON1 A-G haplotype was significantly associated with LDL-C and TC. In non-Hispanic blacks, APOE variant rs7412 and haplotype T-T were strongly associated with LDL-C and TC; whereas, rs5918 of ITGB3 was significantly associated with TG. Several variants and haplotypes of three genes were significantly related to lipids in Mexican Americans: PON1 in relation to HDL-C; APOE and NOS3 in relation to LDL-C; and APOE in relation to TC.

Conclusions

We report the significant associations of blood lipids with variants and haplotypes in APOE, ITGB3, NOS3, and PON1 in the three main race/ethnic groups in the U.S. population using a large, nationally representative and population-based sample survey. Results from our study contribute to a growing body of literature identifying key determinants of plasma lipoprotein concentrations and could provide insight into the biological mechanisms underlying serum lipid and cholesterol concentrations.
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Literature
1.
go back to reference National Institutes of Health: 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 (25): 3143-3421. National Institutes of Health: 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 (25): 3143-3421.
2.
go back to reference Rywik SL, Manolio TA, Pajak A, Piotrowski W, Davis CE, Broda GB, Kawalec E: Association of lipids and lipoprotein level with total mortality and mortality caused by cardiovascular and cancer diseases (Poland and United States collaborative study on cardiovascular epidemiology). Am J Cardiol. 1999, 84 (5): 540-548. 10.1016/S0002-9149(99)00374-4.PubMed Rywik SL, Manolio TA, Pajak A, Piotrowski W, Davis CE, Broda GB, Kawalec E: Association of lipids and lipoprotein level with total mortality and mortality caused by cardiovascular and cancer diseases (Poland and United States collaborative study on cardiovascular epidemiology). Am J Cardiol. 1999, 84 (5): 540-548. 10.1016/S0002-9149(99)00374-4.PubMed
3.
go back to reference Bray M: Genetic and environmental factors in cardiovascular disease. Human Genome Epidemiology. Edited by: Khoury M, Little J, Burke W. 2004, New York: Oxford University Press, Inc, 436-450. Bray M: Genetic and environmental factors in cardiovascular disease. Human Genome Epidemiology. Edited by: Khoury M, Little J, Burke W. 2004, New York: Oxford University Press, Inc, 436-450.
4.
go back to reference Briel M, Ferreira-Gonzalez I, You JJ, Karanicolas PJ, Akl EA, Wu P, Blechacz B, Bassler D, Wei X, Sharman A, Whitt I, Alves da Silva S, Khalid Z, Nordmann AJ, Zhou Q, Walter SD, Vale N, Bhatnagar N, O'Regan C, Mills EJ, Bucher HC, Montori VM, Guyatt GH: Association between change in high density lipoprotein cholesterol and cardiovascular disease morbidity and mortality: systematic review and meta-regression analysis. BMJ. 2009, 338: b92-10.1136/bmj.b92.PubMedPubMedCentral Briel M, Ferreira-Gonzalez I, You JJ, Karanicolas PJ, Akl EA, Wu P, Blechacz B, Bassler D, Wei X, Sharman A, Whitt I, Alves da Silva S, Khalid Z, Nordmann AJ, Zhou Q, Walter SD, Vale N, Bhatnagar N, O'Regan C, Mills EJ, Bucher HC, Montori VM, Guyatt GH: Association between change in high density lipoprotein cholesterol and cardiovascular disease morbidity and mortality: systematic review and meta-regression analysis. BMJ. 2009, 338: b92-10.1136/bmj.b92.PubMedPubMedCentral
5.
go back to reference Asztalos BF, Cupples LA, Demissie S, Horvath KV, Cox CE, Batista MC, Schaefer EJ: High-density lipoprotein subpopulation profile and coronary heart disease prevalence in male participants of the Framingham Offspring Study. Arterioscler Thromb Vasc Biol. 2004, 24 (11): 2181-2187. 10.1161/01.ATV.0000146325.93749.a8.PubMed Asztalos BF, Cupples LA, Demissie S, Horvath KV, Cox CE, Batista MC, Schaefer EJ: High-density lipoprotein subpopulation profile and coronary heart disease prevalence in male participants of the Framingham Offspring Study. Arterioscler Thromb Vasc Biol. 2004, 24 (11): 2181-2187. 10.1161/01.ATV.0000146325.93749.a8.PubMed
6.
go back to reference Castelli WP: Epidemiology of triglycerides: a view from Framingham. Am J Cardiol. 1992, 70 (19): 3H-9H. 10.1016/0002-9149(92)91083-G.PubMed Castelli WP: Epidemiology of triglycerides: a view from Framingham. Am J Cardiol. 1992, 70 (19): 3H-9H. 10.1016/0002-9149(92)91083-G.PubMed
7.
go back to reference Castelli WP: The role of plasma lipids as predictors of risk for coronary heart disease. Drugs. 1990, 40 (Suppl 1): 1-4. 10.2165/00003495-199000401-00003. discussion 5-6.PubMed Castelli WP: The role of plasma lipids as predictors of risk for coronary heart disease. Drugs. 1990, 40 (Suppl 1): 1-4. 10.2165/00003495-199000401-00003. discussion 5-6.PubMed
8.
go back to reference Castelli WP, Anderson K, Wilson PW, Levy D: Lipids and risk of coronary heart disease. The Framingham Study. Ann Epidemiol. 1992, 2 (1-2): 23-28.PubMed Castelli WP, Anderson K, Wilson PW, Levy D: Lipids and risk of coronary heart disease. The Framingham Study. Ann Epidemiol. 1992, 2 (1-2): 23-28.PubMed
9.
go back to reference Heller DA, de Faire U, Pedersen NL, Dahlen G, McClearn GE: Genetic and environmental influences on serum lipid levels in twins. N Engl J Med. 1993, 328 (16): 1150-1156. 10.1056/NEJM199304223281603.PubMed Heller DA, de Faire U, Pedersen NL, Dahlen G, McClearn GE: Genetic and environmental influences on serum lipid levels in twins. N Engl J Med. 1993, 328 (16): 1150-1156. 10.1056/NEJM199304223281603.PubMed
10.
go back to reference Namboodiri KK, Kaplan EB, Heuch I, Elston RC, Green PP, Rao DC, Laskarzewski P, Glueck CJ, Rifkind BM: The Collaborative Lipid Research Clinics Family Study: biological and cultural determinants of familial resemblance for plasma lipids and lipoproteins. Genet Epidemiol. 1985, 2 (3): 227-254. 10.1002/gepi.1370020302.PubMed Namboodiri KK, Kaplan EB, Heuch I, Elston RC, Green PP, Rao DC, Laskarzewski P, Glueck CJ, Rifkind BM: The Collaborative Lipid Research Clinics Family Study: biological and cultural determinants of familial resemblance for plasma lipids and lipoproteins. Genet Epidemiol. 1985, 2 (3): 227-254. 10.1002/gepi.1370020302.PubMed
11.
go back to reference Spielmann N, Leon AS, Rao DC, Rice T, Skinner JS, Bouchard C, Rankinen T: CETP genotypes and HDL-cholesterol phenotypes in the HERITAGE Family Study. Physiol Genomics. 2007, 31 (1): 25-31. 10.1152/physiolgenomics.00281.2006.PubMed Spielmann N, Leon AS, Rao DC, Rice T, Skinner JS, Bouchard C, Rankinen T: CETP genotypes and HDL-cholesterol phenotypes in the HERITAGE Family Study. Physiol Genomics. 2007, 31 (1): 25-31. 10.1152/physiolgenomics.00281.2006.PubMed
12.
go back to reference Choquette AC, Bouchard L, Houde A, Bouchard C, Perusse L, Vohl MC: Associations between USF1 gene variants and cardiovascular risk factors in the Quebec Family Study. Clin Genet. 2007, 71 (3): 245-253. 10.1111/j.1399-0004.2007.00755.x.PubMed Choquette AC, Bouchard L, Houde A, Bouchard C, Perusse L, Vohl MC: Associations between USF1 gene variants and cardiovascular risk factors in the Quebec Family Study. Clin Genet. 2007, 71 (3): 245-253. 10.1111/j.1399-0004.2007.00755.x.PubMed
13.
go back to reference Garenc C, Aubert S, Laroche J, Bergeron J, Gagne C, Rousseau F, Julien P: Gene polymorphisms in the Quebec population: a risk to develop hypertriglyceridemia. Biochem Biophys Res Commun. 2006, 344 (2): 588-596. 10.1016/j.bbrc.2006.03.187.PubMed Garenc C, Aubert S, Laroche J, Bergeron J, Gagne C, Rousseau F, Julien P: Gene polymorphisms in the Quebec population: a risk to develop hypertriglyceridemia. Biochem Biophys Res Commun. 2006, 344 (2): 588-596. 10.1016/j.bbrc.2006.03.187.PubMed
14.
go back to reference Pallaud C, Gueguen R, Sass C, Grow M, Cheng S, Siest G, Visvikis S: Genetic influences on lipid metabolism trait variability within the Stanislas Cohort. J Lipid Res. 2001, 42 (11): 1879-1890.PubMed Pallaud C, Gueguen R, Sass C, Grow M, Cheng S, Siest G, Visvikis S: Genetic influences on lipid metabolism trait variability within the Stanislas Cohort. J Lipid Res. 2001, 42 (11): 1879-1890.PubMed
15.
go back to reference Petrone A, Zavarella S, Iacobellis G, Zampetti S, Vania A, Di Pietro S, Galgani A, Leonetti F, Di Mario U, Buzzetti R: Association of beta2 adrenergic receptor polymorphisms and related haplotypes with triglyceride and LDL-cholesterol levels. Eur J Hum Genet. 2006, 14 (1): 94-100.PubMed Petrone A, Zavarella S, Iacobellis G, Zampetti S, Vania A, Di Pietro S, Galgani A, Leonetti F, Di Mario U, Buzzetti R: Association of beta2 adrenergic receptor polymorphisms and related haplotypes with triglyceride and LDL-cholesterol levels. Eur J Hum Genet. 2006, 14 (1): 94-100.PubMed
16.
go back to reference Dedoussis GV, Maumus S, Choumerianou DM, Skoumas J, Pitsavos C, Stefanadis C, Visvikis-Siest S: Different genes and polymorphisms affecting high-density lipoprotein cholesterol levels in Greek familial hypercholesterolemia patients. Genet Test. 2006, 10 (3): 192-199. 10.1089/gte.2006.10.192.PubMed Dedoussis GV, Maumus S, Choumerianou DM, Skoumas J, Pitsavos C, Stefanadis C, Visvikis-Siest S: Different genes and polymorphisms affecting high-density lipoprotein cholesterol levels in Greek familial hypercholesterolemia patients. Genet Test. 2006, 10 (3): 192-199. 10.1089/gte.2006.10.192.PubMed
17.
go back to reference Pollin TI, Damcott CM, Shen H, Ott SH, Shelton J, Horenstein RB, Post W, McLenithan JC, Bielak LF, Peyser PA, Mitchell BD, Miller M, O'Connell JR, Shuldiner AR: A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. Science. 2008, 322 (5908): 1702-1705. 10.1126/science.1161524.PubMedPubMedCentral Pollin TI, Damcott CM, Shen H, Ott SH, Shelton J, Horenstein RB, Post W, McLenithan JC, Bielak LF, Peyser PA, Mitchell BD, Miller M, O'Connell JR, Shuldiner AR: A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. Science. 2008, 322 (5908): 1702-1705. 10.1126/science.1161524.PubMedPubMedCentral
18.
go back to reference Aulchenko YS, Ripatti S, Lindqvist I, Boomsma D, Heid IM, Pramstaller PP, Penninx BW, Janssens AC, Wilson JF, Spector T, Martin NG, Pedersen NL, Kyvik KO, Kaprio J, Hofman A, Freimer NB, Jarvelin MR, Gyllensten U, Campbell H, Rudan I, Johansson A, Marroni F, Hayward C, Vitart V, Jonasson I, Pattaro C, Wright A, Hastie N, Pichler I, Hicks AA, et al: Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nat Genet. 2009, 41 (1): 47-55. 10.1038/ng.269.PubMed Aulchenko YS, Ripatti S, Lindqvist I, Boomsma D, Heid IM, Pramstaller PP, Penninx BW, Janssens AC, Wilson JF, Spector T, Martin NG, Pedersen NL, Kyvik KO, Kaprio J, Hofman A, Freimer NB, Jarvelin MR, Gyllensten U, Campbell H, Rudan I, Johansson A, Marroni F, Hayward C, Vitart V, Jonasson I, Pattaro C, Wright A, Hastie N, Pichler I, Hicks AA, et al: Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Nat Genet. 2009, 41 (1): 47-55. 10.1038/ng.269.PubMed
19.
go back to reference Kathiresan S, Willer CJ, Peloso GM, Demissie S, Musunuru K, Schadt EE, Kaplan L, Bennett D, Li Y, Tanaka T, Voight BF, Bonnycastle LL, Jackson AU, Crawford G, Surti A, Guiducci C, Burtt NP, Parish S, Clarke R, Zelenika D, Kubalanza KA, Morken MA, Scott LJ, Stringham HM, Galan P, Swift AJ, Kuusisto J, Bergman RN, Sundvall J, Laakso M, et al: Common variants at 30 loci contribute to polygenic dyslipidemia. Nat Genet. 2009, 41 (1): 56-65. 10.1038/ng.291.PubMed Kathiresan S, Willer CJ, Peloso GM, Demissie S, Musunuru K, Schadt EE, Kaplan L, Bennett D, Li Y, Tanaka T, Voight BF, Bonnycastle LL, Jackson AU, Crawford G, Surti A, Guiducci C, Burtt NP, Parish S, Clarke R, Zelenika D, Kubalanza KA, Morken MA, Scott LJ, Stringham HM, Galan P, Swift AJ, Kuusisto J, Bergman RN, Sundvall J, Laakso M, et al: Common variants at 30 loci contribute to polygenic dyslipidemia. Nat Genet. 2009, 41 (1): 56-65. 10.1038/ng.291.PubMed
20.
go back to reference Sabatti C, Service SK, Hartikainen AL, Pouta A, Ripatti S, Brodsky J, Jones CG, Zaitlen NA, Varilo T, Kaakinen M, Sovio U, Ruokonen A, Laitinen J, Jakkula E, Coin L, Hoggart C, Collins A, Turunen H, Gabriel S, Elliot P, McCarthy MI, Daly MJ, Järvelin MR, Freimer NB, Peltonen L: Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. Nat Genet. 2009, 41 (1): 35-46. 10.1038/ng.271.PubMed Sabatti C, Service SK, Hartikainen AL, Pouta A, Ripatti S, Brodsky J, Jones CG, Zaitlen NA, Varilo T, Kaakinen M, Sovio U, Ruokonen A, Laitinen J, Jakkula E, Coin L, Hoggart C, Collins A, Turunen H, Gabriel S, Elliot P, McCarthy MI, Daly MJ, Järvelin MR, Freimer NB, Peltonen L: Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. Nat Genet. 2009, 41 (1): 35-46. 10.1038/ng.271.PubMed
21.
go back to reference Burkhardt R, Kenny EE, Lowe JK, Birkeland A, Josowitz R, Noel M, Salit J, Maller JB, Pe'er I, Daly MJ, Altshuler D, Stoffel M, Friedman JM, Breslow JL: Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13. Arterioscler Thromb Vasc Biol. 2008, 28 (11): 2078-2084. 10.1161/ATVBAHA.108.172288.PubMedPubMedCentral Burkhardt R, Kenny EE, Lowe JK, Birkeland A, Josowitz R, Noel M, Salit J, Maller JB, Pe'er I, Daly MJ, Altshuler D, Stoffel M, Friedman JM, Breslow JL: Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13. Arterioscler Thromb Vasc Biol. 2008, 28 (11): 2078-2084. 10.1161/ATVBAHA.108.172288.PubMedPubMedCentral
22.
go back to reference Sandhu MS, Waterworth DM, Debenham SL, Wheeler E, Papadakis K, Zhao JH, Song K, Yuan X, Johnson T, Ashford S, Inouye M, Luben R, Sims M, Hadley D, McArdle W, Barter P, Kesäniemi YA, Mahley RW, McPherson R, Grundy SM, Wellcome Trust Case Control Consortium, Bingham SA, Khaw KT, Loos RJ, Waeber G, Barroso I, Strachan DP, Deloukas P, Vollenweider P, Wareham NJ, et al: LDL-cholesterol concentrations: a genome-wide association study. Lancet. 2008, 371 (9611): 483-491. 10.1016/S0140-6736(08)60208-1.PubMedPubMedCentral Sandhu MS, Waterworth DM, Debenham SL, Wheeler E, Papadakis K, Zhao JH, Song K, Yuan X, Johnson T, Ashford S, Inouye M, Luben R, Sims M, Hadley D, McArdle W, Barter P, Kesäniemi YA, Mahley RW, McPherson R, Grundy SM, Wellcome Trust Case Control Consortium, Bingham SA, Khaw KT, Loos RJ, Waeber G, Barroso I, Strachan DP, Deloukas P, Vollenweider P, Wareham NJ, et al: LDL-cholesterol concentrations: a genome-wide association study. Lancet. 2008, 371 (9611): 483-491. 10.1016/S0140-6736(08)60208-1.PubMedPubMedCentral
23.
go back to reference Kathiresan S, Melander O, Guiducci C, Surti A, Burtt NP, Rieder MJ, Cooper GM, Roos C, Voight BF, Havulinna AS, Wahlstrand B, Hedner T, Corella D, Tai ES, Ordovas JM, Berglund G, Vartiainen E, Jousilahti P, Hedblad B, Taskinen MR, Newton-Cheh C, Salomaa V, Peltonen L, Groop L, Altshuler DM, Orho-Melander M: Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans. Nat Genet. 2008, 40 (2): 189-197. 10.1038/ng.75.PubMedPubMedCentral Kathiresan S, Melander O, Guiducci C, Surti A, Burtt NP, Rieder MJ, Cooper GM, Roos C, Voight BF, Havulinna AS, Wahlstrand B, Hedner T, Corella D, Tai ES, Ordovas JM, Berglund G, Vartiainen E, Jousilahti P, Hedblad B, Taskinen MR, Newton-Cheh C, Salomaa V, Peltonen L, Groop L, Altshuler DM, Orho-Melander M: Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans. Nat Genet. 2008, 40 (2): 189-197. 10.1038/ng.75.PubMedPubMedCentral
24.
go back to reference Wallace C, Newhouse SJ, Braund P, Zhang F, Tobin M, Falchi M, Ahmadi K, Dobson RJ, Marçano AC, Hajat C, Burton P, Deloukas P, Brown M, Connell JM, Dominiczak A, Lathrop GM, Webster J, Farrall M, Spector T, Samani NJ, Caulfield MJ, Munroe PB: Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. Am J Hum Genet. 2008, 82 (1): 139-149. 10.1016/j.ajhg.2007.11.001.PubMedPubMedCentral Wallace C, Newhouse SJ, Braund P, Zhang F, Tobin M, Falchi M, Ahmadi K, Dobson RJ, Marçano AC, Hajat C, Burton P, Deloukas P, Brown M, Connell JM, Dominiczak A, Lathrop GM, Webster J, Farrall M, Spector T, Samani NJ, Caulfield MJ, Munroe PB: Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. Am J Hum Genet. 2008, 82 (1): 139-149. 10.1016/j.ajhg.2007.11.001.PubMedPubMedCentral
25.
go back to reference Saxena R, Voight BF, Lyssenko V, Burtt NP, de Bakker PI, Chen H, Roix JJ, Kathiresan S, Hirschhorn JN, Daly MJ, Hughes TE, Groop L, Altshuler D, Almgren P, Florez JC, Meyer J, Ardlie K, Bengtsson Boström K, Isomaa B, Lettre G, Lindblad U, Lyon HN, Melander O, Newton-Cheh C, Nilsson P, Orho-Melander M, Råstam L, Speliotes EK, Taskinen MR, Tuomi T, et al: Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science. 2007, 316 (5829): 1331-1336. 10.1126/science.1142358.PubMed Saxena R, Voight BF, Lyssenko V, Burtt NP, de Bakker PI, Chen H, Roix JJ, Kathiresan S, Hirschhorn JN, Daly MJ, Hughes TE, Groop L, Altshuler D, Almgren P, Florez JC, Meyer J, Ardlie K, Bengtsson Boström K, Isomaa B, Lettre G, Lindblad U, Lyon HN, Melander O, Newton-Cheh C, Nilsson P, Orho-Melander M, Råstam L, Speliotes EK, Taskinen MR, Tuomi T, et al: Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science. 2007, 316 (5829): 1331-1336. 10.1126/science.1142358.PubMed
26.
go back to reference Tabet F, Rye KA: High-density lipoproteins, inflammation and oxidative stress. Clin Sci (Lond). 2009, 116 (2): 87-98. 10.1042/CS20080106. Tabet F, Rye KA: High-density lipoproteins, inflammation and oxidative stress. Clin Sci (Lond). 2009, 116 (2): 87-98. 10.1042/CS20080106.
27.
go back to reference Garces C, Lopez-Simon L, Rubio R, Benavente M, Cano B, Ortega H, de Oya M: High-density lipoprotein cholesterol and paraoxonase 1 (PON1) genetics and serum PON1 activity in prepubertal children in Spain. Clin Chem Lab Med. 2008, 46 (6): 809-813. 10.1515/CCLM.2008.163.PubMed Garces C, Lopez-Simon L, Rubio R, Benavente M, Cano B, Ortega H, de Oya M: High-density lipoprotein cholesterol and paraoxonase 1 (PON1) genetics and serum PON1 activity in prepubertal children in Spain. Clin Chem Lab Med. 2008, 46 (6): 809-813. 10.1515/CCLM.2008.163.PubMed
28.
go back to reference National Center for Health Statistics, Centers for Disease Control and Prevention: Plan and Operation of the Third National Health and Nutrition Examination Survey, 1988-94. Hyattsville, MD. National Center for Health Statistics, 1994. Vital and Health Statistics, Series 1: Programs and Collection Procedures, no. 32. DHHS publication no. (PHS) 94-1308. 1994, [http://www.cdc.gov/nchs/data/series/sr_01/sr01_032.pdf] National Center for Health Statistics, Centers for Disease Control and Prevention: Plan and Operation of the Third National Health and Nutrition Examination Survey, 1988-94. Hyattsville, MD. National Center for Health Statistics, 1994. Vital and Health Statistics, Series 1: Programs and Collection Procedures, no. 32. DHHS publication no. (PHS) 94-1308. 1994, [http://​www.​cdc.​gov/​nchs/​data/​series/​sr_​01/​sr01_​032.​pdf]
31.
go back to reference Chang MH, Lindegren ML, Butler MA, Chanock SJ, Dowling NF, Gallagher M, Moonesinghe R, Moore CA, Ned RM, Reichler MR, Sanders CL, Welch R, Yesupriya A, Khoury MJ, CDC/NCI NHANES III Genomics Working Group: Prevalence in the United States of selected candidate gene variants: Third National Health and Nutrition Examination Survey, 1991-1994. Am J Epidemiol. 2009, 169 (1): 54-66. 10.1093/aje/kwn286.PubMed Chang MH, Lindegren ML, Butler MA, Chanock SJ, Dowling NF, Gallagher M, Moonesinghe R, Moore CA, Ned RM, Reichler MR, Sanders CL, Welch R, Yesupriya A, Khoury MJ, CDC/NCI NHANES III Genomics Working Group: Prevalence in the United States of selected candidate gene variants: Third National Health and Nutrition Examination Survey, 1991-1994. Am J Epidemiol. 2009, 169 (1): 54-66. 10.1093/aje/kwn286.PubMed
34.
go back to reference Executive Summary of The 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). JAMA. 2001, 285 (19): 2486-2497. 10.1001/jama.285.19.2486. Executive Summary of The 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). JAMA. 2001, 285 (19): 2486-2497. 10.1001/jama.285.19.2486.
35.
go back to reference Dempster A, Laird N, Rubin D: Maximum likelihood from incomplete data via the EM algorithm. J Royal Statistical Society. 1977, Series B; 39 (1): 1-38. Dempster A, Laird N, Rubin D: Maximum likelihood from incomplete data via the EM algorithm. J Royal Statistical Society. 1977, Series B; 39 (1): 1-38.
36.
go back to reference Schaid DJ: Genetic epidemiology and haplotypes. Genet Epidemiol. 2004, 27 (4): 317-320. 10.1002/gepi.20046.PubMed Schaid DJ: Genetic epidemiology and haplotypes. Genet Epidemiol. 2004, 27 (4): 317-320. 10.1002/gepi.20046.PubMed
37.
go back to reference Zaykin DV, Westfall PH, Young SS, Karnoub MA, Wagner MJ, Ehm MG: Testing association of statistically inferred haplotypes with discrete and continuous traits in samples of unrelated individuals. Hum Hered. 2002, 53 (2): 79-91. 10.1159/000057986.PubMed Zaykin DV, Westfall PH, Young SS, Karnoub MA, Wagner MJ, Ehm MG: Testing association of statistically inferred haplotypes with discrete and continuous traits in samples of unrelated individuals. Hum Hered. 2002, 53 (2): 79-91. 10.1159/000057986.PubMed
38.
go back to reference Schaid DJ: Evaluating associations of haplotypes with traits. Genet Epidemiol. 2004, 27 (4): 348-364. 10.1002/gepi.20037.PubMed Schaid DJ: Evaluating associations of haplotypes with traits. Genet Epidemiol. 2004, 27 (4): 348-364. 10.1002/gepi.20037.PubMed
39.
go back to reference Benjamini Y, Hochberg Y: Controlling the false discovery rate: a practical and powerful approach to multiple testing. J Royal Stat Soc. 1995, Series B (57): 12- Benjamini Y, Hochberg Y: Controlling the false discovery rate: a practical and powerful approach to multiple testing. J Royal Stat Soc. 1995, Series B (57): 12-
40.
go back to reference Keebler ME, Sanders CL, Surti A, Guiducci C, Burtt NP, Kathiresan S: Association of blood lipids with common DNA sequence variants at 19 genetic loci in the multiethnic United States National Health and Nutrition Examination Survey III. Circ Cardiovasc Genet. 2009, 238-243. 10.1161/CIRCGENETICS.108.829473. 2 Keebler ME, Sanders CL, Surti A, Guiducci C, Burtt NP, Kathiresan S: Association of blood lipids with common DNA sequence variants at 19 genetic loci in the multiethnic United States National Health and Nutrition Examination Survey III. Circ Cardiovasc Genet. 2009, 238-243. 10.1161/CIRCGENETICS.108.829473. 2
41.
go back to reference Eichner JE, Dunn ST, Perveen G, Thompson DM, Stewart KE, Stroehla BC: Apolipoprotein E polymorphism and cardiovascular disease: a HuGE review. Am J Epidemiol. 2002, 155 (6): 487-495. 10.1093/aje/155.6.487.PubMed Eichner JE, Dunn ST, Perveen G, Thompson DM, Stewart KE, Stroehla BC: Apolipoprotein E polymorphism and cardiovascular disease: a HuGE review. Am J Epidemiol. 2002, 155 (6): 487-495. 10.1093/aje/155.6.487.PubMed
42.
go back to reference Bennet AM, Di Angelantonio E, Ye Z, Wensley F, Dahlin A, Ahlbom A, Keavney B, Collins R, Wiman B, de Faire U, Danesh J: Association of apolipoprotein E genotypes with lipid levels and coronary risk. JAMA. 2007, 298 (11): 1300-1311. 10.1001/jama.298.11.1300.PubMed Bennet AM, Di Angelantonio E, Ye Z, Wensley F, Dahlin A, Ahlbom A, Keavney B, Collins R, Wiman B, de Faire U, Danesh J: Association of apolipoprotein E genotypes with lipid levels and coronary risk. JAMA. 2007, 298 (11): 1300-1311. 10.1001/jama.298.11.1300.PubMed
43.
go back to reference Mahley RW: Apolipoprotein E: cholesterol transport protein with expanding role in cell biology. Science. 1988, 240 (4852): 622-630. 10.1126/science.3283935.PubMed Mahley RW: Apolipoprotein E: cholesterol transport protein with expanding role in cell biology. Science. 1988, 240 (4852): 622-630. 10.1126/science.3283935.PubMed
44.
go back to reference Davignon J, Gregg RE, Sing CF: Apolipoprotein E polymorphism and atherosclerosis. Arteriosclerosis. 1988, 8 (1): 1-21.PubMed Davignon J, Gregg RE, Sing CF: Apolipoprotein E polymorphism and atherosclerosis. Arteriosclerosis. 1988, 8 (1): 1-21.PubMed
45.
go back to reference Song Y, Stampfer MJ, Liu S: Meta-analysis: apolipoprotein E genotypes and risk for coronary heart disease. Ann Intern Med. 2004, 141 (2): 137-147.PubMed Song Y, Stampfer MJ, Liu S: Meta-analysis: apolipoprotein E genotypes and risk for coronary heart disease. Ann Intern Med. 2004, 141 (2): 137-147.PubMed
46.
go back to reference Sudlow C, Martinez Gonzalez NA, Kim J, Clark C: Does apolipoprotein E genotype influence the risk of ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage? Systematic review and meta-analyses of 31 studies among 5961 cases and 17,965 controls. Stroke. 2006, 37 (2): 364-370. 10.1161/01.STR.0000199065.12908.62.PubMed Sudlow C, Martinez Gonzalez NA, Kim J, Clark C: Does apolipoprotein E genotype influence the risk of ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage? Systematic review and meta-analyses of 31 studies among 5961 cases and 17,965 controls. Stroke. 2006, 37 (2): 364-370. 10.1161/01.STR.0000199065.12908.62.PubMed
47.
go back to reference Willer CJ, Sanna S, Jackson AU, Scuteri A, Bonnycastle LL, Clarke R, Heath SC, Timpson NJ, Najjar SS, Stringham HM, Strait J, Duren WL, Maschio A, Busonero F, Mulas A, Albai G, Swift AJ, Morken MA, Narisu N, Bennett D, Parish S, Shen H, Galan P, Meneton P, Hercberg S, Zelenika D, Chen WM, Li Y, Scott LJ, Scheet PA, et al: Newly identified loci that influence lipid concentrations and risk of coronary artery disease. Nat Genet. 2008, 40 (2): 161-169. 10.1038/ng.76.PubMed Willer CJ, Sanna S, Jackson AU, Scuteri A, Bonnycastle LL, Clarke R, Heath SC, Timpson NJ, Najjar SS, Stringham HM, Strait J, Duren WL, Maschio A, Busonero F, Mulas A, Albai G, Swift AJ, Morken MA, Narisu N, Bennett D, Parish S, Shen H, Galan P, Meneton P, Hercberg S, Zelenika D, Chen WM, Li Y, Scott LJ, Scheet PA, et al: Newly identified loci that influence lipid concentrations and risk of coronary artery disease. Nat Genet. 2008, 40 (2): 161-169. 10.1038/ng.76.PubMed
48.
go back to reference Imamura A, Takahashi R, Murakami R, Kataoka H, Cheng XW, Numaguchi Y, Murohara T, Okumura K: The effects of endothelial nitric oxide synthase gene polymorphisms on endothelial function and metabolic risk factors in healthy subjects: the significance of plasma adiponectin levels. Eur J Endocrinol. 2008, 158 (2): 189-195. 10.1530/EJE-07-0632.PubMed Imamura A, Takahashi R, Murakami R, Kataoka H, Cheng XW, Numaguchi Y, Murohara T, Okumura K: The effects of endothelial nitric oxide synthase gene polymorphisms on endothelial function and metabolic risk factors in healthy subjects: the significance of plasma adiponectin levels. Eur J Endocrinol. 2008, 158 (2): 189-195. 10.1530/EJE-07-0632.PubMed
49.
go back to reference Hoffmann IS, Tavares-Mordwinkin R, Castejon AM, Alfieri AB, Cubeddu LX: Endothelial nitric oxide synthase polymorphism, nitric oxide production, salt sensitivity and cardiovascular risk factors in Hispanics. J Hum Hypertens. 2005, 19 (3): 233-240.PubMed Hoffmann IS, Tavares-Mordwinkin R, Castejon AM, Alfieri AB, Cubeddu LX: Endothelial nitric oxide synthase polymorphism, nitric oxide production, salt sensitivity and cardiovascular risk factors in Hispanics. J Hum Hypertens. 2005, 19 (3): 233-240.PubMed
50.
go back to reference Chrysohoou C, Panagiotakos DB, Pitsavos C, Antoniades C, Skoumas J, Brown M, Stefanadis C: Evidence for association between endothelial nitric oxide synthase gene polymorphism (G894T) and inflammatory markers: the ATTICA study. Am Heart J. 2004, 148 (4): 733-738. 10.1016/j.ahj.2004.04.022.PubMed Chrysohoou C, Panagiotakos DB, Pitsavos C, Antoniades C, Skoumas J, Brown M, Stefanadis C: Evidence for association between endothelial nitric oxide synthase gene polymorphism (G894T) and inflammatory markers: the ATTICA study. Am Heart J. 2004, 148 (4): 733-738. 10.1016/j.ahj.2004.04.022.PubMed
51.
go back to reference Senti M, Tomas M, Elosual R, Sala J, Masia R, Marrugat J: The paraoxonase-1 codon 192 polymorphism is associated with fasting total cholesterol and LDL-cholesterol concentrations only in postmenopausal women. The REGICOR study. Clin Chem Lab Med. 2002, 40 (7): 677-683. 10.1515/CCLM.2002.116.PubMed Senti M, Tomas M, Elosual R, Sala J, Masia R, Marrugat J: The paraoxonase-1 codon 192 polymorphism is associated with fasting total cholesterol and LDL-cholesterol concentrations only in postmenopausal women. The REGICOR study. Clin Chem Lab Med. 2002, 40 (7): 677-683. 10.1515/CCLM.2002.116.PubMed
52.
go back to reference Perez-Herrera N, May-Pech C, Hernandez-Ochoa I, Castro-Mane J, Rojas-Garcia E, Borja-Aburto VH, Castillo-Burguete T, Quintanilla-Vega B: PON1Q192R polymorphism is associated with lipid profile in Mexican men with Mayan ascendancy. Exp Mol Pathol. 2008, 85 (2): 129-134. 10.1016/j.yexmp.2008.05.003.PubMed Perez-Herrera N, May-Pech C, Hernandez-Ochoa I, Castro-Mane J, Rojas-Garcia E, Borja-Aburto VH, Castillo-Burguete T, Quintanilla-Vega B: PON1Q192R polymorphism is associated with lipid profile in Mexican men with Mayan ascendancy. Exp Mol Pathol. 2008, 85 (2): 129-134. 10.1016/j.yexmp.2008.05.003.PubMed
53.
go back to reference Ranade K, Kirchgessner TG, Iakoubova OA, Devlin JJ, DelMonte T, Vishnupad P, Hui L, Tsuchihashi Z, Sacks FM, Sabatine MS, Braunwald E, White TJ, Shaw PM, Dracopoli NC: Evaluation of the paraoxonases as candidate genes for stroke: Gln192Arg polymorphism in the paraoxonase 1 gene is associated with increased risk of stroke. Stroke. 2005, 36 (11): 2346-2350. 10.1161/01.STR.0000185703.88944.7d.PubMed Ranade K, Kirchgessner TG, Iakoubova OA, Devlin JJ, DelMonte T, Vishnupad P, Hui L, Tsuchihashi Z, Sacks FM, Sabatine MS, Braunwald E, White TJ, Shaw PM, Dracopoli NC: Evaluation of the paraoxonases as candidate genes for stroke: Gln192Arg polymorphism in the paraoxonase 1 gene is associated with increased risk of stroke. Stroke. 2005, 36 (11): 2346-2350. 10.1161/01.STR.0000185703.88944.7d.PubMed
54.
go back to reference Lahiry P, Ban MR, Pollex RL, Feldman RD, Sawyez CG, Huff MW, Young TK, Bjerregaard P, Hegele RA: Common variants APOC3, APOA5, APOE and PON1 are associated with variation in plasma lipoprotein traits in Greenlanders. Int J Circumpolar Health. 2007, 66 (5): 390-400.PubMed Lahiry P, Ban MR, Pollex RL, Feldman RD, Sawyez CG, Huff MW, Young TK, Bjerregaard P, Hegele RA: Common variants APOC3, APOA5, APOE and PON1 are associated with variation in plasma lipoprotein traits in Greenlanders. Int J Circumpolar Health. 2007, 66 (5): 390-400.PubMed
55.
go back to reference Gamboa R, Zamora J, Rodriguez-Perez JM, Fragoso JM, Cardoso G, Posadas-Romero C, Vargas-Alarcon G: Distribution of paraoxonase PON1 gene polymorphisms in Mexican populations. Its role in the lipid profile. Exp Mol Pathol. 2006, 80 (1): 85-90.PubMed Gamboa R, Zamora J, Rodriguez-Perez JM, Fragoso JM, Cardoso G, Posadas-Romero C, Vargas-Alarcon G: Distribution of paraoxonase PON1 gene polymorphisms in Mexican populations. Its role in the lipid profile. Exp Mol Pathol. 2006, 80 (1): 85-90.PubMed
56.
go back to reference Blatter Garin MC, Moren X, James RW: Paraoxonase-1 and serum concentrations of HDL-cholesterol and apoA-I. J Lipid Res. 2006, 47 (3): 515-520. 10.1194/jlr.M500281-JLR200.PubMed Blatter Garin MC, Moren X, James RW: Paraoxonase-1 and serum concentrations of HDL-cholesterol and apoA-I. J Lipid Res. 2006, 47 (3): 515-520. 10.1194/jlr.M500281-JLR200.PubMed
57.
go back to reference Srinivasan SR, Li S, Chen W, Tang R, Bond MG, Boerwinkle E, Berenson GS: Q192R polymorphism of the paraoxanase 1 gene and its association with serum lipoprotein variables and carotid artery intima-media thickness in young adults from a biracial community. The Bogalusa Heart Study. Atherosclerosis. 2004, 177 (1): 167-174.PubMed Srinivasan SR, Li S, Chen W, Tang R, Bond MG, Boerwinkle E, Berenson GS: Q192R polymorphism of the paraoxanase 1 gene and its association with serum lipoprotein variables and carotid artery intima-media thickness in young adults from a biracial community. The Bogalusa Heart Study. Atherosclerosis. 2004, 177 (1): 167-174.PubMed
58.
go back to reference Senti M, Tomas M, Marrugat J, Elosua R: Paraoxonase1-192 polymorphism modulates the nonfatal myocardial infarction risk associated with decreased HDLs. Arterioscler Thromb Vasc Biol. 2001, 21 (3): 415-420.PubMed Senti M, Tomas M, Marrugat J, Elosua R: Paraoxonase1-192 polymorphism modulates the nonfatal myocardial infarction risk associated with decreased HDLs. Arterioscler Thromb Vasc Biol. 2001, 21 (3): 415-420.PubMed
59.
go back to reference Turban S, Fuentes F, Ferlic L, Brugada R, Gotto AM, Ballantyne CM, Marian AJ: A prospective study of paraoxonase gene Q/R192 polymorphism and severity, progression and regression of coronary atherosclerosis, plasma lipid levels, clinical events and response to fluvastatin. Atherosclerosis. 2001, 154 (3): 633-640. 10.1016/S0021-9150(00)00495-0.PubMed Turban S, Fuentes F, Ferlic L, Brugada R, Gotto AM, Ballantyne CM, Marian AJ: A prospective study of paraoxonase gene Q/R192 polymorphism and severity, progression and regression of coronary atherosclerosis, plasma lipid levels, clinical events and response to fluvastatin. Atherosclerosis. 2001, 154 (3): 633-640. 10.1016/S0021-9150(00)00495-0.PubMed
60.
go back to reference Manresa JM, Zamora A, Tomás M, Sentí M, Fitó M, Covas MI, Alcántara M, Latorre G, Escurriol V, Domingues S, Marrugat J: Relationship of classical and non-classical risk factors with genetic variants relevant to coronary heart disease. Eur J Cardiovasc Prev Rehabil. 2006, 13 (5): 738-744. 10.1097/01.hjr.0000224484.80349.3f.PubMed Manresa JM, Zamora A, Tomás M, Sentí M, Fitó M, Covas MI, Alcántara M, Latorre G, Escurriol V, Domingues S, Marrugat J: Relationship of classical and non-classical risk factors with genetic variants relevant to coronary heart disease. Eur J Cardiovasc Prev Rehabil. 2006, 13 (5): 738-744. 10.1097/01.hjr.0000224484.80349.3f.PubMed
61.
go back to reference Manresa JM, Tomas M, Ribes E, Pi-Figueras M, Aguilera A, Senti M, Marrugat J: Paraoxonase 1 gene 192 polymorphism, physical activity and lipoprotein in women. Med Clin (Barc). 2004, 122 (4): 126-129. Manresa JM, Tomas M, Ribes E, Pi-Figueras M, Aguilera A, Senti M, Marrugat J: Paraoxonase 1 gene 192 polymorphism, physical activity and lipoprotein in women. Med Clin (Barc). 2004, 122 (4): 126-129.
62.
go back to reference Mikkelsson J, Perola M, Wartiovaara U, Peltonen L, Palotie A, Penttila A, Karhunen PJ: Plasminogen activator inhibitor-1 (PAI-1) 4G/5G polymorphism, coronary thrombosis, and myocardial infarction in middle-aged Finnish men who died suddenly. Thromb Haemost. 2000, 84 (1): 78-82.PubMed Mikkelsson J, Perola M, Wartiovaara U, Peltonen L, Palotie A, Penttila A, Karhunen PJ: Plasminogen activator inhibitor-1 (PAI-1) 4G/5G polymorphism, coronary thrombosis, and myocardial infarction in middle-aged Finnish men who died suddenly. Thromb Haemost. 2000, 84 (1): 78-82.PubMed
63.
go back to reference Weiss EJ, Bray PF, Tayback M, Schulman SP, Kickler TS, Becker LC, Weiss JL, Gerstenblith G, Goldschmidt-Clermont PJ: A polymorphism of a platelet glycoprotein receptor as an inherited risk factor for coronary thrombosis. N Engl J Med. 1996, 334 (17): 1090-1094. 10.1056/NEJM199604253341703.PubMed Weiss EJ, Bray PF, Tayback M, Schulman SP, Kickler TS, Becker LC, Weiss JL, Gerstenblith G, Goldschmidt-Clermont PJ: A polymorphism of a platelet glycoprotein receptor as an inherited risk factor for coronary thrombosis. N Engl J Med. 1996, 334 (17): 1090-1094. 10.1056/NEJM199604253341703.PubMed
64.
go back to reference Carter AM, Catto AJ, Bamford JM, Grant PJ: Platelet GP IIIa PlA and GP Ib variable number tandem repeat polymorphisms and markers of platelet activation in acute stroke. Arterioscler Thromb Vasc Biol. 1998, 18 (7): 1124-1131.PubMed Carter AM, Catto AJ, Bamford JM, Grant PJ: Platelet GP IIIa PlA and GP Ib variable number tandem repeat polymorphisms and markers of platelet activation in acute stroke. Arterioscler Thromb Vasc Biol. 1998, 18 (7): 1124-1131.PubMed
65.
go back to reference Slowik A, Dziedzic T, Turaj W, Pera J, Glodzik-Sobanska L, Szermer P, Malecki MT, Figlewicz DA, Szczudlik A: A2 alelle of GpIIIa gene is a risk factor for stroke caused by large-vessel disease in males. Stroke. 2004, 35 (7): 1589-1593. 10.1161/01.STR.0000132194.24663.3d.PubMed Slowik A, Dziedzic T, Turaj W, Pera J, Glodzik-Sobanska L, Szermer P, Malecki MT, Figlewicz DA, Szczudlik A: A2 alelle of GpIIIa gene is a risk factor for stroke caused by large-vessel disease in males. Stroke. 2004, 35 (7): 1589-1593. 10.1161/01.STR.0000132194.24663.3d.PubMed
66.
go back to reference Weiss LA, Abney M, Parry R, Scanu AM, Cook EH, Ober C: Variation in ITGB3 has sex-specific associations with plasma lipoprotein(a) and whole blood serotonin levels in a population-based sample. Hum Genet. 2005, 117 (1): 81-87. 10.1007/s00439-004-1250-3.PubMed Weiss LA, Abney M, Parry R, Scanu AM, Cook EH, Ober C: Variation in ITGB3 has sex-specific associations with plasma lipoprotein(a) and whole blood serotonin levels in a population-based sample. Hum Genet. 2005, 117 (1): 81-87. 10.1007/s00439-004-1250-3.PubMed
67.
go back to reference Deo RC, Reich D, Tandon A, Akylbekova E, Patterson N, Waliszewska A, Kathiresan S, Sarpong D, Taylor HA, Wilson JG: Genetic differences between the determinants of lipid profile phenotypes in African and European Americans: the Jackson Heart Study. PLoS Genet. 2009, 5 (1): e1000342-10.1371/journal.pgen.1000342.PubMedPubMedCentral Deo RC, Reich D, Tandon A, Akylbekova E, Patterson N, Waliszewska A, Kathiresan S, Sarpong D, Taylor HA, Wilson JG: Genetic differences between the determinants of lipid profile phenotypes in African and European Americans: the Jackson Heart Study. PLoS Genet. 2009, 5 (1): e1000342-10.1371/journal.pgen.1000342.PubMedPubMedCentral
68.
go back to reference Ford ES, Li C, Pearson WS, Zhao G, Mokdad AH: Trends in hypercholesterolemia, treatment and control among United States adults. Int J Cardiol. 2008, 140 (2): 226-235. 10.1016/j.ijcard.2008.11.033.PubMed Ford ES, Li C, Pearson WS, Zhao G, Mokdad AH: Trends in hypercholesterolemia, treatment and control among United States adults. Int J Cardiol. 2008, 140 (2): 226-235. 10.1016/j.ijcard.2008.11.033.PubMed
69.
go back to reference Li M, Ong KL, Tse HF, Cheung BM: Utilization of lipid lowering medications among adults in the United States 1999-2006. Atherosclerosis. 2010, 208 (2): 456-60. 10.1016/j.atherosclerosis.2009.08.001.PubMed Li M, Ong KL, Tse HF, Cheung BM: Utilization of lipid lowering medications among adults in the United States 1999-2006. Atherosclerosis. 2010, 208 (2): 456-60. 10.1016/j.atherosclerosis.2009.08.001.PubMed
70.
go back to reference Reiner-Benaim A: FDR control by the BH procedure for two-sided correlated tests with implications to gene expression data analysis. Biom J. 2007, 49 (1): 107-126. 10.1002/bimj.200510313.PubMed Reiner-Benaim A: FDR control by the BH procedure for two-sided correlated tests with implications to gene expression data analysis. Biom J. 2007, 49 (1): 107-126. 10.1002/bimj.200510313.PubMed
71.
go back to reference Risch N, Burchard E, Ziv E, Tang H: Categorization of humans in biomedical research: genes, race and disease. Genome Biol. 2002, 3 (7): comment2007-10.1186/gb-2002-3-7-comment2007.PubMedPubMedCentral Risch N, Burchard E, Ziv E, Tang H: Categorization of humans in biomedical research: genes, race and disease. Genome Biol. 2002, 3 (7): comment2007-10.1186/gb-2002-3-7-comment2007.PubMedPubMedCentral
72.
go back to reference Tseng M, Williams RC, Maurer KR, Schanfield MS, Knowler WC, Everhart JE: Genetic admixture and gallbladder disease in Mexican Americans. Am J Phys Anthropol. 1998, 106 (3): 361-371. 10.1002/(SICI)1096-8644(199807)106:3<361::AID-AJPA8>3.0.CO;2-P.PubMed Tseng M, Williams RC, Maurer KR, Schanfield MS, Knowler WC, Everhart JE: Genetic admixture and gallbladder disease in Mexican Americans. Am J Phys Anthropol. 1998, 106 (3): 361-371. 10.1002/(SICI)1096-8644(199807)106:3<361::AID-AJPA8>3.0.CO;2-P.PubMed
73.
go back to reference McKeigue PM, Carpenter JR, Parra EJ, Shriver MD: Estimation of admixture and detection of linkage in admixed populations by a Bayesian approach: application to African-American populations. Ann Hum Genet. 2000, 64 (Pt 2): 171-186. 10.1046/j.1469-1809.2000.6420171.x.PubMed McKeigue PM, Carpenter JR, Parra EJ, Shriver MD: Estimation of admixture and detection of linkage in admixed populations by a Bayesian approach: application to African-American populations. Ann Hum Genet. 2000, 64 (Pt 2): 171-186. 10.1046/j.1469-1809.2000.6420171.x.PubMed
74.
go back to reference Salari K, Choudhry S, Tang H, Naqvi M, Lind D, Avila PC, Coyle NE, Ung N, Nazario S, Casal J, Torres-Palacios A, Clark S, Phong A, Gomez I, Matallana H, Pérez-Stable EJ, Shriver MD, Kwok PY, Sheppard D, Rodriguez-Cintron W, Risch NJ, Burchard EG, Ziv E: Genetic admixture and asthma-related phenotypes in Mexican American and Puerto Rican asthmatics. Genet Epidemiol. 2005, 29 (1): 76-86. 10.1002/gepi.20079.PubMed Salari K, Choudhry S, Tang H, Naqvi M, Lind D, Avila PC, Coyle NE, Ung N, Nazario S, Casal J, Torres-Palacios A, Clark S, Phong A, Gomez I, Matallana H, Pérez-Stable EJ, Shriver MD, Kwok PY, Sheppard D, Rodriguez-Cintron W, Risch NJ, Burchard EG, Ziv E: Genetic admixture and asthma-related phenotypes in Mexican American and Puerto Rican asthmatics. Genet Epidemiol. 2005, 29 (1): 76-86. 10.1002/gepi.20079.PubMed
75.
go back to reference Shriver MD, Kennedy GC, Parra EJ, Lawson HA, Sonpar V, Huang J, Akey JM, Jones KW: The genomic distribution of population substructure in four populations using 8,525 autosomal SNPs. Hum Genomics. 2004, 1 (4): 274-286.PubMedPubMedCentral Shriver MD, Kennedy GC, Parra EJ, Lawson HA, Sonpar V, Huang J, Akey JM, Jones KW: The genomic distribution of population substructure in four populations using 8,525 autosomal SNPs. Hum Genomics. 2004, 1 (4): 274-286.PubMedPubMedCentral
76.
go back to reference Rodrigues AC, Rebecchi IM, Bertolami MC, Faludi AA, Hirata MH, Hirata RD: High baseline serum total and LDL cholesterol levels are associated with MDR1 haplotypes in Brazilian hypercholesterolemic individuals of European descent. Braz J Med Biol Res. 2005, 38 (9): 1389-1397. 10.1590/S0100-879X2005000900014.PubMed Rodrigues AC, Rebecchi IM, Bertolami MC, Faludi AA, Hirata MH, Hirata RD: High baseline serum total and LDL cholesterol levels are associated with MDR1 haplotypes in Brazilian hypercholesterolemic individuals of European descent. Braz J Med Biol Res. 2005, 38 (9): 1389-1397. 10.1590/S0100-879X2005000900014.PubMed
77.
go back to reference Hines LM, Hunter DJ, Stampfer MJ, Spiegelman D, Chu NF, Rifai N, Hankinson SE, Rimm EB: Alcohol consumption and high-density lipoprotein levels: the effect of ADH1C genotype, gender and menopausal status. Atherosclerosis. 2005, 182 (2): 293-300. 10.1016/j.atherosclerosis.2005.02.005.PubMed Hines LM, Hunter DJ, Stampfer MJ, Spiegelman D, Chu NF, Rifai N, Hankinson SE, Rimm EB: Alcohol consumption and high-density lipoprotein levels: the effect of ADH1C genotype, gender and menopausal status. Atherosclerosis. 2005, 182 (2): 293-300. 10.1016/j.atherosclerosis.2005.02.005.PubMed
78.
go back to reference Iaccarino G, Trimarco V, Lanni F, Cipolletta E, Izzo R, Arcucci O, De Luca N, Di Renzo G: beta-Blockade and increased dyslipidemia in patients bearing Glu27 variant of beta2 adrenergic receptor gene. Pharmacogenomics J. 2005, 5 (5): 292-297. 10.1038/sj.tpj.6500324.PubMed Iaccarino G, Trimarco V, Lanni F, Cipolletta E, Izzo R, Arcucci O, De Luca N, Di Renzo G: beta-Blockade and increased dyslipidemia in patients bearing Glu27 variant of beta2 adrenergic receptor gene. Pharmacogenomics J. 2005, 5 (5): 292-297. 10.1038/sj.tpj.6500324.PubMed
79.
go back to reference Hallman DM, Srinivasan SR, Chen W, Boerwinkle E, Berenson GS: The beta(2)-adrenergic receptor Arg16-gly polymorphism and interactions involving beta(2)- and beta(3)-adrenergic receptor polymorphisms are associated with variations in longitudinal serum lipid profiles: the Bogalusa Heart Study. Metabolism. 2004, 53 (9): 1184-1191. 10.1016/j.metabol.2004.03.019.PubMed Hallman DM, Srinivasan SR, Chen W, Boerwinkle E, Berenson GS: The beta(2)-adrenergic receptor Arg16-gly polymorphism and interactions involving beta(2)- and beta(3)-adrenergic receptor polymorphisms are associated with variations in longitudinal serum lipid profiles: the Bogalusa Heart Study. Metabolism. 2004, 53 (9): 1184-1191. 10.1016/j.metabol.2004.03.019.PubMed
80.
go back to reference Iwamoto N, Ogawa Y, Kajihara S, Hisatomi A, Yasutake T, Yoshimura T, Mizuta T, Hara T, Ozaki I, Yamamoto K: Gln27Glu beta2-adrenergic receptor variant is associated with hypertriglyceridemia and the development of fatty liver. Clin Chim Acta. 2001, 314 (1-2): 85-91. 10.1016/S0009-8981(01)00633-7.PubMed Iwamoto N, Ogawa Y, Kajihara S, Hisatomi A, Yasutake T, Yoshimura T, Mizuta T, Hara T, Ozaki I, Yamamoto K: Gln27Glu beta2-adrenergic receptor variant is associated with hypertriglyceridemia and the development of fatty liver. Clin Chim Acta. 2001, 314 (1-2): 85-91. 10.1016/S0009-8981(01)00633-7.PubMed
81.
go back to reference Ukkola O, Perusse L, Weisnagel SJ, Bergeron J, Despres JP, Rao DC, Bouchard C: Interactions among the glucocorticoid receptor, lipoprotein lipase, and adrenergic receptor genes and plasma insulin and lipid levels in the Quebec Family Study. Metabolism. 2001, 50 (2): 246-252. 10.1053/meta.2001.18572.PubMed Ukkola O, Perusse L, Weisnagel SJ, Bergeron J, Despres JP, Rao DC, Bouchard C: Interactions among the glucocorticoid receptor, lipoprotein lipase, and adrenergic receptor genes and plasma insulin and lipid levels in the Quebec Family Study. Metabolism. 2001, 50 (2): 246-252. 10.1053/meta.2001.18572.PubMed
82.
go back to reference Dunajska K, Lwow F, Milewicz A, Jedrzejuk D, Laczmanski L, Belowska-Bien K, Urban J, Szuba A: beta(3)-adrenergic receptor polymorphism and metabolic syndrome in postmenopausal women. Gynecol Endocrinol. 2008, 24 (3): 133-138. 10.1080/09513590801921686.PubMed Dunajska K, Lwow F, Milewicz A, Jedrzejuk D, Laczmanski L, Belowska-Bien K, Urban J, Szuba A: beta(3)-adrenergic receptor polymorphism and metabolic syndrome in postmenopausal women. Gynecol Endocrinol. 2008, 24 (3): 133-138. 10.1080/09513590801921686.PubMed
83.
go back to reference Porto PI, Garcia SI, Dieuzeide G, Gonzalez C, Landa MS, Pirola CJ: Clinical features of the metabolic syndrome in adolescents: minor role of the Trp64Arg beta3-adrenergic receptor gene variant. Pediatr Res. 2004, 55 (5): 836-841. 10.1203/01.PDR.0000119367.21770.D7.PubMed Porto PI, Garcia SI, Dieuzeide G, Gonzalez C, Landa MS, Pirola CJ: Clinical features of the metabolic syndrome in adolescents: minor role of the Trp64Arg beta3-adrenergic receptor gene variant. Pediatr Res. 2004, 55 (5): 836-841. 10.1203/01.PDR.0000119367.21770.D7.PubMed
84.
go back to reference Okumura K, Matsui H, Ogawa Y, Takahashi R, Matsubara K, Imai H, Imamura A, Mizuno T, Tsuzuki M, Kitamura Y: The polymorphism of the beta3-adrenergic receptor gene is associated with reduced low-density lipoprotein particle size. Metabolism. 2003, 52 (3): 356-361. 10.1053/meta.2003.50056.PubMed Okumura K, Matsui H, Ogawa Y, Takahashi R, Matsubara K, Imai H, Imamura A, Mizuno T, Tsuzuki M, Kitamura Y: The polymorphism of the beta3-adrenergic receptor gene is associated with reduced low-density lipoprotein particle size. Metabolism. 2003, 52 (3): 356-361. 10.1053/meta.2003.50056.PubMed
85.
go back to reference Manraj M, Francke S, Hebe A, Ramjuttun US, Froguel P: Genetic and environmental nature of the insulin resistance syndrome in Indo-Mauritian subjects with premature coronary heart disease: contribution of beta3-adrenoreceptor gene polymorphism and beta blockers on triglyceride and HDL concentrations. Diabetologia. 2001, 44 (1): 115-122. 10.1007/s001250051588.PubMed Manraj M, Francke S, Hebe A, Ramjuttun US, Froguel P: Genetic and environmental nature of the insulin resistance syndrome in Indo-Mauritian subjects with premature coronary heart disease: contribution of beta3-adrenoreceptor gene polymorphism and beta blockers on triglyceride and HDL concentrations. Diabetologia. 2001, 44 (1): 115-122. 10.1007/s001250051588.PubMed
86.
go back to reference Zuntar I, Antoljak N, Vrkic N, Topic E, Kujundzic N, Demarin V, Vukovic V: Association of methylenetetrahydrofolate (MTHFR) and apolipoprotein E (apo E) genotypes with homocysteine, vitamin and lipid levels in carotid stenosis. Coll Antropol. 2006, 30 (4): 871-878.PubMed Zuntar I, Antoljak N, Vrkic N, Topic E, Kujundzic N, Demarin V, Vukovic V: Association of methylenetetrahydrofolate (MTHFR) and apolipoprotein E (apo E) genotypes with homocysteine, vitamin and lipid levels in carotid stenosis. Coll Antropol. 2006, 30 (4): 871-878.PubMed
87.
go back to reference Loktionov A, Vorster H, O'Neill IK, Nell T, Bingham SA, Runswick SA, Cummings JH: Apolipoprotein E and methylenetetrahydrofolate reductase genetic polymorphisms in relation to other risk factors for cardiovascular disease in UK Caucasians and Black South Africans. Atherosclerosis. 1999, 145 (1): 125-135. 10.1016/S0021-9150(99)00022-2.PubMed Loktionov A, Vorster H, O'Neill IK, Nell T, Bingham SA, Runswick SA, Cummings JH: Apolipoprotein E and methylenetetrahydrofolate reductase genetic polymorphisms in relation to other risk factors for cardiovascular disease in UK Caucasians and Black South Africans. Atherosclerosis. 1999, 145 (1): 125-135. 10.1016/S0021-9150(99)00022-2.PubMed
88.
go back to reference Sawada T, Kishimoto T, Osaki Y, Okamoto M, Tahara A, Kaetu A, Kurosawa Y, Kotani K: Relation of the Glu298Asp polymorphism of the nitric oxide synthase gene to hypertension and serum cholesterol in Japanese workers. Prev Med. 2008, 47 (2): 167-171. 10.1016/j.ypmed.2008.04.006.PubMed Sawada T, Kishimoto T, Osaki Y, Okamoto M, Tahara A, Kaetu A, Kurosawa Y, Kotani K: Relation of the Glu298Asp polymorphism of the nitric oxide synthase gene to hypertension and serum cholesterol in Japanese workers. Prev Med. 2008, 47 (2): 167-171. 10.1016/j.ypmed.2008.04.006.PubMed
89.
go back to reference Mackness B, Mackness MI, Arrol S, Turkie W, Durrington PN: Effect of the human serum paraoxonase 55 and 192 genetic polymorphisms on the protection by high density lipoprotein against low density lipoprotein oxidative modification. FEBS Lett. 1998, 423 (1): 57-60. 10.1016/S0014-5793(98)00064-7.PubMed Mackness B, Mackness MI, Arrol S, Turkie W, Durrington PN: Effect of the human serum paraoxonase 55 and 192 genetic polymorphisms on the protection by high density lipoprotein against low density lipoprotein oxidative modification. FEBS Lett. 1998, 423 (1): 57-60. 10.1016/S0014-5793(98)00064-7.PubMed
90.
go back to reference Chambers JE: PON1 multitasks to protect health. Proc Natl Acad Sci USA. 2008, 105 (35): 12639-12640. 10.1073/pnas.0807062105.PubMedPubMedCentral Chambers JE: PON1 multitasks to protect health. Proc Natl Acad Sci USA. 2008, 105 (35): 12639-12640. 10.1073/pnas.0807062105.PubMedPubMedCentral
91.
go back to reference Fanella S, Harris SB, Young TK, Hanley AJ, Zinman B, Connelly PW, Hegele RA: Association between PON1 L/M55 polymorphism and plasma lipoproteins in two Canadian aboriginal populations. Clin Chem Lab Med. 2000, 38 (5): 413-420. 10.1515/CCLM.2000.060.PubMed Fanella S, Harris SB, Young TK, Hanley AJ, Zinman B, Connelly PW, Hegele RA: Association between PON1 L/M55 polymorphism and plasma lipoproteins in two Canadian aboriginal populations. Clin Chem Lab Med. 2000, 38 (5): 413-420. 10.1515/CCLM.2000.060.PubMed
92.
go back to reference Dedoussis GV, Theodoraki EV, Manios Y, Yiannakouris N, Panagiotakos D, Papoutsakis C, Skenderi K, Zampelas A: The Pro12Ala polymorphism in PPARgamma2 gene affects lipid parameters in Greek primary school children: A case of gene-to-gender interaction. Am J Med Sci. 2007, 333 (1): 10-15. 10.1097/00000441-200701000-00002.PubMed Dedoussis GV, Theodoraki EV, Manios Y, Yiannakouris N, Panagiotakos D, Papoutsakis C, Skenderi K, Zampelas A: The Pro12Ala polymorphism in PPARgamma2 gene affects lipid parameters in Greek primary school children: A case of gene-to-gender interaction. Am J Med Sci. 2007, 333 (1): 10-15. 10.1097/00000441-200701000-00002.PubMed
93.
go back to reference Maeda A, Gohda T, Funabiki K, Horikoshi S, Tomino Y: Peroxisome proliferator-activated receptor gamma gene polymorphism is associated with serum triglyceride levels and body mass index in Japanese type 2 diabetic patients. J Clin Lab Anal. 2004, 18 (6): 317-321. 10.1002/jcla.20045.PubMed Maeda A, Gohda T, Funabiki K, Horikoshi S, Tomino Y: Peroxisome proliferator-activated receptor gamma gene polymorphism is associated with serum triglyceride levels and body mass index in Japanese type 2 diabetic patients. J Clin Lab Anal. 2004, 18 (6): 317-321. 10.1002/jcla.20045.PubMed
94.
go back to reference Tai ES, Corella D, Deurenberg-Yap M, Adiconis X, Chew SK, Tan CE, Ordovas JM: Differential effects of the C1431T and Pro12Ala PPARgamma gene variants on plasma lipids and diabetes risk in an Asian population. J Lipid Res. 2004, 45 (4): 674-685. 10.1194/jlr.M300363-JLR200.PubMed Tai ES, Corella D, Deurenberg-Yap M, Adiconis X, Chew SK, Tan CE, Ordovas JM: Differential effects of the C1431T and Pro12Ala PPARgamma gene variants on plasma lipids and diabetes risk in an Asian population. J Lipid Res. 2004, 45 (4): 674-685. 10.1194/jlr.M300363-JLR200.PubMed
95.
go back to reference Chen S, Tsybouleva N, Ballantyne CM, Gotto AM, Marian AJ: Effects of PPARalpha, gamma and delta haplotypes on plasma levels of lipids, severity and progression of coronary atherosclerosis and response to statin therapy in the lipoprotein coronary atherosclerosis study. Pharmacogenetics. 2004, 14 (1): 61-71. 10.1097/00008571-200401000-00007.PubMed Chen S, Tsybouleva N, Ballantyne CM, Gotto AM, Marian AJ: Effects of PPARalpha, gamma and delta haplotypes on plasma levels of lipids, severity and progression of coronary atherosclerosis and response to statin therapy in the lipoprotein coronary atherosclerosis study. Pharmacogenetics. 2004, 14 (1): 61-71. 10.1097/00008571-200401000-00007.PubMed
96.
go back to reference Eriksson J, Lindi V, Uusitupa M, Forsen T, Laakso M, Osmond C, Barker D: The effects of the Pro12Ala polymorphism of the PPARgamma-2 gene on lipid metabolism interact with body size at birth. Clin Genet. 2003, 64 (4): 366-370. 10.1034/j.1399-0004.2003.00150.x.PubMed Eriksson J, Lindi V, Uusitupa M, Forsen T, Laakso M, Osmond C, Barker D: The effects of the Pro12Ala polymorphism of the PPARgamma-2 gene on lipid metabolism interact with body size at birth. Clin Genet. 2003, 64 (4): 366-370. 10.1034/j.1399-0004.2003.00150.x.PubMed
97.
go back to reference Gonzalez Sanchez JL, Serrano Rios M, Fernandez Perez C, Laakso M, Martinez Larrad MT: Effect of the Pro12Ala polymorphism of the peroxisome proliferator-activated receptor gamma-2 gene on adiposity, insulin sensitivity and lipid profile in the Spanish population. Eur J Endocrinol. 2002, 147 (4): 495-501. 10.1530/eje.0.1470495.PubMed Gonzalez Sanchez JL, Serrano Rios M, Fernandez Perez C, Laakso M, Martinez Larrad MT: Effect of the Pro12Ala polymorphism of the peroxisome proliferator-activated receptor gamma-2 gene on adiposity, insulin sensitivity and lipid profile in the Spanish population. Eur J Endocrinol. 2002, 147 (4): 495-501. 10.1530/eje.0.1470495.PubMed
98.
go back to reference Swarbrick MM, Chapman CM, McQuillan BM, Hung J, Thompson PL, Beilby JP: A Pro12Ala polymorphism in the human peroxisome proliferator-activated receptor-gamma 2 is associated with combined hyperlipidaemia in obesity. Eur J Endocrinol. 2001, 144 (3): 277-282. 10.1530/eje.0.1440277.PubMed Swarbrick MM, Chapman CM, McQuillan BM, Hung J, Thompson PL, Beilby JP: A Pro12Ala polymorphism in the human peroxisome proliferator-activated receptor-gamma 2 is associated with combined hyperlipidaemia in obesity. Eur J Endocrinol. 2001, 144 (3): 277-282. 10.1530/eje.0.1440277.PubMed
99.
go back to reference Kitamura Y, Okumura K, Imamura A, Mizuno T, Tsuzuki M, Numaguchi Y, Matsui H, Murohara T: Association of plasminogen activator inhibitor-1 4G/5G gene polymorphism with variations in the LDL particle size in healthy Japanese men. Clin Chim Acta. 2004, 347 (1-2): 209-216. 10.1016/j.cccn.2004.04.014.PubMed Kitamura Y, Okumura K, Imamura A, Mizuno T, Tsuzuki M, Numaguchi Y, Matsui H, Murohara T: Association of plasminogen activator inhibitor-1 4G/5G gene polymorphism with variations in the LDL particle size in healthy Japanese men. Clin Chim Acta. 2004, 347 (1-2): 209-216. 10.1016/j.cccn.2004.04.014.PubMed
100.
go back to reference Ruiz-Quezada S, Vazquez-Del Mercado M, Parra-Rojas I, Rangel-Villalobos H, Best-Aguilera C, Sanchez-Orozco LV, Munoz-Valle JF: Genotype and allele frequency of PAI-1 promoter polymorphism in healthy subjects from the west of Mexico. Association with biochemical and hematological parameters. Ann Genet. 2004, 47 (2): 155-162.PubMed Ruiz-Quezada S, Vazquez-Del Mercado M, Parra-Rojas I, Rangel-Villalobos H, Best-Aguilera C, Sanchez-Orozco LV, Munoz-Valle JF: Genotype and allele frequency of PAI-1 promoter polymorphism in healthy subjects from the west of Mexico. Association with biochemical and hematological parameters. Ann Genet. 2004, 47 (2): 155-162.PubMed
101.
go back to reference Chen CH, Eng HL, Chang CJ, Tsai TT, Lai ML, Chen HY, Liu CJ, Lin TM: 4G/5G promoter polymorphism of plasminogen activator inhibitor-1, lipid profiles, and ischemic stroke. J Lab Clin Med. 2003, 142 (2): 100-105. 10.1016/S0022-2143(03)00063-5.PubMed Chen CH, Eng HL, Chang CJ, Tsai TT, Lai ML, Chen HY, Liu CJ, Lin TM: 4G/5G promoter polymorphism of plasminogen activator inhibitor-1, lipid profiles, and ischemic stroke. J Lab Clin Med. 2003, 142 (2): 100-105. 10.1016/S0022-2143(03)00063-5.PubMed
102.
go back to reference Lopes C, Dina C, Durand E, Froguel P: PAI-1 polymorphisms modulate phenotypes associated with the metabolic syndrome in obese and diabetic Caucasian population. Diabetologia. 2003, 46 (9): 1284-1290. 10.1007/s00125-003-1170-0.PubMed Lopes C, Dina C, Durand E, Froguel P: PAI-1 polymorphisms modulate phenotypes associated with the metabolic syndrome in obese and diabetic Caucasian population. Diabetologia. 2003, 46 (9): 1284-1290. 10.1007/s00125-003-1170-0.PubMed
103.
go back to reference Parra-Rojas I, Ruiz-Madrigal B, Martinez-Lopez E, Panduro A: Influence of the -308 TNF-alpha and -174 IL-6 polymorphisms on lipid profile in Mexican subjects. Hereditas. 2006, 143 (2006): 167-172. 10.1111/j.2006.0018-0661.01936.x.PubMed Parra-Rojas I, Ruiz-Madrigal B, Martinez-Lopez E, Panduro A: Influence of the -308 TNF-alpha and -174 IL-6 polymorphisms on lipid profile in Mexican subjects. Hereditas. 2006, 143 (2006): 167-172. 10.1111/j.2006.0018-0661.01936.x.PubMed
104.
go back to reference Sookoian SC, Gonzalez C, Pirola CJ: Meta-analysis on the G-308A tumor necrosis factor alpha gene variant and phenotypes associated with the metabolic syndrome. Obes Res. 2005, 13 (12): 2122-2131. 10.1038/oby.2005.263.PubMed Sookoian SC, Gonzalez C, Pirola CJ: Meta-analysis on the G-308A tumor necrosis factor alpha gene variant and phenotypes associated with the metabolic syndrome. Obes Res. 2005, 13 (12): 2122-2131. 10.1038/oby.2005.263.PubMed
105.
go back to reference Davis CL, Wang X, Snieder H, Treiber FA: Genetic and environmental determinants of lipid profile in black and white youth: a study of four candidate genes. Ethn Dis. 2005, 15 (4): 568-577.PubMed Davis CL, Wang X, Snieder H, Treiber FA: Genetic and environmental determinants of lipid profile in black and white youth: a study of four candidate genes. Ethn Dis. 2005, 15 (4): 568-577.PubMed
Metadata
Title
Genetic variants associated with fasting blood lipids in the U.S. population: Third National Health and Nutrition Examination Survey
Authors
Man-huei Chang
Ajay Yesupriya
Renée M Ned
Patricia W Mueller
Nicole F Dowling
Publication date
01-12-2010
Publisher
BioMed Central
Published in
BMC Medical Genetics / Issue 1/2010
Electronic ISSN: 1471-2350
DOI
https://doi.org/10.1186/1471-2350-11-62

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