Skip to main content
Top
Published in: BMC Medical Genetics 1/2013

Open Access 01-12-2013 | Research article

Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study

Authors: Sonali Pechlivanis, Thomas W Mühleisen, Stefan Möhlenkamp, Dirk Schadendorf, Raimund Erbel, Karl-Heinz Jöckel, Per Hoffmann, Markus M Nöthen, André Scherag, Susanne Moebus, for the Heinz Nixdorf Recall Study Investigative Group

Published in: BMC Medical Genetics | Issue 1/2013

Login to get access

Abstract

Background

Atherosclerosis is the primary cause of coronary heart disease (CHD), preceding the onset of cardiovascular disease by decades in most cases. Here we examine the association between single nucleotide polymorphisms (SNPs) integrated on Metabochip and coronary artery calcification (CAC), a valid risk factor for CHD, in an unselected, population-based German cohort.

Methods

The Metabochip is a custom iSELECT array containing >195,000 SNPs that was designed to support large-scale follow-up of putative associations for metabolic and cardiovascular-associated traits. We used generalized linear regression models to explore the impact of Metabochip SNPs on quantitative CAC in 4,329 participants.

Results

The 9p21 variant, rs1537373, was most strongly associated (Beta = 0.30; 95% confidence interval (CI) = 0.21-0.39; p = 4.05x10-11) with quantitative CAC. The second strongest association with CAC was with rs9349379 in the phosphatase and actin regulator 1 gene, PHACTR1, (Beta = 0.30; 95% CI = 0.22-0.40; p = 4.67x10-11). Both SNPs remained nominally significant in dichotomized analyses for the presence of any CAC (odds ratiors1537373 (OR) = 1.19; 95% CI = 1.07-1.31; p = 0.001 and ORrs9349379 = 1.26; 95% CI = 1.14-1.40); p = 1.5x10-5). Fine mapping of the 9p21 and PHACTR1 gene region revealed several other SNPs that were strongly associated with CAC.

Conclusion

We demonstrate that SNPs near 9p21 and in PHACTR1 that have previously been shown to be associated with CHD are strongly associated with CAC in the Heinz Nixdorf Recall Study cohort. Our findings suggest that the 9p21 and 6q24 loci might be involved in cardiac outcome via promoting development of atherosclerosis in the coronary arteries.
Appendix
Available only for authorised users
Literature
1.
go back to reference Kondos GT, Hoff JA, Sevrukov A, Daviglus ML, Garside DB, Devries SS, et al: Electron-beam tomography coronary artery calcium and cardiac events: a 37-month follow-up of 5635 initially asymptomatic low- to intermediate-risk adults. Circulation. 2003, 107: 2571-2576. 10.1161/01.CIR.0000068341.61180.55.CrossRefPubMed Kondos GT, Hoff JA, Sevrukov A, Daviglus ML, Garside DB, Devries SS, et al: Electron-beam tomography coronary artery calcium and cardiac events: a 37-month follow-up of 5635 initially asymptomatic low- to intermediate-risk adults. Circulation. 2003, 107: 2571-2576. 10.1161/01.CIR.0000068341.61180.55.CrossRefPubMed
2.
go back to reference Schmermund A, Schwartz RS, Adamzik M, Sangiorgi G, Pfeifer EA, Rumberger JA, et al: Coronary atherosclerosis in unheralded sudden coronary death under age 50: histo-pathologic comparison with 'healthy' subjects dying out of hospital. Atherosclerosis. 2001, 155: 499-508. 10.1016/S0021-9150(00)00598-0.CrossRefPubMed Schmermund A, Schwartz RS, Adamzik M, Sangiorgi G, Pfeifer EA, Rumberger JA, et al: Coronary atherosclerosis in unheralded sudden coronary death under age 50: histo-pathologic comparison with 'healthy' subjects dying out of hospital. Atherosclerosis. 2001, 155: 499-508. 10.1016/S0021-9150(00)00598-0.CrossRefPubMed
3.
go back to reference Natural history of aortic and coronary atherosclerotic lesions in youth: Findings from the PDAY Study. Pathobiological Determinants of Atherosclerosis in Youth (PDAY) Research Group. Arterioscler Thromb. 1993, 13: 1291-1298.CrossRef Natural history of aortic and coronary atherosclerotic lesions in youth: Findings from the PDAY Study. Pathobiological Determinants of Atherosclerosis in Youth (PDAY) Research Group. Arterioscler Thromb. 1993, 13: 1291-1298.CrossRef
4.
go back to reference Erbel R, Mohlenkamp S, Moebus S, Schmermund A, Lehmann N, Stang A, et al: Coronary risk stratification, discrimination, and reclassification improvement based on quantification of subclinical coronary atherosclerosis: the Heinz Nixdorf Recall study. J Am Coll Cardiol. 2010, 56: 1397-1406. 10.1016/j.jacc.2010.06.030.CrossRefPubMed Erbel R, Mohlenkamp S, Moebus S, Schmermund A, Lehmann N, Stang A, et al: Coronary risk stratification, discrimination, and reclassification improvement based on quantification of subclinical coronary atherosclerosis: the Heinz Nixdorf Recall study. J Am Coll Cardiol. 2010, 56: 1397-1406. 10.1016/j.jacc.2010.06.030.CrossRefPubMed
5.
go back to reference Mohlenkamp S, Schmermund A, Lehmann N, Roggenbuck U, Dragano N, Stang A, et al: Subclinical coronary atherosclerosis and resting ECG abnormalities in an unselected general population. Atherosclerosis. 2008, 196: 786-794. 10.1016/j.atherosclerosis.2007.01.012.CrossRefPubMed Mohlenkamp S, Schmermund A, Lehmann N, Roggenbuck U, Dragano N, Stang A, et al: Subclinical coronary atherosclerosis and resting ECG abnormalities in an unselected general population. Atherosclerosis. 2008, 196: 786-794. 10.1016/j.atherosclerosis.2007.01.012.CrossRefPubMed
6.
go back to reference Fischer M, Broeckel U, Holmer S, Baessler A, Hengstenberg C, Mayer B, et al: Distinct heritable patterns of angiographic coronary artery disease in families with myocardial infarction. Circulation. 2005, 111: 855-862. 10.1161/01.CIR.0000155611.41961.BB.CrossRefPubMed Fischer M, Broeckel U, Holmer S, Baessler A, Hengstenberg C, Mayer B, et al: Distinct heritable patterns of angiographic coronary artery disease in families with myocardial infarction. Circulation. 2005, 111: 855-862. 10.1161/01.CIR.0000155611.41961.BB.CrossRefPubMed
7.
go back to reference Nasir K, Budoff MJ, Wong ND, Scheuner M, Herrington D, Arnett DK, et al: Family history of premature coronary heart disease and coronary artery calcification: Multi-Ethnic Study of Atherosclerosis (MESA). Circulation. 2007, 116: 619-626. 10.1161/CIRCULATIONAHA.107.688739.CrossRefPubMed Nasir K, Budoff MJ, Wong ND, Scheuner M, Herrington D, Arnett DK, et al: Family history of premature coronary heart disease and coronary artery calcification: Multi-Ethnic Study of Atherosclerosis (MESA). Circulation. 2007, 116: 619-626. 10.1161/CIRCULATIONAHA.107.688739.CrossRefPubMed
8.
go back to reference Peyser PA, Bielak LF, Chu JS, Turner ST, Ellsworth DL, Boerwinkle E, et al: Heritability of coronary artery calcium quantity measured by electron beam computed tomography in asymptomatic adults. Circulation. 2002, 106: 304-308. 10.1161/01.CIR.0000022664.21832.5D.CrossRefPubMed Peyser PA, Bielak LF, Chu JS, Turner ST, Ellsworth DL, Boerwinkle E, et al: Heritability of coronary artery calcium quantity measured by electron beam computed tomography in asymptomatic adults. Circulation. 2002, 106: 304-308. 10.1161/01.CIR.0000022664.21832.5D.CrossRefPubMed
9.
go back to reference Erbel R, Delaney JA, Lehmann N, McClelland RL, Mohlenkamp S, Kronmal RA, et al: Signs of subclinical coronary atherosclerosis in relation to risk factor distribution in the Multi-Ethnic Study of Atherosclerosis (MESA) and the Heinz Nixdorf Recall Study (HNR). Eur Heart J. 2008, 29: 2782-2791. 10.1093/eurheartj/ehn439.CrossRefPubMedPubMedCentral Erbel R, Delaney JA, Lehmann N, McClelland RL, Mohlenkamp S, Kronmal RA, et al: Signs of subclinical coronary atherosclerosis in relation to risk factor distribution in the Multi-Ethnic Study of Atherosclerosis (MESA) and the Heinz Nixdorf Recall Study (HNR). Eur Heart J. 2008, 29: 2782-2791. 10.1093/eurheartj/ehn439.CrossRefPubMedPubMedCentral
10.
go back to reference Maher JE, Raz JA, Bielak LF, Sheedy PF, Schwartz RS, Peyser PA: Potential of quantity of coronary artery calcification to identify new risk factors for asymptomatic atherosclerosis. Am J Epidemiol. 1996, 144: 943-953. 10.1093/oxfordjournals.aje.a008864.CrossRefPubMed Maher JE, Raz JA, Bielak LF, Sheedy PF, Schwartz RS, Peyser PA: Potential of quantity of coronary artery calcification to identify new risk factors for asymptomatic atherosclerosis. Am J Epidemiol. 1996, 144: 943-953. 10.1093/oxfordjournals.aje.a008864.CrossRefPubMed
11.
go back to reference Moebus S, Stang A, Mohlenkamp S, Dragano N, Schmermund A, Slomiany U, et al: Association of impaired fasting glucose and coronary artery calcification as a marker of subclinical atherosclerosis in a population-based cohort–results of the Heinz Nixdorf Recall Study. Diabetologia. 2009, 52: 81-89. 10.1007/s00125-008-1173-y.CrossRefPubMed Moebus S, Stang A, Mohlenkamp S, Dragano N, Schmermund A, Slomiany U, et al: Association of impaired fasting glucose and coronary artery calcification as a marker of subclinical atherosclerosis in a population-based cohort–results of the Heinz Nixdorf Recall Study. Diabetologia. 2009, 52: 81-89. 10.1007/s00125-008-1173-y.CrossRefPubMed
12.
go back to reference Wagenknecht LE, Bowden DW, Carr JJ, Langefeld CD, Freedman BI, Rich SS: Familial aggregation of coronary artery calcium in families with type 2 diabetes. Diabetes. 2001, 50: 861-866. 10.2337/diabetes.50.4.861.CrossRefPubMed Wagenknecht LE, Bowden DW, Carr JJ, Langefeld CD, Freedman BI, Rich SS: Familial aggregation of coronary artery calcium in families with type 2 diabetes. Diabetes. 2001, 50: 861-866. 10.2337/diabetes.50.4.861.CrossRefPubMed
13.
go back to reference Burton PR, Clayton DG, Cardon LR, Craddock N, Deloukas P, Duncanson A, et al: Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature. 2007, 447: 661-678. 10.1038/nature05911.CrossRef Burton PR, Clayton DG, Cardon LR, Craddock N, Deloukas P, Duncanson A, et al: Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature. 2007, 447: 661-678. 10.1038/nature05911.CrossRef
14.
go back to reference Peden JF, Hopewell JC, Saleheen D, Chambers JC, Hager J, Soranzo N, et al: A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. Nat Genet. 2011, 43: 339-344. 10.1038/ng.782.CrossRef Peden JF, Hopewell JC, Saleheen D, Chambers JC, Hager J, Soranzo N, et al: A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. Nat Genet. 2011, 43: 339-344. 10.1038/ng.782.CrossRef
15.
go back to reference Ellinor PT, Lunetta KL, Glazer NL, Pfeufer A, Alonso A, Chung MK, et al: Common variants in KCNN3 are associated with lone atrial fibrillation. Nat Genet. 2010, 42: 240-244. 10.1038/ng.537.CrossRefPubMedPubMedCentral Ellinor PT, Lunetta KL, Glazer NL, Pfeufer A, Alonso A, Chung MK, et al: Common variants in KCNN3 are associated with lone atrial fibrillation. Nat Genet. 2010, 42: 240-244. 10.1038/ng.537.CrossRefPubMedPubMedCentral
16.
go back to reference Erdmann J, Grosshennig A, Braund PS, Konig IR, Hengstenberg C, Hall AS, et al: New susceptibility locus for coronary artery disease on chromosome 3q22.3. Nat Genet. 2009, 41: 280-282. 10.1038/ng.307.CrossRefPubMedPubMedCentral Erdmann J, Grosshennig A, Braund PS, Konig IR, Hengstenberg C, Hall AS, et al: New susceptibility locus for coronary artery disease on chromosome 3q22.3. Nat Genet. 2009, 41: 280-282. 10.1038/ng.307.CrossRefPubMedPubMedCentral
17.
go back to reference Erdmann J, Willenborg C, Nahrstaedt J, Preuss M, Konig IR, Baumert J, et al: Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23. Eur Heart J. 2011, 32: 158-168. 10.1093/eurheartj/ehq405.CrossRefPubMed Erdmann J, Willenborg C, Nahrstaedt J, Preuss M, Konig IR, Baumert J, et al: Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23. Eur Heart J. 2011, 32: 158-168. 10.1093/eurheartj/ehq405.CrossRefPubMed
18.
go back to reference Helgadottir A, Thorleifsson G, Manolescu A, Gretarsdottir S, Blondal T, Jonasdottir A, et al: A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science. 2007, 316: 1491-1493. 10.1126/science.1142842.CrossRefPubMed Helgadottir A, Thorleifsson G, Manolescu A, Gretarsdottir S, Blondal T, Jonasdottir A, et al: A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science. 2007, 316: 1491-1493. 10.1126/science.1142842.CrossRefPubMed
19.
go back to reference Helgadottir A, Thorleifsson G, Magnusson KP, Gretarsdottir S, Steinthorsdottir V, Manolescu A, et al: The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. Nat Genet. 2008, 40: 217-224. 10.1038/ng.72.CrossRefPubMed Helgadottir A, Thorleifsson G, Magnusson KP, Gretarsdottir S, Steinthorsdottir V, Manolescu A, et al: The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm. Nat Genet. 2008, 40: 217-224. 10.1038/ng.72.CrossRefPubMed
20.
go back to reference Kathiresan S, Voight BF, Purcell S, Musunuru K, Ardissino D, Mannucci PM, et al: Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet. 2009, 41: 334-341. 10.1038/ng.327.CrossRefPubMed Kathiresan S, Voight BF, Purcell S, Musunuru K, Ardissino D, Mannucci PM, et al: Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat Genet. 2009, 41: 334-341. 10.1038/ng.327.CrossRefPubMed
21.
go back to reference McPherson R, Pertsemlidis A, Kavaslar N, Stewart A, Roberts R, Cox DR, et al: A common allele on chromosome 9 associated with coronary heart disease. Science. 2007, 316: 1488-1491. 10.1126/science.1142447.CrossRefPubMedPubMedCentral McPherson R, Pertsemlidis A, Kavaslar N, Stewart A, Roberts R, Cox DR, et al: A common allele on chromosome 9 associated with coronary heart disease. Science. 2007, 316: 1488-1491. 10.1126/science.1142447.CrossRefPubMedPubMedCentral
22.
go back to reference Samani NJ, Erdmann J, Hall AS, Hengstenberg C, Mangino M, Mayer B, et al: Genomewide association analysis of coronary artery disease. N Engl J Med. 2007, 357: 443-453. 10.1056/NEJMoa072366.CrossRefPubMedPubMedCentral Samani NJ, Erdmann J, Hall AS, Hengstenberg C, Mangino M, Mayer B, et al: Genomewide association analysis of coronary artery disease. N Engl J Med. 2007, 357: 443-453. 10.1056/NEJMoa072366.CrossRefPubMedPubMedCentral
23.
go back to reference Schunkert H, Konig IR, Kathiresan S, Reilly MP, Assimes TL, Holm H, et al: Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet. 2011, 43: 333-338. 10.1038/ng.784.CrossRefPubMedPubMedCentral Schunkert H, Konig IR, Kathiresan S, Reilly MP, Assimes TL, Holm H, et al: Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet. 2011, 43: 333-338. 10.1038/ng.784.CrossRefPubMedPubMedCentral
24.
go back to reference Tregouet DA, Konig IR, Erdmann J, Munteanu A, Braund PS, Hall AS, 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. 10.1038/ng.314.CrossRefPubMed Tregouet DA, Konig IR, Erdmann J, Munteanu A, Braund PS, Hall AS, 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. 10.1038/ng.314.CrossRefPubMed
25.
go back to reference Wild PS, Zeller T, Schillert A, Szymczak S, Sinning CR, Deiseroth A, et al: A Genome-wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease. Circ Cardiovasc Genet. 2011, 4 (4): 403-412. 10.1161/CIRCGENETICS.110.958728.CrossRefPubMedPubMedCentral Wild PS, Zeller T, Schillert A, Szymczak S, Sinning CR, Deiseroth A, et al: A Genome-wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease. Circ Cardiovasc Genet. 2011, 4 (4): 403-412. 10.1161/CIRCGENETICS.110.958728.CrossRefPubMedPubMedCentral
26.
go back to reference O'Donnell CJ, Kavousi M, Smith AV, Kardia SL, Feitosa MF, Hwang SJ, et al: Genome-Wide Association Study for Coronary Artery Calcification With Follow-Up in Myocardial Infarction. Circulation. 2011, 124: 2855-2864. 10.1161/CIRCULATIONAHA.110.974899.CrossRefPubMedPubMedCentral O'Donnell CJ, Kavousi M, Smith AV, Kardia SL, Feitosa MF, Hwang SJ, et al: Genome-Wide Association Study for Coronary Artery Calcification With Follow-Up in Myocardial Infarction. Circulation. 2011, 124: 2855-2864. 10.1161/CIRCULATIONAHA.110.974899.CrossRefPubMedPubMedCentral
28.
go back to reference Schmermund A, Mohlenkamp S, Stang A, Gronemeyer D, Seibel R, Hirche H, et al: Assessment of clinically silent atherosclerotic disease and established and novel risk factors for predicting myocardial infarction and cardiac death in healthy middle-aged subjects: rationale and design of the Heinz Nixdorf RECALL Study. Risk Factors, Evaluation of Coronary Calcium and Lifestyle. Am Heart J. 2002, 144: 212-218. 10.1067/mhj.2002.123579.CrossRefPubMed Schmermund A, Mohlenkamp S, Stang A, Gronemeyer D, Seibel R, Hirche H, et al: Assessment of clinically silent atherosclerotic disease and established and novel risk factors for predicting myocardial infarction and cardiac death in healthy middle-aged subjects: rationale and design of the Heinz Nixdorf RECALL Study. Risk Factors, Evaluation of Coronary Calcium and Lifestyle. Am Heart J. 2002, 144: 212-218. 10.1067/mhj.2002.123579.CrossRefPubMed
29.
go back to reference Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, et al: PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet. 2007, 81: 559-575. 10.1086/519795.CrossRefPubMedPubMedCentral Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, et al: PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet. 2007, 81: 559-575. 10.1086/519795.CrossRefPubMedPubMedCentral
30.
go back to reference Pechlivanis S, Scherag A, Muhleisen TW, Mohlenkamp S, Horsthemke B, Boes T, et al: Coronary artery calcification and its relationship to validated genetic variants for diabetes mellitus assessed in the Heinz Nixdorf recall cohort. Arterioscler Thromb Vasc Biol. 2010, 30: 1867-1872. 10.1161/ATVBAHA.110.208496.CrossRefPubMed Pechlivanis S, Scherag A, Muhleisen TW, Mohlenkamp S, Horsthemke B, Boes T, et al: Coronary artery calcification and its relationship to validated genetic variants for diabetes mellitus assessed in the Heinz Nixdorf recall cohort. Arterioscler Thromb Vasc Biol. 2010, 30: 1867-1872. 10.1161/ATVBAHA.110.208496.CrossRefPubMed
31.
go back to reference Newton-Cheh C, Cook NR, VanDenburgh M, Rimm EB, Ridker PM, Albert CM: A common variant at 9p21 is associated with sudden and arrhythmic cardiac death. Circulation. 2009, 120: 2062-2068. 10.1161/CIRCULATIONAHA.109.879049.CrossRefPubMedPubMedCentral Newton-Cheh C, Cook NR, VanDenburgh M, Rimm EB, Ridker PM, Albert CM: A common variant at 9p21 is associated with sudden and arrhythmic cardiac death. Circulation. 2009, 120: 2062-2068. 10.1161/CIRCULATIONAHA.109.879049.CrossRefPubMedPubMedCentral
32.
go back to reference Harismendy O, Notani D, Song X, Rahim NG, Tanasa B, Heintzman N, et al: 9p21 DNA variants associated with coronary artery disease impair interferon-gamma signalling response. Nature. 2011, 470: 264-268. 10.1038/nature09753.CrossRefPubMedPubMedCentral Harismendy O, Notani D, Song X, Rahim NG, Tanasa B, Heintzman N, et al: 9p21 DNA variants associated with coronary artery disease impair interferon-gamma signalling response. Nature. 2011, 470: 264-268. 10.1038/nature09753.CrossRefPubMedPubMedCentral
33.
go back to reference Battle TE, Lynch RA, Frank DA: Signal transducer and activator of transcription 1 activation in endothelial cells is a negative regulator of angiogenesis. Cancer Res. 2006, 66: 3649-3657. 10.1158/0008-5472.CAN-05-3612.CrossRefPubMed Battle TE, Lynch RA, Frank DA: Signal transducer and activator of transcription 1 activation in endothelial cells is a negative regulator of angiogenesis. Cancer Res. 2006, 66: 3649-3657. 10.1158/0008-5472.CAN-05-3612.CrossRefPubMed
34.
go back to reference Ross R: Atherosclerosis is an inflammatory disease. Am Heart J. 1999, 138: S419-S420. 10.1016/S0002-8703(99)70266-8.CrossRefPubMed Ross R: Atherosclerosis is an inflammatory disease. Am Heart J. 1999, 138: S419-S420. 10.1016/S0002-8703(99)70266-8.CrossRefPubMed
35.
go back to reference Visel A, Zhu Y, May D, Afzal V, Gong E, Attanasio C, et al: Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice. Nature. 2010, 464: 409-412. 10.1038/nature08801.CrossRefPubMedPubMedCentral Visel A, Zhu Y, May D, Afzal V, Gong E, Attanasio C, et al: Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice. Nature. 2010, 464: 409-412. 10.1038/nature08801.CrossRefPubMedPubMedCentral
36.
go back to reference Congrains A, Kamide K, Oguro R, Yasuda O, Miyata K, Yamamoto E, et al: Genetic variants at the 9p21 locus contribute to atherosclerosis through modulation of ANRIL and CDKN2A/B. Atherosclerosis. 2011 Congrains A, Kamide K, Oguro R, Yasuda O, Miyata K, Yamamoto E, et al: Genetic variants at the 9p21 locus contribute to atherosclerosis through modulation of ANRIL and CDKN2A/B. Atherosclerosis. 2011
37.
go back to reference Allen PB, Greenfield AT, Svenningsson P, Haspeslagh DC, Greengard P: Phactrs 1–4: A family of protein phosphatase 1 and actin regulatory proteins. Proc Natl Acad Sci U S A. 2004, 101: 7187-7192. 10.1073/pnas.0401673101.CrossRefPubMedPubMedCentral Allen PB, Greenfield AT, Svenningsson P, Haspeslagh DC, Greengard P: Phactrs 1–4: A family of protein phosphatase 1 and actin regulatory proteins. Proc Natl Acad Sci U S A. 2004, 101: 7187-7192. 10.1073/pnas.0401673101.CrossRefPubMedPubMedCentral
38.
go back to reference Kim C, Ez-Roux AV, Nettleton JA, Polak JF, Post WS, Siscovick DS, et al: Sex differences in subclinical atherosclerosis by race/ethnicity in the multi-ethnic study of atherosclerosis. Am J Epidemiol. 2011, 174: 165-172. 10.1093/aje/kwr088.CrossRefPubMedPubMedCentral Kim C, Ez-Roux AV, Nettleton JA, Polak JF, Post WS, Siscovick DS, et al: Sex differences in subclinical atherosclerosis by race/ethnicity in the multi-ethnic study of atherosclerosis. Am J Epidemiol. 2011, 174: 165-172. 10.1093/aje/kwr088.CrossRefPubMedPubMedCentral
Metadata
Title
Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study
Authors
Sonali Pechlivanis
Thomas W Mühleisen
Stefan Möhlenkamp
Dirk Schadendorf
Raimund Erbel
Karl-Heinz Jöckel
Per Hoffmann
Markus M Nöthen
André Scherag
Susanne Moebus
for the Heinz Nixdorf Recall Study Investigative Group
Publication date
01-12-2013
Publisher
BioMed Central
Published in
BMC Medical Genetics / Issue 1/2013
Electronic ISSN: 1471-2350
DOI
https://doi.org/10.1186/1471-2350-14-23

Other articles of this Issue 1/2013

BMC Medical Genetics 1/2013 Go to the issue