Literature DB >> 12810610

Genetic variation in lectin-like oxidized low-density lipoprotein receptor 1 (LOX1) gene and the risk of coronary artery disease.

Qi Chen1, Steven E Reis, Candace Kammerer, Wendy Y Craig, Sue E LaPierre, Erin Luedecking Zimmer, Dennis M McNamara, Daniel F Pauly, Barry Sharaf, Richard Holubkov, C Noel Bairey Merz, George Sopko, Franklin Bontempo, M Ilyas Kamboh.   

Abstract

BACKGROUND: We examined the association of 3 polymorphisms in the lectin-like oxidized LDL receptor-1 (LOX1 or OLR1) gene with coronary artery disease in the Women's Ischemia Syndrome Evaluation (WISE) study population. METHODS AND
RESULTS: The WISE sample comprised 589 white and 122 black women who underwent angiography for suspected ischemia. The sample was divided into 3 groups: <20% stenosis (38.7%), 20% to 49% stenosis (24.9%), and >or=50% stenosis (35.3%). The three LOX1 polymorphisms (intron 4/G-->A, intron 5/T-->G, and 3' UTR/T-->C) were in linkage disequilibrium and thus behaved as a single polymorphism. The frequency of the 3'UTR/T allele was significantly higher in whites than blacks (49% versus 19%; P<0.0001). Among white women, the frequency of the 3'UTR/T allele carriers (TC+TT genotypes) increased gradually from 67.9% to 75.0% and 79.2% in the <20%, 20% to 49%, and >or=50% stenosis groups, respectively (chi2 trend=6.23; P=0.013). Logistic regression analyses indicated that APOE (odds ratio, 1.90; P=0.007) and LOX1 (odds ratio, 1.67; P=0.025) genotypes were independently associated with the risk of disease and that there was no interaction between the two genes. The 3'UTR/T allele carriers also had significantly higher IgG anti-oxLDL levels than individuals carrying the CC genotype (0.94+/-0.20 versus 0.86+/-0.16; P=0.032). Furthermore, our electrophoretic mobility shift assay data show that the 3'UTR polymorphic sequence affects the binding of a putative transcription factor in an allele-specific manner.
CONCLUSIONS: Our data suggest that common genetic variation in the LOX1 gene may be associated with the risk of coronary artery disease in white women.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12810610     DOI: 10.1161/01.CIR.0000074207.85796.36

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


  24 in total

1.  Complex inheritance of the 5-lipoxygenase locus influencing atherosclerosis in mice.

Authors:  Anatole Ghazalpour; Xuping Wang; Aldons J Lusis; Margarete Mehrabian
Journal:  Genetics       Date:  2006-04-19       Impact factor: 4.562

2.  The oxidized low-density lipoprotein receptor mediates vascular effects of inhaled vehicle emissions.

Authors:  Amie K Lund; JoAnn Lucero; Melissa Harman; Michael C Madden; Jacob D McDonald; Jean Clare Seagrave; Matthew J Campen
Journal:  Am J Respir Crit Care Med       Date:  2011-04-14       Impact factor: 21.405

Review 3.  3' end mRNA processing: molecular mechanisms and implications for health and disease.

Authors:  Sven Danckwardt; Matthias W Hentze; Andreas E Kulozik
Journal:  EMBO J       Date:  2008-02-06       Impact factor: 11.598

Review 4.  LOX-1, a new marker of risk and prognosis in coronary artery disease?

Authors:  Valter Lubrano; Silvana Balzan
Journal:  Mol Cell Biochem       Date:  2013-08-11       Impact factor: 3.396

5.  3'-UTR OLR1/LOX-1 gene polymorphism and endothelial dysfunction: molecular and vascular data in never-treated hypertensive patients.

Authors:  Angela Sciacqua; Ivan Presta; Maria Perticone; Eliezer J Tassone; Francesco Andreozzi; Maria Chiara Quitadamo; Federica Carla Sangiuolo; Giorgio Sesti; Francesco Perticone
Journal:  Intern Emerg Med       Date:  2012-09-29       Impact factor: 3.397

6.  Lack of MEF2A mutations in coronary artery disease.

Authors:  Li Weng; Nihan Kavaslar; Anna Ustaszewska; Heather Doelle; Wendy Schackwitz; Sybil Hébert; Jonathan C Cohen; Ruth McPherson; Len A Pennacchio
Journal:  J Clin Invest       Date:  2005-04       Impact factor: 14.808

7.  A candidate gene study revealed sex-specific association between the OLR1 gene and carotid plaque.

Authors:  Liyong Wang; Danielle Yanuck; Ashley Beecham; Hannah Gardener; Susan Slifer; Susan H Blanton; Ralph L Sacco; Tatjana Rundek
Journal:  Stroke       Date:  2011-01-21       Impact factor: 7.914

8.  Association of anti-oxidized LDL and candidate genes with severity of coronary stenosis in the Women's Ischemia Syndrome Evaluation study.

Authors:  Qi Chen; Steven E Reis; Candace Kammerer; Wendy Craig; Dennis M McNamara; Richard Holubkov; Barry L Sharaf; George Sopko; Daniel F Pauly; C Noel Bairey Merz; M Ilyas Kamboh
Journal:  J Lipid Res       Date:  2011-01-20       Impact factor: 5.922

9.  Apolipoprotein H promoter polymorphisms in relation to lupus and lupus-related phenotypes.

Authors:  Sangita Suresh; F Yesim K Demirci; Erin Jacobs; Amy H Kao; Elisa Y Rhew; Dharambir K Sanghera; Faith Selzer; Kim Sutton-Tyrrell; David McPherson; Franklin A Bontempo; Candace M Kammerer; Rosalind Ramsey-Goldman; Susan Manzi; M Ilyas Kamboh
Journal:  J Rheumatol       Date:  2009-02       Impact factor: 4.666

10.  Associations between Lectin-like, oxidized low-density lipoprotein receptor-1 G501C and 3'-UTR-C188T polymorphisms with coronary artery disease: a meta-analysis.

Authors:  Tian-Ying Feng; Hong-Wei Shan; Rui Lang
Journal:  Int J Clin Exp Med       Date:  2015-06-15
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.