Literature DB >> 26941057

9p21 locus rs10757278 is associated with advanced carotid atherosclerosis in a gender-specific manner.

Ivan Zivotić1, Tamara Djurić1, Aleksandra Stanković1, Ana Djordjević1, Igor Končar2, Lazar Davidović2, Dragan Alavantić1, Maja Zivković3.   

Abstract

Single nucleotide polymorphisms from the chromosome locus 9p21 are reported to carry a risk for various cardiovascular diseases. One of the lead single nucleotide polymorphisms, rs10757278, was mostly investigated in association with coronary artery disease but rarely with carotid atherosclerosis. In this study, we aimed to analyze the association of rs10757278 A/G polymorphism with carotid plaque presence in advanced carotid atherosclerosis. The study included 803 participants, 486 patients with high-grade stenosis (>70%) who were undergoing carotid endarterectomy and 317 controls from Serbian population. Genotypes were determined using the real-time polymerase chain reaction. According to the recessive model of inheritance, GG genotype was significantly and independently associated with carotid plaque in females only (odds ratio 2.42, CI = 1.20-4.90, P = 0.013). Odds ratio was adjusted for age, body mass index, hypertension, TC, LDLC, HDLC and TG, and P value was corrected for multiple comparisons. Our preliminary findings suggest a gender-specific association of rs10757278 polymorphism with carotid plaque. Further studies on larger sample and in genetically and environmentally similar populations are needed.
© 2016 by the Society for Experimental Biology and Medicine.

Entities:  

Keywords:  9p21; carotid plaque; gender specific; gene polymorphism; rs10757278

Mesh:

Year:  2016        PMID: 26941057      PMCID: PMC4950315          DOI: 10.1177/1535370216636718

Source DB:  PubMed          Journal:  Exp Biol Med (Maywood)        ISSN: 1535-3699


  39 in total

1.  The difference between acute coronary heart disease and ischaemic stroke risk with regard to gender and age in Finnish and Swedish populations.

Authors:  Marjukka Hyvärinen; Qing Qiao; Jaakko Tuomilehto; Stefan Söderberg; Mats Eliasson; Coen D A Stehouwer
Journal:  Int J Stroke       Date:  2010-06       Impact factor: 5.266

2.  CVD-associated non-coding RNA, ANRIL, modulates expression of atherogenic pathways in VSMC.

Authors:  Ada Congrains; Kei Kamide; Tomohiro Katsuya; Osamu Yasuda; Ryousuke Oguro; Koichi Yamamoto; Mitsuru Ohishi; Hiromi Rakugi
Journal:  Biochem Biophys Res Commun       Date:  2012-02-20       Impact factor: 3.575

3.  Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.

Authors:  Helen M Broadbent; John F Peden; Stefan Lorkowski; Anuj Goel; Halit Ongen; Fiona Green; Robert Clarke; Rory Collins; Maria Grazia Franzosi; Gianni Tognoni; Udo Seedorf; Stephan Rust; Per Eriksson; Anders Hamsten; Martin Farrall; Hugh Watkins
Journal:  Hum Mol Genet       Date:  2007-11-29       Impact factor: 6.150

4.  A common variant on chromosome 9p21 affects the risk of myocardial infarction.

Authors:  Anna Helgadottir; Gudmar Thorleifsson; Andrei Manolescu; Solveig Gretarsdottir; Thorarinn Blondal; Aslaug Jonasdottir; Adalbjorg Jonasdottir; Asgeir Sigurdsson; Adam Baker; Arnar Palsson; Gisli Masson; Daniel F Gudbjartsson; Kristinn P Magnusson; Karl Andersen; Allan I Levey; Valgerdur M Backman; Sigurborg Matthiasdottir; Thorbjorg Jonsdottir; Stefan Palsson; Helga Einarsdottir; Steinunn Gunnarsdottir; Arnaldur Gylfason; Viola Vaccarino; W Craig Hooper; Muredach P Reilly; Christopher B Granger; Harland Austin; Daniel J Rader; Svati H Shah; Arshed A Quyyumi; Jeffrey R Gulcher; Gudmundur Thorgeirsson; Unnur Thorsteinsdottir; Augustine Kong; Kari Stefansson
Journal:  Science       Date:  2007-05-03       Impact factor: 47.728

5.  Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

Authors:  L M Kunkel; K D Smith; S H Boyer; D S Borgaonkar; S S Wachtel; O J Miller; W R Breg; H W Jones; J M Rary
Journal:  Proc Natl Acad Sci U S A       Date:  1977-03       Impact factor: 11.205

6.  Variants on chromosome 9p21.3 correlated with ANRIL expression contribute to stroke risk and recurrence in a large prospective stroke population.

Authors:  Weili Zhang; Yu Chen; Peng Liu; Jingzhou Chen; Lei Song; Yue Tang; Yuyao Wang; Jibin Liu; Frank B Hu; Rutai Hui
Journal:  Stroke       Date:  2011-10-27       Impact factor: 7.914

7.  Coronary artery disease-associated locus on chromosome 9p21 and early markers of atherosclerosis.

Authors:  Nilesh J Samani; Olli T Raitakari; Kalle Sipilä; Martin D Tobin; Heribert Schunkert; Markus Juonala; Peter S Braund; Jeanette Erdmann; Jorma Viikari; Leena Moilanen; Leena Taittonen; Antti Jula; Eero Jokinen; Tomi Laitinen; Nina Hutri-Kähönen; Markku S Nieminen; Y Antero Kesäniemi; Alistair S Hall; Janne Hulkkonen; Mika Kähönen; Terho Lehtimäki
Journal:  Arterioscler Thromb Vasc Biol       Date:  2008-07-03       Impact factor: 8.311

8.  Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke.

Authors:  Andreas Gschwendtner; Steve Bevan; John W Cole; Anna Plourde; Mar Matarin; Helen Ross-Adams; Thomas Meitinger; Erich Wichmann; Braxton D Mitchell; Karen Furie; Agnieszka Slowik; Stephen S Rich; Paul D Syme; Mary J MacLeod; James F Meschia; Jonathan Rosand; Steve J Kittner; Hugh S Markus; Bertram Müller-Myhsok; Martin Dichgans
Journal:  Ann Neurol       Date:  2009-05       Impact factor: 10.422

9.  Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies.

Authors:  Joanne M Murabito; Charles C White; Maryam Kavousi; Yan V Sun; Mary F Feitosa; Vijay Nambi; Claudia Lamina; Arne Schillert; Stefan Coassin; Joshua C Bis; Linda Broer; Dana C Crawford; Nora Franceschini; Ruth Frikke-Schmidt; Margot Haun; Suzanne Holewijn; Jennifer E Huffman; Shih-Jen Hwang; Stefan Kiechl; Barbara Kollerits; May E Montasser; Ilja M Nolte; Megan E Rudock; Andrea Senft; Alexander Teumer; Pim van der Harst; Veronique Vitart; Lindsay L Waite; Andrew R Wood; Christina L Wassel; Devin M Absher; Matthew A Allison; Najaf Amin; Alice Arnold; Folkert W Asselbergs; Yurii Aulchenko; Stefania Bandinelli; Maja Barbalic; Mladen Boban; Kristin Brown-Gentry; David J Couper; Michael H Criqui; Abbas Dehghan; Martin den Heijer; Benjamin Dieplinger; Jingzhong Ding; Marcus Dörr; Christine Espinola-Klein; Stephan B Felix; Luigi Ferrucci; Aaron R Folsom; Gustav Fraedrich; Quince Gibson; Robert Goodloe; Grgo Gunjaca; Meinhard Haltmayer; Gerardo Heiss; Albert Hofman; Arne Kieback; Lambertus A Kiemeney; Ivana Kolcic; Iftikhar J Kullo; Stephen B Kritchevsky; Karl J Lackner; Xiaohui Li; Wolfgang Lieb; Kurt Lohman; Christa Meisinger; David Melzer; Emile R Mohler; Ivana Mudnic; Thomas Mueller; Gerjan Navis; Friedrich Oberhollenzer; Jeffrey W Olin; Jeff O'Connell; Christopher J O'Donnell; Walter Palmas; Brenda W Penninx; Astrid Petersmann; Ozren Polasek; Bruce M Psaty; Barbara Rantner; Ken Rice; Fernando Rivadeneira; Jerome I Rotter; Adrie Seldenrijk; Marietta Stadler; Monika Summerer; Toshiko Tanaka; Anne Tybjaerg-Hansen; Andre G Uitterlinden; Wiek H van Gilst; Sita H Vermeulen; Sarah H Wild; Philipp S Wild; Johann Willeit; Tanja Zeller; Tatijana Zemunik; Lina Zgaga; Themistocles L Assimes; Stefan Blankenberg; Eric Boerwinkle; Harry Campbell; John P Cooke; Jacqueline de Graaf; David Herrington; Sharon L R Kardia; Braxton D Mitchell; Anna Murray; Thomas Münzel; Anne B Newman; Ben A Oostra; Igor Rudan; Alan R Shuldiner; Harold Snieder; Cornelia M van Duijn; Uwe Völker; Alan F Wright; H-Erich Wichmann; James F Wilson; Jacqueline C M Witteman; Yongmei Liu; Caroline Hayward; Ingrid B Borecki; Andreas Ziegler; Kari E North; L Adrienne Cupples; Florian Kronenberg
Journal:  Circ Cardiovasc Genet       Date:  2011-12-23

10.  Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis.

Authors:  Kenneth Chan; Riyaz S Patel; Paul Newcombe; Christopher P Nelson; Atif Qasim; Stephen E Epstein; Susan Burnett; Viola L Vaccarino; A Maziar Zafari; Svati H Shah; Jeffrey L Anderson; John F Carlquist; Jaana Hartiala; Hooman Allayee; Kunihiko Hinohara; Bok-Soo Lee; Anna Erl; Katrina L Ellis; Anuj Goel; Arne S Schaefer; Nour Eddine El Mokhtari; Benjamin A Goldstein; Mark A Hlatky; Alan S Go; Gong-Qing Shen; Yan Gong; Carl Pepine; Ross C Laxton; John C Whittaker; W H Wilson Tang; Julie A Johnson; Qing K Wang; Themistocles L Assimes; Ute Nöthlings; Martin Farrall; Hugh Watkins; A Mark Richards; Vicky A Cameron; Axel Muendlein; Heinz Drexel; Werner Koch; Jeong Euy Park; Akinori Kimura; Wei-feng Shen; Iain A Simpson; Stanley L Hazen; Benjamin D Horne; Elizabeth R Hauser; Arshed A Quyyumi; Muredach P Reilly; Nilesh J Samani; Shu Ye
Journal:  J Am Coll Cardiol       Date:  2013-01-23       Impact factor: 24.094

View more
  1 in total

1.  Genetic variation in 9p21 is associated with fasting insulin in women but not men.

Authors:  Sara Mahdavi; David J A Jenkins; Ahmed El-Sohemy
Journal:  PLoS One       Date:  2018-08-23       Impact factor: 3.240

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.