Literature DB >> 20605023

Association of an allele on chromosome 9 and abdominal aortic aneurysm.

Erik Biros1, Matthew Cooper, Lyle J Palmer, Philip J Walker, Paul E Norman, Jonathan Golledge.   

Abstract

OBJECTIVE: Abdominal aortic aneurysm (AAA) has been recognized as a multi-factorial disease with both genetic and environmental risk factors. A locus residing within non-coding DNA on chromosome 9p21.3 has recently been associated with AAA. To further investigate the significance of this site for AAA, we performed an association study on a large group of 3371 men aged 65-83 years of whom 513 had an AAA.
METHODS: All men were assessed for other risk factors in a uniform way and an ultrasound of the abdominal aorta was performed.
RESULTS: Our findings validated the strong association of the chromosome 9p21.3 SNPs rs10757278 and rs1333049 with AAA and demonstrated the upregulation of LINE-1 elements at the site of AAA.
CONCLUSION: This study confirms a reproducible association between risk alleles on chromosome 9p21.3 and AAA. We also provide preliminary evidence for an association of LINE-1 elements with AAA which will require further investigation.
Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.

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Year:  2010        PMID: 20605023      PMCID: PMC2952706          DOI: 10.1016/j.atherosclerosis.2010.06.015

Source DB:  PubMed          Journal:  Atherosclerosis        ISSN: 0021-9150            Impact factor:   5.162


  15 in total

1.  Evolutionary analyses of the human genome.

Authors:  W H Li; Z Gu; H Wang; A Nekrutenko
Journal:  Nature       Date:  2001-02-15       Impact factor: 49.962

2.  L1 (LINE-1) retrotransposon evolution and amplification in recent human history.

Authors:  S Boissinot; P Chevret; A V Furano
Journal:  Mol Biol Evol       Date:  2000-06       Impact factor: 16.240

3.  The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm.

Authors:  Anna Helgadottir; Gudmar Thorleifsson; Kristinn P Magnusson; Solveig Grétarsdottir; Valgerdur Steinthorsdottir; Andrei Manolescu; Gregory T Jones; Gabriel J E Rinkel; Jan D Blankensteijn; Antti Ronkainen; Juha E Jääskeläinen; Yoshiki Kyo; Guy M Lenk; Natzi Sakalihasan; Konstantinos Kostulas; Anders Gottsäter; Andrea Flex; Hreinn Stefansson; Torben Hansen; Gitte Andersen; Shantel Weinsheimer; Knut Borch-Johnsen; Torben Jorgensen; Svati H Shah; Arshed A Quyyumi; Christopher B Granger; Muredach P Reilly; Harland Austin; Allan I Levey; Viola Vaccarino; Ebba Palsdottir; G Bragi Walters; Thorbjorg Jonsdottir; Steinunn Snorradottir; Dana Magnusdottir; Gudmundur Gudmundsson; Robert E Ferrell; Sigurlaug Sveinbjornsdottir; Juha Hernesniemi; Mika Niemelä; Raymond Limet; Karl Andersen; Gunnar Sigurdsson; Rafn Benediktsson; Eric L G Verhoeven; Joep A W Teijink; Diederick E Grobbee; Daniel J Rader; David A Collier; Oluf Pedersen; Roberto Pola; Jan Hillert; Bengt Lindblad; Einar M Valdimarsson; Hulda B Magnadottir; Cisca Wijmenga; Gerard Tromp; Annette F Baas; Ynte M Ruigrok; Andre M van Rij; Helena Kuivaniemi; Janet T Powell; Stefan E Matthiasson; Jeffrey R Gulcher; Gudmundur Thorgeirsson; Augustine Kong; Unnur Thorsteinsdottir; Kari Stefansson
Journal:  Nat Genet       Date:  2008-01-06       Impact factor: 38.330

Review 4.  The genetic basis of abdominal aortic aneurysms: a review.

Authors:  R M Sandford; M J Bown; N J London; R D Sayers
Journal:  Eur J Vasc Endovasc Surg       Date:  2007-02-02       Impact factor: 7.069

5.  Screening for abdominal aortic aneurysm: lessons from a population-based study.

Authors:  K Jamrozik; P E Norman; C A Spencer; R W Parsons; R Tuohy; M M Lawrence-Brown; J A Dickinson
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Review 6.  Biology of mammalian L1 retrotransposons.

Authors:  E M Ostertag; H H Kazazian
Journal:  Annu Rev Genet       Date:  2001       Impact factor: 16.830

7.  High frequency retrotransposition in cultured mammalian cells.

Authors:  J V Moran; S E Holmes; T P Naas; R J DeBerardinis; J D Boeke; H H Kazazian
Journal:  Cell       Date:  1996-11-29       Impact factor: 41.582

8.  Relationship between two sequence variations in the gene for peroxisome proliferator-activated receptor-gamma and plasma homocysteine concentration. Health in men study.

Authors:  Jonathan Golledge; Paul E Norman
Journal:  Hum Genet       Date:  2007-11-13       Impact factor: 4.132

9.  Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice.

Authors:  Axel Visel; Yiwen Zhu; Dalit May; Veena Afzal; Elaine Gong; Catia Attanasio; Matthew J Blow; Jonathan C Cohen; Edward M Rubin; Len A Pennacchio
Journal:  Nature       Date:  2010-02-21       Impact factor: 49.962

10.  L1 retrotransposition can occur early in human embryonic development.

Authors:  José A J M van den Hurk; Iwan C Meij; Maria del Carmen Seleme; Hiroki Kano; Konstantinos Nikopoulos; Lies H Hoefsloot; Erik A Sistermans; Ilse J de Wijs; Arijit Mukhopadhyay; Astrid S Plomp; Paulus T V M de Jong; Haig H Kazazian; Frans P M Cremers
Journal:  Hum Mol Genet       Date:  2007-05-04       Impact factor: 6.150

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  12 in total

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Authors:  Ian M Nordon; Robert J Hinchliffe; Ian M Loftus; Matt M Thompson
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2.  The rs1333049 polymorphism on locus 9p21.3 and extreme longevity in Spanish and Japanese cohorts.

Authors:  Tomàs Pinós; Noriyuki Fuku; Yolanda Cámara; Yasumichi Arai; Yukiko Abe; Gabriel Rodríguez-Romo; Nuria Garatachea; Alejandro Santos-Lozano; Elisabet Miro-Casas; Marisol Ruiz-Meana; Imanol Otaegui; Haruka Murakami; Motohiko Miyachi; David Garcia-Dorado; Kunihiko Hinohara; Antoni L Andreu; Akinori Kimura; Nobuyoshi Hirose; Alejandro Lucia
Journal:  Age (Dordr)       Date:  2013-10-28

Review 3.  Long non-coding RNA ANRIL in gene regulation and its duality in atherosclerosis.

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4.  Expression of linear and novel circular forms of an INK4/ARF-associated non-coding RNA correlates with atherosclerosis risk.

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5.  Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk.

Authors:  Tatiana Foroud; Daniel L Koller; Dongbing Lai; Laura Sauerbeck; Craig Anderson; Nerissa Ko; Ranjan Deka; Thomas H Mosley; Myriam Fornage; Daniel Woo; Charles J Moomaw; Richard Hornung; John Huston; Irene Meissner; Joan E Bailey-Wilson; Carl Langefeld; Guy Rouleau; E Sander Connolly; Bradford B Worrall; Dawn Kleindorfer; Matthew L Flaherty; Sharyl Martini; Jason Mackey; Felipe De Los Rios La Rosa; Robert D Brown; Joseph P Broderick
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Review 6.  TGFB1 genetic polymorphisms and coronary heart disease risk: a meta-analysis.

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7.  Genomic research to identify novel pathways in the development of abdominal aortic aneurysm.

Authors:  Seamus C Harrison; Anastasia Z Kalea; Michael V Holmes; Obi Agu; Steve E Humphries
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8.  Association of arterial stiffness with single nucleotide polymorphism rs1333049 and metabolic risk factors.

Authors:  Suphawadee Phababpha; Upa Kukongviriyapan; Poungrat Pakdeechote; Laddawan Senggunprai; Veerapol Kukongviriyapan; Chatri Settasatian; Pyatat Tatsanavivat; Phongsak Intharaphet; Vichai Senthong; Nantarat Komanasin; Nongnuch Settasatian; Stephen E Greenwald
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9.  Analysis of the 9p21.3 sequence associated with coronary artery disease reveals a tendency for duplication in a CAD patient.

Authors:  Mikhail Liskovykh; Nicholas C O Lee; Natalay Kouprina; Vladimir N Noskov; Joshua J Waterfall; Robert L Walker; Paul S Meltzer; Eric J Topol; Vladimir Larionov
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Review 10.  Genetic and Epigenetic Mechanisms Underlying Vascular Smooth Muscle Cell Phenotypic Modulation in Abdominal Aortic Aneurysm.

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