Literature DB >> 15710764

Distinct heritable patterns of angiographic coronary artery disease in families with myocardial infarction.

Marcus Fischer1, Ulrich Broeckel, Stephan Holmer, Andrea Baessler, Christian Hengstenberg, Bjoern Mayer, Jeanette Erdmann, Gernot Klein, Guenter Riegger, Howard J Jacob, Heribert Schunkert.   

Abstract

BACKGROUND: Coronary artery disease (CAD) and myocardial infarction (MI) are significantly determined by genetic background. Whether distinct angiographic features of CAD are affected by inherited factors has never been investigated. Thus, we analyzed comprehensively the extent to which various aspects of CAD, including disease severity, distribution of lesions, presence of coronary calcification, morphology of stenoses, and anatomic characteristics, are under genetic control. METHODS AND
RESULTS: We retrospectively studied the coronary angiograms of 882 siblings with CAD from 401 families. These families were ascertained through index patients defined by MI before the age of 60 years and at least 1 sibling with MI or coronary revascularization procedures. Heritability calculations were performed with variance-component analysis. Additionally, recurrence risks to siblings were analyzed. Traditional cardiovascular risk factors and age at the first coronary event displayed significant heritable components. After adjustment for age and sex, significant heritabilities were identified for proximal stenoses, in particular, left main CAD (h2=0.49+/-0.12; P=0.01), coronary calcification (h2=0.51+/-0.17; P=0.001), and ectatic coronary lesions (h2=0.52+/-0.07; P=0.001). In contrast, no heritability was found for distal disease (h2=0.05+/-0.19; NS), the pattern of coronary arterial blood supply, or the number of diseased vessels. Calculation of recurrence risks in siblings largely confirmed the heritability estimates.
CONCLUSIONS: Distinct morphological characteristics associated with CAD show different degrees of heritability. Notably, the most hazardous localizations, like left main or proximal disease, display a high heritability. In contrast, some features of coronary morphology, such as distal disease, do not appear to be markedly influenced by heritable factors.

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Year:  2005        PMID: 15710764     DOI: 10.1161/01.CIR.0000155611.41961.BB

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


  54 in total

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Authors:  Elina Nikkola; Arthur Ko; Marcus Alvarez; Rita M Cantor; Kristina Garske; Elliot Kim; Stephanie Gee; Alejandra Rodriguez; Reinhard Muxel; Niina Matikainen; Sanni Söderlund; Mahdi M Motazacker; Jan Borén; Claudia Lamina; Florian Kronenberg; Wolfgang J Schneider; Aarno Palotie; Markku Laakso; Marja-Riitta Taskinen; Päivi Pajukanta
Journal:  Atherosclerosis       Date:  2017-07-22       Impact factor: 5.162

2.  The chromosome 9p21 risk locus is associated with angiographic severity and progression of coronary artery disease.

Authors:  Riyaz S Patel; Shaoyong Su; Ian J Neeland; Ayushi Ahuja; Emir Veledar; Jinying Zhao; Anna Helgadottir; Hilma Holm; Jeffrey R Gulcher; Kari Stefansson; Salina Waddy; Viola Vaccarino; A Maziar Zafari; Arshed A Quyyumi
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Review 3.  Genome-wide association studies of late-onset cardiovascular disease.

Authors:  J Gustav Smith; Christopher Newton-Cheh
Journal:  J Mol Cell Cardiol       Date:  2015-04-11       Impact factor: 5.000

Review 4.  Genetic causes of myocardial infarction: new insights from genome-wide association studies.

Authors:  Jeanette Erdmann; Patrick Linsel-Nitschke; Heribert Schunkert
Journal:  Dtsch Arztebl Int       Date:  2010-10-08       Impact factor: 5.594

Review 5.  The genetics of heart attack.

Authors:  Eric J Topol
Journal:  Heart       Date:  2006-06       Impact factor: 5.994

Review 6.  Genetics and heritability of coronary artery disease and myocardial infarction.

Authors:  Björn Mayer; Jeanette Erdmann; Heribert Schunkert
Journal:  Clin Res Cardiol       Date:  2006-10-10       Impact factor: 5.460

7.  Heritability of carotid intima-media thickness: a twin study.

Authors:  Jinying Zhao; Faiz A Cheema; J Douglas Bremner; Jack Goldberg; Shaoyong Su; Harold Snieder; Carisa Maisano; Linda Jones; Farhan Javed; Nancy Murrah; Ngoc-Anh Le; Viola Vaccarino
Journal:  Atherosclerosis       Date:  2007-09-06       Impact factor: 5.162

8.  Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease.

Authors:  David-Alexandre Trégouët; Inke R König; Jeanette Erdmann; Alexandru Munteanu; Peter S Braund; Alistair S Hall; Anika Grosshennig; Patrick Linsel-Nitschke; Claire Perret; Maylis DeSuremain; Thomas Meitinger; Ben J Wright; Michael Preuss; Anthony J Balmforth; Stephen G Ball; Christa Meisinger; Cécile Germain; Alun Evans; Dominique Arveiler; Gérald Luc; Jean-Bernard Ruidavets; Caroline Morrison; Pim van der Harst; Stefan Schreiber; Katharina Neureuther; Arne Schäfer; Peter Bugert; Nour E El Mokhtari; Jürgen Schrezenmeir; Klaus Stark; Diana Rubin; H-Erich Wichmann; Christian Hengstenberg; Willem Ouwehand; Andreas Ziegler; Laurence Tiret; John R Thompson; Francois Cambien; Heribert Schunkert; Nilesh J Samani
Journal:  Nat Genet       Date:  2009-02-08       Impact factor: 38.330

9.  A pre-microRNA-149 (miR-149) genetic variation affects miR-149 maturation and its ability to regulate the Puma protein in apoptosis.

Authors:  Su-Ling Ding; Jian-Xun Wang; Jian-Qin Jiao; Xin Tu; Qing Wang; Fang Liu; Qian Li; Jie Gao; Qun-Yong Zhou; Dong-Feng Gu; Pei-Feng Li
Journal:  J Biol Chem       Date:  2013-07-19       Impact factor: 5.157

10.  Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease.

Authors:  Benjamin D Horne; John F Carlquist; Joseph B Muhlestein; Tami L Bair; Jeffrey L Anderson
Journal:  Circ Cardiovasc Genet       Date:  2008-12
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