Literature DB >> 17021678

Genetics and heritability of coronary artery disease and myocardial infarction.

Björn Mayer1, Jeanette Erdmann, Heribert Schunkert.   

Abstract

A positive family history is frequently reported by patients with coronary artery disease (CAD) or myocardial infarction. For risk stratification, it is crucial to distinguish between accidental reoccurrence of sporadic cases and cases with a true heritable component of the conditions. A familial predisposition is assumed when a myocardial infarction is diagnosed by a male first degree relative before the 55th year of life or a female first degree relative before the 65th year of life. The current manuscript reviews major studies from which a familial risk of CAD or myocardial infarction can be inferred. Moreover, a brief overview summarizes the current results of molecular genetic research on chromosomal loci and genes relevant for CAD and myocardial infarction.

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Year:  2006        PMID: 17021678     DOI: 10.1007/s00392-006-0447-y

Source DB:  PubMed          Journal:  Clin Res Cardiol        ISSN: 1861-0684            Impact factor:   5.460


  44 in total

1.  Old and simple tools may do better--sometimes.

Authors:  H Schunkert; M Fischer
Journal:  Eur Heart J       Date:  2002-12       Impact factor: 29.983

Review 2.  Clinical application of genetic risk assessment strategies for coronary artery disease: genotypes, phenotypes, and family history.

Authors:  Maren T Scheuner
Journal:  Prim Care       Date:  2004-09       Impact factor: 2.907

3.  Regional cardiac dysfunction is associated with specific alterations in inflammatory cytokines and matrix metalloproteinases after acute myocardial infarction in sheep.

Authors:  Gabrielle Gallagher; Stuart Menzie; Yifei Huang; Chris Jackson; Stephen N Hunyor
Journal:  Basic Res Cardiol       Date:  2006-07-04       Impact factor: 17.165

Review 4.  Controversial association of left ventricular hypertrophy and the ACE I/D polymorphism--is the mist clearing up?

Authors:  H Schunkert
Journal:  Nephrol Dial Transplant       Date:  1998-05       Impact factor: 5.992

5.  Parental history is an independent risk factor for coronary artery disease: the Framingham Study.

Authors:  R H Myers; D K Kiely; L A Cupples; W B Kannel
Journal:  Am Heart J       Date:  1990-10       Impact factor: 4.749

6.  The joint impact of family history of myocardial infarction and other risk factors on 12-year coronary heart disease mortality.

Authors:  J M Boer; E J Feskens; W M Verschuren; J C Seidell; D Kromhout
Journal:  Epidemiology       Date:  1999-11       Impact factor: 4.822

7.  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

8.  After myocardial infarction carvedilol improves insulin resistance compared to metoprolol.

Authors:  Okcan Basat; Sema Ucak; Selcuk Seber; Erkan Oztekin; Yuksel Altuntas
Journal:  Clin Res Cardiol       Date:  2006-02-06       Impact factor: 5.460

9.  Prevalence, awareness and treatment of hypercholesterolaemia in 32 populations: results from the WHO MONICA Project.

Authors:  Hanna Tolonen; Ulrich Keil; Marco Ferrario; Alun Evans
Journal:  Int J Epidemiol       Date:  2005-02       Impact factor: 7.196

10.  Genetic susceptibility to death from coronary heart disease in a study of twins.

Authors:  M E Marenberg; N Risch; L F Berkman; B Floderus; U de Faire
Journal:  N Engl J Med       Date:  1994-04-14       Impact factor: 91.245

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  37 in total

Review 1.  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

2.  Major depression and coronary artery disease in the Swedish twin registry: phenotypic, genetic, and environmental sources of comorbidity.

Authors:  Kenneth S Kendler; Charles O Gardner; Amy Fiske; Margaret Gatz
Journal:  Arch Gen Psychiatry       Date:  2009-08

Review 3.  Molecular signatures of cardiovascular disease risk: potential for test development and clinical application.

Authors:  Heribert Schunkert; Inke R König; Jeanette Erdmann
Journal:  Mol Diagn Ther       Date:  2008       Impact factor: 4.074

4.  Association between microRNA polymorphisms and coronary heart disease : A meta-analysis.

Authors:  X Xie; X Shi; X Xun; L Rao
Journal:  Herz       Date:  2016-11-10       Impact factor: 1.443

5.  Correlation between genetic polymorphisms within the MAPK1/HIF-1/HO-1 signaling pathway and risk or prognosis of perimenopausal coronary artery disease.

Authors:  Nan Guo; Nan Zhang; Liqiu Yan; Xufen Cao; Jiawang Wang; Yunfei Wang
Journal:  Clin Cardiol       Date:  2017-04-26       Impact factor: 2.882

Review 6.  The enigma of genetics etiology of atherosclerosis in the post-GWAS era.

Authors:  A J Marian
Journal:  Curr Atheroscler Rep       Date:  2012-08       Impact factor: 5.113

Review 7.  Genetics of coronary artery disease and myocardial infarction--2013.

Authors:  Thorsten Kessler; Jeanette Erdmann; Heribert Schunkert
Journal:  Curr Cardiol Rep       Date:  2013-06       Impact factor: 2.931

8.  Incidence of coronary artery disease in siblings of patients with premature coronary artery disease: 10 years of follow-up.

Authors:  Dhananjay Vaidya; Lisa R Yanek; Taryn F Moy; Thomas A Pearson; Lewis C Becker; Diane M Becker
Journal:  Am J Cardiol       Date:  2007-08-16       Impact factor: 2.778

9.  Analyses of C-Reactive Protein, Endothelial Nitric Oxide Synthase and Interleukin-6 Gene Polymorphisms in Adolescents with a Family History of Premature Coronary Artery Disease: A Pilot Study.

Authors:  Ataç Çelik; Mustafa Özçetin; Ömer Ateş; Fatih Altunkaş; Kayıhan Karaman; İlker Akar; İlker İnce; Murat Yalçın; Metin Karayakalı; Köksal Ceyhan; Fatih Koç
Journal:  Balkan Med J       Date:  2015-10-01       Impact factor: 2.021

10.  A novel stop mutation truncating critical regions of the cardiac transcription factor NKX2-5 in a large family with autosomal-dominant inherited congenital heart disease.

Authors:  S Pabst; B Wollnik; E Rohmann; Y Hintz; K Glänzer; H Vetter; G Nickenig; C Grohé
Journal:  Clin Res Cardiol       Date:  2007-09-25       Impact factor: 5.460

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