Document Detail


Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction.
MedLine Citation:
PMID:  18592168     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Coronary artery disease (CAD) and myocardial infarction (MI) have a genetic basis, but the precise genetic underpinning remains controversial. Recently, an association of the LRP8 R952Q polymorphism (rs5174) with familial premature CAD/MI was reported. We analysed rs5174 (or the perfect proxy rs5177) in 1,210 patients with familial MI and 1,015 controls from the German MI Family study, in 1,926 familial CAD (1,377 with MI) patients and 2,938 controls from the Wellcome Trust Case Control Consortium (WTCCC) MI/CAD cohort, in 346 CAD patients and 351 controls from the AtheroGene study and in 295 men with incident CAD and 301 controls from the Prospective Epidemiological Study of MI study and found no evidence for association in any of the populations studied. In the WTCCC and the German MI Family studies, additional single-nucleotide polymorphisms in the LRP8 gene were analysed and displayed no evidence for association either.
Authors:
Wolfgang Lieb; Tanja Zeller; Massimo Mangino; Anika Götz; Peter Braund; Juergen J Wenzel; Christian Horn; Carole Proust; Patrick Linsel-Nitschke; Philippe Amouyel; Petra Bruse; Dominique Arveiler; Inke R König; Jean Ferrières; Andreas Ziegler; Anthony J Balmforth; Alun Evans; Pierre Ducimetière; Francois Cambien; Christian Hengstenberg; Klaus Stark; Alistair S Hall; Heribert Schunkert; Stefan Blankenberg; Nilesh J Samani; Jeanette Erdmann; Laurence Tiret
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2008-07-01
Journal Detail:
Title:  Journal of molecular medicine (Berlin, Germany)     Volume:  86     ISSN:  0946-2716     ISO Abbreviation:  J. Mol. Med.     Publication Date:  2008 Oct 
Date Detail:
Created Date:  2008-09-23     Completed Date:  2009-03-31     Revised Date:  2011-07-08    
Medline Journal Info:
Nlm Unique ID:  9504370     Medline TA:  J Mol Med (Berl)     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  1163-70     Citation Subset:  IM    
Affiliation:
Medizinische Klinik II, Universität zu Lübeck, Ratzeburger Allee 160, 23538 Lübeck, Germany.
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MeSH Terms
Descriptor/Qualifier:
Coronary Artery Disease / genetics*
Family Health
Female
Gene Frequency
Genetic Predisposition to Disease / genetics
Genotype
Germany
Humans
Male
Middle Aged
Myocardial Infarction / genetics*
Polymorphism, Single Nucleotide*
Receptors, Lipoprotein / genetics*
Grant Support
ID/Acronym/Agency:
//British Heart Foundation
Chemical
Reg. No./Substance:
0/Receptors, Lipoprotein; 0/low density lipoprotein receptor-related protein 8

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