Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
1998-1-22
pubmed:abstractText
The biological role of the very low density lipoprotein receptor (VLDL-R) in humans is not yet elucidated. This cellular receptor binds apolipoprotein E (apoE)-containing lipoparticles and is mainly expressed in peripheral tissues. The VLDL-R gene contains a polymorphic triplet (CGG) repeat located 19 bp upstream of the initiation codon. We explored the allelic distribution of this repeat in 1384 subjects of European Caucasian origin, 609 of them surviving a myocardial infarction. Six alleles corresponding to 5, 6, 7, 8, 9, and 11 repeats were detected in this population. The alleles 5, 8, and 9 were the most frequent, with frequencies of 0.413, 0.275, and 0.292, respectively. No association was found between the VLDL-R polymorphism and myocardial infarction. In controls without lipid lowering treatment, a statistically significant interaction between VLDL-R genotype and apoE phenotype was found for plasma triglycerides (P < .04), suggesting a gene-gene interaction. There was also a main effect of the VLDL-R polymorphism on LpE:B and LpA-I. The VLDL-R 9 allele was associated with lower levels of plasma LpE:B (P < .05) and higher concentrations of plasma LpA-I (P < .01) than the other alleles. These results suggest that VLDL-R has a modest influence on circulating lipoproteins in humans.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1079-5642
pubmed:author
pubmed:issnType
Print
pubmed:volume
17
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2759-64
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:9409253-Adult, pubmed-meshheading:9409253-Alleles, pubmed-meshheading:9409253-Apolipoproteins E, pubmed-meshheading:9409253-Asian Continental Ancestry Group, pubmed-meshheading:9409253-Body Mass Index, pubmed-meshheading:9409253-Comorbidity, pubmed-meshheading:9409253-Europe, pubmed-meshheading:9409253-European Continental Ancestry Group, pubmed-meshheading:9409253-Gene Frequency, pubmed-meshheading:9409253-Genetic Variation, pubmed-meshheading:9409253-Genotype, pubmed-meshheading:9409253-Humans, pubmed-meshheading:9409253-Hyperlipidemias, pubmed-meshheading:9409253-Hypolipidemic Agents, pubmed-meshheading:9409253-Japan, pubmed-meshheading:9409253-Lipids, pubmed-meshheading:9409253-Lipoproteins, pubmed-meshheading:9409253-Male, pubmed-meshheading:9409253-Middle Aged, pubmed-meshheading:9409253-Myocardial Infarction, pubmed-meshheading:9409253-Obesity, pubmed-meshheading:9409253-Phenotype, pubmed-meshheading:9409253-Receptors, LDL, pubmed-meshheading:9409253-Retrospective Studies, pubmed-meshheading:9409253-Survivors, pubmed-meshheading:9409253-Trinucleotide Repeats, pubmed-meshheading:9409253-United States
pubmed:year
1997
pubmed:articleTitle
The role of a triplet repeat sequence of the very low density lipoprotein receptor gene in plasma lipid and lipoprotein level variability in humans.
pubmed:affiliation
Service d'Epidémiologie et de Santé Publique-INSERM CJF 95-05, Institut Pasteur de Lille, France.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't, Multicenter Study