Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
18
pubmed:dateCreated
2008-8-27
pubmed:abstractText
Recent genome-wide association (GWA) studies have identified new genetic determinants of complex quantitative traits, including plasma triglyceride (TG). We hypothesized that common variants associated with mild TG variation identified in GWA studies would also be associated with severe hypertriglyceridemia (HTG). We studied 132 patients of European ancestry with severe HTG (fasting plasma TG > 10 mmol/l), who had no mutations found by resequencing of candidate genes, and 351 matched normolipidemic controls. We determined genotypes for: GALNT2 rs4846914, TBL2/MLXIPL rs17145738, TRIB1 rs17321515, ANGPTL3 rs12130333, GCKR rs780094, APOA5 rs3135506 (S19W), APOA5 rs662799 (-1131T > C), APOE (isoforms) and LPL rs328 (S447X). We found that: (i) genotypes, including those of APOA5 S19W, APOA5 -1131T > C, APOE, GCKR, TRIB1 and TBL2/MLXIPL, were significantly associated with severe HTG; (ii) odds ratios for these genetic variables were significant in both univariate and multivariate regression analyses, irrespective of the presence or absence of diabetes or obesity; (iii) a significant fraction-about one-quarter-of the explained variation in disease status was associated with these genotypes. Therefore, common SNPs (single nucleotide polymorphisms) that are associated with mild TG variation in GWA studies of normolipidemic subjects are also associated with severe HTG. Our findings are consistent with the emerging model of a complex genetic trait. At the extremes of a quantitative trait, such as severe HTG, are found the cumulative contributions of both multiple rare alleles with large genetic effects and common alleles with small effects.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Adaptor Proteins, Signal Transducing, http://linkedlifedata.com/resource/pubmed/chemical/Apolipoproteins, http://linkedlifedata.com/resource/pubmed/chemical/GCKR protein, human, http://linkedlifedata.com/resource/pubmed/chemical/GTP-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Intracellular Signaling Peptides..., http://linkedlifedata.com/resource/pubmed/chemical/N-Acetylgalactosaminyltransferases, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/TBL2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/TRIB1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Triglycerides, http://linkedlifedata.com/resource/pubmed/chemical/polypeptide...
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1460-2083
pubmed:author
pubmed:issnType
Electronic
pubmed:day
15
pubmed:volume
17
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2894-9
pubmed:meshHeading
pubmed-meshheading:18596051-Adaptor Proteins, Signal Transducing, pubmed-meshheading:18596051-Adult, pubmed-meshheading:18596051-Apolipoproteins, pubmed-meshheading:18596051-Case-Control Studies, pubmed-meshheading:18596051-European Continental Ancestry Group, pubmed-meshheading:18596051-Female, pubmed-meshheading:18596051-GTP-Binding Proteins, pubmed-meshheading:18596051-Genetic Predisposition to Disease, pubmed-meshheading:18596051-Genotype, pubmed-meshheading:18596051-Humans, pubmed-meshheading:18596051-Hypertriglyceridemia, pubmed-meshheading:18596051-Intracellular Signaling Peptides and Proteins, pubmed-meshheading:18596051-Male, pubmed-meshheading:18596051-Middle Aged, pubmed-meshheading:18596051-Multifactorial Inheritance, pubmed-meshheading:18596051-Multivariate Analysis, pubmed-meshheading:18596051-N-Acetylgalactosaminyltransferases, pubmed-meshheading:18596051-Protein-Serine-Threonine Kinases, pubmed-meshheading:18596051-Triglycerides
pubmed:year
2008
pubmed:articleTitle
Polygenic determinants of severe hypertriglyceridemia.
pubmed:affiliation
Vascular Biology Research Group 2 Clinical Trials Group, Robarts Research Institute and Schulich School of Medicine and Dentistry, University of Western Ontario, London, Ontario, Canada.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't