Genome-wide linkage scan for loci influencing plasma triglycerides


Autoria(s): Middelberg, Rita P.; Martin, Nicholas G.; Montgomery, Grant W.; Whitfield, John B.
Contribuinte(s)

A. H. Wu

J. Delanghe

Data(s)

01/01/2006

Resumo

Background: Plasma triglyceride concentration is known to be a significant risk factor for cardiovascular disease (CVD). Previous studies have found that the level of triglycerides is strongly influenced by genetic factors. Methods: To identify quantitative trait loci influencing triglycerides, we conducted a genome-wide linkage scan on data from 485 Australian adult dizygotic twin pairs. Prior to linkage analysis, triglyceride values were adjusted for the effects of covariates including age, sex, time since last meal, time of blood collection (CT) and time to plasma separation. Results: The heritability estimate for ln(triglyceride) adjusted for all above fixed effects was 0.49. The highest multipoint LOD score observed was 2.94 (genome-wide p=0.049) on chromosome 7 (at 65cM). This 7p region contains several candidate genes. Two other regions with suggestive multipoint LOD scores were also identified on chromosome 4 (LOD score=2.26 at 62cM) and chromosome X (LOD score=2.01 at 81cM). Conclusions: The linkage peaks found represent newly identified regions for more detailed study, in particular the significant linkage observed on chromosome 7p13. \ (c) 2006 Elsevier B.V. All rights reserved.

Identificador

http://espace.library.uq.edu.au/view/UQ:81591

Idioma(s)

eng

Publicador

Elsevier

Palavras-Chave #Medical Laboratory Technology #Triglycerides #Cardiovascular Disease #Genetics #Quantitative Loci #Genome Scan #Coronary-artery-disease #Tg/hdl-c Ratio #Insulin-resistance #Serum Triglyceride #Mexican-americans #Hdl-cholesterol #Complex Traits #Increased Risk #Twin Families #Lipid Traits #C1 #321011 Medical Genetics #730107 Inherited diseases (incl. gene therapy)
Tipo

Journal Article