Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
19
pubmed:dateCreated
2003-9-16
pubmed:abstractText
The apolipoprotein A5 gene (APOA5 ) has been shown to play an important role in determining plasma triglyceride concentrations in humans. We describe here a novel variant, c.553G>T, in the apolipoprotein A5 gene that is associated with hypertriglyceridemia. In contrast to some other polymorphisms, which occur in non-coding regions of the gene, this variant occurs within the coding region and causes the change of amino acid sequence (a substitution of a cysteine for a glycine residue). The minor allele frequencies were 0.042 and 0.27 (P<0.001) for control and hypertriglyceridemic patients, respectively. The serum triglyceride level was significantly different among the genotypic groups (G/G 92.5+/-37.8 mg/dl, G/T 106.6+/-34.8 mg/dl, T/T 183.0 mg/dl, P=0.014) in control subjects. Multiple logistic regression revealed individuals carrying the minor allele had age, gender and BMI (body mass index)-adjusted odds ratio of 11.73 (95% confidence interval of 6.617-20.793; P<0.0001) for developing hypertriglyceridemia in comparison to individuals without that allele. These findings suggest the possible use of c.553G>T polymorphisms in APOA5 as prognostic indicators for hypertriglyceridemia susceptibility in Chinese.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0964-6906
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
12
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2533-9
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:12915450-Age Factors, pubmed-meshheading:12915450-Amino Acid Substitution, pubmed-meshheading:12915450-Apolipoproteins A, pubmed-meshheading:12915450-Asian Continental Ancestry Group, pubmed-meshheading:12915450-Body Mass Index, pubmed-meshheading:12915450-Cholesterol, pubmed-meshheading:12915450-Cholesterol, HDL, pubmed-meshheading:12915450-Cholesterol, LDL, pubmed-meshheading:12915450-Female, pubmed-meshheading:12915450-Gene Frequency, pubmed-meshheading:12915450-Genetic Predisposition to Disease, pubmed-meshheading:12915450-Genetic Variation, pubmed-meshheading:12915450-Glycine, pubmed-meshheading:12915450-Haplotypes, pubmed-meshheading:12915450-Humans, pubmed-meshheading:12915450-Hypertriglyceridemia, pubmed-meshheading:12915450-Linkage Disequilibrium, pubmed-meshheading:12915450-Logistic Models, pubmed-meshheading:12915450-Male, pubmed-meshheading:12915450-Odds Ratio, pubmed-meshheading:12915450-Polymorphism, Genetic, pubmed-meshheading:12915450-Sex Ratio
pubmed:year
2003
pubmed:articleTitle
A novel genetic variant in the apolipoprotein A5 gene is associated with hypertriglyceridemia.
pubmed:affiliation
School and Graduate Institute of Medical Technology, College of Medicine, and Department of Laboratory Medicine, University Hospital, National Taiwan University, No. 7, Chung-Shan S. Rd, Taipei, 100 Taiwan. jtkao@ha.mc.ntu.edu.tw
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't