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Association between HaeIII polymorphism of scavenger receptor class B type I gene and plasma HDL-cholesterol concentration.

Authors :
Seung Ho Hong
Young-Ree Kim
Yeo Min Yoon
Won Ki Min
Sa Il Chun
Kim, Jin Q.
Source :
Annals of Clinical Biochemistry; Sep2002, Vol. 39 Issue 5, p478-481, 4p, 2 Charts
Publication Year :
2002

Abstract

Background: Evidence has recently been found for significant associations between genetic variation within the scavenger receptor class B type I gene (SR-BI), plasma lipids and anthropometric measurements in healthy Caucasians. The present case-control study was conducted to determine whether there is an association between three polymorphisms identified by the restriction endonucleases HaeIII, AluI and ApaI of SR-BI and coronary artery disease (CAD) in Korean subjects. Methods: DNA was extracted from 137 subjects with CAD and 124 age-matched controls; it was amplified using the polymerase chain reaction. Individual alleles at each of the three polymorphic sites were identified by digestion with the appropriate restriction enzyme. Results: Only a single allele was identified at the AluI and ApaI polymorphic sites. The frequency of the common (+) allele at the HaeIII polymorphic site was higher in CAD patients than in the controls (P = 0·001). The concentrations of plasma HDL-cholesterol and apolipoprotein AI also varied significantly among HaeIII genotypes in the CAD patients. The common (+) allele of the HaeIII polymorphism was associated with a lower body mass index in female controls. Conclusions: Allele frequencies of the AluI and ApaI polymorphisms in this study were different to those in a Caucasian population studied previously, suggesting a difference in the genetic background. Further comparative studies of SR-BI polymorphism in other racial or ethnic groups should therefore prove to be of value. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00045632
Volume :
39
Issue :
5
Database :
Complementary Index
Journal :
Annals of Clinical Biochemistry
Publication Type :
Academic Journal
Accession number :
22630605
Full Text :
https://doi.org/10.1258/000456302320314485