| Literature DB >> 3113537 |
R C Trembath, D J Thomas, T J Hendra, J S Yudkin, D J Galton.
Abstract
The prevalence of an uncommon allelic variant (S2) of the apoprotein AI-CIII-AIV gene cluster was determined in non-insulin-dependent diabetics with or without evidence of coronary heart disease and in controls. Frequencies of the S2 allele were 14% for diabetics with coronary heart disease compared with 2% for non-diabetics with no clinical evidence of occlusive vascular disease. No subject with the S2 allele was detected among a further group of matched diabetics without clinical features of macrovascular disease. The results suggest that a genetic component contributes to the susceptibility to coronary heart disease in non-insulin-dependent diabetics. Whether the observed deoxyribonucleic acid variant is aetiological for atherosclerosis or in linkage disequilibrium with other atherogenic loci on chromosome 11 remains to be clarified.Entities:
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Year: 1987 PMID: 3113537 PMCID: PMC1246727 DOI: 10.1136/bmj.294.6587.1577
Source DB: PubMed Journal: Br Med J (Clin Res Ed) ISSN: 0267-0623