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The influence of the polymorphism in apolipoprotein B codon 2488 on insulin and lipid levels in a Danish twin population
Author(s) -
Bentzen J.,
Poulsen P.,
Vaag A.,
BeckNielsen H.,
Fenger M.
Publication year - 2002
Publication title -
diabetic medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.474
H-Index - 145
eISSN - 1464-5491
pISSN - 0742-3071
DOI - 10.1046/j.0742-3071.2001.00602.x
Subject(s) - endocrinology , medicine , insulin resistance , triglyceride , insulin , genotype , apolipoprotein b , allele , type 2 diabetes , population , genetics , cholesterol , diabetes mellitus , biology , gene , environmental health
Aims The apolipoprotein B codon 2488 polymorphism has been associated with the metabolism of lipoproteins in subjects with Type 2 diabetes. However, no data are available on the influence of the polymorphism on insulin or glucose metabolism. This study examines the impact of the polymorphism on parameters associated with the insulin resistance syndrome in Danish twins. Methods The effect of the polymorphism on lipid, glucose and insulin measures was studied in 548 same sex twins aged 55–74 years. Results The codon 2488 polymorphism influenced fasting triglyceride levels, as well as insulin, as measured at 120 min in an oral glucose tolerance test. Subjects with the genotype T2488T had 14% higher triglyceride levels ( P = 0.02) and 31% higher insulin levels ( P = 0.004) than subjects with genotype C2488C. In twins discordant for genotype, the T‐allele was associated with higher levels of triglyceride ( P = 0.04) and insulin ( P = 0.02) and lower levels of HDL‐cholesterol ( P = 0.04). Conclusion The T‐allele of the codon 2488 polymorphism influenced parameters related to the insulin resistance syndrome, i.e. increased levels of insulin, increased levels of triglyceride and decreased levels of HDL. As the polymorphism is silent, these effects must be mediated through linkage to other polymorphisms in apolipoprotein B or other genes on chromosome 2.