Effect of Microsomal Triglyceride Transfer Protein gene variants (-493G > T, Q95H and H297Q) on plasma lipid levels in healthy middle-aged UK men.
ANN HUM GENET
269 - 276.
Microsomal triglyceride transfer protein (MTP) plays a central role in the synthesis of lipoproteins by shuttling lipids between phospholipid membranes to apoB. We have examined the effect of three MTP gene variants, -493G > T, Q95H and H297Q, in 2831 healthy UK middle-aged men. The rare allele frequencies were: 0.25 (95 % CI 0.24-0.26) for -493T, 0.054 (95 % CI 0.05-0.06) for 95H and 0.32 (95 % CI 0.31-0.33) for 297Q. The three variants were in strong allelic association in all pairwise combinations (p < 0.001). None of the variant sites were associated with significant differences in cholesterol, triglyceride, apoB or apoAI levels. When stratified by tertiles of triglycerides for the H297Q variant alone there was a significant effect on apoB levels in men in the top tertile (p = 0.01). Considering the -493G > T and H297Q genotype in combination on baseline levels, individuals with three or four rare alleles had 6.6% higher mean apoB levels compared to the rest (p = 0.007). Therefore, homozygosity for 297Q at higher triglyceride (Tg) levels, or in combination with -493G: > T, is associated with a. raising effect on apoB levels, suggesting the importance of modest differences in MTP activity in determining hepatic secretion of lipoproteins in healthy men.
|Title:||Effect of Microsomal Triglyceride Transfer Protein gene variants (-493G > T, Q95H and H297Q) on plasma lipid levels in healthy middle-aged UK men|
|Keywords:||B-CONTAINING LIPOPROTEINS, APOLIPOPROTEIN-B, FAMILIAL HYPERCHOLESTEROLEMIA, HEPG2 CELLS, ABETALIPOPROTEINEMIA, PHENOTYPE, SECRETION, DISEASE, POLYMORPHISM, METABOLISM|
|UCL classification:||UCL > School of Life and Medical Sciences
UCL > School of Life and Medical Sciences > Faculty of Population Health Sciences > Institute of Cardiovascular Science
UCL > School of Life and Medical Sciences > Faculty of Population Health Sciences > Institute of Cardiovascular Science > Centre for Cardiovascular Genetics
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