Literature DB >> 11398140

Association between the TaqIB polymorphism in the cholesteryl ester transfer protein gene locus and plasma lipoprotein levels in familial hypercholesterolemia.

R Carmena-Ramón1, J F Ascaso, J T Real, G Nájera, J M Ordovás, R Carmena.   

Abstract

Cholesteryl ester transfer protein (CETP) facilitates the exchange of triglycerides (TG) and cholesteryl ester between lipoprotein particles. Subjects with familial hypercholesterolemia (FH) have been reported to have higher CETP activities, which could contribute to the lower high-density lipoprotein-cholesterol (HDL-C) levels and increased cardiovascular risk observed in some of these patients. Several polymorphisms have been reported in the CETP locus; the common TaqlB polymorphism is associated, in normolipidemic subjects, with decreased CETP activity and levels and with increased HDL-C levels. No data is available on the influence of this polymorphism in FH subjects. We have examined the TaqIB polymorphism in a group of 101 FH heterozygotes from Valencia, Spain. We have observed a frequency of 0.43 for the B2 allele, similar to those reported in the general population. Based on analysis of variance (ANOVA), we found significant associations between the presence of the B2 allele and increased plasma HDL-C (P <.04) and apolipoprotein A-I (apoA-I) levels (P <.01). An opposite association was observed for low-density lipoprotein-cholesterol (LDL-C) levels, with the B2/B2 subjects having lower levels than B1/B1 and B1/B2 subjects. The plasma apoB levels followed the same trend as those for LDL-C. In addition, the response to a National Cholesterol Education Program (NCEP)-I diet was studied in 77 of these subjects. The TaqlB polymorphism did not have a significant effect over the individual dietary response for any of the variables examined, as demonstrated by the lack of significant gene by diet interactions. In summary, the CETP TaqlB polymorphism is associated with a less atherogenic lipid profile, consisting of lower LDL-C, higher HDL-C levels, and a lower LDL-C/HDL-C ratio in heterozygous FH subjects. Moreover, the B2 allele was associated with a lower appearance of arcus cornealis, xanthomata, and clinical arteriosclerotic disease in these subjects. Copyright 2001 by W.B. Saunders Company

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Year:  2001        PMID: 11398140     DOI: 10.1053/meta.2001.23289

Source DB:  PubMed          Journal:  Metabolism        ISSN: 0026-0495            Impact factor:   8.694


  4 in total

1.  Familial hypercholesterolaemia.

Authors:  A David Marais
Journal:  Clin Biochem Rev       Date:  2004-02

2.  Gene-environment interactions of CETP gene variation in a high cardiovascular risk Mediterranean population.

Authors:  Dolores Corella; Paula Carrasco; Montserrat Fitó; Miguel Angel Martínez-González; Jordi Salas-Salvadó; Fernando Arós; José Lapetra; Marisa Guillén; Carolina Ortega-Azorín; Julia Warnberg; Miquel Fiol; Valentina Ruiz-Gutierrez; Lluís Serra-Majem; J Alfredo Martínez; Emilio Ros; Ramón Estruch
Journal:  J Lipid Res       Date:  2010-06-25       Impact factor: 5.922

3.  CETP genotype and changes in lipid levels in response to weight-loss diet intervention in the POUNDS LOST and DIRECT randomized trials.

Authors:  Qibin Qi; Ronen Durst; Dan Schwarzfuchs; Eran Leitersdorf; Shoshi Shpitzen; Yanping Li; Hongyu Wu; Catherine M Champagne; Frank B Hu; Meir J Stampfer; George A Bray; Frank M Sacks; Iris Shai; Lu Qi
Journal:  J Lipid Res       Date:  2014-12-29       Impact factor: 5.922

4.  Cholesterol ester transfer protein (CETP) gene polymorphism and selected parameters of lipid metabolism in children from families with history of cardiovascular system diseases.

Authors:  Elżbieta Pac-Kożuchowska; Paulina Krawiec
Journal:  Med Sci Monit       Date:  2013-10-04
  4 in total

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