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Cholesteryl Ester Transfer Protein Gene Polymorphisms and Longevity Syndrome
PURPOSE: High levels of high density lipoprotein (HDL) cholesterol are associated with a decreased risk of coronary heart disease (CHD). Subjects with high levels of HDL cholesterol (>70 mg/dl; 1.79 mmol/l) as well as high levels of low density lipoprotein (LDL) cholesterol, could represent a gro...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Bentham Open
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2831192/ https://www.ncbi.nlm.nih.gov/pubmed/20200605 http://dx.doi.org/10.2174/1874192401004010014 |
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author | Kolovou, Genovefa Stamatelatou, Marianna Anagnostopoulou, Katherine Kostakou, Peggy Kolovou, Vana Mihas, Constantinos Vasiliadis, Ioannis Diakoumakou, Olga Mikhailidis, Dimitri P Cokkinos, Dennis V |
author_facet | Kolovou, Genovefa Stamatelatou, Marianna Anagnostopoulou, Katherine Kostakou, Peggy Kolovou, Vana Mihas, Constantinos Vasiliadis, Ioannis Diakoumakou, Olga Mikhailidis, Dimitri P Cokkinos, Dennis V |
author_sort | Kolovou, Genovefa |
collection | PubMed |
description | PURPOSE: High levels of high density lipoprotein (HDL) cholesterol are associated with a decreased risk of coronary heart disease (CHD). Subjects with high levels of HDL cholesterol (>70 mg/dl; 1.79 mmol/l) as well as high levels of low density lipoprotein (LDL) cholesterol, could represent a group with longevity syndrome (LS). Since HDL particles are influenced by cholesteryl ester transfer protein (CETP) activity, it is worth studying the CETP polymorphism. The aim of the study was to detect whether 2 genetic variants of the CETP are associated with the LS. SUBJECTS AND METHODS: The study population consisted of 136 unrelated men and women with no personal and family history of CHD; 69 met the criteria for LS and 67 did not meet these criteria and had “normal” HDL cholesterol (>40 and <70 mg/dl; >1.03 and <1.79 mmol/l). All patients were genotyped for the TaqIB and I405V polymorphisms. RESULTS: The B2 allele frequency of TaqIB polymorphism was higher in the LS in comparison with the non-LS group (p=0.03) whereas B1 allele frequency was higher in the non-LS group (p=0.03). CONCLUSIONS: Gene polymorphisms could help decide whether individuals who have increased levels of both LDL cholesterol and HDL cholesterol require treatment. Some of the prerequisites could include that subjects with LS should not only have very high levels of HDL cholesterol but also favorable gene polymorphisms. However, further investigations with a larger sample and including other gene polymorphisms, are needed. |
format | Text |
id | pubmed-2831192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Bentham Open |
record_format | MEDLINE/PubMed |
spelling | pubmed-28311922010-03-03 Cholesteryl Ester Transfer Protein Gene Polymorphisms and Longevity Syndrome Kolovou, Genovefa Stamatelatou, Marianna Anagnostopoulou, Katherine Kostakou, Peggy Kolovou, Vana Mihas, Constantinos Vasiliadis, Ioannis Diakoumakou, Olga Mikhailidis, Dimitri P Cokkinos, Dennis V Open Cardiovasc Med J Article PURPOSE: High levels of high density lipoprotein (HDL) cholesterol are associated with a decreased risk of coronary heart disease (CHD). Subjects with high levels of HDL cholesterol (>70 mg/dl; 1.79 mmol/l) as well as high levels of low density lipoprotein (LDL) cholesterol, could represent a group with longevity syndrome (LS). Since HDL particles are influenced by cholesteryl ester transfer protein (CETP) activity, it is worth studying the CETP polymorphism. The aim of the study was to detect whether 2 genetic variants of the CETP are associated with the LS. SUBJECTS AND METHODS: The study population consisted of 136 unrelated men and women with no personal and family history of CHD; 69 met the criteria for LS and 67 did not meet these criteria and had “normal” HDL cholesterol (>40 and <70 mg/dl; >1.03 and <1.79 mmol/l). All patients were genotyped for the TaqIB and I405V polymorphisms. RESULTS: The B2 allele frequency of TaqIB polymorphism was higher in the LS in comparison with the non-LS group (p=0.03) whereas B1 allele frequency was higher in the non-LS group (p=0.03). CONCLUSIONS: Gene polymorphisms could help decide whether individuals who have increased levels of both LDL cholesterol and HDL cholesterol require treatment. Some of the prerequisites could include that subjects with LS should not only have very high levels of HDL cholesterol but also favorable gene polymorphisms. However, further investigations with a larger sample and including other gene polymorphisms, are needed. Bentham Open 2010-01-29 /pmc/articles/PMC2831192/ /pubmed/20200605 http://dx.doi.org/10.2174/1874192401004010014 Text en © Kolovou et al.; Licensee Bentham Open. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Article Kolovou, Genovefa Stamatelatou, Marianna Anagnostopoulou, Katherine Kostakou, Peggy Kolovou, Vana Mihas, Constantinos Vasiliadis, Ioannis Diakoumakou, Olga Mikhailidis, Dimitri P Cokkinos, Dennis V Cholesteryl Ester Transfer Protein Gene Polymorphisms and Longevity Syndrome |
title | Cholesteryl Ester Transfer Protein Gene Polymorphisms and Longevity Syndrome |
title_full | Cholesteryl Ester Transfer Protein Gene Polymorphisms and Longevity Syndrome |
title_fullStr | Cholesteryl Ester Transfer Protein Gene Polymorphisms and Longevity Syndrome |
title_full_unstemmed | Cholesteryl Ester Transfer Protein Gene Polymorphisms and Longevity Syndrome |
title_short | Cholesteryl Ester Transfer Protein Gene Polymorphisms and Longevity Syndrome |
title_sort | cholesteryl ester transfer protein gene polymorphisms and longevity syndrome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2831192/ https://www.ncbi.nlm.nih.gov/pubmed/20200605 http://dx.doi.org/10.2174/1874192401004010014 |
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