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Relationship between CETP gene polymorphisms with coronary artery disease in Polish population
The cholesteryl ester transfer protein (CETP) gene encodes a hydrophobic glycoprotein that plays a crucial role in the reverse transport of cholesterol. The aim of the present study was to determine whether CETP polymorphisms (rs1532624, rs247616 and rs708272) are associated with coronary artery dis...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6267260/ https://www.ncbi.nlm.nih.gov/pubmed/30178218 http://dx.doi.org/10.1007/s11033-018-4342-1 |
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author | Iwanicka, Joanna Iwanicki, Tomasz Niemiec, Paweł Balcerzyk, Anna Krauze, Jolanta Górczyńska-Kosiorz, Sylwia Ochalska-Tyka, Anna Grzeszczak, Władysław Żak, Iwona |
author_facet | Iwanicka, Joanna Iwanicki, Tomasz Niemiec, Paweł Balcerzyk, Anna Krauze, Jolanta Górczyńska-Kosiorz, Sylwia Ochalska-Tyka, Anna Grzeszczak, Władysław Żak, Iwona |
author_sort | Iwanicka, Joanna |
collection | PubMed |
description | The cholesteryl ester transfer protein (CETP) gene encodes a hydrophobic glycoprotein that plays a crucial role in the reverse transport of cholesterol. The aim of the present study was to determine whether CETP polymorphisms (rs1532624, rs247616 and rs708272) are associated with coronary artery disease (CAD) in a Polish population. Serum lipid levels and single nucleotide polymorphisms of CETP genes were determined in 494 subjects: 248 patients with premature CAD and 246 blood donors as controls. Selected polymorphisms were examined using TaqMan PCR analysis. We found that CAD risk was significantly higher for CC homozygotes and C allele carriers of the rs247616 polymorphism than for carriers with the T allele (OR 1.89, 95% CI 1.29–2.76, p = 0.001 and OR 1.51, 95% CI 1.14–1.99, p = 0.003) and likewise for the CC genotype of the rs1532624 polymorphism than for those with the A allele (OR 1.59, 95% CI 1.05–2.40, p = 0.026). Moreover, T allele carriers of the rs708272 polymorphism had significantly higher total cholesterol levels compared to CC homozygotes (p < 0.05) in the healthy controls. We also observed an allelic pattern, C((rs2477616))C((rs708272))C((rs1532624),) which increased susceptibility to CAD by 43% (OR = 1.43, 95% CI 1.10–1.85, p = 0.006). In conclusion, the rs247616 and rs1532624 polymorphisms of CETP may modulate the risk of CAD in Polish population. |
format | Online Article Text |
id | pubmed-6267260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-62672602018-12-11 Relationship between CETP gene polymorphisms with coronary artery disease in Polish population Iwanicka, Joanna Iwanicki, Tomasz Niemiec, Paweł Balcerzyk, Anna Krauze, Jolanta Górczyńska-Kosiorz, Sylwia Ochalska-Tyka, Anna Grzeszczak, Władysław Żak, Iwona Mol Biol Rep Original Article The cholesteryl ester transfer protein (CETP) gene encodes a hydrophobic glycoprotein that plays a crucial role in the reverse transport of cholesterol. The aim of the present study was to determine whether CETP polymorphisms (rs1532624, rs247616 and rs708272) are associated with coronary artery disease (CAD) in a Polish population. Serum lipid levels and single nucleotide polymorphisms of CETP genes were determined in 494 subjects: 248 patients with premature CAD and 246 blood donors as controls. Selected polymorphisms were examined using TaqMan PCR analysis. We found that CAD risk was significantly higher for CC homozygotes and C allele carriers of the rs247616 polymorphism than for carriers with the T allele (OR 1.89, 95% CI 1.29–2.76, p = 0.001 and OR 1.51, 95% CI 1.14–1.99, p = 0.003) and likewise for the CC genotype of the rs1532624 polymorphism than for those with the A allele (OR 1.59, 95% CI 1.05–2.40, p = 0.026). Moreover, T allele carriers of the rs708272 polymorphism had significantly higher total cholesterol levels compared to CC homozygotes (p < 0.05) in the healthy controls. We also observed an allelic pattern, C((rs2477616))C((rs708272))C((rs1532624),) which increased susceptibility to CAD by 43% (OR = 1.43, 95% CI 1.10–1.85, p = 0.006). In conclusion, the rs247616 and rs1532624 polymorphisms of CETP may modulate the risk of CAD in Polish population. Springer Netherlands 2018-09-03 2018 /pmc/articles/PMC6267260/ /pubmed/30178218 http://dx.doi.org/10.1007/s11033-018-4342-1 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Iwanicka, Joanna Iwanicki, Tomasz Niemiec, Paweł Balcerzyk, Anna Krauze, Jolanta Górczyńska-Kosiorz, Sylwia Ochalska-Tyka, Anna Grzeszczak, Władysław Żak, Iwona Relationship between CETP gene polymorphisms with coronary artery disease in Polish population |
title | Relationship between CETP gene polymorphisms with coronary artery disease in Polish population |
title_full | Relationship between CETP gene polymorphisms with coronary artery disease in Polish population |
title_fullStr | Relationship between CETP gene polymorphisms with coronary artery disease in Polish population |
title_full_unstemmed | Relationship between CETP gene polymorphisms with coronary artery disease in Polish population |
title_short | Relationship between CETP gene polymorphisms with coronary artery disease in Polish population |
title_sort | relationship between cetp gene polymorphisms with coronary artery disease in polish population |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6267260/ https://www.ncbi.nlm.nih.gov/pubmed/30178218 http://dx.doi.org/10.1007/s11033-018-4342-1 |
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