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Interaction Effects of Lipoprotein Lipase Polymorphisms with Lifestyle on Lipid Levels in a Korean Population: A Cross-sectional Study

Lipoprotein lipase (LPL) plays an essential role in the regulation of high-density lipoprotein cholesterol (HDLC) and triglyceride levels, which have been closely associated with cardiovascular diseases. Genetic studies in European have shown that LPL single-nucleotide polymorphisms (SNPs) are stron...

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Autores principales: Pyun, Jung-A, Kim, Sunshin, Park, KyungChae, Baik, Inkyung, Cho, Nam H, Koh, InSong, Lee, Jong-Young, Cho, Yoon Shin, Kim, Young Jin, Go, Min Jin, Shim, Eugene, Kwack, KyuBum, Shin, Chol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korea Genome Organization 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3480683/
https://www.ncbi.nlm.nih.gov/pubmed/23105935
http://dx.doi.org/10.5808/GI.2012.10.2.88
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author Pyun, Jung-A
Kim, Sunshin
Park, KyungChae
Baik, Inkyung
Cho, Nam H
Koh, InSong
Lee, Jong-Young
Cho, Yoon Shin
Kim, Young Jin
Go, Min Jin
Shim, Eugene
Kwack, KyuBum
Shin, Chol
author_facet Pyun, Jung-A
Kim, Sunshin
Park, KyungChae
Baik, Inkyung
Cho, Nam H
Koh, InSong
Lee, Jong-Young
Cho, Yoon Shin
Kim, Young Jin
Go, Min Jin
Shim, Eugene
Kwack, KyuBum
Shin, Chol
author_sort Pyun, Jung-A
collection PubMed
description Lipoprotein lipase (LPL) plays an essential role in the regulation of high-density lipoprotein cholesterol (HDLC) and triglyceride levels, which have been closely associated with cardiovascular diseases. Genetic studies in European have shown that LPL single-nucleotide polymorphisms (SNPs) are strongly associated with lipid levels. However, studies about the influence of interactions between LPL SNPs and lifestyle factors have not been sufficiently performed. Here, we examine if LPL polymorphisms, as well as their interaction with lifestyle factors, influence lipid concentrations in a Korean population. A two-stage association study was performed using genotype data for SNPs on the LPL gene, including the 3' flanking region from 7,536 (stage 1) and 3,703 (stage 2) individuals. The association study showed that 15 SNPs and 4 haplotypes were strongly associated with HDLC (lowest p = 2.86 × 10(-22)) and triglyceride levels (lowest p = 3.0 × 10(-15)). Interactions between LPL polymorphisms and lifestyle factors (lowest p = 9.6 × 10(-4)) were also observed on lipid concentrations. These findings suggest that there are interaction effects of LPL polymorphisms with lifestyle variables, including energy intake, fat intake, smoking, and alcohol consumption, as well as effects of LPL polymorphisms themselves, on lipid concentrations in a Korean population.
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spelling pubmed-34806832012-10-26 Interaction Effects of Lipoprotein Lipase Polymorphisms with Lifestyle on Lipid Levels in a Korean Population: A Cross-sectional Study Pyun, Jung-A Kim, Sunshin Park, KyungChae Baik, Inkyung Cho, Nam H Koh, InSong Lee, Jong-Young Cho, Yoon Shin Kim, Young Jin Go, Min Jin Shim, Eugene Kwack, KyuBum Shin, Chol Genomics Inf Article Lipoprotein lipase (LPL) plays an essential role in the regulation of high-density lipoprotein cholesterol (HDLC) and triglyceride levels, which have been closely associated with cardiovascular diseases. Genetic studies in European have shown that LPL single-nucleotide polymorphisms (SNPs) are strongly associated with lipid levels. However, studies about the influence of interactions between LPL SNPs and lifestyle factors have not been sufficiently performed. Here, we examine if LPL polymorphisms, as well as their interaction with lifestyle factors, influence lipid concentrations in a Korean population. A two-stage association study was performed using genotype data for SNPs on the LPL gene, including the 3' flanking region from 7,536 (stage 1) and 3,703 (stage 2) individuals. The association study showed that 15 SNPs and 4 haplotypes were strongly associated with HDLC (lowest p = 2.86 × 10(-22)) and triglyceride levels (lowest p = 3.0 × 10(-15)). Interactions between LPL polymorphisms and lifestyle factors (lowest p = 9.6 × 10(-4)) were also observed on lipid concentrations. These findings suggest that there are interaction effects of LPL polymorphisms with lifestyle variables, including energy intake, fat intake, smoking, and alcohol consumption, as well as effects of LPL polymorphisms themselves, on lipid concentrations in a Korean population. Korea Genome Organization 2012-06 2012-06-30 /pmc/articles/PMC3480683/ /pubmed/23105935 http://dx.doi.org/10.5808/GI.2012.10.2.88 Text en Copyright © 2012 by The Korea Genome Organization http://creativecommons.org/licenses/by-nc/3.0 It is identical to the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/).
spellingShingle Article
Pyun, Jung-A
Kim, Sunshin
Park, KyungChae
Baik, Inkyung
Cho, Nam H
Koh, InSong
Lee, Jong-Young
Cho, Yoon Shin
Kim, Young Jin
Go, Min Jin
Shim, Eugene
Kwack, KyuBum
Shin, Chol
Interaction Effects of Lipoprotein Lipase Polymorphisms with Lifestyle on Lipid Levels in a Korean Population: A Cross-sectional Study
title Interaction Effects of Lipoprotein Lipase Polymorphisms with Lifestyle on Lipid Levels in a Korean Population: A Cross-sectional Study
title_full Interaction Effects of Lipoprotein Lipase Polymorphisms with Lifestyle on Lipid Levels in a Korean Population: A Cross-sectional Study
title_fullStr Interaction Effects of Lipoprotein Lipase Polymorphisms with Lifestyle on Lipid Levels in a Korean Population: A Cross-sectional Study
title_full_unstemmed Interaction Effects of Lipoprotein Lipase Polymorphisms with Lifestyle on Lipid Levels in a Korean Population: A Cross-sectional Study
title_short Interaction Effects of Lipoprotein Lipase Polymorphisms with Lifestyle on Lipid Levels in a Korean Population: A Cross-sectional Study
title_sort interaction effects of lipoprotein lipase polymorphisms with lifestyle on lipid levels in a korean population: a cross-sectional study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3480683/
https://www.ncbi.nlm.nih.gov/pubmed/23105935
http://dx.doi.org/10.5808/GI.2012.10.2.88
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