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KCNQ1 gene polymorphisms are associated with lipid parameters in a Chinese Han population

BACKGROUND: Four single nucleotide polymorphisms (SNPs) (rs2237892, rs2237895, rs2237897, and rs2283228) in KCNQ1 are reported to be associated with type 2 diabetes mellitus (T2DM), possibly caused by a reduction in insulin secretion and higher fasting glucose, but the results are inconsistent. We i...

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Autores principales: Chen, Zhong, Yin, Quanzhong, Ma, Genshan, Qian, Qi
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2925337/
https://www.ncbi.nlm.nih.gov/pubmed/20701788
http://dx.doi.org/10.1186/1475-2840-9-35
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author Chen, Zhong
Yin, Quanzhong
Ma, Genshan
Qian, Qi
author_facet Chen, Zhong
Yin, Quanzhong
Ma, Genshan
Qian, Qi
author_sort Chen, Zhong
collection PubMed
description BACKGROUND: Four single nucleotide polymorphisms (SNPs) (rs2237892, rs2237895, rs2237897, and rs2283228) in KCNQ1 are reported to be associated with type 2 diabetes mellitus (T2DM), possibly caused by a reduction in insulin secretion and higher fasting glucose, but the results are inconsistent. We investigated whether these 4 genetic markers are associated with serum lipid metabolism in a middle-aged Chinese Han population. METHODS: We enrolled 398 consecutive patients, including 180 with premature coronary artery disease (CAD) (male < 55 years, female < 65 years) and 218 controls without documented CAD. All subjects were genotyped for 4 SNPs by using the ligase detection reaction method. Fasting blood sugar (FBS) and plasma concentrations of total cholesterol, triglycerides (TG), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), apolipoprotein A1(apo A1), and apolipoprotein B (apo B) were determined by standard biochemical methods. Main anthropometric and metabolic characteristics are analyzed among 3 genotypes at rs2283228, rs2237895, rs2237897, or rs2237892 in KCNQ1. RESULTS: The 3 genotypes AA, AC, and CC were present in rs2283228 and rs2237895, and the 3 genotypes CC, CT, and TT were present in rs2237897 and rs2237892. The minor genotypes CC at rs2283228 and TT at rs2237892 were associated with higher levels of TG (P = 0.007 and 0.026, respectively). Furthermore, subjects with the CC genotype at rs2283228 had lower levels of HDL-C and apo A1 than in the other 2 genotype groups (P = 0.052 and 0.055, respectively). No other associations were detected between these 4 SNPs and FBS or other lipid parameters. CONCLUSIONS: Our data suggest that rs2283228 and rs2237892 in KCNQ1 are associated with lipid metabolism in a middle-aged Chinese Han population.
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spelling pubmed-29253372010-08-24 KCNQ1 gene polymorphisms are associated with lipid parameters in a Chinese Han population Chen, Zhong Yin, Quanzhong Ma, Genshan Qian, Qi Cardiovasc Diabetol Original Investigation BACKGROUND: Four single nucleotide polymorphisms (SNPs) (rs2237892, rs2237895, rs2237897, and rs2283228) in KCNQ1 are reported to be associated with type 2 diabetes mellitus (T2DM), possibly caused by a reduction in insulin secretion and higher fasting glucose, but the results are inconsistent. We investigated whether these 4 genetic markers are associated with serum lipid metabolism in a middle-aged Chinese Han population. METHODS: We enrolled 398 consecutive patients, including 180 with premature coronary artery disease (CAD) (male < 55 years, female < 65 years) and 218 controls without documented CAD. All subjects were genotyped for 4 SNPs by using the ligase detection reaction method. Fasting blood sugar (FBS) and plasma concentrations of total cholesterol, triglycerides (TG), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), apolipoprotein A1(apo A1), and apolipoprotein B (apo B) were determined by standard biochemical methods. Main anthropometric and metabolic characteristics are analyzed among 3 genotypes at rs2283228, rs2237895, rs2237897, or rs2237892 in KCNQ1. RESULTS: The 3 genotypes AA, AC, and CC were present in rs2283228 and rs2237895, and the 3 genotypes CC, CT, and TT were present in rs2237897 and rs2237892. The minor genotypes CC at rs2283228 and TT at rs2237892 were associated with higher levels of TG (P = 0.007 and 0.026, respectively). Furthermore, subjects with the CC genotype at rs2283228 had lower levels of HDL-C and apo A1 than in the other 2 genotype groups (P = 0.052 and 0.055, respectively). No other associations were detected between these 4 SNPs and FBS or other lipid parameters. CONCLUSIONS: Our data suggest that rs2283228 and rs2237892 in KCNQ1 are associated with lipid metabolism in a middle-aged Chinese Han population. BioMed Central 2010-08-11 /pmc/articles/PMC2925337/ /pubmed/20701788 http://dx.doi.org/10.1186/1475-2840-9-35 Text en Copyright ©2010 Chen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Investigation
Chen, Zhong
Yin, Quanzhong
Ma, Genshan
Qian, Qi
KCNQ1 gene polymorphisms are associated with lipid parameters in a Chinese Han population
title KCNQ1 gene polymorphisms are associated with lipid parameters in a Chinese Han population
title_full KCNQ1 gene polymorphisms are associated with lipid parameters in a Chinese Han population
title_fullStr KCNQ1 gene polymorphisms are associated with lipid parameters in a Chinese Han population
title_full_unstemmed KCNQ1 gene polymorphisms are associated with lipid parameters in a Chinese Han population
title_short KCNQ1 gene polymorphisms are associated with lipid parameters in a Chinese Han population
title_sort kcnq1 gene polymorphisms are associated with lipid parameters in a chinese han population
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2925337/
https://www.ncbi.nlm.nih.gov/pubmed/20701788
http://dx.doi.org/10.1186/1475-2840-9-35
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