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Endothelin Type A Receptor Genotype is a Determinant of Quantitative Traits of Metabolic Syndrome in Asian Hypertensive Families: A SAPPHIRe Study
Co-heritability of hypertension and insulin resistance (IR) within families not only implies genetic susceptibility may be responsible for these complex traits but also suggests a rational that biological candidate genes for hypertension may serve as markers for features of the metabolic syndrome (M...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842518/ https://www.ncbi.nlm.nih.gov/pubmed/24348460 http://dx.doi.org/10.3389/fendo.2013.00172 |
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author | Ho, Low-Tone Hsu, Yung-Pei Hsiao, Chin-Fu Ting, Chih-Tai Shih, Kuang-Chung Chuang, Lee-Ming Masaki, Kamal Grove, John Quertermous, Thomas Juan, Chi-Chung Lin, Ming-Wei Chiang, Shu-Chiung Chen, Yii-Der I. |
author_facet | Ho, Low-Tone Hsu, Yung-Pei Hsiao, Chin-Fu Ting, Chih-Tai Shih, Kuang-Chung Chuang, Lee-Ming Masaki, Kamal Grove, John Quertermous, Thomas Juan, Chi-Chung Lin, Ming-Wei Chiang, Shu-Chiung Chen, Yii-Der I. |
author_sort | Ho, Low-Tone |
collection | PubMed |
description | Co-heritability of hypertension and insulin resistance (IR) within families not only implies genetic susceptibility may be responsible for these complex traits but also suggests a rational that biological candidate genes for hypertension may serve as markers for features of the metabolic syndrome (MetS). Thus we determined whether the T323C polymorphism (rs5333) of endothelin type A (ET(A)) receptor, a predominant receptor evoking potent vasoconstrictive action of endothelin-1, contributes to susceptibility to IR-associated hypertension in 1694 subjects of Chinese and Japanese origins. Blood pressures (BPs) and biochemistries were measured. Fasting insulin level, insulin-resistance homeostasis model assessment (HOMA(IR)) score, and area under curve of insulin concentration (AUC(INS)) were selected for assessing insulin sensitivity. Genotypes were obtained by methods of polymerase chain reaction-restriction fragment length polymorphism. Foremost findings were that minor allele frequency of the T323C polymorphism was noticeable lower in our overall Asian subjects compared to multi-national population reported in gene database; moreover both the genotypic and allelic frequencies of the polymorphism were significantly different between the two ethnic groups we studied. The genotype distributions at TT/TC/CC were 65, 31, 4% in Chinese and 51, 41, 8% in Japanese, respectively (p < 0.0001). Additionally, carriers of the C homozygote revealed characteristics of IR, namely significantly higher levels of fasting insulin, HOMA(IR) score, and AUC(INS) at 29.3, 35.3, and 39.3%, respectively, when compared to their counterparts with TT/TC genotypes in Chinese. Meanwhile, the CC genotype was associated with a higher level of high density lipoprotein cholesterol in Japanese. No association of the polymorphism with BP was observed. This study demonstrated for the first time that T323C polymorphism of ET(A) receptor gene was associated with an adverse insulin response in Chinese and a favorite atherogenic index in Japanese. |
format | Online Article Text |
id | pubmed-3842518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-38425182013-12-13 Endothelin Type A Receptor Genotype is a Determinant of Quantitative Traits of Metabolic Syndrome in Asian Hypertensive Families: A SAPPHIRe Study Ho, Low-Tone Hsu, Yung-Pei Hsiao, Chin-Fu Ting, Chih-Tai Shih, Kuang-Chung Chuang, Lee-Ming Masaki, Kamal Grove, John Quertermous, Thomas Juan, Chi-Chung Lin, Ming-Wei Chiang, Shu-Chiung Chen, Yii-Der I. Front Endocrinol (Lausanne) Endocrinology Co-heritability of hypertension and insulin resistance (IR) within families not only implies genetic susceptibility may be responsible for these complex traits but also suggests a rational that biological candidate genes for hypertension may serve as markers for features of the metabolic syndrome (MetS). Thus we determined whether the T323C polymorphism (rs5333) of endothelin type A (ET(A)) receptor, a predominant receptor evoking potent vasoconstrictive action of endothelin-1, contributes to susceptibility to IR-associated hypertension in 1694 subjects of Chinese and Japanese origins. Blood pressures (BPs) and biochemistries were measured. Fasting insulin level, insulin-resistance homeostasis model assessment (HOMA(IR)) score, and area under curve of insulin concentration (AUC(INS)) were selected for assessing insulin sensitivity. Genotypes were obtained by methods of polymerase chain reaction-restriction fragment length polymorphism. Foremost findings were that minor allele frequency of the T323C polymorphism was noticeable lower in our overall Asian subjects compared to multi-national population reported in gene database; moreover both the genotypic and allelic frequencies of the polymorphism were significantly different between the two ethnic groups we studied. The genotype distributions at TT/TC/CC were 65, 31, 4% in Chinese and 51, 41, 8% in Japanese, respectively (p < 0.0001). Additionally, carriers of the C homozygote revealed characteristics of IR, namely significantly higher levels of fasting insulin, HOMA(IR) score, and AUC(INS) at 29.3, 35.3, and 39.3%, respectively, when compared to their counterparts with TT/TC genotypes in Chinese. Meanwhile, the CC genotype was associated with a higher level of high density lipoprotein cholesterol in Japanese. No association of the polymorphism with BP was observed. This study demonstrated for the first time that T323C polymorphism of ET(A) receptor gene was associated with an adverse insulin response in Chinese and a favorite atherogenic index in Japanese. Frontiers Media S.A. 2013-11-28 /pmc/articles/PMC3842518/ /pubmed/24348460 http://dx.doi.org/10.3389/fendo.2013.00172 Text en Copyright © 2013 Ho, Hsu, Hsiao, Ting, Shih, Chuang, Masaki, Grove, Quertermous, Juan, Lin, Chiang and Chen. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Ho, Low-Tone Hsu, Yung-Pei Hsiao, Chin-Fu Ting, Chih-Tai Shih, Kuang-Chung Chuang, Lee-Ming Masaki, Kamal Grove, John Quertermous, Thomas Juan, Chi-Chung Lin, Ming-Wei Chiang, Shu-Chiung Chen, Yii-Der I. Endothelin Type A Receptor Genotype is a Determinant of Quantitative Traits of Metabolic Syndrome in Asian Hypertensive Families: A SAPPHIRe Study |
title | Endothelin Type A Receptor Genotype is a Determinant of Quantitative Traits of Metabolic Syndrome in Asian Hypertensive Families: A SAPPHIRe Study |
title_full | Endothelin Type A Receptor Genotype is a Determinant of Quantitative Traits of Metabolic Syndrome in Asian Hypertensive Families: A SAPPHIRe Study |
title_fullStr | Endothelin Type A Receptor Genotype is a Determinant of Quantitative Traits of Metabolic Syndrome in Asian Hypertensive Families: A SAPPHIRe Study |
title_full_unstemmed | Endothelin Type A Receptor Genotype is a Determinant of Quantitative Traits of Metabolic Syndrome in Asian Hypertensive Families: A SAPPHIRe Study |
title_short | Endothelin Type A Receptor Genotype is a Determinant of Quantitative Traits of Metabolic Syndrome in Asian Hypertensive Families: A SAPPHIRe Study |
title_sort | endothelin type a receptor genotype is a determinant of quantitative traits of metabolic syndrome in asian hypertensive families: a sapphire study |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842518/ https://www.ncbi.nlm.nih.gov/pubmed/24348460 http://dx.doi.org/10.3389/fendo.2013.00172 |
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