Type 2 diabetes associated variants of KCNQ1 strongly confer the risk of cardiovascular disease among the Saudi Arabian population

Abstract Genome-wide association studies have identified several loci associated with an increased risk for cardiovascular disease (CVD) and type 2 diabetes (T2D). Polymorphisms within the KCNQ1 (potassium voltage-gated channel, KQT-like subfamily, member 1) gene are consistently associated with T2D...

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Main Authors: Maha S. Al-Shammari, Rhaya Al-Ali, Nader Al-Balawi, Mansour S. Al-Enazi, Ali A. Al-Muraikhi, Fadi N. Busaleh, Ali S. Al-Sahwan, Abdulmohsen Al-Elq, Awatif N. Al-Nafaie, Jesu Francis Borgio, Sayed AbdulAzeez, Amein Al-Ali, Sadananda Acharya
Format: Article
Language:English
Published: Sociedade Brasileira de Genética 2017-08-01
Series:Genetics and Molecular Biology
Subjects:
T2D
CVD
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572017000400586&lng=en&tlng=en
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spelling doaj-73a9fe912f344490a06bbed236ec32492020-11-25T02:39:27ZengSociedade Brasileira de GenéticaGenetics and Molecular Biology1678-46852017-08-0140358659010.1590/1678-4685-gmb-2017-0005S1415-47572017000400586Type 2 diabetes associated variants of KCNQ1 strongly confer the risk of cardiovascular disease among the Saudi Arabian populationMaha S. Al-ShammariRhaya Al-AliNader Al-BalawiMansour S. Al-EnaziAli A. Al-MuraikhiFadi N. BusalehAli S. Al-SahwanAbdulmohsen Al-ElqAwatif N. Al-NafaieJesu Francis BorgioSayed AbdulAzeezAmein Al-AliSadananda AcharyaAbstract Genome-wide association studies have identified several loci associated with an increased risk for cardiovascular disease (CVD) and type 2 diabetes (T2D). Polymorphisms within the KCNQ1 (potassium voltage-gated channel, KQT-like subfamily, member 1) gene are consistently associated with T2D in a number of populations. The current study was undertaken to evaluate the association of 3 polymorphisms of KCNQ1 (rs2237892, rs151290 and rs2237895) with T2D and/or CVD. Patients diagnosed with either T2D (320 patients), CVD (250 patients) or both (60 patients) and 516 healthy controls were genotyped by TaqMan assay run on a real time PCR thermocycler. A statistically significant association was found for SNPs rs151290 (OR = 1.76; 95%CI = 1.02-3.05; p = 0.0435) and rs2237895 (OR = 2.49; 95%CI = 1.72-3.61; p < 0.0001) with CVD. SNP rs151290 (OR = 7.43; 95%CI = 1.00-55.22; p = 0.0499) showed a strong association in patients with both T2D and CVD. None of the SNPs showed any significant association with T2D. Haploview analysis showed that the ACC (rs151290, rs2237892 and rs2237895) haplotype is the most significant risk allele combination for CVD, while CCA is the most significant risk haplotype for co-morbidity with T2D. KCNQ1 polymorphism at SNPs rs151290 and rs2237895 is strongly associated with CVD in this population, but presented no association with T2D.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572017000400586&lng=en&tlng=enT2DCVDKCNQ1genetic associationSaudi population
collection DOAJ
language English
format Article
sources DOAJ
author Maha S. Al-Shammari
Rhaya Al-Ali
Nader Al-Balawi
Mansour S. Al-Enazi
Ali A. Al-Muraikhi
Fadi N. Busaleh
Ali S. Al-Sahwan
Abdulmohsen Al-Elq
Awatif N. Al-Nafaie
Jesu Francis Borgio
Sayed AbdulAzeez
Amein Al-Ali
Sadananda Acharya
spellingShingle Maha S. Al-Shammari
Rhaya Al-Ali
Nader Al-Balawi
Mansour S. Al-Enazi
Ali A. Al-Muraikhi
Fadi N. Busaleh
Ali S. Al-Sahwan
Abdulmohsen Al-Elq
Awatif N. Al-Nafaie
Jesu Francis Borgio
Sayed AbdulAzeez
Amein Al-Ali
Sadananda Acharya
Type 2 diabetes associated variants of KCNQ1 strongly confer the risk of cardiovascular disease among the Saudi Arabian population
Genetics and Molecular Biology
T2D
CVD
KCNQ1
genetic association
Saudi population
author_facet Maha S. Al-Shammari
Rhaya Al-Ali
Nader Al-Balawi
Mansour S. Al-Enazi
Ali A. Al-Muraikhi
Fadi N. Busaleh
Ali S. Al-Sahwan
Abdulmohsen Al-Elq
Awatif N. Al-Nafaie
Jesu Francis Borgio
Sayed AbdulAzeez
Amein Al-Ali
Sadananda Acharya
author_sort Maha S. Al-Shammari
title Type 2 diabetes associated variants of KCNQ1 strongly confer the risk of cardiovascular disease among the Saudi Arabian population
title_short Type 2 diabetes associated variants of KCNQ1 strongly confer the risk of cardiovascular disease among the Saudi Arabian population
title_full Type 2 diabetes associated variants of KCNQ1 strongly confer the risk of cardiovascular disease among the Saudi Arabian population
title_fullStr Type 2 diabetes associated variants of KCNQ1 strongly confer the risk of cardiovascular disease among the Saudi Arabian population
title_full_unstemmed Type 2 diabetes associated variants of KCNQ1 strongly confer the risk of cardiovascular disease among the Saudi Arabian population
title_sort type 2 diabetes associated variants of kcnq1 strongly confer the risk of cardiovascular disease among the saudi arabian population
publisher Sociedade Brasileira de Genética
series Genetics and Molecular Biology
issn 1678-4685
publishDate 2017-08-01
description Abstract Genome-wide association studies have identified several loci associated with an increased risk for cardiovascular disease (CVD) and type 2 diabetes (T2D). Polymorphisms within the KCNQ1 (potassium voltage-gated channel, KQT-like subfamily, member 1) gene are consistently associated with T2D in a number of populations. The current study was undertaken to evaluate the association of 3 polymorphisms of KCNQ1 (rs2237892, rs151290 and rs2237895) with T2D and/or CVD. Patients diagnosed with either T2D (320 patients), CVD (250 patients) or both (60 patients) and 516 healthy controls were genotyped by TaqMan assay run on a real time PCR thermocycler. A statistically significant association was found for SNPs rs151290 (OR = 1.76; 95%CI = 1.02-3.05; p = 0.0435) and rs2237895 (OR = 2.49; 95%CI = 1.72-3.61; p < 0.0001) with CVD. SNP rs151290 (OR = 7.43; 95%CI = 1.00-55.22; p = 0.0499) showed a strong association in patients with both T2D and CVD. None of the SNPs showed any significant association with T2D. Haploview analysis showed that the ACC (rs151290, rs2237892 and rs2237895) haplotype is the most significant risk allele combination for CVD, while CCA is the most significant risk haplotype for co-morbidity with T2D. KCNQ1 polymorphism at SNPs rs151290 and rs2237895 is strongly associated with CVD in this population, but presented no association with T2D.
topic T2D
CVD
KCNQ1
genetic association
Saudi population
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572017000400586&lng=en&tlng=en
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