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Age-and sex-dependent mRNA expression of KCNQ1 and HERG in patients with long QT syndrome type 1 and 2

INTRODUCTION: The main goal of this study was to examine the patient age and sex dependent expression of KCNQ1 and HERG genes that encode potassium channels responsible for the occurrence of long QT syndrome (LQTS). MATERIAL AND METHODS: The study enrolled 43 families whose members suffered from LQT...

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Autores principales: Moric-Janiszewska, Ewa, Głogowska-Ligus, Joanna, Paul-Samojedny, Monika, Węglarz, Ludmiła, Markiewicz-Łoskot, Grażyna, Szydłowski, Lesław
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3264984/
https://www.ncbi.nlm.nih.gov/pubmed/22328875
http://dx.doi.org/10.5114/aoms.2011.26604
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author Moric-Janiszewska, Ewa
Głogowska-Ligus, Joanna
Paul-Samojedny, Monika
Węglarz, Ludmiła
Markiewicz-Łoskot, Grażyna
Szydłowski, Lesław
author_facet Moric-Janiszewska, Ewa
Głogowska-Ligus, Joanna
Paul-Samojedny, Monika
Węglarz, Ludmiła
Markiewicz-Łoskot, Grażyna
Szydłowski, Lesław
author_sort Moric-Janiszewska, Ewa
collection PubMed
description INTRODUCTION: The main goal of this study was to examine the patient age and sex dependent expression of KCNQ1 and HERG genes that encode potassium channels responsible for the occurrence of long QT syndrome (LQTS). MATERIAL AND METHODS: The study enrolled 43 families whose members suffered from LQTS type 1 (LQTS1) or 2 (LQTS2) or were healthy. The study attempted to prove that β-actin is a good endogenous control when determining the expression of the studied genes. Examination of gene expression was achieved with quantitative real-time PCR (QRT-PCR). Expression of the investigated genes was inferred from the analysis of the number of mRNA copies per 1 μg total RNA isolated from whole blood. RESULTS: Significantly lower KCNQ1 and KCNH2 mRNA levels in healthy females than healthy males were observed (p = 0.032; p = 0.02). In male patients both transcripts were expressed at a lower level (p = 0.0084; p = 0.035). The comparison of transcriptional activity of KCNQ1 and KCNH2 in healthy adults and children revealed higher KCNQ1 and lower KCNH2 mRNA levels in healthy adults (p = 0.033; p = 0.04), higher KCNQ1 and lower KCNH2 mRNA levels in adult patients below 55 years old than in adults over 55 years old (p=0.036; p = 0.044), and significantly higher KCNQ1 and lower KCNH2 mRNA levels in adult patients (over 55 years) than in paediatric patients (below 15 years) (p=0.047; p = 0.08). CONCLUSIONS: The results support the hypothesis that KCNQ1 and HERG gene expression is influenced by age and gender in human patients with long QT syndrome and in healthy subjects.
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spelling pubmed-32649842012-02-10 Age-and sex-dependent mRNA expression of KCNQ1 and HERG in patients with long QT syndrome type 1 and 2 Moric-Janiszewska, Ewa Głogowska-Ligus, Joanna Paul-Samojedny, Monika Węglarz, Ludmiła Markiewicz-Łoskot, Grażyna Szydłowski, Lesław Arch Med Sci Basic Research INTRODUCTION: The main goal of this study was to examine the patient age and sex dependent expression of KCNQ1 and HERG genes that encode potassium channels responsible for the occurrence of long QT syndrome (LQTS). MATERIAL AND METHODS: The study enrolled 43 families whose members suffered from LQTS type 1 (LQTS1) or 2 (LQTS2) or were healthy. The study attempted to prove that β-actin is a good endogenous control when determining the expression of the studied genes. Examination of gene expression was achieved with quantitative real-time PCR (QRT-PCR). Expression of the investigated genes was inferred from the analysis of the number of mRNA copies per 1 μg total RNA isolated from whole blood. RESULTS: Significantly lower KCNQ1 and KCNH2 mRNA levels in healthy females than healthy males were observed (p = 0.032; p = 0.02). In male patients both transcripts were expressed at a lower level (p = 0.0084; p = 0.035). The comparison of transcriptional activity of KCNQ1 and KCNH2 in healthy adults and children revealed higher KCNQ1 and lower KCNH2 mRNA levels in healthy adults (p = 0.033; p = 0.04), higher KCNQ1 and lower KCNH2 mRNA levels in adult patients below 55 years old than in adults over 55 years old (p=0.036; p = 0.044), and significantly higher KCNQ1 and lower KCNH2 mRNA levels in adult patients (over 55 years) than in paediatric patients (below 15 years) (p=0.047; p = 0.08). CONCLUSIONS: The results support the hypothesis that KCNQ1 and HERG gene expression is influenced by age and gender in human patients with long QT syndrome and in healthy subjects. Termedia Publishing House 2011-12-30 2011-12-31 /pmc/articles/PMC3264984/ /pubmed/22328875 http://dx.doi.org/10.5114/aoms.2011.26604 Text en Copyright © 2011 Termedia & Banach http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Basic Research
Moric-Janiszewska, Ewa
Głogowska-Ligus, Joanna
Paul-Samojedny, Monika
Węglarz, Ludmiła
Markiewicz-Łoskot, Grażyna
Szydłowski, Lesław
Age-and sex-dependent mRNA expression of KCNQ1 and HERG in patients with long QT syndrome type 1 and 2
title Age-and sex-dependent mRNA expression of KCNQ1 and HERG in patients with long QT syndrome type 1 and 2
title_full Age-and sex-dependent mRNA expression of KCNQ1 and HERG in patients with long QT syndrome type 1 and 2
title_fullStr Age-and sex-dependent mRNA expression of KCNQ1 and HERG in patients with long QT syndrome type 1 and 2
title_full_unstemmed Age-and sex-dependent mRNA expression of KCNQ1 and HERG in patients with long QT syndrome type 1 and 2
title_short Age-and sex-dependent mRNA expression of KCNQ1 and HERG in patients with long QT syndrome type 1 and 2
title_sort age-and sex-dependent mrna expression of kcnq1 and herg in patients with long qt syndrome type 1 and 2
topic Basic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3264984/
https://www.ncbi.nlm.nih.gov/pubmed/22328875
http://dx.doi.org/10.5114/aoms.2011.26604
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