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Health status in patients at risk of inherited arrhythmias and sudden unexpected death compared to the general population

BACKGROUND: The possibilities in the molecular genetics of long QT syndrome (LQTS) and hypertrophic cardiomyopathy (HCM) has made family screening, with diagnostic and predictive genetic testing part of the health care offer in genetic counselling of inherited arrhythmias, potentially affecting the...

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Autores principales: Hamang, Anniken, Eide, Geir Egil, Nordin, Karin, Rokne, Berit, Bjorvatn, Cathrine, Øyen, Nina
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2836315/
https://www.ncbi.nlm.nih.gov/pubmed/20163700
http://dx.doi.org/10.1186/1471-2350-11-27
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author Hamang, Anniken
Eide, Geir Egil
Nordin, Karin
Rokne, Berit
Bjorvatn, Cathrine
Øyen, Nina
author_facet Hamang, Anniken
Eide, Geir Egil
Nordin, Karin
Rokne, Berit
Bjorvatn, Cathrine
Øyen, Nina
author_sort Hamang, Anniken
collection PubMed
description BACKGROUND: The possibilities in the molecular genetics of long QT syndrome (LQTS) and hypertrophic cardiomyopathy (HCM) has made family screening, with diagnostic and predictive genetic testing part of the health care offer in genetic counselling of inherited arrhythmias, potentially affecting the subjective health among these individuals. The study compared health status among patients at risk of arrhythmia because of family history or clinical diagnosis of LQTS and HCM with reference health status scores of the general population. METHODS: In the period 2005-2007, 127 patients (mean age 45 years, 53.5% women), with a family history of arrhythmia (n = 95) or a clinical diagnosis of LQTS (n = 12) or HCM (n = 19) referred for genetic counselling at the medical genetic departments in Norway filled in a questionnaire (Short Form Health Survey SF-36) measuring health status on eight domains. The patient SF-36 scores were compared to expected scores of the general population by t-test, and the relationship between the socio-demographic variables, clinical status, and SF-36 domains were analysed by multiple linear regression. RESULTS: The total sample reported significant lower SF-36 score as compared to the general population scores for the domain of general health (mean difference -7.3 (<0.001). When analysing the sample in subgroups according to clinical status, the general health was still significant lower for the group of family risk and in the group of HCM. In addition the physical functioning, role physical, vitality and role emotional domains were reduced for the latter group. In general, employment, higher education and being referred to genetic counselling through a family member were associated with better scores on the health status domains. CONCLUSIONS: Having a genetic risk of arrhythmia affects general health significantly. In addition, patients with a clinical diagnosis of HCM demonstrate a significantly poorer health in both physical and mental domains.
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spelling pubmed-28363152010-03-11 Health status in patients at risk of inherited arrhythmias and sudden unexpected death compared to the general population Hamang, Anniken Eide, Geir Egil Nordin, Karin Rokne, Berit Bjorvatn, Cathrine Øyen, Nina BMC Med Genet Research Article BACKGROUND: The possibilities in the molecular genetics of long QT syndrome (LQTS) and hypertrophic cardiomyopathy (HCM) has made family screening, with diagnostic and predictive genetic testing part of the health care offer in genetic counselling of inherited arrhythmias, potentially affecting the subjective health among these individuals. The study compared health status among patients at risk of arrhythmia because of family history or clinical diagnosis of LQTS and HCM with reference health status scores of the general population. METHODS: In the period 2005-2007, 127 patients (mean age 45 years, 53.5% women), with a family history of arrhythmia (n = 95) or a clinical diagnosis of LQTS (n = 12) or HCM (n = 19) referred for genetic counselling at the medical genetic departments in Norway filled in a questionnaire (Short Form Health Survey SF-36) measuring health status on eight domains. The patient SF-36 scores were compared to expected scores of the general population by t-test, and the relationship between the socio-demographic variables, clinical status, and SF-36 domains were analysed by multiple linear regression. RESULTS: The total sample reported significant lower SF-36 score as compared to the general population scores for the domain of general health (mean difference -7.3 (<0.001). When analysing the sample in subgroups according to clinical status, the general health was still significant lower for the group of family risk and in the group of HCM. In addition the physical functioning, role physical, vitality and role emotional domains were reduced for the latter group. In general, employment, higher education and being referred to genetic counselling through a family member were associated with better scores on the health status domains. CONCLUSIONS: Having a genetic risk of arrhythmia affects general health significantly. In addition, patients with a clinical diagnosis of HCM demonstrate a significantly poorer health in both physical and mental domains. BioMed Central 2010-02-17 /pmc/articles/PMC2836315/ /pubmed/20163700 http://dx.doi.org/10.1186/1471-2350-11-27 Text en Copyright ©2010 Hamang 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 Research Article
Hamang, Anniken
Eide, Geir Egil
Nordin, Karin
Rokne, Berit
Bjorvatn, Cathrine
Øyen, Nina
Health status in patients at risk of inherited arrhythmias and sudden unexpected death compared to the general population
title Health status in patients at risk of inherited arrhythmias and sudden unexpected death compared to the general population
title_full Health status in patients at risk of inherited arrhythmias and sudden unexpected death compared to the general population
title_fullStr Health status in patients at risk of inherited arrhythmias and sudden unexpected death compared to the general population
title_full_unstemmed Health status in patients at risk of inherited arrhythmias and sudden unexpected death compared to the general population
title_short Health status in patients at risk of inherited arrhythmias and sudden unexpected death compared to the general population
title_sort health status in patients at risk of inherited arrhythmias and sudden unexpected death compared to the general population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2836315/
https://www.ncbi.nlm.nih.gov/pubmed/20163700
http://dx.doi.org/10.1186/1471-2350-11-27
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