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Predisposition of functional genetic variants of A-kinase anchoring protein 10 toward acquired repolarization disorders in high-risk vascular surgery patients

PURPOSE: We aimed at assessing the predisposition of A-kinase anchoring protein 10 (AKAP10) polymorphism toward acquired repolarization disorders in high-risk vascular surgery patients. PATIENTS AND METHODS: One hundred adult patients (age =44–85 years), scheduled for an elective high-risk “open” va...

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Autores principales: Biernawska, Jowita, Solek-Pastuszka, Joanna, Kazimierczak, Arkadiusz, Safranow, Krzysztof, Kaczmarczyk, Mariusz, Zegan-Baranska, Malgorzata, Zukowski, Maciej, Kotfis, Katarzyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6067797/
https://www.ncbi.nlm.nih.gov/pubmed/30100729
http://dx.doi.org/10.2147/TCRM.S167086
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author Biernawska, Jowita
Solek-Pastuszka, Joanna
Kazimierczak, Arkadiusz
Safranow, Krzysztof
Kaczmarczyk, Mariusz
Zegan-Baranska, Malgorzata
Zukowski, Maciej
Kotfis, Katarzyna
author_facet Biernawska, Jowita
Solek-Pastuszka, Joanna
Kazimierczak, Arkadiusz
Safranow, Krzysztof
Kaczmarczyk, Mariusz
Zegan-Baranska, Malgorzata
Zukowski, Maciej
Kotfis, Katarzyna
author_sort Biernawska, Jowita
collection PubMed
description PURPOSE: We aimed at assessing the predisposition of A-kinase anchoring protein 10 (AKAP10) polymorphism toward acquired repolarization disorders in high-risk vascular surgery patients. PATIENTS AND METHODS: One hundred adult patients (age =44–85 years), scheduled for an elective high-risk “open” vascular surgery procedure, were recruited. The electrocardiogram Holter monitor was used to assess repolarization stability from the beginning of the operation up to 24 hours afterward. The AKAP10 gene rs203462 polymorphism and cardiac complications were analyzed. RESULTS: Repolarization disturbances defined as QT interval duration corrected for heart rate (QTc) interval prolongation >500 ms and QTc interval dispersion >65 ms were recorded in 46 patients. A model of multivariate logistic regression showed that only the presence of allele G of the AKAP10 polymorphism was an independent risk factor for repolarization disturbances in the perioperative period (odds ratio =14.35; 95% CI =4.65–44.23; p<0.0001). CONCLUSION: When the acquired QTc interval prolongation or QTc dispersion is associated with AKAP10 polymorphism, it may remain clinically silent.
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spelling pubmed-60677972018-08-10 Predisposition of functional genetic variants of A-kinase anchoring protein 10 toward acquired repolarization disorders in high-risk vascular surgery patients Biernawska, Jowita Solek-Pastuszka, Joanna Kazimierczak, Arkadiusz Safranow, Krzysztof Kaczmarczyk, Mariusz Zegan-Baranska, Malgorzata Zukowski, Maciej Kotfis, Katarzyna Ther Clin Risk Manag Original Research PURPOSE: We aimed at assessing the predisposition of A-kinase anchoring protein 10 (AKAP10) polymorphism toward acquired repolarization disorders in high-risk vascular surgery patients. PATIENTS AND METHODS: One hundred adult patients (age =44–85 years), scheduled for an elective high-risk “open” vascular surgery procedure, were recruited. The electrocardiogram Holter monitor was used to assess repolarization stability from the beginning of the operation up to 24 hours afterward. The AKAP10 gene rs203462 polymorphism and cardiac complications were analyzed. RESULTS: Repolarization disturbances defined as QT interval duration corrected for heart rate (QTc) interval prolongation >500 ms and QTc interval dispersion >65 ms were recorded in 46 patients. A model of multivariate logistic regression showed that only the presence of allele G of the AKAP10 polymorphism was an independent risk factor for repolarization disturbances in the perioperative period (odds ratio =14.35; 95% CI =4.65–44.23; p<0.0001). CONCLUSION: When the acquired QTc interval prolongation or QTc dispersion is associated with AKAP10 polymorphism, it may remain clinically silent. Dove Medical Press 2018-07-26 /pmc/articles/PMC6067797/ /pubmed/30100729 http://dx.doi.org/10.2147/TCRM.S167086 Text en © 2018 Biernawska et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Biernawska, Jowita
Solek-Pastuszka, Joanna
Kazimierczak, Arkadiusz
Safranow, Krzysztof
Kaczmarczyk, Mariusz
Zegan-Baranska, Malgorzata
Zukowski, Maciej
Kotfis, Katarzyna
Predisposition of functional genetic variants of A-kinase anchoring protein 10 toward acquired repolarization disorders in high-risk vascular surgery patients
title Predisposition of functional genetic variants of A-kinase anchoring protein 10 toward acquired repolarization disorders in high-risk vascular surgery patients
title_full Predisposition of functional genetic variants of A-kinase anchoring protein 10 toward acquired repolarization disorders in high-risk vascular surgery patients
title_fullStr Predisposition of functional genetic variants of A-kinase anchoring protein 10 toward acquired repolarization disorders in high-risk vascular surgery patients
title_full_unstemmed Predisposition of functional genetic variants of A-kinase anchoring protein 10 toward acquired repolarization disorders in high-risk vascular surgery patients
title_short Predisposition of functional genetic variants of A-kinase anchoring protein 10 toward acquired repolarization disorders in high-risk vascular surgery patients
title_sort predisposition of functional genetic variants of a-kinase anchoring protein 10 toward acquired repolarization disorders in high-risk vascular surgery patients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6067797/
https://www.ncbi.nlm.nih.gov/pubmed/30100729
http://dx.doi.org/10.2147/TCRM.S167086
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