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Published on: March 12, 2013
KCNQ1 Polymorphism in the Context of Ischemic Cardiomyopathy: A Potential Key to Decision-Making for Device
Uğur Özkan1, Metin Budak2, Muhammet Gürdoğan1
1Department of Cardiology, School of Medicine, Trakya University, Turkey.
Insights
Specific KCNQ1 gene variations (rs2237892 and rs2237895) are linked to ventricular tachyarrhythmia (VTA) in ischemic cardiomyopathy (ICM) patients. These genetic markers may aid in predicting VTA risk and guiding implantable cardioverter-defibrillator (ICD) decisions.
Area of Science:
- Cardiovascular Genetics
- Electrophysiology
- Molecular Cardiology
Background:
- Ventricular tachyarrhythmia (VTA) poses a significant risk in ischemic cardiomyopathy (ICM).
- Genetic factors and electrical remodeling are key influences on VTA development in ICM.
- Accurate risk stratification is crucial for managing VTA and guiding device implantation.
Purpose of the Study:
- To investigate the association between KCNQ1 gene polymorphisms (rs2237892 and rs2237895) and VTA in ICM patients.
- To evaluate the potential of these polymorphisms as biomarkers for VTA risk stratification.
- To inform decisions regarding implantable cardioverter-defibrillator (ICD) implantation in ICM patients.
Main Methods:
- A single-center study involving 213 ICM patients with ICDs for primary VTA prevention.
- Genetic analysis of KCNQ1 polymorphisms (rs2237892, rs2237895) using real-time PCR.
- Correlation and logistic regression analyses to assess the association between genotypes and VTA risk.
Main Results:
- Patients with VTA showed significantly higher QT dispersion, frontal QRS-T angle, and T-wave peak-to-end interval.
- The TT genotype of rs2237892 and AC genotype of rs2237895 were significantly associated with increased VTA risk (p < 0.001).
- These KCNQ1 genotypes were confirmed as independent predictors of VTA in multivariate analysis.
Conclusions:
- KCNQ1 gene polymorphisms rs2237892 and rs2237895 are strongly associated with VTA in ICM.
- These polymorphisms may serve as valuable biomarkers for VTA risk stratification in ICM patients.
- Findings can help personalize ICD implantation strategies and improve patient outcomes.
Background:
Ventricular tachyarrhythmia (VTA) in ischemic cardiomyopathy (ICM) is a life-threatening condition influenced by genetic factors and electrical remodeling. This study investigated the association between KCNQ1 gene polymorphisms (rs2237892 and rs2237895) and the development of VTA in ICM patients to improve risk stratification and guide device implantation decisions.
Methods:
This single-center study included 213 ICM patients with implantable cardioverter-defibrillators (ICD) for primary prevention of VTA. Patients were divided into arrhythmia and control groups based on device interrogation findings. Genetic analysis for rs2237892 and rs2237895 polymorphisms was performed using real-time polymerase chain reaction (PCR). Clinical, electrocardiographic, and laboratory parameters were analyzed. Correlation and logistic regression analyses evaluated the association between KCNQ1 polymorphisms and VTA risk.
Results:
The arrhythmia group demonstrated significantly higher QT dispersion, frontal QRS-T angle, and T-wave peak-to-end interval compared to the control group. The TT genotype of rs2237892 and the AC genotype of rs2237895 were significantly associated with increased VTA risk (p < 0.001). Multivariate analysis confirmed these genotypes as independent predictors of VTA. No significant differences in other clinical or laboratory risk factors were observed.
Conclusions:
KCNQ1 gene polymorphisms (rs2237892 and rs2237895) are strongly associated with VTA in ICM patients, suggesting a potential role as biomarkers for risk stratification. These findings may assist in tailoring ICD implantation decisions and improving patient outcomes.
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