8 results on '"Zumhagen, Sven"'
Search Results
2. Sodium permeable and 'hypersensitive' TREK-1 channels cause ventricular tachycardia.
- Author
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Decher, Niels, Ortiz‐Bonnin, Beatriz, Friedrich, Corinna, Schewe, Marcus, Kiper, Aytug K, Rinné, Susanne, Seemann, Gunnar, Peyronnet, Rémi, Zumhagen, Sven, Bustos, Daniel, Kockskämper, Jens, Kohl, Peter, Just, Steffen, González, Wendy, Baukrowitz, Thomas, Stallmeyer, Birgit, and Schulze‐Bahr, Eric
- Abstract
In a patient with right ventricular outflow tract ( RVOT) tachycardia, we identified a heterozygous point mutation in the selectivity filter of the stretch-activated K
2P potassium channel TREK-1 ( KCNK2 or K2P 2.1). This mutation introduces abnormal sodium permeability to TREK-1. In addition, mutant channels exhibit a hypersensitivity to stretch-activation, suggesting that the selectivity filter is directly involved in stretch-induced activation and desensitization. Increased sodium permeability and stretch-sensitivity of mutant TREK-1 channels may trigger arrhythmias in areas of the heart with high physical strain such as the RVOT. We present a pharmacological strategy to rescue the selectivity defect of the TREK-1 pore. Our findings provide important insights for future studies of K2P channel stretch-activation and the role of TREK-1 in mechano-electrical feedback in the heart. [ABSTRACT FROM AUTHOR]- Published
- 2017
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3. Improved Clinical Risk Stratification in Patients with Long QT Syndrome? Novel Insights from Multi-Channel ECGs.
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Samol, Alexander, Gönes, Mehmet, Zumhagen, Sven, Bruns, Hans-Jürgen, Paul, Matthias, Vahlhaus, Christian, Waltenberger, Johannes, Schulze-Bahr, Eric, Eckardt, Lars, and Mönnig, Gerold
- Subjects
HEART disease diagnosis ,HEART diseases ,THERAPEUTICS ,ELECTROCARDIOGRAPHY ,CARDIAC arrest ,BODY surface area ,RECEIVER operating characteristic curves - Abstract
Background: We investigated whether multichannel ECG-recordings are useful to risk-stratify patients with congenital long-QT syndrome (LQTS) for risk of sudden cardiac death under optimized medical treatment. Methods: In 34 LQTS-patients (11 male; age 31±13 years, QTc 478±51ms; LQT1 n = 8, LQT2 n = 15) we performed a standard 12-channel ECG and a 120-channel body surface potential mapping. The occurrence of clinical events (CE; syncope, torsade de pointes (TdP), sudden cardiac arrest (SCA)) was documented and correlated with different ECG-parameters in all lead positions. Results: Seven patients developed TdP, four survived SCA and 12 experienced syncope. 12/34 had at least one CE. CE was associated with a longer QTc-interval (519±43ms vs. 458±42ms; p = 0.001), a lower T-wave integral (TWI) on the left upper chest (-1.2±74.4mV*ms vs. 63.0±29.7mV*ms; p = 0.001), a lower range of T-wave amplitude (TWA) in the region of chest lead V8 (0.10±0.08mV vs. 0.18±0.07mV; p = 0.008) and a longer T-peak-T-end time (TpTe) in lead V1 (98±23ms vs. 78±26ms; p = 0.04). Receiver-operating-characteristic (ROC) analyses revealed a sensitivity of 96% and a specificity of 75% (area under curve (AUC) 0.89±0.06, p = 0.001) at a cut-off value of 26.8mV*ms for prediction of CE by TWI, a sensitivity of 86% and a specificity of 83% at a cut-off value of 0.11mV (AUC 0.83±0.09, p = 0.002) for prediction of CE by TWA and a sensitivity of 83% and a specificity of 73% at a cut-off value of 87ms (AUC 0.80±0.07, p = 0.005) for prediction of CE by TpTe. Conclusions: Occurrence of CE in LQTS-patients seems to be associated with a prolonged, low-amplitude T-wave. [ABSTRACT FROM AUTHOR]
- Published
- 2016
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4. Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2.
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Postema, Pieter G., Koopmann, Tamara T., Kolder, Iris C. R. M., Bezzina, Connie R., Wilde, Arthur A. M., Barc, Julien, Hofman, Nynke, Pfeufer, Arne, Lichtner, Peter, Meitinger, Thomas, Myerburg, Robert J., Bishopric, Nanette H., Roden, Dan M., Tanck, Michael W. T., Schott, Jean-Jacques, Sinner, Moritz F., Beckmann, Britt M., Kääb, Stefan, Zumhagen, Sven, and Husemann, Anja
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LONG QT syndrome ,ION channels ,ARRHYTHMIA ,GENETICS - Abstract
Background--Considerable interest exists in the identification of genetic modifiers of disease severity in the long-QT syndrome (LQTS) as their identification may contribute to refinement of risk stratification. Methods and Results--We searched for single-nucleotide polymorphisms (SNPs) that modulate the corrected QT (QTc)- interval and the occurrence of cardiac events in 639 patients harboring different mutations in KCNH2. We analyzed 1201 SNPs in and around 18 candidate genes, and in another approach investigated 22 independent SNPs previously identified as modulators of QTc-interval in genome-wide association studies in the general population. In an analysis for quantitative effects on the QTc-interval, 3 independent SNPs at NOS1AP (rs10494366, P=9.5×10
-8 ; rs12143842, P=4.8×10-7 ; and rs2880058, P=8.6×10-7 ) were strongly associated with the QTc-interval with marked effects (>12 ms/allele). Analysis of patients versus general population controls uncovered enrichment of QTc-prolonging alleles in patients for 2 SNPs, located respectively at NOS1AP (rs12029454; odds ratio, 1.85; 95% confidence interval, 1.32-2.59; P=3×10-4 ) and KCNQ1 (rs12576239; odds ratio, 1.84; 95% confidence interval, 1.31-2.60; P=5×10-4 ). An analysis of the cumulative effect of the 6 NOS1AP SNPs by means of a multilocus genetic risk score (GRSNOS1AP ) uncovered a strong linear relationship between GRSNOS1AP and the QTc-interval (P=4.2×10-7 ). Furthermore, patients with a GRSNOS1AP in the lowest quartile had a lower relative risk of cardiac events compared with patients in the other quartiles combined (P=0.039). Conclusions--We uncovered unexpectedly large effects of NOS1AP SNPs on the QTc-interval and a trend for effects on risk of cardiac events. For the first time, we linked common genetic variation at KCNQ1 with risk of long-QT syndrome. [ABSTRACT FROM AUTHOR]- Published
- 2015
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5. Gain-of-function mutation in TASK-4 channels and severe cardiac conduction disorder.
- Author
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Friedrich, Corinna, Rinné, Susanne, Zumhagen, Sven, Kiper, Aytug K, Silbernagel, Nicole, Netter, Michael F, Stallmeyer, Birgit, Schulze‐Bahr, Eric, and Decher, Niels
- Abstract
Analyzing a patient with progressive and severe cardiac conduction disorder combined with idiopathic ventricular fibrillation ( IVF), we identified a splice site mutation in the sodium channel gene SCN5A. Due to the severe phenotype, we performed whole-exome sequencing ( WES) and identified an additional mutation in the KCNK17 gene encoding the K
2P potassium channel TASK-4. The heterozygous change (c.262G>A) resulted in the p.Gly88Arg mutation in the first extracellular pore loop. Mutant TASK-4 channels generated threefold increased currents, while surface expression was unchanged, indicating enhanced conductivity. When co-expressed with wild-type channels, the gain-of-function by G88R was conferred in a dominant-active manner. We demonstrate that KCNK17 is strongly expressed in human Purkinje cells and that overexpression of G88R leads to a hyperpolarization and strong slowing of the upstroke velocity of spontaneously beating HL-1 cells. Thus, we propose that a gain-of-function by TASK-4 in the conduction system might aggravate slowed conductivity by the loss of sodium channel function. Moreover, WES supports a second hit-hypothesis in severe arrhythmia cases and identified KCNK17 as a novel arrhythmia gene. [ABSTRACT FROM AUTHOR]- Published
- 2014
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6. Overlapping Cardiac Phenotype Associated with a Familial Mutation in the Voltage Sensor of the KCNQ1 Channel.
- Author
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Henrion, Ulrike, Zumhagen, Sven, Steinke, Katja, Strutz-Seebohm, Nathalie, Stallmeyer, Birgit, Lang, Florian, Schulze-Bahr, Eric, and Seebohm, Guiscard
- Abstract
Background: Cardiac action potential repolarisation is determined by K+ currents including IKs. IKs channels are heteromeric channels composed of KCNQ1 and KCNE β-subunits. Mutations in KCNQ1 are associated with sinus bradycardia, familial atrial fibrillation (fAF) and/or short QT syndrome as a result of gain-offunction, and long QT syndrome (LQTS) due to lossof- function in the ventricles. Here, we report that the missense mutation R231C located in S4 voltage sensor domain is associated with a combined clinical phenotype of sinus bradycardia, fAF and LQTS. We aim to understand the molecular basis of the complex clinical phenotype. Methods: We expressed and functionally analyzed the respective channels kinetics in Xenopus laevis oocytes. The molecular nature of the residue R231 was studied by homology modeling and molecular dynamics simulation. Results: As a result, the mutation reduced voltage sensitivity of channels, possibly due to neutralization of the positive charge of the arginine side chain substituted by cysteine. Modeling suggested that the charge carrying side chain of R231 is positioned suitably to transfer transmembrane voltages into conformational energy. Further, the mutation altered the functional interactions with KCNE subunits. Conclusion: The mutation acted in a β-subunit dependent manner, suggesting IKs function altered by the presence of different KCNE subunits in sinus node, atria and ventricles as the molecular basis of sinus bradycardia, fAF and LQTS in mutation carriers. [ABSTRACT FROM AUTHOR]
- Published
- 2012
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7. POPDC2 a novel susceptibility gene for conduction disorders.
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Rinné, Susanne, Ortiz-Bonnin, Beatriz, Stallmeyer, Birgit, Kiper, Aytug K., Fortmüller, Lisa, Schindler, Roland F.R., Herbort-Brand, Ursula, Kabir, Nashitha S., Dittmann, Sven, Friedrich, Corinna, Zumhagen, Sven, Gualandi, Francesca, Selvatici, Rita, Rapezzi, Claudio, Arbustini, Eloisa, Ferlini, Alessandra, Fabritz, Larissa, Schulze-Bahr, Eric, Brand, Thomas, and Decher, Niels
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VENTRICULAR arrhythmia , *ATRIOVENTRICULAR node , *TWINS , *MYOCARDIUM , *GENETIC mutation , *SINOATRIAL node , *RECESSIVE genes - Abstract
Despite recent progress in the understanding of cardiac ion channel function and its role in inherited forms of ventricular arrhythmias, the molecular basis of cardiac conduction disorders often remains unresolved. We aimed to elucidate the genetic background of familial atrioventricular block (AVB) using a whole exome sequencing (WES) approach. In monozygotic twins with a third-degree AVB and in another, unrelated family with first-degree AVB, we identified a heterozygous nonsense mutation in the POPDC2 gene causing a premature stop at position 188 (POPDC2W188⁎), deleting parts of its cAMP binding-domain. Popeye-domain containing (POPDC) proteins are predominantly expressed in the skeletal muscle and the heart, with particularly high expression of POPDC2 in the sinoatrial node of the mouse. We now show by quantitative PCR experiments that in the human heart the POPDC-modulated two-pore domain potassium (K 2P) channel TREK-1 is preferentially expressed in the atrioventricular node. Co-expression studies in Xenopus oocytes revealed that POPDC2W188⁎ causes a loss-of-function with impaired TREK-1 modulation. Consistent with the high expression level of POPDC2 in the murine sinoatrial node, POPDC2W188⁎ knock-in mice displayed stress-induced sinus bradycardia and pauses, a phenotype that was previously also reported for POPDC2 and TREK-1 knock-out mice. We propose that the POPDC2W188⁎ loss-of-function mutation contributes to AVB pathogenesis by an aberrant modulation of TREK-1, highlighting that POPDC2 represents a novel arrhythmia gene for cardiac conduction disorders. [ABSTRACT FROM AUTHOR]
- Published
- 2020
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8. Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome.
- Author
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Wemhöner, Konstantin, Friedrich, Corinna, Stallmeyer, Birgit, Coffey, Alison J., Grace, Andrew, Zumhagen, Sven, Seebohm, Guiscard, Ortiz-Bonnin, Beatriz, Rinné, Susanne, Sachse, Frank B., Schulze-Bahr, Eric, and Decher, Niels
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GAIN-of-function mutations , *CALCIUM channels , *HEART diseases , *ETIOLOGY of diseases , *COMPUTER simulation , *EXONS (Genetics) , *ARRHYTHMIA - Abstract
Gain-of-function mutations in CACNA1C , encoding the L-type Ca 2 + channel Cav1.2, cause Timothy syndrome (TS), a multi-systemic disorder with dysmorphic features, long-QT syndrome (LQTS) and autism spectrum disorders. TS patients have heterozygous mutations (G402S and G406R) located in the alternatively spliced exon 8, causing a gain-of-function by reduced voltage-dependence of inactivation. Screening 540 unrelated patients with non-syndromic forms of LQTS, we identified six functional relevant CACNA1C mutations in different regions of the channel. All these mutations caused a gain-of-function combining different mechanisms, including changes in current amplitude, rate of inactivation and voltage-dependence of activation or inactivation, similar as in TS. Computer simulations support the theory that the novel CACNA1C mutations prolong action potential duration. We conclude that genotype-negative LQTS patients should be investigated for mutations in CACNA1C , as a gain-of-function in Cav1.2 is likely to cause LQTS and only specific and rare mutations, i.e. in exon 8, cause the multi-systemic TS. [ABSTRACT FROM AUTHOR]
- Published
- 2015
- Full Text
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