» Articles » PMID: 29953465

Reduced T Wave Alternans in Heart Failure Responders to Cardiac Resynchronization Therapy: Evidence of Electrical Remodeling

Overview
Journal PLoS One
Date 2018 Jun 29
PMID 29953465
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Background: T-wave alternans (TWA), a marker of electrical instability, can be modulated by cardiac resynchronization therapy (CRT). The relationship between TWA and heart failure response to CRT has not been clearly defined.

Methods And Results: In 40-patients (age 65±11 years, left ventricular ejection-fraction [LVEF] 23±7%), TWA was evaluated prospectively at median of 2 months (baseline) and 8 months (follow-up) post-CRT implant. TWA-magnitude (Valt >0μV, k≥3), its duration (d), and burden (Valt ·d) were quantified in moving 128-beat segments during incremental atrial (AAI, native-TWA) and atrio-biventricular (DDD-CRT) pacing. The immediate and long-term effect of CRT on TWA was examined. Clinical response to CRT was defined as an increase in LVEF of ≥5%. Native-TWA was clinically significant (Valt ≥1.9μV, k≥3) in 68% of subjects at baseline. Compared to native-TWA at baseline, DDD-CRT pacing at baseline and follow-up reduced the number of positive TWA segments, peak-magnitude, longest-duration and peak-burden of TWA (44±5 to 33±5 to 28±4%, p = 0.02 and 0.002; 5.9±0.8 to 4.1±0.7 to 3.8±0.7μV, p = 0.01 and 0.01; 97±9 to 76±8 to 67±8sec, p = 0.004 and <0.001; and 334±65 to 178±58 to 146±54μV.sec, p = 0.01 and 0.004). In addition, the number of positive segments and longest-duration of native-TWA diminished during follow-up (44±5 to 35±6%, p = 0.044; and 97±9 to 81±9sec, p = 0.02). Clinical response to CRT was observed in 71% of patients; the reduction in DDD-CRT paced TWA both at baseline and follow-up was present only in responders (interaction p-values <0.1).

Conclusion: Long-term CRT reduces the prevalence and magnitude of TWA. This CRT induced beneficial electrical remodeling is a marker of clinical response after CRT.

Citing Articles

Microvolt QRS Alternans in Hypertrophic Cardiomyopathy: A Novel Risk Marker of Late Ventricular Arrhythmias.

Chakraborty P, Suszko A, Viswanathan K, Sheikholeslami K, Spears D, Adler A J Am Heart Assoc. 2021; 10(23):e022036.

PMID: 34854315 PMC: 9075383. DOI: 10.1161/JAHA.121.022036.


Microvolt QRS Alternans Without Microvolt T-Wave Alternans in Human Cardiomyopathy: A Novel Risk Marker of Late Ventricular Arrhythmias.

Suszko A, Nayyar S, Labos C, Nanthakumar K, Pinter A, Crystal E J Am Heart Assoc. 2020; 9(17):e016461.

PMID: 32806990 PMC: 7660784. DOI: 10.1161/JAHA.119.016461.

References
1.
Walker M, Wan X, Kirsch G, Rosenbaum D . Hysteresis effect implicates calcium cycling as a mechanism of repolarization alternans. Circulation. 2003; 108(21):2704-9. DOI: 10.1161/01.CIR.0000093276.10885.5B. View

2.
Selvaraj R, Picton P, Nanthakumar K, Mak S, Chauhan V . Endocardial and epicardial repolarization alternans in human cardiomyopathy: evidence for spatiotemporal heterogeneity and correlation with body surface T-wave alternans. J Am Coll Cardiol. 2007; 49(3):338-46. DOI: 10.1016/j.jacc.2006.08.056. View

3.
Weiss J, Karma A, Shiferaw Y, Chen P, Garfinkel A, Qu Z . From pulsus to pulseless: the saga of cardiac alternans. Circ Res. 2006; 98(10):1244-53. DOI: 10.1161/01.RES.0000224540.97431.f0. View

4.
Verrier R, Nieminen T, Josephson M . Antiarrhythmic drug effects on microvolt T-wave alternans: measurement nuisance or indicator of therapeutic action?. J Cardiovasc Electrophysiol. 2010; 21(11):E79. DOI: 10.1111/j.1540-8167.2010.01901.x. View

5.
Anh D, Srivatsa U, Bui H, Vasconcellos S, Narayan S . Biventricular pacing attenuates T-wave alternans and T-wave amplitude compared to other pacing modes. Pacing Clin Electrophysiol. 2008; 31(6):714-21. DOI: 10.1111/j.1540-8159.2008.01074.x. View