Ge Gao1, Vikram Brahmanandam1, Mihai Raicu1, Lianzhi Gu1, Li Zhou1, Srinivasan Kasturirangan1, Anish Shah2, Smita I Negi3, Melissa R Wood1, Ankit A Desai4, Antone Tatooles5, Alan Schwartz6, Samuel C Dudley7. 1. Section of Cardiology and the Jesse Brown VAMC, University of Illinois at Chicago, Chicago, Illinois. 2. University of Illinois at Chicago College of Medicine, Chicago, Illinois. 3. The University of Texas Health Science Center, Houston, Texas. 4. Section of Cardiology and the Jesse Brown VAMC, University of Illinois at Chicago, Chicago, Illinois; Institute for Personalized Respiratory Medicine and Center for Cardiovascular Research, University of Illinois at Chicago, Chicago, Illinois. 5. Transplant/Mechanical Assist, Advocate Christ Medical Center, Oak Lawn, Illinois. 6. Departments of Medical Education and Pediatrics, University of Illinois at Chicago, Chicago, Illinois. 7. Section of Cardiology and the Jesse Brown VAMC, University of Illinois at Chicago, Chicago, Illinois. Electronic address: samuel_dudley@brown.edu.
Abstract
OBJECTIVES: The aim of this study was to determine the association of SCN5A cardiac sodium (Na(+)) channel mRNA splice variants in white blood cells (WBCs) with risk of arrhythmias in heart failure (HF). BACKGROUND: HF is associated with upregulation of two cardiac SCN5A mRNA splice variants that encode prematurely truncated, nonfunctional Na(+) channels. Because circulating WBCs demonstrate similar SCN5A splicing patterns, we hypothesized that these WBC-derived splice variants might further stratify patients with HF who are at risk for arrhythmias. METHODS: Simultaneously obtained myocardial core samples and WBCs were compared for SCN5A variants C (VC) and D (VD). Circulating variant levels were compared among patients with HF, divided into three groups: HF without an implantable cardioverter-defibrillator (ICD), HF with an ICD without appropriate intervention, and HF with an ICD with appropriate intervention. RESULTS: Myocardial tissue-derived SCN5A variant expression levels strongly correlated with circulating WBC samples for both VC and VD variants (r = 0.78 and 0.75, respectively). After controlling for covariates, patients with HF who had received an appropriate ICD intervention had higher expression levels of both WBC-derived SCN5A variants compared with patients with HF with ICDs who had not received appropriate ICD intervention (odds ratio, 3.25; 95% CI, 1.64-6.45; p = 0.001). Receiver operating characteristic analysis revealed that circulating SCN5A variant levels were highly associated with the risk for appropriate ICD intervention (area under the curve ≥0.97). CONCLUSIONS: Circulating expression levels of SCN5A variants were strongly associated with myocardial tissue levels. Furthermore, circulating variant levels were correlative with arrhythmic risk as measured by ICD events in an HF population within 1 year. (Sodium Channel Splicing in Heart Failure Trial [SOCS-HEFT]; NCT01185587).
OBJECTIVES: The aim of this study was to determine the association of SCN5A cardiac sodium (Na(+)) channel mRNA splice variants in white blood cells (WBCs) with risk of arrhythmias in heart failure (HF). BACKGROUND: HF is associated with upregulation of two cardiac SCN5A mRNA splice variants that encode prematurely truncated, nonfunctional Na(+) channels. Because circulating WBCs demonstrate similar SCN5A splicing patterns, we hypothesized that these WBC-derived splice variants might further stratify patients with HF who are at risk for arrhythmias. METHODS: Simultaneously obtained myocardial core samples and WBCs were compared for SCN5A variants C (VC) and D (VD). Circulating variant levels were compared among patients with HF, divided into three groups: HF without an implantable cardioverter-defibrillator (ICD), HF with an ICD without appropriate intervention, and HF with an ICD with appropriate intervention. RESULTS: Myocardial tissue-derived SCN5A variant expression levels strongly correlated with circulating WBC samples for both VC and VD variants (r = 0.78 and 0.75, respectively). After controlling for covariates, patients with HF who had received an appropriate ICD intervention had higher expression levels of both WBC-derived SCN5A variants compared with patients with HF with ICDs who had not received appropriate ICD intervention (odds ratio, 3.25; 95% CI, 1.64-6.45; p = 0.001). Receiver operating characteristic analysis revealed that circulating SCN5A variant levels were highly associated with the risk for appropriate ICD intervention (area under the curve ≥0.97). CONCLUSIONS: Circulating expression levels of SCN5A variants were strongly associated with myocardial tissue levels. Furthermore, circulating variant levels were correlative with arrhythmic risk as measured by ICD events in an HF population within 1 year. (Sodium Channel Splicing in Heart Failure Trial [SOCS-HEFT]; NCT01185587).
Authors: Véronique L Roger; Alan S Go; Donald M Lloyd-Jones; Emelia J Benjamin; Jarett D Berry; William B Borden; Dawn M Bravata; Shifan Dai; Earl S Ford; Caroline S Fox; Heather J Fullerton; Cathleen Gillespie; Susan M Hailpern; John A Heit; Virginia J Howard; Brett M Kissela; Steven J Kittner; Daniel T Lackland; Judith H Lichtman; Lynda D Lisabeth; Diane M Makuc; Gregory M Marcus; Ariane Marelli; David B Matchar; Claudia S Moy; Dariush Mozaffarian; Michael E Mussolino; Graham Nichol; Nina P Paynter; Elsayed Z Soliman; Paul D Sorlie; Nona Sotoodehnia; Tanya N Turan; Salim S Virani; Nathan D Wong; Daniel Woo; Melanie B Turner Journal: Circulation Date: 2011-12-15 Impact factor: 29.690
Authors: Luis Ferreira Santos; Bruno Rodrigues; Davide Moreira; Emanuel Correia; Luis Nunes; Antonio Costa; Luis Elvas; Telmo Pereira; Jose Carlos Machado; Sergio Castedo; Carla Henriques; Ana Matos; Jorge Oliveira Santos Journal: Europace Date: 2012-01-25 Impact factor: 5.214
Authors: Dan Hu; Hector Barajas-Martínez; Argelia Medeiros-Domingo; Lia Crotti; Christian Veltmann; Rainer Schimpf; Janire Urrutia; Aintzane Alday; Oscar Casis; Ryan Pfeiffer; Elena Burashnikov; Gabriel Caceres; David J Tester; Christian Wolpert; Martin Borggrefe; Peter Schwartz; Michael J Ackerman; Charles Antzelevitch Journal: Heart Rhythm Date: 2011-12-07 Impact factor: 6.343
Authors: Ge Gao; An Xie; Shu-Ching Huang; Anyu Zhou; Jianhua Zhang; Amanda M Herman; Sassan Ghassemzadeh; Euy-Myoung Jeong; Srinivasan Kasturirangan; Mihai Raicu; Michael A Sobieski; Geetha Bhat; Antone Tatooles; Edward J Benz; Timothy J Kamp; Samuel C Dudley Journal: Circulation Date: 2011-08-22 Impact factor: 29.690
Authors: Ronald J Kanter; Ryan Pfeiffer; Dan Hu; Héctor Barajas-Martinez; Michael P Carboni; Charles Antzelevitch Journal: Circulation Date: 2011-11-16 Impact factor: 29.690
Authors: Bo Gregers Winkel; Maiken Kudahl Larsen; Knut Erik Berge; Trond Paul Leren; Peter Henrik Nissen; Morten Salling Olesen; Mads Vilhelm Hollegaard; Thomas Jespersen; Lei Yuan; Nikolaj Nielsen; Stig Haunsø; Jesper Hastrup Svendsen; Yinman Wang; Ingrid Bayer Kristensen; Henrik Kjaerulf Jensen; Jacob Tfelt-Hansen; Jytte Banner Journal: J Cardiovasc Electrophysiol Date: 2012-08-06
Authors: Ge Gao; An Xie; Jianhua Zhang; Amanda M Herman; Euy-Myoung Jeong; Lianzhi Gu; Man Liu; Kai-Chien Yang; Timothy J Kamp; Samuel C Dudley Journal: Circ Arrhythm Electrophysiol Date: 2013-09-13
Authors: Adam M Noyes; Anyu Zhou; Ge Gao; Lianzhi Gu; Sharlene Day; J Andrew Wasserstrom; Samuel C Dudley Journal: Int J Cardiol Date: 2017-09-07 Impact factor: 4.164
Authors: Debasree Banerjee; Tom N Grammatopoulos; Amy Palmisciano; James R Klinger; Ipsita Krishnan; Mary Whittenhall; Anyu Zhou; Samuel Dudley; Corey E Ventetuolo Journal: Chest Date: 2020-02-26 Impact factor: 9.410
Authors: Ning Jiang; Anyu Zhou; Hafiz Imran; Guangbin Shi; Bahaa Kaseer; Vincent Siu; Antony F Chu; David M Donaldson; Malcolm M Kirk; Binu B Philips; Samuel C Dudley Journal: JACC Clin Electrophysiol Date: 2021-08-25
Authors: Ning Jiang; Anyu Zhou; Bharati Prasad; Li Zhou; Jimmy Doumit; Guangbin Shi; Hafiz Imran; Bahaa Kaseer; Richard Millman; Samuel C Dudley Journal: J Am Heart Assoc Date: 2016-08-19 Impact factor: 5.501