Journal article
Myocardial Recovery in Patients With Systolic Heart Failure and Autoantibodies Against beta(1)-Adrenergic Receptors
Journal of the American College of Cardiology, Vol.69(8), pp.968-977
02/28/2017
DOI: 10.1016/j.jacc.2016.11.067
PMCID: PMC5330212
PMID: 28231950
Abstract
BACKGROUND Among various cardiac autoantibodies (AAbs), those recognizing the beta(1)-adrenergic receptor (beta(1)AR) demonstrate agonist-like effects and induce myocardial damage that can be reversed by beta-blockers and immunoglobulin G3 (IgG3) immunoadsorption.
OBJECTIVES The goal of this study was to investigate the role of beta(1)AR-AAbs belonging to the IgG3 subclass in patients with recent-onset cardiomyopathy.
METHODS Peripheral blood samples were drawn at enrollment in patients with recent-onset cardiomyopathy (left ventricular ejection fraction [LVEF] <= 0.40; <6 months). The presence of IgG and IgG3-beta(1)AR-AAb was determined, and echocardiograms were assessed, at baseline and 6 months. Patients were followed up for <= 48 months.
RESULTS Among the 353 patients who had blood samples adequate for the analysis, 62 (18%) were positive for IgG3-beta(1)AR-AAbs (IgG3 group), 58 (16%) were positive for IgG but not IgG3 (non-IgG3 group), and the remaining were negative. There were no significant differences in baseline systolic blood pressure, heart rate, or LVEF among the groups at baseline. Left ventricular end-diastolic and end-systolic diameters were significantly larger in the non-IgG3 group compared with the other groups (left ventricular end-diastolic diameter, p < 0.01; left ventricular end-systolic diameter, p = 0.03). At 6 months, LVEF was significantly higher in the IgG3 group (p = 0.007). Multiple regression analysis showed that IgG3-beta(1)AR-AAb was an independent predictor of LVEF at 6 months and change in LVEF over 6 months, even after multivariable adjustment (LVEF at 6 months, beta = 0.20, p = 0.01; change in LVEF, beta = 0.20, p = 0.008). In patients with high New York Heart Association functional class (III or IV) at baseline, the IgG3 group had a lower incidence of the composite endpoint of all-cause death, cardiac transplantation, and hospitalization due to heart failure, whereas the non-IgG3 group had the highest incidence of the composite endpoint.
CONCLUSIONS IgG3-beta(1)AR-AAbs were associated with more favorable myocardial recovery in patients with recent-onset cardiomyopathy. (C) 2017 by the American College of Cardiology Foundation.
Details
- Title: Subtitle
- Myocardial Recovery in Patients With Systolic Heart Failure and Autoantibodies Against beta(1)-Adrenergic Receptors
- Creators
- Yuji Nagatomo - Cleveland ClinicDennis M. McNamara - University of PittsburghJeffrey D. Alexis - University of RochesterLeslie T. Cooper - Mayo Clinic in FloridaG. William Dec - Harvard University ,Daniel F. Pauly - Truman Medical CenterRichard Sheppard - Jewish General HospitalRandall C. Starling - Cleveland ClinicW. H. Wilson Tang - Cleveland ClinicIMAC-2 Investigators
- Contributors
- Barry London (Contributor) - University of Iowa, Internal Medicine
- Resource Type
- Journal article
- Publication Details
- Journal of the American College of Cardiology, Vol.69(8), pp.968-977
- DOI
- 10.1016/j.jacc.2016.11.067
- PMID
- 28231950
- PMCID
- PMC5330212
- NLM abbreviation
- J Am Coll Cardiol
- ISSN
- 0735-1097
- eISSN
- 1558-3597
- Publisher
- Elsevier
- Number of pages
- 10
- Grant note
- 1R01HL103931 / National Institutes of Health; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA Cleveland Clinic Research Programs Committee R01HL086918 / NATIONAL HEART, LUNG, AND BLOOD INSTITUTE; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Heart Lung & Blood Institute (NHLBI) MYF1401MF / Myocarditis Foundation National Institutes of Health; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA HL075038; HL086918; HL69912 / National Heart, Lung, and Blood Institute; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Heart Lung & Blood Institute (NHLBI)
- Language
- English
- Date published
- 02/28/2017
- Academic Unit
- Molecular Physiology and Biophysics; Cardiovascular Medicine; Internal Medicine
- Record Identifier
- 9984297506602771
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