Myocardial Recovery in Patients With Systolic Heart Failure and Autoantibodies Against β1-Adrenergic Receptors

被引:28
作者
Nagatomo, Yuji [1 ,2 ]
McNamara, Dennis M. [3 ]
Alexis, Jeffrey D. [4 ]
Cooper, Leslie T. [5 ]
Dec, G. William [6 ]
Pauly, Daniel F. [7 ]
Sheppard, Richard [8 ]
Starling, Randall C. [1 ]
Tang, W. H. Wilson [1 ]
机构
[1] Cleveland Clin Fdn, Heart & Vasc Inst, 9500 Euclid Ave, Cleveland, OH 44195 USA
[2] Sakakibara Heart Inst, Fuchu, Tokyo, Japan
[3] Univ Pittsburgh, Med Ctr, Heart & Vasc Inst, Pittsburgh, PA USA
[4] Univ Rochester, Med Ctr, Sch Med & Dent, Rochester, NY 14642 USA
[5] Mayo Clin Florida, Jacksonville, FL USA
[6] Massachusetts Gen Hosp, Boston, MA 02114 USA
[7] Univ Missouri, Truman Med Ctr, Kansas City, MO USA
[8] Jewish Gen Hosp, Montreal, PQ, Canada
基金
美国国家卫生研究院;
关键词
autoantibody; beta-blocker; IgG3; recent-onset cardiomyopathy; IDIOPATHIC DILATED CARDIOMYOPATHY; 2ND EXTRACELLULAR LOOP; ISOLATED CARDIOMYOCYTES; BETA-1-ADRENERGIC RECEPTOR; CARDIAC DYSFUNCTION; AUTOIMMUNE EPITOPE; POTENTIAL ROLE; ANTIBODIES; IMMUNOADSORPTION; IMMUNOGLOBULIN;
D O I
10.1016/j.jacc.2016.11.067
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
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.
引用
收藏
页码:968 / 977
页数:10
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