PMID- 27890513 OWN - NLM STAT- MEDLINE DCOM- 20170609 LR - 20181202 IS - 1876-4738 (Electronic) IS - 0914-5087 (Linking) VI - 69 IP - 2 DP - 2017 Feb TI - Therapeutic effect of immunoadsorption and subsequent immunoglobulin substitution in patients with dilated cardiomyopathy: Results from the observational prospective Bad Berka Registry. PG - 409-416 LID - S0914-5087(16)30161-7 [pii] LID - 10.1016/j.jjcc.2016.07.014 [doi] AB - BACKGROUND: Elimination of cardiac autoantibodies, frequently detected in patients with dilated cardiomyopathy (DCM), with immunoadsorption (IA) improves functional capacity and left ventricular (LV) function. This study aimed to prospectively address this issue in a large cohort of unselected patients. METHODS: Consecutive patients undergoing IA followed by IgG substitution were included. Clinical and echocardiographic parameters were assessed at baseline (BL) and 12-month follow-up (FU). Patients were classified as IA responders when >/=2 of the following criteria were achieved: improvement in the Minnesota Living with Heart Failure Questionnaire (MLHFQ) >/=5 points, symptoms [>/=1 New York Heart Association (NYHA) class], LV ejection fraction (EF) >/=10% or decrease in LV end-diastolic diameter (EDD) >/=10%, or N-terminal pro B-type natriuretic peptide (NT-pro-BNP) >/=50%. RESULTS: 93 patients (median age 61 years, LVEF 30%, duration of symptoms 14 months, 87% in NYHA class III/IV, >90% treated with beta-blocker/angiotensin-converting enzyme inhibitor) were included. When the entire cohort was analyzed, a significant improvement in MLHFQ (50 vs. 26 points), NYHA-class (median 3.0 vs. 2.0), LVEF (30% vs. 38%), LVEDD (62 vs. 59mm), NT-pro-BNP (892 vs. 523pg/ml) was observed at FU (p<0.05 for all). 48% (n=43) were classified as responders. Those were characterized by a shorter disease duration (11 vs. 22 months), larger BL LVEDD (64 vs. 60mm), presence of >1 viral genome, and higher values of mononuclear inflammatory cells at endomyocardial biopsy. Sixteen (17.2%) patients experienced IA related complications. CONCLUSIONS: A positive response is observed in 48% of inflammatory DCM patients undergoing IA, and this translates into a significant improvement in clinical and echocardiographic parameters. CI - Copyright (c) 2016 Japanese College of Cardiology. Published by Elsevier Ltd. All rights reserved. FAU - Ohlow, Marc-Alexander AU - Ohlow MA AD - Department of Cardiology, Zentralklinik Bad Berka, Bad Berka, Germany. Electronic address: marc.ohlow@zentralklinik.de. FAU - Brunelli, Michele AU - Brunelli M AD - Department of Invasive and Interventional Electrophysiology, Zentralklinik Bad Berka, Germany. FAU - Schreiber, Matthias AU - Schreiber M AD - Department of Cardiology, Zentralklinik Bad Berka, Bad Berka, Germany. FAU - Lauer, Bernward AU - Lauer B AD - Department of Cardiology, Zentralklinik Bad Berka, Bad Berka, Germany. LA - eng PT - Journal Article PT - Observational Study DEP - 20161124 PL - Netherlands TA - J Cardiol JT - Journal of cardiology JID - 8804703 RN - 0 (Adrenergic beta-Antagonists) RN - 0 (Angiotensin-Converting Enzyme Inhibitors) RN - 0 (Autoantibodies) RN - 0 (Immunoglobulin G) RN - 0 (Peptide Fragments) RN - 0 (pro-brain natriuretic peptide (1-76)) RN - 114471-18-0 (Natriuretic Peptide, Brain) SB - IM MH - Adrenergic beta-Antagonists/therapeutic use MH - Aged MH - Angiotensin-Converting Enzyme Inhibitors/therapeutic use MH - Autoantibodies/*metabolism MH - Cardiomyopathy, Dilated/*therapy MH - Cohort Studies MH - Diastole MH - Echocardiography MH - Female MH - Heart Ventricles/diagnostic imaging MH - Humans MH - Immunoglobulin G/*immunology MH - *Immunosorbent Techniques MH - Male MH - Middle Aged MH - Natriuretic Peptide, Brain/blood MH - Peptide Fragments/blood MH - *Quality of Life MH - Registries MH - Stroke Volume MH - Ventricular Dysfunction, Left/therapy OTO - NOTNLM OT - Dilated cardiomyopathy OT - Immunoadsorption OT - Inflammatory OT - Quality of life EDAT- 2016/11/29 06:00 MHDA- 2017/06/10 06:00 CRDT- 2016/11/29 06:00 PHST- 2016/02/14 00:00 [received] PHST- 2016/07/08 00:00 [revised] PHST- 2016/07/22 00:00 [accepted] PHST- 2016/11/29 06:00 [pubmed] PHST- 2017/06/10 06:00 [medline] PHST- 2016/11/29 06:00 [entrez] AID - S0914-5087(16)30161-7 [pii] AID - 10.1016/j.jjcc.2016.07.014 [doi] PST - ppublish SO - J Cardiol. 2017 Feb;69(2):409-416. doi: 10.1016/j.jjcc.2016.07.014. Epub 2016 Nov 24.