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(Circulation. 2000;101:385.)
© 2000 American Heart Association, Inc.

Clinical Investigation and Reports

Immunoglobulin Adsorption in Patients With Idiopathic Dilated Cardiomyopathy

Johannes Müller, MD; Gerd Wallukat, PhD; Michael Dandel, MD; Heidrun Bieda, MD; Kersten Brandes, MD; Susanne Spiegelsberger, MD; Eberhard Nissen, PhD; Rudolf Kunze, PhD; Roland Hetzer, MD

From the German Heart Institute Berlin (J.M., M.D., H.B., K.B., S.S., R.H.); Max-Delbrück-Center (G.W., E.N.); and IMTOX, Immunbiologische Forschungs GmbH (R.K.), Berlin, Germany.

Correspondence to Johannes Müller, MD, German Heart Institute Berlin (Deutsches Herzzentrum Berlin), Augustenburger Platz 1, 13353 Berlin, Germany. E-mail jmueller{at}dhzb.de

Background—Idiopathic dilated cardiomyopathy (IDC) frequently is a progressive disease without causative therapy options. Following the hypothesis that in certain patients autoantibodies against cardiac structures may induce, maintain, or promote the progression of the disease, we investigated whether the elimination of these autoantibodies through immunoadsorption would improve cardiac function.

Methods and Results—This prospective case-control study included 34 patients with IDC. Each patient presented with moderate to severe heart failure and evidence of autoantibodies directed against ß₁-adrenoceptors (ß₁-AABs). Seventeen patients received standard medical therapy (control group), whereas 17 were also treated with immunoadsorption (treatment group) to eliminate ß₁-AABs. A 1-year follow-up included echocardiographic assessment of left ventricular ejection fraction and internal diameters, ß₁-AAB levels, and clinical status every 3 months. Within 1 year, the mean±SD left ventricular ejection fraction rose from 22.3±3.3% to 37.9±7.9% (P=0.0001) in the treatment group, with a relative increase of 69.9%. However, in the control group, no overall increase was seen (from 23.8±3.0% to 25.2±5.9%, P=0.3154). Left ventricular diameter in diastole decreased by 14.5% from 74.5±7.1 to 63.7±6.0 mm in the treatment group (P=0.0001) and by 3.8% (P=0.2342) in the control group. In the treatment group, the NYHA functional rating improved after immunoadsorption (P=0.0001). ß₁-AABs did not increase anew.

Conclusions—In IDC, the use of immunoadsorption is superior to the use of standard medical therapy. It significantly improves cardiac performance and clinical status.

Key Words: dilated cardiomyopathy • autoantibodies

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