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J Am Coll Cardiol, 2004; 44:829-836, doi:10.1016/j.jacc.2004.04.055
© 2004 by the American College of Cardiology Foundation
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Potential role of humoral immunity in cardiac dysfunction of patients suffering from dilated cardiomyopathy

Alexander Staudt, MD*,*, Yvonne Staudt, MD*, Marcus Dörr, MD*, Marco Böhm, MD{dagger}, Fabian Knebel, MD{dagger}, Astrid Hummel, MD*, Lydia Wunderle, MD*, Malte Tiburcy, MD*, Klaus D. Wernecke, PhD{ddagger}, Gert Baumann, MD{dagger} and Stephan B. Felix, MD*

* Klinik für Innere Medizin B, Ernst-Moritz-Arndt-Universität, Greifswald, Germany
{dagger} Medizinische Klinik I, Charité, Humboldt-Universität, Berlin, Germany
{ddagger} Institut für Medizinische Biometrie, Charité, Humboldt-Universität, Berlin, Germany



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Figure 1 Individual effects of purified antibodies (IgG 300 mg/l) on isolated field-stimulated rat cardiomyocytes. Changes of Ca2+ transients (A) and systolic cell shortening (B) during superfusion (% changes from baseline): antibodies from plasma of healthy blood donors (controls, n = 45). Antibodies from dilated cardiomyopathy (DCM) patients that induced cardiodepressant effects (cardiodepressant group, n = 29). Antibodies from DCM patients that did not influence Ca2+ transients and systolic cell shortening (non-cardiodepressant group, n = 16). ###p < 0.001 significantly different from controls; +++p < 0.001 significantly different from non-cardiodepressant group.

 


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Figure 2 Changes in cardiac index in the cardiodepressant group (solid bars, n = 29) and in the non-cardiodepressant group (open bars, n = 16). ***p < 0.001 significantly different from baseline; +++p < 0.001 significantly different from non-cardiodepressant group. IA = immunoadsorption.

 


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Figure 3 Changes in stroke volume index in the cardiodepressant group (solid bars, n = 29) and in the non-cardiodepressant group (open bars, n = 16). ***p < 0.001 significantly different from baseline; +++p < 0.001 significantly different from non-cardiodepressant group. IA = immunoadsorption.

 


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Figure 4 Changes in systemic vascular resistance (SVR) in the cardiodepressant group (solid bars, n = 29)and in the non-cardiodepressant group (open bars, n = 16). ***p < 0.001 significantly different from baseline; +++p < 0.001 significantly different from non-cardiodepressant group. IA = immunoadsorption.

 


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Figure 5 Changes in LV ejection fraction as assessed by echocardiography in the cardiodepressant group (solid bars, n = 29) and in the non-cardiodepressant group (open bars, n = 16). ***p < 0.001 significantly different from baseline; ++p < 0.01 significantly different from non-cardiodepressant group. IA = immunoadsorption.

 




 
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