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Measurement of Antibody Effects on Cellular Function of Isolated Cardiomyocytes
Published on: March 8, 2013
Immunoadsorption can improve cardiac function in transplant candidates with non-ischemic dilated cardiomyopathy
Michael Dandel1, Angela Englert1, Gerd Wallukat1
1Department of Cardiothoracic and Vascular Surgery, Deutsches Herzzentrum Berlin, Germany.
Insights
Immunoadsorption (IA) improves heart function and survival for patients with diabetes and dilated cardiomyopathy (DCM). This therapy may reduce the need for heart transplantation (HTx) in high-risk diabetic patients.
Area of Science:
- Cardiology
- Immunology
- Endocrinology
Background:
- Diabetes mellitus (DM) increases mortality risk in patients with dilated cardiomyopathy (DCM), a condition often leading to heart failure (HF).
- Diabetic patients face reduced eligibility and increased mortality risk associated with heart transplantation (HTx), necessitating alternative therapies.
- Immunoadsorption (IA) shows potential for improving cardiac function in DCM, but its efficacy in DM-associated DCM requires investigation.
Purpose of the Study:
- To assess the effectiveness of immunoadsorption (IA) in treating diabetic patients with end-stage dilated cardiomyopathy (DCM).
- To compare cardiac function, exercise tolerance, and heart transplantation (HTx)-free survival between diabetic and non-diabetic DCM patients undergoing IA.
Main Methods:
- Cardiac function and HTx-free survival were evaluated in diabetic DCM patients who underwent IA (Globaffin) between 2003-2012.
- Non-diabetic DCM patients receiving IA during the same period served as controls.
- Serum β1-autoantibodies (β1-AABs) were measured before and after IA in both groups.
Main Results:
- IA treatment led to significant improvements in left ventricular (LV) size, ejection fraction (LVEF), and NYHA class within the first year for both diabetic and non-diabetic groups.
- Three-year HTx-free survival rates were comparable between diabetic (81.3 ± 8%) and non-diabetic (78.4 ± 8%) patients post-IA.
- The prevalence of responders to IA and freedom from β1-AAB reappearance were similar in both groups, suggesting IA's broad efficacy.
Conclusions:
- Immunoadsorption (IA) effectively improves cardiac function, exercise tolerance, and heart transplantation (HTx)-free survival in diabetic patients with end-stage dilated cardiomyopathy (DCM).
- IA therapy may help delay the need for HTx, improve outcomes for patients on waiting lists, and potentially spare some diabetic patients from transplantation.
- These findings are particularly significant given the high pre- and post-HTx mortality risks associated with diabetes in DCM patients.
Background:
Diabetes mellitus (DM) is a risk factor for death from heart failure (HF) in patients with dilated cardiomyopathy (DCM) but DM patients are less eligible for heart transplantation (HTx) and DM is a risk factor for death also after HTx. New therapies are therefore necessary to improve survival of diabetic DCM patients. Immunoadsorption (IA) can improve heart function in DCM but its usefulness for therapy of DM-associated DCM is unknown. We assessed this aspect.
Methods:
Cardiac function and HTx-free survival were evaluated in diabetic HTx-candidates with DCM who underwent IA (Globaffin(®), a broadband-immunoadsorber containing synthetic peptide-GAM(®)) in 6/2003-6/2012 (follow-up 1-10 yrs). Non-diabetic HTx-candidates with DCM who received IA in the same time-period served as controls. Before and after IA patients were tested for serum β1-autoantibodies (β1-AABs).
Results:
We evaluated 31 patients with and 31 without DM. Before IA there were no differences between the 2 groups in LV size, LVEF and β1-AAB levels. However, DM patients were older, their HF duration was longer and their peak oxygen-uptake was lower (p < 0.005). During the 1st post-IA year in both groups there was a decrease in LV size and improvement in both LVEF and NYHA-class (p < 0.05). Post-IA 3-year HTx-free survival and prevalence of responders to IA in patients with and without DM was 81.3 ± 8% and 78.4 ± 8%, respectively and 73.3% and 67.7%, respectively. Post-IA 3-year freedom from β1-AAB reappearance in patients with and without DM reached 72.1 ± 9.0% and 71.1 ± 8.6%, respectively.
Conclusions:
IA improves heart function, exercise tolerance and Tx-free survival in patients with DM-associated end-stage DCM. Our results also suggest that IA can delay HTx-listing, improve survival on HTx lists and even spare some diabetic patients from HTx, benefits of particular importance for these patients who are at high risk for pre-HTx and post-HTx mortality.
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