Related Experiment Video
Updated: Feb 7, 2026

A Doxorubicin-Induced Murine Model of Dilated Cardiomyopathy In Vivo
Published on: May 16, 2020
Comparison of Mesenchymal Stem Cell Efficacy in Ischemic Versus Nonischemic Dilated Cardiomyopathy
Bryon A Tompkins1,2, Angela C Rieger1, Victoria Florea1
1Interdisciplinary Stem Cell Institute, University of Miami Miller School of Medicine, Miami, FL.
Insights
Mesenchymal stem cell therapy benefits both ischemic cardiomyopathy (ICM) and dilated cardiomyopathy (DCM) patients. While cardiac function improved more in DCM, ICM patients showed reverse remodeling, with both groups experiencing enhanced quality of life.
Area of Science:
- Cardiology
- Regenerative Medicine
- Stem Cell Therapy
Background:
- Ischemic cardiomyopathy (ICM) and dilated cardiomyopathy (DCM) are distinct heart conditions.
- Mesenchymal stem cell (MSC) therapy is safe and shows cardiovascular benefits in both ICM and DCM.
- A direct comparison of MSC efficacy between ICM and DCM was previously lacking.
Purpose of the Study:
- To compare the efficacy of transendocardial mesenchymal stem cell (MSC) delivery in patients with ICM versus DCM.
- To analyze differences in cardiac structure, function, and quality of life outcomes between ICM and DCM patients post-MSC therapy.
Main Methods:
- A pooled analysis of 3 randomized, blinded clinical trials (TAC-HFT, POSEIDON, POSEIDON-DCM) was performed.
- 46 ICM patients and 33 DCM patients receiving autologous or allogeneic MSCs were included.
- Cardiac structure, function, and quality-of-life data were assessed at baseline and 1-year follow-up.
Main Results:
- Ejection fraction and stroke volume improved significantly in DCM, but not in ICM.
- ICM patients showed improvements in end-diastolic volume, sphericity index, and end-diastolic mass (reverse remodeling).
- Both ICM and DCM patients demonstrated significant improvements in the 6-minute walk test, NYHA class, and quality of life.
Conclusions:
- Mesenchymal stem cell therapy is beneficial for both DCM and ICM, yielding distinct cardiac remodeling effects.
- DCM patients experienced preferential improvements in cardiac function, while ICM patients underwent reverse remodeling.
- MSC therapy effectively enhances functional capacity and quality of life in patients with both etiologies of cardiomyopathy.
Background:
Ischemic cardiomyopathy (ICM) and dilated cardiomyopathy (DCM) differ in histopathology and prognosis. Although transendocardial delivery of mesenchymal stem cells is safe and provides cardiovascular benefits in both, a comparison of mesenchymal stem cell efficacy in ICM versus DCM has not been done.
Methods And Results:
We conducted a subanalysis of 3 single-center, randomized, and blinded clinical trials: (1) TAC-HFT (Transendocardial Autologous Mesenchymal Stem Cells and Mononuclear Bone Marrow Cells in Ischemic Heart Failure Trial); (2) POSEIDON (A Phase I/II, Randomized Pilot Study of the Comparative Safety and Efficacy of Transendocardial Injection of Autologous Mesenchymal Stem Cells Versus Allogeneic Mesenchymal Stem Cells in Patients With Chronic Ischemic Left Ventricular Dysfunction Secondary to Myocardial Infarction); and (3) POSEIDON-DCM (Percutaneous Stem Cell Injection Delivery Effects on Neomyogenesis in Dilated Cardiomyopathy). Baseline and 1-year cardiac structure and function and quality-of-life data were compared in a post hoc pooled analysis including ICM (n=46) and DCM (n=33) patients who received autologous or allogeneic mesenchymal stem cells. Ejection fraction improved in DCM by 7% (within-group, P=0.002) compared to ICM (1.5%; within-group, P=0.14; between-group, P=0.003). Similarly, stroke volume increased in DCM by 10.59 mL (P=0.046) versus ICM (-0.2 mL; P=0.73; between-group, P=0.02). End-diastolic volume improved only in ICM (10.6 mL; P=0.04) and end-systolic volume improved only in DCM (17.8 mL; P=0.049). The sphericity index decreased only in ICM (-0.04; P=0.0002). End-diastolic mass increased in ICM (23.1 g; P<0.0001) versus DCM (-4.1 g; P=0.34; between-group, P=0.007). The 6-minute walk test improved in DCM (31.1 m; P=0.009) and ICM (36.3 m; P=0.006) with no between-group difference (P=0.79). The New York Heart Association class improved in DCM (P=0.005) and ICM (P=0.02; between-group P=0.20). The Minnesota Living with Heart Failure Questionnaire improved in DCM (-19.5; P=0.002) and ICM (-6.4; P=0.03; δ between-group difference P=0.042) patients.
Conclusions:
Mesenchymal stem cell therapy is beneficial in DCM and ICM patients, despite variable effects on cardiac phenotypic outcomes. Whereas cardiac function improved preferentially in DCM patients, ICM patients experienced reverse remodeling. Mesenchymal stem cell therapy enhanced quality of life and functional capacity in both etiologies.
Clinical Trial Registration:
URL: http://www.clinicaltrials.gov. Unique identifiers: TAC-HFT: NCT00768066, POSEIDON: NCT01087996, POSEIDON-DCM: NCT01392625.
More Related Videos
09:16Isolation and Characterization of Cardiac Mesenchymal Stromal Cells from Endomyocardial Bioptic Samples of Arrhythmogenic Cardiomyopathy Patients
Published on: February 28, 2018
08:09Isolation of Rat Adipose Tissue Mesenchymal Stem Cells for Differentiation into Insulin-producing Cells
Published on: August 29, 2022
Related Concept Videos
Cardiomyopathy II: Dilated Cardiomyopathy
Mesenchymal Stem Cells
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy IV: Restrictive Cardiomyopathy
Adult Stem Cells
Embryonic Stem Cells