Cardiac Magnetic Resonance Imaging used for Evaluation of Adipose-Derived Stromal Cell Therapy in Patients with Chronic Ischemic Heart Disease
- PMID: 31698917
- PMCID: PMC6923551
- DOI: 10.1177/0963689719883592
Cardiac Magnetic Resonance Imaging used for Evaluation of Adipose-Derived Stromal Cell Therapy in Patients with Chronic Ischemic Heart Disease
Abstract
Adipose-derived stromal cell (ASC) therapy is currently investigated as a new treatment option for patients with ischemic heart disease (IHD). The aim of this study was to evaluate the effect of ASC therapy in patients with chronic IHD measuring myocardial perfusion and cardiac function using cardiac magnetic resonance imaging (CMRI). Patients were included in MyStromalCell trial, a phase II, randomized, double-blinded, placebo-controlled study investigated the effect of ASCs in patients with chronic IHD with preserved left ventricular ejection fraction (LVEF). In total, 41 of 60 patients underwent cine, late enhancement, rest and stress imaging with CMRI. There was a non-significant difference between stress and rest values in maximal signal intensity, a measure of myocardial perfusion, from baseline to follow-up comparing placebo with ASC group (-52.52 ± 88.61 and 3.05 ± 63.17, p = 0.061, respectively). LVEF, myocardial mass, stroke volume, left ventricle end-diastolic volume and end-systolic volume changed non-significantly (-0.5 ± 4.7%, -3.5 ± 13.1 g, -0.7 ± 8.6 mL, 1.9 ± 25.1 mL and 2.6 ± 16.5 mL, respectively) in the placebo group and in the ASC group (0.7 ± 8.6%, 0.9 ± 10.8 g, -0.3 ± 26.1 mL, -3.0 ± 31.5 mL and -2.7 ± 20.4 mL, respectively) from baseline to 6 months follow-up. The amount of scar tissue was unchanged in the placebo group by 0.0 ± 1.6 g, p = 1.0 and in the ASC group with -0.3 ± 2.3 g, p = 0.540. There was no difference between the groups. There was a non-significant trend toward increased myocardial perfusion but no significant changes in functional parameters or amount of scar tissue in patients treated with ASCs compared with patients allocated into the placebo group.
Keywords: adipose-derived stromal cell; cardiac magnetic resonance imaging; coronary artery disease; mesenchymal; randomized clinical trial; stem cell therapy.
Conflict of interest statement
Figures
Similar articles
-
Danish phase II trial using adipose tissue derived mesenchymal stromal cells for patients with ischaemic heart failure.ESC Heart Fail. 2023 Apr;10(2):1170-1183. doi: 10.1002/ehf2.14281. Epub 2023 Jan 13. ESC Heart Fail. 2023. PMID: 36638837 Free PMC article. Clinical Trial.
-
Autologous adipose-derived stromal cell treatment for patients with refractory angina (MyStromalCell Trial): 3-years follow-up results.J Transl Med. 2019 Nov 12;17(1):360. doi: 10.1186/s12967-019-2110-1. J Transl Med. 2019. PMID: 31711513 Free PMC article. Clinical Trial.
-
Cryopreserved Off-the-Shelf Allogeneic Adipose-Derived Stromal Cells for Therapy in Patients with Ischemic Heart Disease and Heart Failure-A Safety Study.Stem Cells Transl Med. 2017 Nov;6(11):1963-1971. doi: 10.1002/sctm.17-0040. Epub 2017 Sep 7. Stem Cells Transl Med. 2017. PMID: 28880460 Free PMC article. Clinical Trial.
-
Adipose-derived mesenchymal stromal cells for chronic myocardial ischemia (MyStromalCell Trial): study design.Regen Med. 2012 May;7(3):421-8. doi: 10.2217/rme.12.17. Regen Med. 2012. PMID: 22594332 Review.
-
Is the measurement of left ventricular ejection fraction the proper end point for cell therapy trials? An analysis of the effect of bone marrow mononuclear stem cell administration on left ventricular ejection fraction after ST-segment elevation myocardial infarction when evaluated by cardiac magnetic resonance imaging.Am Heart J. 2011 Oct;162(4):671-7. doi: 10.1016/j.ahj.2011.06.019. Am Heart J. 2011. PMID: 21982659 Review.
Cited by
-
Aging and Metabolic Reprogramming of Adipose-Derived Stem Cells Affect Molecular Mechanisms Related to Cardiovascular Diseases.Cells. 2023 Dec 7;12(24):2785. doi: 10.3390/cells12242785. Cells. 2023. PMID: 38132104 Free PMC article. Review.
-
Regenerative Medicine for the Treatment of Ischemic Heart Disease; Status and Future Perspectives.Front Cell Dev Biol. 2021 Sep 10;9:704903. doi: 10.3389/fcell.2021.704903. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 34568321 Free PMC article. Review.
-
Mesenchymal Stem Cell Transplantation for Ischemic Diseases: Mechanisms and Challenges.Tissue Eng Regen Med. 2021 Aug;18(4):587-611. doi: 10.1007/s13770-021-00334-3. Epub 2021 Apr 21. Tissue Eng Regen Med. 2021. PMID: 33884577 Free PMC article. Review.
References
-
- Nesto RW, Kowalchuk GJ. The ischemic cascade: temporal sequence of hemodynamic, electrocardiographic and symptomatic expressions of ischemia. Am J Cardiol. 1987;59(7):23C–30C. - PubMed
-
- Aaberge L, Rootwelt K, Smith HJ, Nordstrand K, Forfang K. Effects of transmyocardial revascularization on myocardial perfusion and systolic function assessed by nuclear and magnetic resonance imaging methods. Scand Cardiovasc J. 2001;35(1):8–13. - PubMed
-
- Hopp E, Lunde K, Solheim S, Aakhus S, Arnesen H, Forfang K, Edvardsen T, Smith HJ. Regional myocardial function after intracoronary bone marrow cell injection in reperfused anterior wall infarction - a cardiovascular magnetic resonance tagging study. J Cardiovasc Magn Reson. 2011;13:22. - PMC - PubMed
-
- Thuesen L, Andersen HR, Bagger H, Bøtker HE, Dalsgaard D, Kristensen SD, Krusell LR, Munkholm H. Long genuine coronary artery lesions treated with stiff tubular or flexible coiled stents. A randomized angiographic follow-up study. Scand Cardiovasc J. 2002;36(2):91–94. - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous
