Graber M, Gollmann-Tepeköylü C, Schweiger V, Hirsch J, Pölzl L, Nägele F, et al. Modulation of cell fate by shock wave therapy in ischaemic heart disease. Eur Heart J Open. 2025;5(2):oeaf011.
Coronary artery bypass graft surgery (CABG) and interventional implantation of coronary artery stents are current state-of-the-art techniques for revascularization and restoration of blood supply of infarcted myocardium. However, these treatment options remain some kind of palliative as already established impairment of heart function due to irreversibly damaged myocardium cannot be reversed3. Regenerative therapies such as stem cell or gene therapy aim to retrieve lost cardiac muscle to restore heart function. Both strategies have shown promising results in pre-clinical and clinical trials. Nevertheless, despite huge research efforts during the last decades stem cell and gene therapy have not yet gained broad clinical routine use. Reasons thereof include complexity in preparation and application, side effects as well as ethical concerns4,5. Therefore, clinicians and their patients, as well as public healthcare systems, are still in urgent need of alternative treatment options for heart muscle regeneration after myocardial infarction.
Thereby, the target area of all regenerative therapies in ischemic heart disease (after myocardial infarction) is the so-called peri-infarction zone, the border zone of the infarction. Whereas the infarct area with a total loss of blood supply completely loses its function and gets transformed into fibrotic scar tissue, this border zone remains still vital but chronically undersupplied. It is therefore also called the “hibernating myocardium”. During contraction of the heart muscle, the fibrotic scar tissue evades (Dyskinesia) and thereby causes dead space for blood. By regenerating and strengthening the hibernating myocardium it gets capable of pulling the fibrotic scar inside (Akinesia) during contraction, thereby increasing the amount of blood pumped out of the heart (ejection fraction).
Graber M, Gollmann-Tepeköylü C, Schweiger V, Hirsch J, Pölzl L, Nägele F, et al. Modulation of cell fate by shock wave therapy in ischaemic heart disease. Eur Heart J Open. 2025;5(2):oeaf011.
Holfeld J, Nägele F, Pölzl L, Engler C, Graber M, Hirsch J, et al. Cardiac shockwave therapy in addition to coronary bypass surgery improves myocardial function in ischaemic heart failure: the CAST-HF trial. Eur Heart J. 2024;45(29):2634-43.
Nägele F, Pölzl L, Graber M, Hirsch J, Mayr A, Pamminger M, et al. Safety and efficacy of direct cardiac shockwave therapy in patients with ischemic cardiomyopathy undergoing coronary artery bypass grafting (the CAST-HF trial): study protocol for a randomized controlled trial-an update. Trials. 2022;23(1):988.
Graber M, Nägele F, Röhrs BT, Hirsch J, Pölzl L, Moriggl B, et al. Prevention of oxidative damage in spinal cord ischemia upon aortic surgery: First-in-human results of shock wave therapy prove safety and feasibility. J Am Heart Assoc. 2022;11(20):e026076.
Graber M, Nägele F, Hirsch J, Pölzl L, Schweiger V, Lechner S, et al. Cardiac shockwave therapy – A novel therapy for ischemic cardiomyopathy? Front Cardiovasc Med. 2022;9:875965.
Lobenwein D, Huber R, Kerbler L, Gratl A, Wipper S, Gollmann-Tepeköylü C, et al. Neuronal pre- and postconditioning via Toll-like receptor 3 agonist or extracorporeal shock wave therapy as new treatment strategies for spinal cord ischemia: An in vitro study. J Clin Med. 2022;11(8):2115.