Abstract
Background: The therapeutic potential of the human amnion has been known since the early twentieth century. Subsequent study has revealed the further therapeutic potential of all elements of the amnion—membrane, cells, fluid—in the treatment of cardiac disease. Materials and Methods: A systematic review was performed utilizing PubMed/MEDLINE and Embase with search terms including “amniotic fluid,” “cardiovascular disease,” “cardiac disease,” “amnion,” “amniotic membrane,” and “heart.” Results were reviewed by each author to ensure inclusion of all relevant articles. Animal studies were included for evaluation of existing preclinical models, and the few available clinical studies of amniotic products were included. Results: Preclinical studies addressing organ function, assessment, and enhancement of cardiac performance in response to injury, and regenerative potential are included, as are the few clinical studies utilizing amniotic products for the treatment of cardiac disease. Therapeutic approaches include reduction of inflammation, immunomodulation, and the promotion of myocardial regeneration via cellular therapy to target the most common mechanisms underlying myocardial injury. Conclusions: The components of the human amnion have anti-inflammatory, immunomodulatory, and pro-differentiation abilities which lend the ability to attenuate myocardial ischemia-reperfusion injury, temper cardiac fibrosis, and promote activation of progenitor cells to induce regeneration. Preclinical studies have focused heavily on cellular therapy, but clinical experience has yielded little success. The acellular components of the amnion have fueled more recent investigation and represent a new source of enthusiasm for clinical translation of amniotic products in the treatment of cardiac disease.
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Nickel, I., Mitchell, G., Javan, H., Pierce, J., Ripoll, C. V., & Selzman, C. H. (2025, January 1). Cardiovascular Therapeutic Applications of the Human Amnion: Membrane, Cells, and Beyond. Journal of Cardiovascular Pharmacology and Therapeutics. SAGE Publications Ltd. https://doi.org/10.1177/10742484251380914
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