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Updated: Oct 19, 2025

Modeling and Evaluation of Murine Diabetic Cardiomyopathy Model
Published on: November 29, 2024
Aortic valve disease in diabetes: Molecular mechanisms and novel therapies
Ileana Manduteanu1, Dan Simionescu2, Agneta Simionescu2
1Institute of Cellular Biology and Pathology "Nicolae Simionescu" of the Romanian Academy, Bucharest, Romania.
Insights
Diabetes accelerates calcific aortic valve disease (CAVD) progression, increasing cardiovascular risks. Understanding these mechanisms is crucial for developing new therapies to manage this growing global health burden.
Area of Science:
- Cardiovascular Research
- Diabetology
- Pathology
Background:
- Calcific aortic valve disease (CAVD) and diabetes mellitus (DM) are progressive global health burdens, particularly in aging populations.
- Diabetic patients exhibit a higher risk of cardiovascular disorders and accelerated degeneration of bioprosthetic aortic valves compared to non-diabetic individuals.
- Current pharmacological treatments to reverse or slow aortic valve disease progression in diabetes are lacking.
Purpose of the Study:
- To review current basic research on CAVD in the context of diabetes.
- To elucidate the mechanisms underlying diabetes-induced aortic valve disease progression.
- To identify potential biomarkers, therapeutic targets, and novel treatment strategies for CAVD in diabetic patients.
Main Methods:
- Review of existing literature on CAVD and diabetes.
- Analysis of experimental data from diabetic-hyperlipemic hamster models.
- Exploration of cell and molecular alterations in the aortic valve.
Main Results:
- Diabetes induces progressive cell and molecular alterations in the aortic valve, leading to calcification and CAVD.
- Identified potential biomarkers for assessing disease evolution and therapeutic response.
- Highlighted advancements in targeted nanotherapies, tissue engineering, and the role of circulating endothelial progenitor cells.
Conclusions:
- Diabetes significantly exacerbates CAVD, necessitating urgent research into underlying mechanisms.
- Novel biomarkers and therapeutic strategies, including nanotherapies and tissue engineering, show promise for managing CAVD in diabetic patients.
- Further research is critical to develop effective treatments for this complex condition.
Abstract:
Valve disease and particularly calcific aortic valve disease (CAVD) and diabetes (DM) are progressive diseases constituting a global health burden for all aging societies (Progress in Cardiovascular Diseases. 2014;56(6):565: Circulation Research. 2021;128(9):1344). Compared to non-diabetic individuals (The Lancet. 2008;371(9626):1800: The American Journal of Cardiology. 1983;51(3):403: Journal of the American College of Cardiology. 2017;69(12):1523), the diabetic patients have a significantly greater propensity for cardiovascular disorders and faster degeneration of implanted bioprosthetic aortic valves. Previously, using an original experimental model, the diabetic-hyperlipemic hamsters, we have shown that the earliest alterations induced by these conditions occur at the level of the aortic valves and, with time these changes lead to calcifications and CAVD. However, there are no pharmacological treatments available to reverse or retard the progression of aortic valve disease in diabetes, despite the significant advances in the field. Therefore, it is critical to uncover the mechanisms of valve disease progression, find biomarkers for diagnosis and new targets for therapies. This review aims at presenting an update on the basic research in CAVD in the context of diabetes. We provide an insight into the accumulated data including our results on diabetes-induced progressive cell and molecular alterations in the aortic valve, new potential biomarkers to assess the evolution and therapy of the disease, advancement in targeted nanotherapies, tissue engineering and the potential use of circulating endothelial progenitor cells in CAVD.
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