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Updated: Oct 9, 2025

Author Spotlight: Development of a Minimally Invasive Large-Animal Model for Reliable and Reproducible Cardiovascular Research
Published on: October 20, 2023
Towards Personalized Therapy of Aortic Stenosis
Piotr Mazur1,2, Magdalena Kopytek2,3, Michał Ząbczyk2,3
1Department of Cardiovascular Surgery, Mayo Clinic, Rochester, MN 55902, USA.
Abstract:
Calcific aortic stenosis (CAS) is the most common cause of acquired valvular heart disease in adults with no available pharmacological treatment to inhibit the disease progression to date. This review provides an up-to-date overview of current knowledge of molecular mechanisms underlying CAS pathobiology and the related treatment pathways. Particular attention is paid to current randomized trials investigating medical treatment of CAS, including strategies based on lipid-lowering and antihypertensive therapies, phosphate and calcium metabolism, and novel therapeutic targets such as valvular oxidative stress, coagulation proteins, matrix metalloproteinases, and accumulation of advanced glycation end products.
Insights
Calcific aortic stenosis (CAS) lacks pharmacological treatments. This review details CAS molecular mechanisms and explores emerging therapies targeting lipid metabolism, oxidative stress, and advanced glycation end products.
Area of Science:
- Cardiovascular Medicine
- Molecular Biology
- Pharmacology
Background:
- Calcific aortic stenosis (CAS) is the leading cause of acquired valvular heart disease in adults.
- Currently, no pharmacological treatments exist to halt the progression of CAS.
Purpose of the Study:
- To provide an updated overview of the molecular mechanisms driving CAS pathobiology.
- To review current and emerging treatment strategies for CAS.
Main Methods:
- Literature review of current knowledge on CAS molecular mechanisms.
- Analysis of ongoing randomized trials for medical treatment of CAS.
- Examination of novel therapeutic targets and pathways.
Main Results:
- CAS involves complex molecular pathways including lipid metabolism, inflammation, and calcification.
- Investigated treatments include lipid-lowering, antihypertensive, and phosphate/calcium metabolism modulation.
- Emerging targets include oxidative stress, coagulation, matrix metalloproteinases, and advanced glycation end products.
Conclusions:
- Understanding CAS molecular mechanisms is crucial for developing effective treatments.
- Multiple therapeutic strategies are under investigation, offering hope for future pharmacological interventions.
- Targeting novel pathways may inhibit CAS progression and improve patient outcomes.
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