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Isolation and Characterization of Primary Rat Valve Interstitial Cells: A New Model to Study Aortic Valve Calcification
Published on: November 20, 2017
Novel pharmacological targets for calcific aortic valve disease: Prevention and treatments
Veronika A Myasoedova1, Alessio L Ravani1, Beatrice Frigerio1
1Centro Cardiologico Monzino IRCCS, Milan, Italy.
Insights
Calcific aortic valve disease (CAVD) affects 3% of Western adults, progressing from sclerosis to stenosis. This review explores novel therapeutic targets for CAVD, offering hope beyond current surgical interventions.
Area of Science:
- Cardiovascular Medicine
- Pathology
- Pharmacology
Background:
- Calcific aortic valve disease (CAVD) is a prevalent valvular disorder in the elderly.
- It progresses from aortic valve sclerosis (AVSc) to aortic valve stenosis (AS), involving complex pathological mechanisms.
- Current treatments for severe CAVD are limited to surgical or transcatheter interventions.
Purpose of the Study:
- To review current literature on pathological mechanisms of CAVD.
- To identify and discuss potential future pharmacological therapeutic targets for CAVD.
- To highlight the need for effective medical treatments for this condition.
Main Methods:
- Comprehensive literature review of existing research on CAVD.
- Analysis of pathological cellular and molecular mechanisms implicated in CAVD.
- Identification and evaluation of emerging therapeutic targets based on current evidence.
Main Results:
- CAVD pathogenesis involves matrix degradation, fibrosis, mineralization, inflammation, lipid accumulation, and neo-angiogenesis.
- Clinical risk factors for CAVD overlap significantly with atherosclerosis.
- Several potential therapeutic targets, including PCSK9, P2Y2 receptor, cadherin 11, and DDP-4, have been identified.
Conclusions:
- No approved pharmacological treatments currently exist for CAVD.
- Emerging therapeutic targets show promise for future medical interventions in CAVD.
- Further research into these targets could lead to novel treatments for this debilitating disease.
Abstract:
Calcific aortic valve disease (CAVD) is the most common valvular disorder in the elderly, with the incidence of 3% in general population of Western countries. The initial phase of CAVD is characterized by leaflet thickening and possible spotty calcification (i.e. aortic valve sclerosis (AVSc)), while advanced stages have leaflets structure degeneration (i.e. aortic valve stenosis (AS)). The pathological cellular and molecular mechanisms, involved in CAVD, are extracellular matrix degradation, aberrant matrix deposition, fibrosis, mineralization, inflammation, lipid accumulation, and neo-angiogenesis. CAVD clinical risk shares considerable overlap with those of atherosclerosis and they include hypertension, smoking habits, and hyperlipidemia. Unfortunately, surgical aortic valve replacement and transcatheter aortic valve implantation are the only available treatments when the disease become severe and symptoms occur. Indeed, no approved pharmacological approach is available for CAVD patients. In this review, we describe the current literature evidence on possible future therapeutic targets for this debilitating and fatal disease such as PCSK9, P2Y2 receptor, cadherin 11, and DDP-4.
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