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Tissue resident C reactive protein in degenerative aortic valves: correlation with serum C reactive protein
D Skowasch1, S Schrempf, C J Preusse
1Heart Centre University of Bonn, Bonn, Germany. Dirk.Skowasch@ukb.uni-bonn.de
Insights
C-reactive protein (CRP) is present in degenerative aortic valves, particularly bioprostheses. Statin use was associated with lower CRP levels in both valves and serum, suggesting a role in aortic stenosis management.
Area of Science:
- Cardiovascular Research
- Inflammation Biology
- Biomaterials Science
Background:
- Degenerative aortic valve disease involves complex inflammatory processes.
- C-reactive protein (CRP) is a key inflammatory marker, but its role in aortic valve pathology is not fully understood.
- Bioprosthetic valves may elicit distinct inflammatory responses compared to native valves.
Purpose of the Study:
- To investigate the presence and location of CRP in native degenerative aortic valves and bioprosthetic valves.
- To determine the relationship between CRP levels in valve tissue and serum.
- To explore the impact of statin medication on CRP expression in aortic valves and serum.
Main Methods:
- Analysis of degenerative aortic valve tissue (native stenosis and bioprostheses) and control valves using immunostaining and morphometry.
- Preoperative measurement of serum CRP concentrations.
- Comparison of CRP levels between patients with and without statin treatment.
Main Results:
- CRP was detected in the majority of native degenerative aortic valves and bioprosthetic valves, primarily in the fibrosa layer.
- CRP expression was significantly higher in bioprosthetic valves compared to native aortic stenosis valves.
- Serum CRP levels were elevated in bioprosthetic valve patients and correlated significantly with valvar CRP.
- Patients receiving statin treatment exhibited lower valvar and serum CRP concentrations compared to non-statin users.
Conclusions:
- C-reactive protein is a common finding in degenerative aortic valves, with higher prevalence in bioprosthetic valves.
- Serum CRP levels may serve as a biomarker for underlying aortic valve inflammation.
- The observed reduction in CRP with statin use suggests a potential mechanism for the pleiotropic benefits of statins in aortic stenosis.
Objective:
To assess aortic valve probes for valvar C reactive protein (CRP) presence, the relation between valvar and serum CRP, and a possible modification of CRP by statin medication.
Setting:
Tertiary referral centre.
Patients And Design:
End stage, degenerative valve tissue was taken from 81 patients, 57 with non-rheumatic aortic valve stenosis (AS) and 24 with degenerative aortic valve bioprosthesis (BP). Five non-stenosed valves served as controls. Tissue from four non-implanted bioprostheses was also examined. The presence and location of CRP was analysed by use of immunostaining and morphometry. Serum CRP concentrations were measured preoperatively.
Results:
The majority of AS and BP valves exhibited CRP labelled cells, predominantly localised to the valvar fibrosa. The expression of CRP was much higher in BP than in AS (by a factor of 3.7, p = 0.03). Notably, non-stenosed aortic valves and non-implanted bioprostheses did not have CRP signalling. Serum CRP was also increased with BP (by a factor of 2.5, p = 0.02) and was significantly correlated with valvar CRP expression (r = 0.54, p < 0.001). The main finding in patients with (n = 26) and without statin treatment (n = 55) was that both valvar CRP expression (p = 0.02) and serum CRP concentrations (p = 0.04) were lower in the statin treated group.
Conclusions:
CRP was found in a large series of degenerative aortic valves, more often in bioprostheses than in native cusps. Serum CRP concentrations may reflect inflammatory processes within the aortic valve. The association of statin treatment with decreases in both valvar and serum CRP concentrations may explain known pleiotropic effects of statins in patients with aortic stenosis.
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