Blood vessels and lymphatics in calcific aortic stenosis--in support of its inflammatory pathogenesis

I Steiner1, L Krbal, J Dominik

  • 1The Fingerland Department of Pathology, Charles University Faculty of Medicine and Faculty Hospital Hradec Králové, Czech Republic. steiner@lfhk.cuni.cz

Ceskoslovenska Patologie
|February 1, 2011
PubMed

Insights

Calcific aortic stenosis (CAS), a common heart valve disease, involves inflammation. This study found blood and lymphatic vessels with inflammatory cells in diseased aortic valves, supporting an inflammatory cause for CAS.

Area of Science:

  • Cardiovascular Pathology
  • Immunology
  • Vascular Biology

Background:

  • Calcific aortic stenosis (CAS) is the most prevalent acquired valvular heart disease in developed nations.
  • CAS is increasingly recognized as an inflammatory process, akin to atherosclerosis.
  • Etiologically, CAS is typically categorized as senile (degenerative) or related to a bicuspid aortic valve.

Purpose of the Study:

  • To investigate the presence and significance of vascularization and inflammation within calcified aortic valve cusps.
  • To compare the vascular and inflammatory patterns in senile versus bicuspid aortic valve types of CAS.
  • To provide evidence supporting the inflammatory theory of CAS pathogenesis.

Main Methods:

  • Histological examination and immunohistochemistry were performed on 28 human calcific aortic stenosis cases.
  • Specific markers CD31 (for blood vessels) and D2-40 (for lymphatics) were utilized.
  • Cases were classified into senile, bicuspid, or indeterminable types.

Main Results:

  • Blood vessels were identified in all 28 examined calcified aortic valve cusps.
  • Lymphatic vessels were present in 14 of the cases.
  • Vascularization was consistently associated with lymphocytic infiltrates in 24 cases, irrespective of CAS type.

Conclusions:

  • The presence of both blood and lymphatic vessels, alongside inflammatory cell infiltration, in calcified aortic cusps strongly supports an inflammatory mechanism in CAS pathogenesis.
  • These findings contribute to understanding the etiology of this common valvular disease.
  • The vascular and inflammatory patterns did not differ significantly between senile and bicuspid aortic valve types.

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