Table 1.
Parameter | Explanation | Ref. |
---|---|---|
Passive calcification mechanism | Both native and bioprosthetic heart valves involve passive calcification mechanisms. However, bioprosthetic valves, the effect of the debris of untreated dead cells is more pronounced. | [24] |
The effect of the crosslinking agent “glutaraldehyde” |
The presence of glutaraldehyde in bioprosthetic valves showed some procalcifying events: -Deactivation of membranes pumps allowing Ca2+ leakage from the mitochondrial membranes. -Increasing exposed areas through formation of void spaces. -Non-neutralized residues of glutaraldehyde. -Exposing larger numbers of more negative charges due to crosslinking of basic amino acids. |
[27] |
Bioprosthetic heart valve is accelerated version of native calcification | The calcification of native heart valves is a slowly proceeding disease. However, the bioprosthetic heart valves show a faster rate of progression in both children and elders. | [21] |
Age prevalence of incidence | For non-pathological conditions, elders are under high risk of calcification of heart valves in comparison to children. In contrast, with bioprosthetic heart valves substitutes, the children would develop much faster calcification. | [28, 29] |
Structural differences of calcific deposits | The solubility of mineral deposits of bioprosthetic heart valves is higher than in the corresponding deposits in the native valves. | [32] |
Immunological consideration | Several immune responses have been involved in calcification of native heart valves. However, there is no sufficient evidences to support their role in calcification of bioprosthetic heart valves. | [21] |