Table 2.
High (RR 80–90%) | - Previous recurrence - Pathogenic mutations in CFH - CFH/CFHR1 hybrid genes. >80 of recurrence rate. High graft loss risk (45, 114) - CFB > 80% of recurrence risk - TBHD = 80% (46, 47) |
Moderate (RR 40–75%) | - Isolated CFI mutations. 40–60% recurrence risk (11, 39, 41, 44) - C3. 30–70%* - Detectable circulating Anti–CFH antibodies (48–50) - Two at risk CFH haplotypes (39) - Negative complement genetic study 30% (11) - Complement gene mutation of unknown significance |
Low (RR <20%) | - Isolated MCP mutation+(41) - DGKε mutation (13) - Negative Anti–CFH antibodies at the time of transplantation (48–50) |
Recurrence risk varies depending on the different series.
Recurrences in patients with MCP account for patient with combined mutation/risk polimorphisms.
RR, recurrence risk; CFH, complement factor H; CFHR1 complement factor H related protein 1; CFB, complement factor B; TBHD, thrombomodulin; CFI, complement factor I; MCP, membrane cofactor protein; DGKε, diacylglycerol kinase epsilon.