Cumulative Kaplan-Meier estimates of the rates of first event (ESRF or death). The fractions of patients free of ESRF or still alive at any time point according to the presence of mutations in CFH, CFI, C3, THBD, MCP, or CFH autoantibodies or without mutations (Non mut) are shown. The MCP group was chosen as the reference group. Hazard ratios and 95% confidence intervals calculated using the Cox proportional hazards regression model are shown. P values were calculated using the log-rank test. The comparisons that were statistically significant after Bonferroni correction are shown in the table. °Follow-up < 120 months.

Outcome of kidney transplantation. The outcome at 1 year of 64 transplanted kidneys in genotyped patients of the International Registry of HUS/TTP is reported, according to the absence or presence of a mutation. Plasma prophylaxis was used in three patients with CFH mutation, in one patient with C3 mutation, and in one patient with CFI mutation (*), all with good outcomes. Plasma was given to treat aHUS recurrences in 20 grafts. Remission was achieved in only three (°). The numbers of transplanted organs are shown above each column.

Summary of CFH (A), CFI (B), C3 (C), CFB (D), MCP (E), and THBD (F) variants and of combined mutations (G) in aHUS patients from the International Registry of Recurrent and Familial HUS/TTP. Already published mutations are reported in black; new mutations are in red; and polymorphisms are in green (newly described polymorphisms are in italic). Mutations found only in familial aHUS patients are in dark gray squares, those found both in familial and sporadic cases are in gray squares, and mutations found only in sporadic cases are in light gray squares. A, B, E, and F include also mutational events in patients with combined mutations. (A) CFH: 69% of the overall independent mutations in CFH cluster in the C terminus short consensus repeat (SCR) 20. Another cluster of mutations is located in SCRs 15 to 16 (15.5%). Six mutations resulted in truncated proteins at SCR8 (n = 1), SCR15 (n = 1), SCR17 (n = 1), and SCR20 (n = 3). The aHUS-associated polymorphism in SCR16 (E936D) is marked in green. To complete CFH genetic analysis, we also screened exon 10, which produces factor H-like 1, a splice variant containing the first eight SCRs of CFH, including the complement regulatory domain. No mutations and/or polymorphisms were found. (B) CFI: 6 mutations (58%) cluster in the serine-protease domain of CFI. Of note, the intronic change 1534 + 5 G>T that was previously reported by us as a HUS-associated mutation (15) is indicated in the figure as a polymorphism because, in this report, we found this variant in a healthy control. (C) C3: the mutations are spread all over the gene; however, a hot spot is evidenced in the thioester-containing domain (TED domain) with five independent mutations (42%). (D) CFB: only one heterozygous mutation (in SCR2) has been found. Eight polymorphic variants were identified. (E) MCP: 17 independent mutations (94%) cluster in the four SCRs at the N terminus of MCP, and 55.5% are located within SCR1, confirming the importance of this region for complement regulation. The R59X and C35Y mutations were identified four and three times, respectively, suggesting that they may represent a mutational hot spot in MCP. A L139L sinonymous polymorphism has been found in MCP in a sporadic patient, but it was not found in healthy controls. This subject carries also a mutation in CFH. The amino acid syntax of MCP that takes into account the signal peptide has been adopted. (F) THBD: three independent mutational events cluster in the lectin-like domain and six cluster in the serine threonine rich (ST-rich) peptide. (G) Diagram showing the number of patients with single or combined mutations from the International Registry of Recurrent and Familial HUS/TTP is reported. Numbers of patients with mutations in CFH, MCP, CFI, and THBD alone are shown in the circles. The numbers of patients carrying combined mutations are shown in the overlapping areas; the amino acid changes are reported in the corresponding boxes.

Cumulative Kaplan-Meier estimates of the rates of death. Fractions of patients still alive at any time point according to the presence of mutations in CFH, CFI, C3, THBD, MCP, or CFH autoantibodies or without mutations (Non mut) are shown. The CFH and THBD groups were chosen as reference groups. When feasible, hazard ratios and 95% confidence intervals were calculated by means of Cox proportional hazards regression model and shown in the figure. P values were calculated by means of the log-rank test after Bonferroni's correction. The most relevant comparisons are shown in the table. *Statistically significant after Bonferroni correction. °Follow-up < 120 months.