Thrombotic microangiopathy after kidney transplantation: Analysis of the Brazilian Atypical Hemolytic Uremic Syndrome cohort
Main Author: | |
---|---|
Publication Date: | 2021 |
Other Authors: | , , , , , , , , |
Format: | Article |
Language: | eng |
Source: | Repositório Institucional da UNESP |
Download full: | http://dx.doi.org/10.1371/journal.pone.0258319 http://hdl.handle.net/11449/222832 |
Summary: | Background Atypical Hemolytic Uremic Syndrome (aHUS) is an ultra-rare disease that potentially leads to kidney graft failure due to ongoing Thrombotic Microangiopathy (TMA). The aim was evaluating the frequency of TMA after kidney transplantation in patients with aHUS in a Brazilian cohort stratified by the use of the specific complement-inhibitor eculizumab. Methods This was a multicenter retrospective cohort study including kidney transplant patients diagnosed with aHUS. We collected data from 118 transplant centers in Brazil concerning aHUS transplanted patients between 01/01/2007 and 12/31/2019. Patients were stratified into three groups: no use of eculizumab (No Eculizumab Group), use of eculizumab for treatment of after transplantation TMA (Therapeutic Group), and use of eculizumab for prophylaxis of aHUS recurrence (Prophylactic Group). Results Thirty-eight patients with aHUS who received kidney transplantation were enrolled in the study. Patients' mean age was 30 years (24-40), and the majority of participants was women (63% of cases). In the No Eculizumab Group (n = 11), there was a 91% graft loss due to the TMA. The hazard ratio of TMA graft loss was 0.07 [0.01-0.55], p = 0.012 in the eculizumab Prophylactic Group and 0.04 [0.00-0.28], p = 0.002 in the eculizumab Therapeutic Group. Conclusion The TMA graft loss in the absence of a specific complement-inhibitor was higher among the Brazilian cohort of kidney transplant patients. This finding reinforces the need of eculizumab use for treatment of aHUS kidney transplant patients. Cost optimization analysis and the early access to C5 inhibitors are suggested, especially in low-medium income countries. |
id |
UNSP_6469a5c63b5f9a1ae8bb10462ff1dffc |
---|---|
oai_identifier_str |
oai:repositorio.unesp.br:11449/222832 |
network_acronym_str |
UNSP |
network_name_str |
Repositório Institucional da UNESP |
repository_id_str |
2946 |
spelling |
Thrombotic microangiopathy after kidney transplantation: Analysis of the Brazilian Atypical Hemolytic Uremic Syndrome cohortBackground Atypical Hemolytic Uremic Syndrome (aHUS) is an ultra-rare disease that potentially leads to kidney graft failure due to ongoing Thrombotic Microangiopathy (TMA). The aim was evaluating the frequency of TMA after kidney transplantation in patients with aHUS in a Brazilian cohort stratified by the use of the specific complement-inhibitor eculizumab. Methods This was a multicenter retrospective cohort study including kidney transplant patients diagnosed with aHUS. We collected data from 118 transplant centers in Brazil concerning aHUS transplanted patients between 01/01/2007 and 12/31/2019. Patients were stratified into three groups: no use of eculizumab (No Eculizumab Group), use of eculizumab for treatment of after transplantation TMA (Therapeutic Group), and use of eculizumab for prophylaxis of aHUS recurrence (Prophylactic Group). Results Thirty-eight patients with aHUS who received kidney transplantation were enrolled in the study. Patients' mean age was 30 years (24-40), and the majority of participants was women (63% of cases). In the No Eculizumab Group (n = 11), there was a 91% graft loss due to the TMA. The hazard ratio of TMA graft loss was 0.07 [0.01-0.55], p = 0.012 in the eculizumab Prophylactic Group and 0.04 [0.00-0.28], p = 0.002 in the eculizumab Therapeutic Group. Conclusion The TMA graft loss in the absence of a specific complement-inhibitor was higher among the Brazilian cohort of kidney transplant patients. This finding reinforces the need of eculizumab use for treatment of aHUS kidney transplant patients. Cost optimization analysis and the early access to C5 inhibitors are suggested, especially in low-medium income countries.Department of Internal Medicine-UNESP Univ Estadual PaulistaDepartamento de Pediatria Hospital de Clinicas Universidade Estadual de Campinas, SPTransplant Unit São Jose Rio Preto/FAMERPTransplant Unit Santa Casa de Misericórdia de Porto Alegre-ISCMPASanta Casa de Belo HorizonteDepartment of Internal Medicine-UNESP Univ Estadual PaulistaUniversidade Estadual Paulista (UNESP)Universidade Estadual de Campinas (UNICAMP)Transplant Unit São Jose Rio Preto/FAMERPTransplant Unit Santa Casa de Misericórdia de Porto Alegre-ISCMPASanta Casa de Belo HorizonteNga, Hong Si [UNESP]Palma, Lilian Monteiro PereiraNeto, Miguel Ernandes [UNESP]Fernandes-Charpiot, Ida Maria MaximinaGarcia, Valter DuroKist, RogerMiranda, Silvana Maria Carvalhode Souza, Pedro Augusto MacedoPereira, Gerson MarquesDe Andrade, Luis Gustavo Modelli [UNESP]2022-04-28T19:47:04Z2022-04-28T19:47:04Z2021-11-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1371/journal.pone.0258319PLoS ONE, v. 16, n. 11 November, 2021.1932-6203http://hdl.handle.net/11449/22283210.1371/journal.pone.02583192-s2.0-85118838536Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPLoS ONEinfo:eu-repo/semantics/openAccess2022-04-28T19:47:04Zoai:repositorio.unesp.br:11449/222832Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462022-04-28T19:47:04Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Thrombotic microangiopathy after kidney transplantation: Analysis of the Brazilian Atypical Hemolytic Uremic Syndrome cohort |
title |
Thrombotic microangiopathy after kidney transplantation: Analysis of the Brazilian Atypical Hemolytic Uremic Syndrome cohort |
spellingShingle |
Thrombotic microangiopathy after kidney transplantation: Analysis of the Brazilian Atypical Hemolytic Uremic Syndrome cohort Nga, Hong Si [UNESP] |
title_short |
Thrombotic microangiopathy after kidney transplantation: Analysis of the Brazilian Atypical Hemolytic Uremic Syndrome cohort |
title_full |
Thrombotic microangiopathy after kidney transplantation: Analysis of the Brazilian Atypical Hemolytic Uremic Syndrome cohort |
title_fullStr |
Thrombotic microangiopathy after kidney transplantation: Analysis of the Brazilian Atypical Hemolytic Uremic Syndrome cohort |
title_full_unstemmed |
Thrombotic microangiopathy after kidney transplantation: Analysis of the Brazilian Atypical Hemolytic Uremic Syndrome cohort |
title_sort |
Thrombotic microangiopathy after kidney transplantation: Analysis of the Brazilian Atypical Hemolytic Uremic Syndrome cohort |
author |
Nga, Hong Si [UNESP] |
author_facet |
Nga, Hong Si [UNESP] Palma, Lilian Monteiro Pereira Neto, Miguel Ernandes [UNESP] Fernandes-Charpiot, Ida Maria Maximina Garcia, Valter Duro Kist, Roger Miranda, Silvana Maria Carvalho de Souza, Pedro Augusto Macedo Pereira, Gerson Marques De Andrade, Luis Gustavo Modelli [UNESP] |
author_role |
author |
author2 |
Palma, Lilian Monteiro Pereira Neto, Miguel Ernandes [UNESP] Fernandes-Charpiot, Ida Maria Maximina Garcia, Valter Duro Kist, Roger Miranda, Silvana Maria Carvalho de Souza, Pedro Augusto Macedo Pereira, Gerson Marques De Andrade, Luis Gustavo Modelli [UNESP] |
author2_role |
author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (UNESP) Universidade Estadual de Campinas (UNICAMP) Transplant Unit São Jose Rio Preto/FAMERP Transplant Unit Santa Casa de Misericórdia de Porto Alegre-ISCMPA Santa Casa de Belo Horizonte |
dc.contributor.author.fl_str_mv |
Nga, Hong Si [UNESP] Palma, Lilian Monteiro Pereira Neto, Miguel Ernandes [UNESP] Fernandes-Charpiot, Ida Maria Maximina Garcia, Valter Duro Kist, Roger Miranda, Silvana Maria Carvalho de Souza, Pedro Augusto Macedo Pereira, Gerson Marques De Andrade, Luis Gustavo Modelli [UNESP] |
description |
Background Atypical Hemolytic Uremic Syndrome (aHUS) is an ultra-rare disease that potentially leads to kidney graft failure due to ongoing Thrombotic Microangiopathy (TMA). The aim was evaluating the frequency of TMA after kidney transplantation in patients with aHUS in a Brazilian cohort stratified by the use of the specific complement-inhibitor eculizumab. Methods This was a multicenter retrospective cohort study including kidney transplant patients diagnosed with aHUS. We collected data from 118 transplant centers in Brazil concerning aHUS transplanted patients between 01/01/2007 and 12/31/2019. Patients were stratified into three groups: no use of eculizumab (No Eculizumab Group), use of eculizumab for treatment of after transplantation TMA (Therapeutic Group), and use of eculizumab for prophylaxis of aHUS recurrence (Prophylactic Group). Results Thirty-eight patients with aHUS who received kidney transplantation were enrolled in the study. Patients' mean age was 30 years (24-40), and the majority of participants was women (63% of cases). In the No Eculizumab Group (n = 11), there was a 91% graft loss due to the TMA. The hazard ratio of TMA graft loss was 0.07 [0.01-0.55], p = 0.012 in the eculizumab Prophylactic Group and 0.04 [0.00-0.28], p = 0.002 in the eculizumab Therapeutic Group. Conclusion The TMA graft loss in the absence of a specific complement-inhibitor was higher among the Brazilian cohort of kidney transplant patients. This finding reinforces the need of eculizumab use for treatment of aHUS kidney transplant patients. Cost optimization analysis and the early access to C5 inhibitors are suggested, especially in low-medium income countries. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-11-01 2022-04-28T19:47:04Z 2022-04-28T19:47:04Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1371/journal.pone.0258319 PLoS ONE, v. 16, n. 11 November, 2021. 1932-6203 http://hdl.handle.net/11449/222832 10.1371/journal.pone.0258319 2-s2.0-85118838536 |
url |
http://dx.doi.org/10.1371/journal.pone.0258319 http://hdl.handle.net/11449/222832 |
identifier_str_mv |
PLoS ONE, v. 16, n. 11 November, 2021. 1932-6203 10.1371/journal.pone.0258319 2-s2.0-85118838536 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
PLoS ONE |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
_version_ |
1834484489029419008 |