Clinical Features, Treatment and Prognostic Factors of Post-Transplant Immunoglobulin A Nephropathy

Detalhes bibliográficos
Autor(a) principal: Cabral, Diogo Buarque Cordeiro [UNIFESP]
Data de Publicação: 2018
Outros Autores: Sandes-Freitas, Taina Veras de [UNIFESP], Pestana, Jose Osmar Medina [UNIFESP], Kirsztajn, Gianna Mastroianni [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.12659/AOT.907167
https://repositorio.unifesp.br/handle/11600/55825
Resumo: Background: Initially described as a relatively benign condition, recent studies report graft loss in up to 50% of the patients with post-transplant IgA nephropathy. There is no evidence for the best therapeutic approach, and prognostic factors remain to be elucidated. Material/Methods: Single center retrospective analysis of patients >12 years old, with clinically relevant post-transplant IgA nephropathy (proteinuria >= 1.0g/g and/or graft dysfunction) and >= 6 months follow-up after diagnosis (n=47). Results: Living donor transplants represented 85% of cases. Dysmorphic hematuria (100%), blood pressure elevation (95.7%), renal dysfunction (70.2%) and subnephrotic proteinuria (60.6%) predominated at presentation. Using the Oxford Classification, mesangial proliferation was the main histological lesion (91%). Treatment consisted mostly of blockade of the renin angiotensin system (89.4%) and modification of immunosuppression (85.1%), mainly by increasing oral steroids dose (83%), with venous pulse therapy in 63.8% of cases. Partial and complete remission occurred in 48.9% and 17% of cases, respectively. One patient died (sepsis) and 15 patients (31.9%) lost their grafts due to nephropathy. The percentage of decrease in glomerular filtration rate at diagnosis was independently associated with partial remission (HR 0.97, 95% CI 0.94-0.99, p=0.01) and graft loss (HR 1.13, 95% CI 1.06-1.20, p<0.001). Deceased donor (HR 28.04, 95% CI 4.41-178.39, p<0.001) and donor age (HR 1.1, 95% CI 1.04-1.16, p=0.001) were also risk factors for graft loss. Conclusions: Despite treatment, most patients with post-transplant IgA nephropathy in this cohort study presented unfavorable outcomes, and graft dysfunction at diagnosis appeared to be the main prognostic marker.
id UFSP_8ae9db6295621cc4b10432261a1ac55f
oai_identifier_str oai:repositorio.unifesp.br/:11600/55825
network_acronym_str UFSP
network_name_str Repositório Institucional da UNIFESP
repository_id_str 3465
spelling Clinical Features, Treatment and Prognostic Factors of Post-Transplant Immunoglobulin A NephropathyGlomerulonephritis, IgAImmunosuppressive AgentsKidney TransplantationPrognosisBackground: Initially described as a relatively benign condition, recent studies report graft loss in up to 50% of the patients with post-transplant IgA nephropathy. There is no evidence for the best therapeutic approach, and prognostic factors remain to be elucidated. Material/Methods: Single center retrospective analysis of patients >12 years old, with clinically relevant post-transplant IgA nephropathy (proteinuria >= 1.0g/g and/or graft dysfunction) and >= 6 months follow-up after diagnosis (n=47). Results: Living donor transplants represented 85% of cases. Dysmorphic hematuria (100%), blood pressure elevation (95.7%), renal dysfunction (70.2%) and subnephrotic proteinuria (60.6%) predominated at presentation. Using the Oxford Classification, mesangial proliferation was the main histological lesion (91%). Treatment consisted mostly of blockade of the renin angiotensin system (89.4%) and modification of immunosuppression (85.1%), mainly by increasing oral steroids dose (83%), with venous pulse therapy in 63.8% of cases. Partial and complete remission occurred in 48.9% and 17% of cases, respectively. One patient died (sepsis) and 15 patients (31.9%) lost their grafts due to nephropathy. The percentage of decrease in glomerular filtration rate at diagnosis was independently associated with partial remission (HR 0.97, 95% CI 0.94-0.99, p=0.01) and graft loss (HR 1.13, 95% CI 1.06-1.20, p<0.001). Deceased donor (HR 28.04, 95% CI 4.41-178.39, p<0.001) and donor age (HR 1.1, 95% CI 1.04-1.16, p=0.001) were also risk factors for graft loss. Conclusions: Despite treatment, most patients with post-transplant IgA nephropathy in this cohort study presented unfavorable outcomes, and graft dysfunction at diagnosis appeared to be the main prognostic marker.Fed Univ Sao Paulo UNIFESP, Nephrol Div, Glomerulopathies Sect, Sao Paulo, SP, BrazilFed Univ Sao Paulo UNIFESP, Nephrol Div, Transplantat Sect, Sao Paulo, SP, BrazilHosp Rim, Sao Paulo, SP, BrazilFed Univ Sao Paulo UNIFESP, Nephrol Div, Glomerulopathies Sect, Sao Paulo, SP, BrazilFed Univ Sao Paulo UNIFESP, Nephrol Div, Transplantat Sect, Sao Paulo, SP, BrazilWeb of ScienceInt Scientific Literature, Inc2020-07-20T16:31:15Z2020-07-20T16:31:15Z2018info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion166-175application/pdfhttp://dx.doi.org/10.12659/AOT.907167Annals Of Transplantation. Smithtown, v. 23, p. 166-175, 2018.10.12659/AOT.907167WOS000427524500001.pdf1425-9524https://repositorio.unifesp.br/handle/11600/55825WOS:000427524500001engAnnals Of TransplantationSmithtowninfo:eu-repo/semantics/openAccessCabral, Diogo Buarque Cordeiro [UNIFESP]Sandes-Freitas, Taina Veras de [UNIFESP]Pestana, Jose Osmar Medina [UNIFESP]Kirsztajn, Gianna Mastroianni [UNIFESP]reponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-03T08:36:10Zoai:repositorio.unifesp.br/:11600/55825Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-03T08:36:10Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Clinical Features, Treatment and Prognostic Factors of Post-Transplant Immunoglobulin A Nephropathy
title Clinical Features, Treatment and Prognostic Factors of Post-Transplant Immunoglobulin A Nephropathy
spellingShingle Clinical Features, Treatment and Prognostic Factors of Post-Transplant Immunoglobulin A Nephropathy
Cabral, Diogo Buarque Cordeiro [UNIFESP]
Glomerulonephritis, IgA
Immunosuppressive Agents
Kidney Transplantation
Prognosis
title_short Clinical Features, Treatment and Prognostic Factors of Post-Transplant Immunoglobulin A Nephropathy
title_full Clinical Features, Treatment and Prognostic Factors of Post-Transplant Immunoglobulin A Nephropathy
title_fullStr Clinical Features, Treatment and Prognostic Factors of Post-Transplant Immunoglobulin A Nephropathy
title_full_unstemmed Clinical Features, Treatment and Prognostic Factors of Post-Transplant Immunoglobulin A Nephropathy
title_sort Clinical Features, Treatment and Prognostic Factors of Post-Transplant Immunoglobulin A Nephropathy
author Cabral, Diogo Buarque Cordeiro [UNIFESP]
author_facet Cabral, Diogo Buarque Cordeiro [UNIFESP]
Sandes-Freitas, Taina Veras de [UNIFESP]
Pestana, Jose Osmar Medina [UNIFESP]
Kirsztajn, Gianna Mastroianni [UNIFESP]
author_role author
author2 Sandes-Freitas, Taina Veras de [UNIFESP]
Pestana, Jose Osmar Medina [UNIFESP]
Kirsztajn, Gianna Mastroianni [UNIFESP]
author2_role author
author
author
dc.contributor.author.fl_str_mv Cabral, Diogo Buarque Cordeiro [UNIFESP]
Sandes-Freitas, Taina Veras de [UNIFESP]
Pestana, Jose Osmar Medina [UNIFESP]
Kirsztajn, Gianna Mastroianni [UNIFESP]
dc.subject.por.fl_str_mv Glomerulonephritis, IgA
Immunosuppressive Agents
Kidney Transplantation
Prognosis
topic Glomerulonephritis, IgA
Immunosuppressive Agents
Kidney Transplantation
Prognosis
description Background: Initially described as a relatively benign condition, recent studies report graft loss in up to 50% of the patients with post-transplant IgA nephropathy. There is no evidence for the best therapeutic approach, and prognostic factors remain to be elucidated. Material/Methods: Single center retrospective analysis of patients >12 years old, with clinically relevant post-transplant IgA nephropathy (proteinuria >= 1.0g/g and/or graft dysfunction) and >= 6 months follow-up after diagnosis (n=47). Results: Living donor transplants represented 85% of cases. Dysmorphic hematuria (100%), blood pressure elevation (95.7%), renal dysfunction (70.2%) and subnephrotic proteinuria (60.6%) predominated at presentation. Using the Oxford Classification, mesangial proliferation was the main histological lesion (91%). Treatment consisted mostly of blockade of the renin angiotensin system (89.4%) and modification of immunosuppression (85.1%), mainly by increasing oral steroids dose (83%), with venous pulse therapy in 63.8% of cases. Partial and complete remission occurred in 48.9% and 17% of cases, respectively. One patient died (sepsis) and 15 patients (31.9%) lost their grafts due to nephropathy. The percentage of decrease in glomerular filtration rate at diagnosis was independently associated with partial remission (HR 0.97, 95% CI 0.94-0.99, p=0.01) and graft loss (HR 1.13, 95% CI 1.06-1.20, p<0.001). Deceased donor (HR 28.04, 95% CI 4.41-178.39, p<0.001) and donor age (HR 1.1, 95% CI 1.04-1.16, p=0.001) were also risk factors for graft loss. Conclusions: Despite treatment, most patients with post-transplant IgA nephropathy in this cohort study presented unfavorable outcomes, and graft dysfunction at diagnosis appeared to be the main prognostic marker.
publishDate 2018
dc.date.none.fl_str_mv 2018
2020-07-20T16:31:15Z
2020-07-20T16:31:15Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.12659/AOT.907167
Annals Of Transplantation. Smithtown, v. 23, p. 166-175, 2018.
10.12659/AOT.907167
WOS000427524500001.pdf
1425-9524
https://repositorio.unifesp.br/handle/11600/55825
WOS:000427524500001
url http://dx.doi.org/10.12659/AOT.907167
https://repositorio.unifesp.br/handle/11600/55825
identifier_str_mv Annals Of Transplantation. Smithtown, v. 23, p. 166-175, 2018.
10.12659/AOT.907167
WOS000427524500001.pdf
1425-9524
WOS:000427524500001
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Annals Of Transplantation
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 166-175
application/pdf
dc.coverage.none.fl_str_mv Smithtown
dc.publisher.none.fl_str_mv Int Scientific Literature, Inc
publisher.none.fl_str_mv Int Scientific Literature, Inc
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
_version_ 1814268321294450688