Proximal tubular dysfunction as an indicator of chronic graft dysfunction
Autor(a) principal: | |
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Data de Publicação: | 2009 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2009000300003 http://repositorio.unifesp.br/handle/11600/4911 |
Resumo: | New strategies are being devised to limit the impact of renal sclerosis on graft function. Individualization of immunosuppression, specifically the interruption of calcineurin-inhibitors has been tried in order to promote better graft survival once chronic graft dysfunction has been established. However, the long-term impact of these approaches is still not totally clear. Nevertheless, patients at higher risk for tubular atrophy and interstitial fibrosis (TA/IF) development should be carefully monitored for tubular function as well as glomerular performance. Since tubular-interstitial impairment is an early event in TA/IF pathogenesis and associated with graft function, it seems reasonable that strategies directed at assessing tubular structural integrity and function would yield important functional and prognostic data. The measurement of small proteins in urine such as α-1-microglobulin, N-acetyl-beta-D-glucosaminidase, alpha/pi S-glutathione transferases, β-2 microglobulin, and retinol binding protein is associated with proximal tubular cell dysfunction. Therefore, its straightforward assessment could provide a powerful tool in patient monitoring and ongoing clinical assessment of graft function, ultimately helping to facilitate longer patient and graft survival associated with good graft function. |
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Proximal tubular dysfunction as an indicator of chronic graft dysfunctionRenal transplantationTubular proteinsProximal tubular dysfunctionChronic allograft nephropathyRetinol binding proteinNew strategies are being devised to limit the impact of renal sclerosis on graft function. Individualization of immunosuppression, specifically the interruption of calcineurin-inhibitors has been tried in order to promote better graft survival once chronic graft dysfunction has been established. However, the long-term impact of these approaches is still not totally clear. Nevertheless, patients at higher risk for tubular atrophy and interstitial fibrosis (TA/IF) development should be carefully monitored for tubular function as well as glomerular performance. Since tubular-interstitial impairment is an early event in TA/IF pathogenesis and associated with graft function, it seems reasonable that strategies directed at assessing tubular structural integrity and function would yield important functional and prognostic data. The measurement of small proteins in urine such as α-1-microglobulin, N-acetyl-beta-D-glucosaminidase, alpha/pi S-glutathione transferases, β-2 microglobulin, and retinol binding protein is associated with proximal tubular cell dysfunction. Therefore, its straightforward assessment could provide a powerful tool in patient monitoring and ongoing clinical assessment of graft function, ultimately helping to facilitate longer patient and graft survival associated with good graft function.Universidade Federal de São Paulo (UNIFESP) Escola Paulista de Medicina Hospital do Rim e HipertensãoUniversidade Federal de São Paulo (UNIFESP) Instituto de Ciências Biomédicas IV Departamento de ImunologiaHarvard University Massachusetts General HospitalInstituto Israelita de Ensino e Pesquisa Hospital Albert Einstein Unidade de Transplante RenalUNIFESP, EPM, Hospital do Rim e HipertensãoUNIFESP, Instituto de Ciências Biomédicas IV Depto. de ImunologiaSciELOAssociação Brasileira de Divulgação CientíficaUniversidade Federal de São Paulo (UNIFESP)Harvard University Massachusetts General HospitalInstituto Israelita de Ensino e Pesquisa Hospital Albert Einstein Unidade de Transplante RenalCâmara, Niels Olsen Saraiva [UNIFESP]Williams Jr., W.w.Pacheco-Silva, Alvaro [UNIFESP]2015-06-14T13:39:06Z2015-06-14T13:39:06Z2009-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion229-236application/pdfhttp://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2009000300003Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 42, n. 3, p. 229-236, 2009.S0100-879X2009000300003.pdf0100-879XS0100-879X2009000300003http://repositorio.unifesp.br/handle/11600/4911WOS:000264200100003engBrazilian Journal of Medical and Biological Researchinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-29T18:29:32Zoai:repositorio.unifesp.br/:11600/4911Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-29T18:29:32Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Proximal tubular dysfunction as an indicator of chronic graft dysfunction |
title |
Proximal tubular dysfunction as an indicator of chronic graft dysfunction |
spellingShingle |
Proximal tubular dysfunction as an indicator of chronic graft dysfunction Câmara, Niels Olsen Saraiva [UNIFESP] Renal transplantation Tubular proteins Proximal tubular dysfunction Chronic allograft nephropathy Retinol binding protein |
title_short |
Proximal tubular dysfunction as an indicator of chronic graft dysfunction |
title_full |
Proximal tubular dysfunction as an indicator of chronic graft dysfunction |
title_fullStr |
Proximal tubular dysfunction as an indicator of chronic graft dysfunction |
title_full_unstemmed |
Proximal tubular dysfunction as an indicator of chronic graft dysfunction |
title_sort |
Proximal tubular dysfunction as an indicator of chronic graft dysfunction |
author |
Câmara, Niels Olsen Saraiva [UNIFESP] |
author_facet |
Câmara, Niels Olsen Saraiva [UNIFESP] Williams Jr., W.w. Pacheco-Silva, Alvaro [UNIFESP] |
author_role |
author |
author2 |
Williams Jr., W.w. Pacheco-Silva, Alvaro [UNIFESP] |
author2_role |
author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) Harvard University Massachusetts General Hospital Instituto Israelita de Ensino e Pesquisa Hospital Albert Einstein Unidade de Transplante Renal |
dc.contributor.author.fl_str_mv |
Câmara, Niels Olsen Saraiva [UNIFESP] Williams Jr., W.w. Pacheco-Silva, Alvaro [UNIFESP] |
dc.subject.por.fl_str_mv |
Renal transplantation Tubular proteins Proximal tubular dysfunction Chronic allograft nephropathy Retinol binding protein |
topic |
Renal transplantation Tubular proteins Proximal tubular dysfunction Chronic allograft nephropathy Retinol binding protein |
description |
New strategies are being devised to limit the impact of renal sclerosis on graft function. Individualization of immunosuppression, specifically the interruption of calcineurin-inhibitors has been tried in order to promote better graft survival once chronic graft dysfunction has been established. However, the long-term impact of these approaches is still not totally clear. Nevertheless, patients at higher risk for tubular atrophy and interstitial fibrosis (TA/IF) development should be carefully monitored for tubular function as well as glomerular performance. Since tubular-interstitial impairment is an early event in TA/IF pathogenesis and associated with graft function, it seems reasonable that strategies directed at assessing tubular structural integrity and function would yield important functional and prognostic data. The measurement of small proteins in urine such as α-1-microglobulin, N-acetyl-beta-D-glucosaminidase, alpha/pi S-glutathione transferases, β-2 microglobulin, and retinol binding protein is associated with proximal tubular cell dysfunction. Therefore, its straightforward assessment could provide a powerful tool in patient monitoring and ongoing clinical assessment of graft function, ultimately helping to facilitate longer patient and graft survival associated with good graft function. |
publishDate |
2009 |
dc.date.none.fl_str_mv |
2009-03-01 2015-06-14T13:39:06Z 2015-06-14T13:39:06Z |
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://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2009000300003 Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 42, n. 3, p. 229-236, 2009. S0100-879X2009000300003.pdf 0100-879X S0100-879X2009000300003 http://repositorio.unifesp.br/handle/11600/4911 WOS:000264200100003 |
url |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2009000300003 http://repositorio.unifesp.br/handle/11600/4911 |
identifier_str_mv |
Brazilian Journal of Medical and Biological Research. Associação Brasileira de Divulgação Científica, v. 42, n. 3, p. 229-236, 2009. S0100-879X2009000300003.pdf 0100-879X S0100-879X2009000300003 WOS:000264200100003 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Brazilian Journal of Medical and Biological Research |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
229-236 application/pdf |
dc.publisher.none.fl_str_mv |
Associação Brasileira de Divulgação Científica |
publisher.none.fl_str_mv |
Associação Brasileira de Divulgação Científica |
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_ |
1814268396498321408 |