Functional and morphologic evaluation of kidney proximal tubuli and correlation with renal allograft prognosis

Summary Renal transplant patients with stable graft function and proximal tubular dysfunction (PTD) have an increased risk for chronic allograft nephropathy (CAN). In this study, we investigated the histologic pattern associated with PTD and its correlation with graft outcome. Forty‐nine transplant...

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Veröffentlicht in:Transplant international 2010-05, Vol.23 (5), p.493-499
Hauptverfasser: De Matos, Ana Cristina Carvalho, Câmara, Niels Olsen Saraiva, De Oliveira, Ana Francisca Franco, Franco, Marcello F., Moura, Luiz Antonio Ribeiro, Nishida, Sonia, Pereira, Aparecido Bernardo, Pacheco‐Silva, Alvaro
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container_end_page 499
container_issue 5
container_start_page 493
container_title Transplant international
container_volume 23
creator De Matos, Ana Cristina Carvalho
Câmara, Niels Olsen Saraiva
De Oliveira, Ana Francisca Franco
Franco, Marcello F.
Moura, Luiz Antonio Ribeiro
Nishida, Sonia
Pereira, Aparecido Bernardo
Pacheco‐Silva, Alvaro
description Summary Renal transplant patients with stable graft function and proximal tubular dysfunction (PTD) have an increased risk for chronic allograft nephropathy (CAN). In this study, we investigated the histologic pattern associated with PTD and its correlation with graft outcome. Forty‐nine transplant patients with stable graft function were submitted to a biopsy. Simultaneously, urinary retinol‐binding protein (uRBP) was measured and creatinine clearance was also determined. Banff’s score and semi‐quantitative histologic analyses were performed to assess tubulointerstitial alterations. Patients were followed for 24.0 ± 7.8 months. At biopsy time, mean serum creatinine was 1.43 ± 0.33 mg/dl. Twelve patients (24.5%) had uRBP ≥1 mg/l, indicating PTD and 67% of biopsies had some degree of tubulointerstitial injury. At the end of the study period, 18 (36.7%) patients had lost renal function. uRBP levels were not associated with morphologic findings of interstitial fibrosis and tubular atrophy (IF/TA), interstitial fibrosis measured by Sirius red or tubulointerstitial damage. However, in multivariate analysis, the only variable associated with the loss of renal function was uRBP level ≥1 mg/l, determining a risk of 5.290 of loss of renal function (P = 0.003). Renal transplant patients who present PTD have functional alteration, which is not associated with morphologic alteration. This functional alteration is associated to progressive decrease in renal function.
doi_str_mv 10.1111/j.1432-2277.2009.01005.x
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In this study, we investigated the histologic pattern associated with PTD and its correlation with graft outcome. Forty‐nine transplant patients with stable graft function were submitted to a biopsy. Simultaneously, urinary retinol‐binding protein (uRBP) was measured and creatinine clearance was also determined. Banff’s score and semi‐quantitative histologic analyses were performed to assess tubulointerstitial alterations. Patients were followed for 24.0 ± 7.8 months. At biopsy time, mean serum creatinine was 1.43 ± 0.33 mg/dl. Twelve patients (24.5%) had uRBP ≥1 mg/l, indicating PTD and 67% of biopsies had some degree of tubulointerstitial injury. At the end of the study period, 18 (36.7%) patients had lost renal function. uRBP levels were not associated with morphologic findings of interstitial fibrosis and tubular atrophy (IF/TA), interstitial fibrosis measured by Sirius red or tubulointerstitial damage. However, in multivariate analysis, the only variable associated with the loss of renal function was uRBP level ≥1 mg/l, determining a risk of 5.290 of loss of renal function (P = 0.003). Renal transplant patients who present PTD have functional alteration, which is not associated with morphologic alteration. This functional alteration is associated to progressive decrease in renal function.</description><identifier>ISSN: 0934-0874</identifier><identifier>EISSN: 1432-2277</identifier><identifier>DOI: 10.1111/j.1432-2277.2009.01005.x</identifier><identifier>PMID: 19929858</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult ; Biopsy ; chronic allograft nephropathy ; Female ; Fibrosis ; Graft Survival ; Humans ; Kidney - metabolism ; kidney transplantation ; Kidney Transplantation - methods ; Kidney Tubules - pathology ; Male ; Middle Aged ; Multivariate analysis ; Prognosis ; proximal tubular function ; Retinol-Binding Proteins, Cellular - metabolism ; retinol‐binding protein ; surrogate marker ; Transplantation, Homologous - methods ; Transplants &amp; implants ; Treatment Outcome ; tubulointerstitial injury</subject><ispartof>Transplant international, 2010-05, Vol.23 (5), p.493-499</ispartof><rights>2009 The Authors. 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In this study, we investigated the histologic pattern associated with PTD and its correlation with graft outcome. Forty‐nine transplant patients with stable graft function were submitted to a biopsy. Simultaneously, urinary retinol‐binding protein (uRBP) was measured and creatinine clearance was also determined. Banff’s score and semi‐quantitative histologic analyses were performed to assess tubulointerstitial alterations. Patients were followed for 24.0 ± 7.8 months. At biopsy time, mean serum creatinine was 1.43 ± 0.33 mg/dl. Twelve patients (24.5%) had uRBP ≥1 mg/l, indicating PTD and 67% of biopsies had some degree of tubulointerstitial injury. At the end of the study period, 18 (36.7%) patients had lost renal function. uRBP levels were not associated with morphologic findings of interstitial fibrosis and tubular atrophy (IF/TA), interstitial fibrosis measured by Sirius red or tubulointerstitial damage. However, in multivariate analysis, the only variable associated with the loss of renal function was uRBP level ≥1 mg/l, determining a risk of 5.290 of loss of renal function (P = 0.003). Renal transplant patients who present PTD have functional alteration, which is not associated with morphologic alteration. This functional alteration is associated to progressive decrease in renal function.</description><subject>Adult</subject><subject>Biopsy</subject><subject>chronic allograft nephropathy</subject><subject>Female</subject><subject>Fibrosis</subject><subject>Graft Survival</subject><subject>Humans</subject><subject>Kidney - metabolism</subject><subject>kidney transplantation</subject><subject>Kidney Transplantation - methods</subject><subject>Kidney Tubules - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Multivariate analysis</subject><subject>Prognosis</subject><subject>proximal tubular function</subject><subject>Retinol-Binding Proteins, Cellular - metabolism</subject><subject>retinol‐binding protein</subject><subject>surrogate marker</subject><subject>Transplantation, Homologous - methods</subject><subject>Transplants &amp; implants</subject><subject>Treatment Outcome</subject><subject>tubulointerstitial injury</subject><issn>0934-0874</issn><issn>1432-2277</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkUtLxDAUhYMoOj7-ghRcuGrNs2kWLkR8DAiCjOuQSdOZ1LQZk1Zn_r3tjA_wbnLhfPfccA8ACYIZGuqqzhAlOMWY8wxDKDKIIGTZeg9MfoV9MIGC0BQWnB6B4xhrCCEuGDwER0gILApWTEB737e6s75VLlFtmTQ-rJbe-YXViflQrlejmPgqebNlazbJKvi1bQa66-e9s9sh7UMwbkd-2m6ZBLP1c4NPUFU3Di1aH208BQeVctGcfb8n4PX-bnb7mD49P0xvb55STShnqZ5jTZASnHJealMqwipSqTyvMBFEYGRKakpGc4KxRpgSUolCCcrMXBeMFuQEXO58h83vvYmdbGzUxjnVGt9HyQkhiPOcDeTFP7L2fRi-HyXieV6IHIrR7_yb6ueNKeUqDDcIG_lzyAG43gGf1pnNnw7lGJis5ZiLHHORY2ByG5hcy9nLdOzIF3fqimI</recordid><startdate>201005</startdate><enddate>201005</enddate><creator>De Matos, Ana Cristina Carvalho</creator><creator>Câmara, Niels Olsen Saraiva</creator><creator>De Oliveira, Ana Francisca Franco</creator><creator>Franco, Marcello F.</creator><creator>Moura, Luiz Antonio Ribeiro</creator><creator>Nishida, Sonia</creator><creator>Pereira, Aparecido Bernardo</creator><creator>Pacheco‐Silva, Alvaro</creator><general>Blackwell Publishing Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QO</scope><scope>7T5</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201005</creationdate><title>Functional and morphologic evaluation of kidney proximal tubuli and correlation with renal allograft prognosis</title><author>De Matos, Ana Cristina Carvalho ; Câmara, Niels Olsen Saraiva ; De Oliveira, Ana Francisca Franco ; Franco, Marcello F. ; Moura, Luiz Antonio Ribeiro ; Nishida, Sonia ; Pereira, Aparecido Bernardo ; Pacheco‐Silva, Alvaro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3475-cb2c31a97477dceda35f3fa66f2393921ed4ed546322c12433f98a945ebc85483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adult</topic><topic>Biopsy</topic><topic>chronic allograft nephropathy</topic><topic>Female</topic><topic>Fibrosis</topic><topic>Graft Survival</topic><topic>Humans</topic><topic>Kidney - metabolism</topic><topic>kidney transplantation</topic><topic>Kidney Transplantation - methods</topic><topic>Kidney Tubules - pathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Multivariate analysis</topic><topic>Prognosis</topic><topic>proximal tubular function</topic><topic>Retinol-Binding Proteins, Cellular - metabolism</topic><topic>retinol‐binding protein</topic><topic>surrogate marker</topic><topic>Transplantation, Homologous - methods</topic><topic>Transplants &amp; 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In this study, we investigated the histologic pattern associated with PTD and its correlation with graft outcome. Forty‐nine transplant patients with stable graft function were submitted to a biopsy. Simultaneously, urinary retinol‐binding protein (uRBP) was measured and creatinine clearance was also determined. Banff’s score and semi‐quantitative histologic analyses were performed to assess tubulointerstitial alterations. Patients were followed for 24.0 ± 7.8 months. At biopsy time, mean serum creatinine was 1.43 ± 0.33 mg/dl. Twelve patients (24.5%) had uRBP ≥1 mg/l, indicating PTD and 67% of biopsies had some degree of tubulointerstitial injury. At the end of the study period, 18 (36.7%) patients had lost renal function. uRBP levels were not associated with morphologic findings of interstitial fibrosis and tubular atrophy (IF/TA), interstitial fibrosis measured by Sirius red or tubulointerstitial damage. However, in multivariate analysis, the only variable associated with the loss of renal function was uRBP level ≥1 mg/l, determining a risk of 5.290 of loss of renal function (P = 0.003). Renal transplant patients who present PTD have functional alteration, which is not associated with morphologic alteration. This functional alteration is associated to progressive decrease in renal function.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>19929858</pmid><doi>10.1111/j.1432-2277.2009.01005.x</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Biopsy
chronic allograft nephropathy
Female
Fibrosis
Graft Survival
Humans
Kidney - metabolism
kidney transplantation
Kidney Transplantation - methods
Kidney Tubules - pathology
Male
Middle Aged
Multivariate analysis
Prognosis
proximal tubular function
Retinol-Binding Proteins, Cellular - metabolism
retinol‐binding protein
surrogate marker
Transplantation, Homologous - methods
Transplants & implants
Treatment Outcome
tubulointerstitial injury
title Functional and morphologic evaluation of kidney proximal tubuli and correlation with renal allograft prognosis
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