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Clinicopathologic characteristics, treatment, and outcomes of tubulointerstitial nephritis and uveitis syndrome in adults: A national retrospective strobe-compliant study
Tubulointerstitial nephritis and uveitis (TINU) syndrome is a rare disease, defined by the association of idiopathic acute TINU. The aim of our work was to determine the characteristics of adult TINU syndrome in France, and to assess factors (including treatment) influencing medium-term prognosis. W...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937908/ https://www.ncbi.nlm.nih.gov/pubmed/27367994 http://dx.doi.org/10.1097/MD.0000000000003964 |
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author | Legendre, Mathieu Devilliers, Hervé Perard, Laurent Groh, Matthieu Nefti, Habdelamid Dussol, Bertrand Trad, Salim Touré, Fatouma Abad, Sébastien Boffa, Jean-Jacques Frimat, Luc Torner, Stéphane Seidowsky, Alexandre Massy, Ziad André Saadoun, David Rieu, Virginie Schoindre, Yoland Heron, Emmanuel Frouget, Thierry Lionet, Arnaud Glowacki, François Arnaud, Laurent Mousson, Christiane Besancenot, Jean-François Rebibou, Jean-Michel Bielefeld, Philip |
author_facet | Legendre, Mathieu Devilliers, Hervé Perard, Laurent Groh, Matthieu Nefti, Habdelamid Dussol, Bertrand Trad, Salim Touré, Fatouma Abad, Sébastien Boffa, Jean-Jacques Frimat, Luc Torner, Stéphane Seidowsky, Alexandre Massy, Ziad André Saadoun, David Rieu, Virginie Schoindre, Yoland Heron, Emmanuel Frouget, Thierry Lionet, Arnaud Glowacki, François Arnaud, Laurent Mousson, Christiane Besancenot, Jean-François Rebibou, Jean-Michel Bielefeld, Philip |
author_sort | Legendre, Mathieu |
collection | PubMed |
description | Tubulointerstitial nephritis and uveitis (TINU) syndrome is a rare disease, defined by the association of idiopathic acute TINU. The aim of our work was to determine the characteristics of adult TINU syndrome in France, and to assess factors (including treatment) influencing medium-term prognosis. We conducted a nationwide study including 20 French hospitals. Clinical, laboratory, and renal histopathologic data of 41 biopsy-proven TINU syndromes were retrospectively collected. The patients were diagnosed between January 1, 1999 and December 1, 2015. Twenty-five females and 16 males were included (F/M ratio: 1.6:1). The median age at disease onset was 46.8 years (range 16.8–77.4) with a median serum creatinine level at 207 μmol/L (range 100–1687) and a median estimated glomerular filtration rate (eGFR) at 27 mL/min per 1.73 m(2) (range 2–73). Twenty-nine patients (71%) had a bilateral anterior uveitis and 24 (59%) had deterioration in general health at presentation. Moderate proteinuria was found in 32 patients (78%) (median proteinuria 0.52 g/24 h; range 0.10–2.10), aseptic leukocyturia in 25/36 patients (70%). The evaluation of renal biopsies revealed 41 patients (100%) with an acute tubulointerstitial nephritis, 19/39 patients (49%) with light to moderate fibrosis and 5 patients (12%) with an acute tubular necrosis. Thirty-six patients (88%) were treated with oral corticosteroids. After 1 year of follow-up, the median eGFR was 76 mL/min per 1.73 m(2) (range 17–119) and 32% of the patients suffered from moderate to severe chronic kidney disease. Serum creatinine (P < 0.001, r = −0.54), serum bicarbonate and phosphate levels (respectively, P = 0.01, r = 0.53; and P = 0.04, r = 0.46), and age (P = 0.03, r = −0.37) at the 1st symptoms were associated with eGFR after 1 year. During the 1st year 40% of patients had uveitis relapses. The use of oral corticosteroids was not associated with a better kidney function but was associated with fewer uveitis relapses (P = 0.44 and 0.02, respectively). In our study, 32% of patients were suffering from moderate to severe chronic kidney disease after 1 year of follow-up, and 40% had uveitis relapses during this follow-up. This work also suggests that oral corticosteroids are effective for the treatment of TINU syndrome's uveitis. |
format | Online Article Text |
id | pubmed-4937908 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-49379082016-08-18 Clinicopathologic characteristics, treatment, and outcomes of tubulointerstitial nephritis and uveitis syndrome in adults: A national retrospective strobe-compliant study Legendre, Mathieu Devilliers, Hervé Perard, Laurent Groh, Matthieu Nefti, Habdelamid Dussol, Bertrand Trad, Salim Touré, Fatouma Abad, Sébastien Boffa, Jean-Jacques Frimat, Luc Torner, Stéphane Seidowsky, Alexandre Massy, Ziad André Saadoun, David Rieu, Virginie Schoindre, Yoland Heron, Emmanuel Frouget, Thierry Lionet, Arnaud Glowacki, François Arnaud, Laurent Mousson, Christiane Besancenot, Jean-François Rebibou, Jean-Michel Bielefeld, Philip Medicine (Baltimore) 5200 Tubulointerstitial nephritis and uveitis (TINU) syndrome is a rare disease, defined by the association of idiopathic acute TINU. The aim of our work was to determine the characteristics of adult TINU syndrome in France, and to assess factors (including treatment) influencing medium-term prognosis. We conducted a nationwide study including 20 French hospitals. Clinical, laboratory, and renal histopathologic data of 41 biopsy-proven TINU syndromes were retrospectively collected. The patients were diagnosed between January 1, 1999 and December 1, 2015. Twenty-five females and 16 males were included (F/M ratio: 1.6:1). The median age at disease onset was 46.8 years (range 16.8–77.4) with a median serum creatinine level at 207 μmol/L (range 100–1687) and a median estimated glomerular filtration rate (eGFR) at 27 mL/min per 1.73 m(2) (range 2–73). Twenty-nine patients (71%) had a bilateral anterior uveitis and 24 (59%) had deterioration in general health at presentation. Moderate proteinuria was found in 32 patients (78%) (median proteinuria 0.52 g/24 h; range 0.10–2.10), aseptic leukocyturia in 25/36 patients (70%). The evaluation of renal biopsies revealed 41 patients (100%) with an acute tubulointerstitial nephritis, 19/39 patients (49%) with light to moderate fibrosis and 5 patients (12%) with an acute tubular necrosis. Thirty-six patients (88%) were treated with oral corticosteroids. After 1 year of follow-up, the median eGFR was 76 mL/min per 1.73 m(2) (range 17–119) and 32% of the patients suffered from moderate to severe chronic kidney disease. Serum creatinine (P < 0.001, r = −0.54), serum bicarbonate and phosphate levels (respectively, P = 0.01, r = 0.53; and P = 0.04, r = 0.46), and age (P = 0.03, r = −0.37) at the 1st symptoms were associated with eGFR after 1 year. During the 1st year 40% of patients had uveitis relapses. The use of oral corticosteroids was not associated with a better kidney function but was associated with fewer uveitis relapses (P = 0.44 and 0.02, respectively). In our study, 32% of patients were suffering from moderate to severe chronic kidney disease after 1 year of follow-up, and 40% had uveitis relapses during this follow-up. This work also suggests that oral corticosteroids are effective for the treatment of TINU syndrome's uveitis. Wolters Kluwer Health 2016-07-01 /pmc/articles/PMC4937908/ /pubmed/27367994 http://dx.doi.org/10.1097/MD.0000000000003964 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 5200 Legendre, Mathieu Devilliers, Hervé Perard, Laurent Groh, Matthieu Nefti, Habdelamid Dussol, Bertrand Trad, Salim Touré, Fatouma Abad, Sébastien Boffa, Jean-Jacques Frimat, Luc Torner, Stéphane Seidowsky, Alexandre Massy, Ziad André Saadoun, David Rieu, Virginie Schoindre, Yoland Heron, Emmanuel Frouget, Thierry Lionet, Arnaud Glowacki, François Arnaud, Laurent Mousson, Christiane Besancenot, Jean-François Rebibou, Jean-Michel Bielefeld, Philip Clinicopathologic characteristics, treatment, and outcomes of tubulointerstitial nephritis and uveitis syndrome in adults: A national retrospective strobe-compliant study |
title | Clinicopathologic characteristics, treatment, and outcomes of tubulointerstitial nephritis and uveitis syndrome in adults: A national retrospective strobe-compliant study |
title_full | Clinicopathologic characteristics, treatment, and outcomes of tubulointerstitial nephritis and uveitis syndrome in adults: A national retrospective strobe-compliant study |
title_fullStr | Clinicopathologic characteristics, treatment, and outcomes of tubulointerstitial nephritis and uveitis syndrome in adults: A national retrospective strobe-compliant study |
title_full_unstemmed | Clinicopathologic characteristics, treatment, and outcomes of tubulointerstitial nephritis and uveitis syndrome in adults: A national retrospective strobe-compliant study |
title_short | Clinicopathologic characteristics, treatment, and outcomes of tubulointerstitial nephritis and uveitis syndrome in adults: A national retrospective strobe-compliant study |
title_sort | clinicopathologic characteristics, treatment, and outcomes of tubulointerstitial nephritis and uveitis syndrome in adults: a national retrospective strobe-compliant study |
topic | 5200 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937908/ https://www.ncbi.nlm.nih.gov/pubmed/27367994 http://dx.doi.org/10.1097/MD.0000000000003964 |
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