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Gastrointestinal bleeding is associated with renal prognosis in adult patients with IgA vasculitis with nephritis

BACKGROUND: Although the prediction of renal prognosis in patients with IgA vasculitis with nephritis (IgAVN) is important, the association between gastrointestinal bleeding (GIB) and its renal prognosis is unknown. This study investigated the effect of GIB on the progression to end‐stage kidney dis...

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Autores principales: Shimamura, Yoshinosuke, Maeda, Takuto, Nishizawa, Keitaro, Ogawa, Yayoi, Takizawa, Hideki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942937/
https://www.ncbi.nlm.nih.gov/pubmed/31911884
http://dx.doi.org/10.1002/jgf2.285
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author Shimamura, Yoshinosuke
Maeda, Takuto
Nishizawa, Keitaro
Ogawa, Yayoi
Takizawa, Hideki
author_facet Shimamura, Yoshinosuke
Maeda, Takuto
Nishizawa, Keitaro
Ogawa, Yayoi
Takizawa, Hideki
author_sort Shimamura, Yoshinosuke
collection PubMed
description BACKGROUND: Although the prediction of renal prognosis in patients with IgA vasculitis with nephritis (IgAVN) is important, the association between gastrointestinal bleeding (GIB) and its renal prognosis is unknown. This study investigated the effect of GIB on the progression to end‐stage kidney disease (ESKD) in patients with IgAVN. METHODS: We compared the clinicopathological findings at diagnosis, therapy, and clinical outcomes between 10 patients with GIB and 20 patients without GIB in 30 patients with IgAVN aged ≥18 years at the renal biopsy. The primary outcome was the incidence of ESKD. Secondary outcomes included clinical remission and all‐cause mortality. The outcomes and factors affecting the progression to ESKD were evaluated using the Kaplan‐Meier method with log‐rank test and Cox proportional hazards models. RESULTS: End‐stage kidney disease, clinical remission, and deaths from any related cause occurred in 6, 17, and 2 patients, respectively. In Kaplan‐Meier analyses, the GIB group showed a higher incidence of ESKD (50% vs 5%, P = .003) and a lower incidence of clinical remission (20% vs 75%, P = .003). Although the numbers were not statistically significant, this group tended to have a greater number of deaths than the non‐GIB group (7% vs 0%, P = .07). In a multivariable Cox model adjusted for hypertension and urinary proteinuria, GIB could not demonstrate a significant association with ESKD (hazard ratio, 4.51; 95% confidence interval, 0.39‐52.7; P = .23). CONCLUSION: IgAVN with GIB has worse renal outcome, but GIB does not have a statistically significant association with progression to ESKD.
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spelling pubmed-69429372020-01-07 Gastrointestinal bleeding is associated with renal prognosis in adult patients with IgA vasculitis with nephritis Shimamura, Yoshinosuke Maeda, Takuto Nishizawa, Keitaro Ogawa, Yayoi Takizawa, Hideki J Gen Fam Med Original Articles BACKGROUND: Although the prediction of renal prognosis in patients with IgA vasculitis with nephritis (IgAVN) is important, the association between gastrointestinal bleeding (GIB) and its renal prognosis is unknown. This study investigated the effect of GIB on the progression to end‐stage kidney disease (ESKD) in patients with IgAVN. METHODS: We compared the clinicopathological findings at diagnosis, therapy, and clinical outcomes between 10 patients with GIB and 20 patients without GIB in 30 patients with IgAVN aged ≥18 years at the renal biopsy. The primary outcome was the incidence of ESKD. Secondary outcomes included clinical remission and all‐cause mortality. The outcomes and factors affecting the progression to ESKD were evaluated using the Kaplan‐Meier method with log‐rank test and Cox proportional hazards models. RESULTS: End‐stage kidney disease, clinical remission, and deaths from any related cause occurred in 6, 17, and 2 patients, respectively. In Kaplan‐Meier analyses, the GIB group showed a higher incidence of ESKD (50% vs 5%, P = .003) and a lower incidence of clinical remission (20% vs 75%, P = .003). Although the numbers were not statistically significant, this group tended to have a greater number of deaths than the non‐GIB group (7% vs 0%, P = .07). In a multivariable Cox model adjusted for hypertension and urinary proteinuria, GIB could not demonstrate a significant association with ESKD (hazard ratio, 4.51; 95% confidence interval, 0.39‐52.7; P = .23). CONCLUSION: IgAVN with GIB has worse renal outcome, but GIB does not have a statistically significant association with progression to ESKD. John Wiley and Sons Inc. 2019-10-15 /pmc/articles/PMC6942937/ /pubmed/31911884 http://dx.doi.org/10.1002/jgf2.285 Text en © 2019 The Authors. Journal of General and Family Medicine published by John Wiley & Sons Australia, Ltd on behalf of Japan Primary Care Association This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Shimamura, Yoshinosuke
Maeda, Takuto
Nishizawa, Keitaro
Ogawa, Yayoi
Takizawa, Hideki
Gastrointestinal bleeding is associated with renal prognosis in adult patients with IgA vasculitis with nephritis
title Gastrointestinal bleeding is associated with renal prognosis in adult patients with IgA vasculitis with nephritis
title_full Gastrointestinal bleeding is associated with renal prognosis in adult patients with IgA vasculitis with nephritis
title_fullStr Gastrointestinal bleeding is associated with renal prognosis in adult patients with IgA vasculitis with nephritis
title_full_unstemmed Gastrointestinal bleeding is associated with renal prognosis in adult patients with IgA vasculitis with nephritis
title_short Gastrointestinal bleeding is associated with renal prognosis in adult patients with IgA vasculitis with nephritis
title_sort gastrointestinal bleeding is associated with renal prognosis in adult patients with iga vasculitis with nephritis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942937/
https://www.ncbi.nlm.nih.gov/pubmed/31911884
http://dx.doi.org/10.1002/jgf2.285
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