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Hepatic steatosis index at diagnosis has the potential for forecasting end-stage kidney disease in patients with antineutrophil cytoplasmic antibody-associated vasculitis

OBJECTIVE: This study evaluated whether the hepatic steatosis index (HSI) at antineutrophil cytoplasmic antibody-associated vasculitis (AAV) diagnosis could forecast poor outcomes during the disease course in AAV patients. METHODS: This study included 260 AAV patients. The equation for HSI is as fol...

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Autores principales: Choi, Hyun Joon, Park, Pil Gyu, Park, Yong-Beom, Huh, Ji Hye, Lee, Sang-Won, Ph.D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean College of Rheumatology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509637/
https://www.ncbi.nlm.nih.gov/pubmed/37736592
http://dx.doi.org/10.4078/jrd.2023.0032
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author Choi, Hyun Joon
Park, Pil Gyu
Park, Yong-Beom
Huh, Ji Hye
Lee, Sang-Won
Ph.D
author_facet Choi, Hyun Joon
Park, Pil Gyu
Park, Yong-Beom
Huh, Ji Hye
Lee, Sang-Won
Ph.D
author_sort Choi, Hyun Joon
collection PubMed
description OBJECTIVE: This study evaluated whether the hepatic steatosis index (HSI) at antineutrophil cytoplasmic antibody-associated vasculitis (AAV) diagnosis could forecast poor outcomes during the disease course in AAV patients. METHODS: This study included 260 AAV patients. The equation for HSI is as follows HSI=8×(alanine aminotransferase/aspartate aminotransferase)+body mass index+(2, diabetes mellitus)+(2, female). The cut-off of HSI was obtained using the receiver operating characteristic curve. RESULTS: The median age of the 260 patients was 59.5 years, and 65.0% were female. Among the continuous variables excluding the parameters composing the equation for HSI, HSI was significantly correlated with Birmingham vasculitis activity score, five-factor score, haemoglobin, blood urea nitrogen, serum creatinine, and total cholesterol. Among poor outcomes, the area under the curve of HSI for end-stage renal disease (ESRD) was significant, and the cut-off of HSI for ESRD was set at ≤30.82. AAV patients with HSI ≤30.82 exhibited a significantly higher risk of ESRD (relative risk 3.489) and a significantly lower cumulative ESRD-free survival rate than those with HSI >30.82. CONCLUSION: This study is the first to demonstrate that HSI at AAV diagnosis could forecast ESRD during the disease course in AAV patients.
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spelling pubmed-105096372023-09-21 Hepatic steatosis index at diagnosis has the potential for forecasting end-stage kidney disease in patients with antineutrophil cytoplasmic antibody-associated vasculitis Choi, Hyun Joon Park, Pil Gyu Park, Yong-Beom Huh, Ji Hye Lee, Sang-Won Ph.D J Rheum Dis Original Article OBJECTIVE: This study evaluated whether the hepatic steatosis index (HSI) at antineutrophil cytoplasmic antibody-associated vasculitis (AAV) diagnosis could forecast poor outcomes during the disease course in AAV patients. METHODS: This study included 260 AAV patients. The equation for HSI is as follows HSI=8×(alanine aminotransferase/aspartate aminotransferase)+body mass index+(2, diabetes mellitus)+(2, female). The cut-off of HSI was obtained using the receiver operating characteristic curve. RESULTS: The median age of the 260 patients was 59.5 years, and 65.0% were female. Among the continuous variables excluding the parameters composing the equation for HSI, HSI was significantly correlated with Birmingham vasculitis activity score, five-factor score, haemoglobin, blood urea nitrogen, serum creatinine, and total cholesterol. Among poor outcomes, the area under the curve of HSI for end-stage renal disease (ESRD) was significant, and the cut-off of HSI for ESRD was set at ≤30.82. AAV patients with HSI ≤30.82 exhibited a significantly higher risk of ESRD (relative risk 3.489) and a significantly lower cumulative ESRD-free survival rate than those with HSI >30.82. CONCLUSION: This study is the first to demonstrate that HSI at AAV diagnosis could forecast ESRD during the disease course in AAV patients. Korean College of Rheumatology 2023-10-01 2023-08-31 /pmc/articles/PMC10509637/ /pubmed/37736592 http://dx.doi.org/10.4078/jrd.2023.0032 Text en Copyright © 2023 by The Korean College of Rheumatology. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Choi, Hyun Joon
Park, Pil Gyu
Park, Yong-Beom
Huh, Ji Hye
Lee, Sang-Won
Ph.D
Hepatic steatosis index at diagnosis has the potential for forecasting end-stage kidney disease in patients with antineutrophil cytoplasmic antibody-associated vasculitis
title Hepatic steatosis index at diagnosis has the potential for forecasting end-stage kidney disease in patients with antineutrophil cytoplasmic antibody-associated vasculitis
title_full Hepatic steatosis index at diagnosis has the potential for forecasting end-stage kidney disease in patients with antineutrophil cytoplasmic antibody-associated vasculitis
title_fullStr Hepatic steatosis index at diagnosis has the potential for forecasting end-stage kidney disease in patients with antineutrophil cytoplasmic antibody-associated vasculitis
title_full_unstemmed Hepatic steatosis index at diagnosis has the potential for forecasting end-stage kidney disease in patients with antineutrophil cytoplasmic antibody-associated vasculitis
title_short Hepatic steatosis index at diagnosis has the potential for forecasting end-stage kidney disease in patients with antineutrophil cytoplasmic antibody-associated vasculitis
title_sort hepatic steatosis index at diagnosis has the potential for forecasting end-stage kidney disease in patients with antineutrophil cytoplasmic antibody-associated vasculitis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10509637/
https://www.ncbi.nlm.nih.gov/pubmed/37736592
http://dx.doi.org/10.4078/jrd.2023.0032
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