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Validation of the Oxford Classification of IgA Nephropathy: A Single-Center Study in Korean Adults

BACKGROUND/AIMS: The recently published Oxford classification of IgA nephropathy (IgAN) proposed a split system for histological grading, based on prognostic pathological features. This new classification system must be validated in a variety of cohorts. We investigated whether these pathological fe...

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Autores principales: Lee, Hoyoung, Yi, Sul Hee, Seo, Mi Seon, Hyun, Jin Nam, Jeon, Jin Seok, Noh, Hyunjin, Han, Dong Cheol, Hwang, Seung Duk, Jin, So Young, Kwon, Soon Hyo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Association of Internal Medicine 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443722/
https://www.ncbi.nlm.nih.gov/pubmed/23019394
http://dx.doi.org/10.3904/kjim.2012.27.3.293
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author Lee, Hoyoung
Yi, Sul Hee
Seo, Mi Seon
Hyun, Jin Nam
Jeon, Jin Seok
Noh, Hyunjin
Han, Dong Cheol
Hwang, Seung Duk
Jin, So Young
Kwon, Soon Hyo
author_facet Lee, Hoyoung
Yi, Sul Hee
Seo, Mi Seon
Hyun, Jin Nam
Jeon, Jin Seok
Noh, Hyunjin
Han, Dong Cheol
Hwang, Seung Duk
Jin, So Young
Kwon, Soon Hyo
author_sort Lee, Hoyoung
collection PubMed
description BACKGROUND/AIMS: The recently published Oxford classification of IgA nephropathy (IgAN) proposed a split system for histological grading, based on prognostic pathological features. This new classification system must be validated in a variety of cohorts. We investigated whether these pathological features were applicable to an adult Korean population. METHODS: In total, 69 adult Korean patients with IgAN were analyzed using the Oxford classification system at Soonchunhyang University Hospital, Seoul, Korea. All cases were categorized according to Lee's classification. Renal biopsies from all patients were scored by a pathologist who was blinded to the clinical data for pathological variables. Inclusion criteria were age greater than 18 years and at least 36 months of follow-up. We excluded cases with secondary IgAN, diabetic nephropathy combined other glomerulopathies, less than 36 months of follow-up, and those that progressed rapidly. RESULTS: The median age of the patients was 34 years (range, 27 to 45). Mean arterial blood pressure was 97 ± 10 mmHg at the time of biopsy. The median follow-up period was 85 months (range, 60 to 114). Kaplan-Meier analysis showed significant prognostic predictions for M, E, and T lesions. A Cox proportional hazard regression analysis also revealed prognostic predictions for E and T lesions. CONCLUSIONS: Using the Oxford classification in IgAN, E, and T lesions predicted renal outcome in Korean adults after taking clinical variables into account.
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spelling pubmed-34437222012-09-27 Validation of the Oxford Classification of IgA Nephropathy: A Single-Center Study in Korean Adults Lee, Hoyoung Yi, Sul Hee Seo, Mi Seon Hyun, Jin Nam Jeon, Jin Seok Noh, Hyunjin Han, Dong Cheol Hwang, Seung Duk Jin, So Young Kwon, Soon Hyo Korean J Intern Med Original Article BACKGROUND/AIMS: The recently published Oxford classification of IgA nephropathy (IgAN) proposed a split system for histological grading, based on prognostic pathological features. This new classification system must be validated in a variety of cohorts. We investigated whether these pathological features were applicable to an adult Korean population. METHODS: In total, 69 adult Korean patients with IgAN were analyzed using the Oxford classification system at Soonchunhyang University Hospital, Seoul, Korea. All cases were categorized according to Lee's classification. Renal biopsies from all patients were scored by a pathologist who was blinded to the clinical data for pathological variables. Inclusion criteria were age greater than 18 years and at least 36 months of follow-up. We excluded cases with secondary IgAN, diabetic nephropathy combined other glomerulopathies, less than 36 months of follow-up, and those that progressed rapidly. RESULTS: The median age of the patients was 34 years (range, 27 to 45). Mean arterial blood pressure was 97 ± 10 mmHg at the time of biopsy. The median follow-up period was 85 months (range, 60 to 114). Kaplan-Meier analysis showed significant prognostic predictions for M, E, and T lesions. A Cox proportional hazard regression analysis also revealed prognostic predictions for E and T lesions. CONCLUSIONS: Using the Oxford classification in IgAN, E, and T lesions predicted renal outcome in Korean adults after taking clinical variables into account. The Korean Association of Internal Medicine 2012-09 2012-09-01 /pmc/articles/PMC3443722/ /pubmed/23019394 http://dx.doi.org/10.3904/kjim.2012.27.3.293 Text en Copyright © 2012 The Korean Association of Internal Medicine http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Hoyoung
Yi, Sul Hee
Seo, Mi Seon
Hyun, Jin Nam
Jeon, Jin Seok
Noh, Hyunjin
Han, Dong Cheol
Hwang, Seung Duk
Jin, So Young
Kwon, Soon Hyo
Validation of the Oxford Classification of IgA Nephropathy: A Single-Center Study in Korean Adults
title Validation of the Oxford Classification of IgA Nephropathy: A Single-Center Study in Korean Adults
title_full Validation of the Oxford Classification of IgA Nephropathy: A Single-Center Study in Korean Adults
title_fullStr Validation of the Oxford Classification of IgA Nephropathy: A Single-Center Study in Korean Adults
title_full_unstemmed Validation of the Oxford Classification of IgA Nephropathy: A Single-Center Study in Korean Adults
title_short Validation of the Oxford Classification of IgA Nephropathy: A Single-Center Study in Korean Adults
title_sort validation of the oxford classification of iga nephropathy: a single-center study in korean adults
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443722/
https://www.ncbi.nlm.nih.gov/pubmed/23019394
http://dx.doi.org/10.3904/kjim.2012.27.3.293
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