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Clinical and pathological characteristics of non-diabetic renal disease in type 2 diabetes patients

BACKGROUND: Renal involvement in type 2 diabetes is mainly due to diabetic nephropathy (DN). Nevertheless, a sizable proportion of diabetic patients could actually have nondiabetic renal diseases (NDRDs) or DN plus NDRDs. This study aimed to explore the pathological features of NDRD in diabetic pati...

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Autores principales: Kritmetapak, Kittrawee, Anutrakulchai, Sirirat, Pongchaiyakul, Chatlert, Puapairoj, Anucha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007236/
https://www.ncbi.nlm.nih.gov/pubmed/29942497
http://dx.doi.org/10.1093/ckj/sfx111
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author Kritmetapak, Kittrawee
Anutrakulchai, Sirirat
Pongchaiyakul, Chatlert
Puapairoj, Anucha
author_facet Kritmetapak, Kittrawee
Anutrakulchai, Sirirat
Pongchaiyakul, Chatlert
Puapairoj, Anucha
author_sort Kritmetapak, Kittrawee
collection PubMed
description BACKGROUND: Renal involvement in type 2 diabetes is mainly due to diabetic nephropathy (DN). Nevertheless, a sizable proportion of diabetic patients could actually have nondiabetic renal diseases (NDRDs) or DN plus NDRDs. This study aimed to explore the pathological features of NDRD in diabetic patients and to assess the predictability of diagnosing NDRD (±DN) versus isolated DN on the basis of clinical parameters. METHODS: Medical records of type 2 diabetes patients who underwent renal biopsy under suspicion of NDRD from January 2011 through November 2015 were analyzed retrospectively. RESULTS: A total of 101 patients were enrolled in this study. The most frequent indication for renal biopsy was recent onset of nephrotic syndrome (41%), followed by rapidly progressive renal failure (29%) and active urinary sediment (21%). On renal biopsy, 51% of patients had isolated DN, 20% had isolated NDRD and 29% had DN plus NDRD. IgA nephropathy was the most common cause of isolated NDRD, whereas acute tubular necrosis (39%) and acute interstitial nephritis (33%) were the main causes of NDRD superimposed on DN. Male gender, short-duration diabetes (<8 years), lower glycated hemoglobin and active urinary sediment (≥10 red and white blood cells per high-power field) were independent predictors of NDRD according to multiple logistic regression analysis. CONCLUSIONS: Judicious use of renal biopsy revealed NDRD (±DN) in nearly half of type 2 diabetes patients with atypical renal presentation, especially in male patients with well-controlled diabetes, those who have had diabetes for a short duration and those with active urinary sediment.
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spelling pubmed-60072362018-06-25 Clinical and pathological characteristics of non-diabetic renal disease in type 2 diabetes patients Kritmetapak, Kittrawee Anutrakulchai, Sirirat Pongchaiyakul, Chatlert Puapairoj, Anucha Clin Kidney J Clinical Nephrology BACKGROUND: Renal involvement in type 2 diabetes is mainly due to diabetic nephropathy (DN). Nevertheless, a sizable proportion of diabetic patients could actually have nondiabetic renal diseases (NDRDs) or DN plus NDRDs. This study aimed to explore the pathological features of NDRD in diabetic patients and to assess the predictability of diagnosing NDRD (±DN) versus isolated DN on the basis of clinical parameters. METHODS: Medical records of type 2 diabetes patients who underwent renal biopsy under suspicion of NDRD from January 2011 through November 2015 were analyzed retrospectively. RESULTS: A total of 101 patients were enrolled in this study. The most frequent indication for renal biopsy was recent onset of nephrotic syndrome (41%), followed by rapidly progressive renal failure (29%) and active urinary sediment (21%). On renal biopsy, 51% of patients had isolated DN, 20% had isolated NDRD and 29% had DN plus NDRD. IgA nephropathy was the most common cause of isolated NDRD, whereas acute tubular necrosis (39%) and acute interstitial nephritis (33%) were the main causes of NDRD superimposed on DN. Male gender, short-duration diabetes (<8 years), lower glycated hemoglobin and active urinary sediment (≥10 red and white blood cells per high-power field) were independent predictors of NDRD according to multiple logistic regression analysis. CONCLUSIONS: Judicious use of renal biopsy revealed NDRD (±DN) in nearly half of type 2 diabetes patients with atypical renal presentation, especially in male patients with well-controlled diabetes, those who have had diabetes for a short duration and those with active urinary sediment. Oxford University Press 2018-06 2017-09-18 /pmc/articles/PMC6007236/ /pubmed/29942497 http://dx.doi.org/10.1093/ckj/sfx111 Text en © The Author 2017. Published by Oxford University Press on behalf of ERA-EDTA. http://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/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Clinical Nephrology
Kritmetapak, Kittrawee
Anutrakulchai, Sirirat
Pongchaiyakul, Chatlert
Puapairoj, Anucha
Clinical and pathological characteristics of non-diabetic renal disease in type 2 diabetes patients
title Clinical and pathological characteristics of non-diabetic renal disease in type 2 diabetes patients
title_full Clinical and pathological characteristics of non-diabetic renal disease in type 2 diabetes patients
title_fullStr Clinical and pathological characteristics of non-diabetic renal disease in type 2 diabetes patients
title_full_unstemmed Clinical and pathological characteristics of non-diabetic renal disease in type 2 diabetes patients
title_short Clinical and pathological characteristics of non-diabetic renal disease in type 2 diabetes patients
title_sort clinical and pathological characteristics of non-diabetic renal disease in type 2 diabetes patients
topic Clinical Nephrology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007236/
https://www.ncbi.nlm.nih.gov/pubmed/29942497
http://dx.doi.org/10.1093/ckj/sfx111
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