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Clinicopathological correlates of chronic kidney disease of unknown etiology in Sri Lanka
Chronic kidney disease of unknown etiology (CKDu) is a major healthcare issue in Sri Lanka. This study included 125 consecutive patients with a diagnosis of CKDu undergoing renal biopsy at one hospital from 2008 to 2012. Associations between renal outcome parameters, epidemiological data, and histop...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015515/ https://www.ncbi.nlm.nih.gov/pubmed/27795631 http://dx.doi.org/10.4103/0971-4065.167280 |
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author | Selvarajah, M. Weeratunga, P. Sivayoganthan, S. Rathnatunga, N. Rajapakse, S. |
author_facet | Selvarajah, M. Weeratunga, P. Sivayoganthan, S. Rathnatunga, N. Rajapakse, S. |
author_sort | Selvarajah, M. |
collection | PubMed |
description | Chronic kidney disease of unknown etiology (CKDu) is a major healthcare issue in Sri Lanka. This study included 125 consecutive patients with a diagnosis of CKDu undergoing renal biopsy at one hospital from 2008 to 2012. Associations between renal outcome parameters, epidemiological data, and histopathological findings were examined and regression models constructed based on univariate associations with outcome variables as serum creatinine >1.2 and stage of CKD >3. The mean patient age was 46.21 years (standard deviation = 11.64). A marked male predominance was noted. A positive family history of CKD was seen in 35.8%. Prominent histopathological features were glomerular sclerosis (94.8%), interstitial infiltration (76%) with lymphocytic infiltration, interstitial fibrosis (71.2%), and tubular atrophy (70.4%). Importantly, significant histological changes were seen in patients with early CKDu. For CKD stage >3 independent associations were: interstitial fibrosis [P = 0.005; odds ratio (OR) =0.153] and interstitial infiltrate (P = 0.030; OR = 0.2440. For serum creatinine >1.2, independent predictors were >50% glomerular sclerosis (P = 0.041; OR = 0.92), tubular atrophy (P = 0.034; OR = 0.171, and more than 40 residential life years (P = 0.009; OR = 9.229). Chronic tubulointerstitial nephritis (TIN) appears to be the predominant histopathological finding in patients with CKDu, with significant renal pathology established early on in the course of the disease. Interstitial infiltration appears to be an independent association of advancing CKD, CKDu, histopathology, histology, and TIN. |
format | Online Article Text |
id | pubmed-5015515 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-50155152016-10-28 Clinicopathological correlates of chronic kidney disease of unknown etiology in Sri Lanka Selvarajah, M. Weeratunga, P. Sivayoganthan, S. Rathnatunga, N. Rajapakse, S. Indian J Nephrol Original Article Chronic kidney disease of unknown etiology (CKDu) is a major healthcare issue in Sri Lanka. This study included 125 consecutive patients with a diagnosis of CKDu undergoing renal biopsy at one hospital from 2008 to 2012. Associations between renal outcome parameters, epidemiological data, and histopathological findings were examined and regression models constructed based on univariate associations with outcome variables as serum creatinine >1.2 and stage of CKD >3. The mean patient age was 46.21 years (standard deviation = 11.64). A marked male predominance was noted. A positive family history of CKD was seen in 35.8%. Prominent histopathological features were glomerular sclerosis (94.8%), interstitial infiltration (76%) with lymphocytic infiltration, interstitial fibrosis (71.2%), and tubular atrophy (70.4%). Importantly, significant histological changes were seen in patients with early CKDu. For CKD stage >3 independent associations were: interstitial fibrosis [P = 0.005; odds ratio (OR) =0.153] and interstitial infiltrate (P = 0.030; OR = 0.2440. For serum creatinine >1.2, independent predictors were >50% glomerular sclerosis (P = 0.041; OR = 0.92), tubular atrophy (P = 0.034; OR = 0.171, and more than 40 residential life years (P = 0.009; OR = 9.229). Chronic tubulointerstitial nephritis (TIN) appears to be the predominant histopathological finding in patients with CKDu, with significant renal pathology established early on in the course of the disease. Interstitial infiltration appears to be an independent association of advancing CKD, CKDu, histopathology, histology, and TIN. Medknow Publications & Media Pvt Ltd 2016-09 /pmc/articles/PMC5015515/ /pubmed/27795631 http://dx.doi.org/10.4103/0971-4065.167280 Text en Copyright: © Indian Journal of Nephrology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Selvarajah, M. Weeratunga, P. Sivayoganthan, S. Rathnatunga, N. Rajapakse, S. Clinicopathological correlates of chronic kidney disease of unknown etiology in Sri Lanka |
title | Clinicopathological correlates of chronic kidney disease of unknown etiology in Sri Lanka |
title_full | Clinicopathological correlates of chronic kidney disease of unknown etiology in Sri Lanka |
title_fullStr | Clinicopathological correlates of chronic kidney disease of unknown etiology in Sri Lanka |
title_full_unstemmed | Clinicopathological correlates of chronic kidney disease of unknown etiology in Sri Lanka |
title_short | Clinicopathological correlates of chronic kidney disease of unknown etiology in Sri Lanka |
title_sort | clinicopathological correlates of chronic kidney disease of unknown etiology in sri lanka |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015515/ https://www.ncbi.nlm.nih.gov/pubmed/27795631 http://dx.doi.org/10.4103/0971-4065.167280 |
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