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A Systematic Review of Renal Pathology in Chronic Kidney Disease of Uncertain Etiology

INTRODUCTION: Despite much research on chronic kidney disease of uncertain etiology (CKDu) in Sri Lanka and the Mesoamerican nephropathy, the etiology and pathogenesis of this disease remains elusive. The pathology has broadly been described as chronic tubulointerstitial nephritis and no specific si...

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Autores principales: Gunawardena, Sameera, Dayaratne, Maleesha, Wijesinghe, Harshima, Wijewickrama, Eranga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207327/
https://www.ncbi.nlm.nih.gov/pubmed/34169213
http://dx.doi.org/10.1016/j.ekir.2021.03.898
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author Gunawardena, Sameera
Dayaratne, Maleesha
Wijesinghe, Harshima
Wijewickrama, Eranga
author_facet Gunawardena, Sameera
Dayaratne, Maleesha
Wijesinghe, Harshima
Wijewickrama, Eranga
author_sort Gunawardena, Sameera
collection PubMed
description INTRODUCTION: Despite much research on chronic kidney disease of uncertain etiology (CKDu) in Sri Lanka and the Mesoamerican nephropathy, the etiology and pathogenesis of this disease remains elusive. The pathology has broadly been described as chronic tubulointerstitial nephritis and no specific signature lesions have been identified. METHODS: A scoping review was conducted through MEDLINE and Google Scholar databases for peer-reviewed publications on biopsy studies related to CKDu – Sri Lanka and Mesoamerican nephropathy to develop a comparative and critical analysis of the renal pathology found in these patients. RESULTS: Thirteen studies met the selection criteria. Interstitial fibrosis was the predominant lesion in all the studies. Tubulointerstitial and glomerular abnormalities showed a more variable distribution. No characteristic histopathological feature was reported other than a proximal tubular lysosomal inclusion body which was claimed to indicate a toxic etiology. Three main pathogenetic mechanisms were postulated: repeated acute insults leading to scarring, low-grade chronic insults leading to non-inflammatory fibrosis, and tubulointerstitial damage in combination with glomerular injury. The main limitations in the interpretation and comparative analysis of these studies were the heterogeneity in case selection and biopsy reporting. CONCLUSIONS: Although no characteristic histopathological feature could be found in CKDu–Sri Lanka or Mesoamerican nephropathy, there are noticeable differences between these two groups in the frequency and severity of the glomerular and tubulointerstitial changes which warrant more explorative studies preferably on kidneys in early stages of the disease. Future strategies should ensure that more uniform selection criteria and reporting methods are used.
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spelling pubmed-82073272021-06-23 A Systematic Review of Renal Pathology in Chronic Kidney Disease of Uncertain Etiology Gunawardena, Sameera Dayaratne, Maleesha Wijesinghe, Harshima Wijewickrama, Eranga Kidney Int Rep Clinical Research INTRODUCTION: Despite much research on chronic kidney disease of uncertain etiology (CKDu) in Sri Lanka and the Mesoamerican nephropathy, the etiology and pathogenesis of this disease remains elusive. The pathology has broadly been described as chronic tubulointerstitial nephritis and no specific signature lesions have been identified. METHODS: A scoping review was conducted through MEDLINE and Google Scholar databases for peer-reviewed publications on biopsy studies related to CKDu – Sri Lanka and Mesoamerican nephropathy to develop a comparative and critical analysis of the renal pathology found in these patients. RESULTS: Thirteen studies met the selection criteria. Interstitial fibrosis was the predominant lesion in all the studies. Tubulointerstitial and glomerular abnormalities showed a more variable distribution. No characteristic histopathological feature was reported other than a proximal tubular lysosomal inclusion body which was claimed to indicate a toxic etiology. Three main pathogenetic mechanisms were postulated: repeated acute insults leading to scarring, low-grade chronic insults leading to non-inflammatory fibrosis, and tubulointerstitial damage in combination with glomerular injury. The main limitations in the interpretation and comparative analysis of these studies were the heterogeneity in case selection and biopsy reporting. CONCLUSIONS: Although no characteristic histopathological feature could be found in CKDu–Sri Lanka or Mesoamerican nephropathy, there are noticeable differences between these two groups in the frequency and severity of the glomerular and tubulointerstitial changes which warrant more explorative studies preferably on kidneys in early stages of the disease. Future strategies should ensure that more uniform selection criteria and reporting methods are used. Elsevier 2021-04-20 /pmc/articles/PMC8207327/ /pubmed/34169213 http://dx.doi.org/10.1016/j.ekir.2021.03.898 Text en © 2021 International Society of Nephrology. Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Clinical Research
Gunawardena, Sameera
Dayaratne, Maleesha
Wijesinghe, Harshima
Wijewickrama, Eranga
A Systematic Review of Renal Pathology in Chronic Kidney Disease of Uncertain Etiology
title A Systematic Review of Renal Pathology in Chronic Kidney Disease of Uncertain Etiology
title_full A Systematic Review of Renal Pathology in Chronic Kidney Disease of Uncertain Etiology
title_fullStr A Systematic Review of Renal Pathology in Chronic Kidney Disease of Uncertain Etiology
title_full_unstemmed A Systematic Review of Renal Pathology in Chronic Kidney Disease of Uncertain Etiology
title_short A Systematic Review of Renal Pathology in Chronic Kidney Disease of Uncertain Etiology
title_sort systematic review of renal pathology in chronic kidney disease of uncertain etiology
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8207327/
https://www.ncbi.nlm.nih.gov/pubmed/34169213
http://dx.doi.org/10.1016/j.ekir.2021.03.898
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