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Increased Rates of Supplement-Associated Oxalate Nephropathy During COVID-19 Pandemic

INTRODUCTION: Causes of secondary oxalate nephropathy include enteric dysfunction and excessive intake of oxalate or oxalate precursors. During the COVID-19 pandemic, there has been a dramatic rise in sales of supplements and vitamin C, during which time we observed an apparent increase in the propo...

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Autores principales: Fong, Peter, Wusirika, Raghav, Rueda, Jose, Raphael, Kalani L., Rehman, Shehzad, Stack, Megan, de Mattos, Angelo, Gupta, Renu, Michels, Kendall, Khoury, Firas G., Kung, Vanderlene, Andeen, Nicole K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9464307/
https://www.ncbi.nlm.nih.gov/pubmed/36120391
http://dx.doi.org/10.1016/j.ekir.2022.09.002
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author Fong, Peter
Wusirika, Raghav
Rueda, Jose
Raphael, Kalani L.
Rehman, Shehzad
Stack, Megan
de Mattos, Angelo
Gupta, Renu
Michels, Kendall
Khoury, Firas G.
Kung, Vanderlene
Andeen, Nicole K.
author_facet Fong, Peter
Wusirika, Raghav
Rueda, Jose
Raphael, Kalani L.
Rehman, Shehzad
Stack, Megan
de Mattos, Angelo
Gupta, Renu
Michels, Kendall
Khoury, Firas G.
Kung, Vanderlene
Andeen, Nicole K.
author_sort Fong, Peter
collection PubMed
description INTRODUCTION: Causes of secondary oxalate nephropathy include enteric dysfunction and excessive intake of oxalate or oxalate precursors. During the COVID-19 pandemic, there has been a dramatic rise in sales of supplements and vitamin C, during which time we observed an apparent increase in the proportion of ingestion-associated oxalate nephropathy. METHODS: We retrospectively reviewed secondary oxalate nephropathy and compared pre-pandemic (2018–2019) and pandemic (2020–early 2022) time periods. RESULTS: We identified 35 patients with kidney biopsy proven (30 native, 5 allograft) oxalate nephropathy at a single academic institution. Supplement-associated oxalate nephropathy comprised a significantly higher proportion of cases during COVID-19 pandemic compared with the preceding 2 years (44% vs. 0%, P = 0.002), and was associated with use of vitamin C, dietary changes, and supplements. Oxalate nephropathy in the kidney allograft, in contrast, remained associated with enteric hyperoxaluria, antibiotic use, and dehydration. Many patients had diabetes mellitus (57%), hypertension (40%) and/or pre-existing chronic kidney disease (CKD, 49%). Of 9 patients in which the potentially causative ingestion was identified and removed, 8 experienced improvement in kidney function. CONCLUSION: There was a shift toward supplements rather than enteric hyperoxaluria as a leading cause of secondary oxalate nephropathy during the COVID-19 pandemic. Kidney outcomes are better than those observed for enteric hyperoxaluria, if the offending agent is identified and removed.
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spelling pubmed-94643072022-09-12 Increased Rates of Supplement-Associated Oxalate Nephropathy During COVID-19 Pandemic Fong, Peter Wusirika, Raghav Rueda, Jose Raphael, Kalani L. Rehman, Shehzad Stack, Megan de Mattos, Angelo Gupta, Renu Michels, Kendall Khoury, Firas G. Kung, Vanderlene Andeen, Nicole K. Kidney Int Rep Clinical Research INTRODUCTION: Causes of secondary oxalate nephropathy include enteric dysfunction and excessive intake of oxalate or oxalate precursors. During the COVID-19 pandemic, there has been a dramatic rise in sales of supplements and vitamin C, during which time we observed an apparent increase in the proportion of ingestion-associated oxalate nephropathy. METHODS: We retrospectively reviewed secondary oxalate nephropathy and compared pre-pandemic (2018–2019) and pandemic (2020–early 2022) time periods. RESULTS: We identified 35 patients with kidney biopsy proven (30 native, 5 allograft) oxalate nephropathy at a single academic institution. Supplement-associated oxalate nephropathy comprised a significantly higher proportion of cases during COVID-19 pandemic compared with the preceding 2 years (44% vs. 0%, P = 0.002), and was associated with use of vitamin C, dietary changes, and supplements. Oxalate nephropathy in the kidney allograft, in contrast, remained associated with enteric hyperoxaluria, antibiotic use, and dehydration. Many patients had diabetes mellitus (57%), hypertension (40%) and/or pre-existing chronic kidney disease (CKD, 49%). Of 9 patients in which the potentially causative ingestion was identified and removed, 8 experienced improvement in kidney function. CONCLUSION: There was a shift toward supplements rather than enteric hyperoxaluria as a leading cause of secondary oxalate nephropathy during the COVID-19 pandemic. Kidney outcomes are better than those observed for enteric hyperoxaluria, if the offending agent is identified and removed. Elsevier 2022-09-11 /pmc/articles/PMC9464307/ /pubmed/36120391 http://dx.doi.org/10.1016/j.ekir.2022.09.002 Text en © 2022 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
Fong, Peter
Wusirika, Raghav
Rueda, Jose
Raphael, Kalani L.
Rehman, Shehzad
Stack, Megan
de Mattos, Angelo
Gupta, Renu
Michels, Kendall
Khoury, Firas G.
Kung, Vanderlene
Andeen, Nicole K.
Increased Rates of Supplement-Associated Oxalate Nephropathy During COVID-19 Pandemic
title Increased Rates of Supplement-Associated Oxalate Nephropathy During COVID-19 Pandemic
title_full Increased Rates of Supplement-Associated Oxalate Nephropathy During COVID-19 Pandemic
title_fullStr Increased Rates of Supplement-Associated Oxalate Nephropathy During COVID-19 Pandemic
title_full_unstemmed Increased Rates of Supplement-Associated Oxalate Nephropathy During COVID-19 Pandemic
title_short Increased Rates of Supplement-Associated Oxalate Nephropathy During COVID-19 Pandemic
title_sort increased rates of supplement-associated oxalate nephropathy during covid-19 pandemic
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9464307/
https://www.ncbi.nlm.nih.gov/pubmed/36120391
http://dx.doi.org/10.1016/j.ekir.2022.09.002
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