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Plasma Vitamin B(12) and Folate Alter the Association of Blood Lead and Cadmium and Total Urinary Arsenic Levels with Chronic Kidney Disease in a Taiwanese Population

Heavy metals causing chronic nephrotoxicity may play a key role in the pathogenesis of chronic kidney disease (CKD). This study hypothesized that plasma folate and vitamin B(12) would modify the association of CKD with total urinary arsenic and blood lead and cadmium levels. We recruited 220 patient...

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Autores principales: Hsueh, Yu-Mei, Huang, Ya-Li, Lin, Yuh-Feng, Shiue, Horng-Sheng, Lin, Ying-Chin, Chen, Hsi-Hsien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8625054/
https://www.ncbi.nlm.nih.gov/pubmed/34836097
http://dx.doi.org/10.3390/nu13113841
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author Hsueh, Yu-Mei
Huang, Ya-Li
Lin, Yuh-Feng
Shiue, Horng-Sheng
Lin, Ying-Chin
Chen, Hsi-Hsien
author_facet Hsueh, Yu-Mei
Huang, Ya-Li
Lin, Yuh-Feng
Shiue, Horng-Sheng
Lin, Ying-Chin
Chen, Hsi-Hsien
author_sort Hsueh, Yu-Mei
collection PubMed
description Heavy metals causing chronic nephrotoxicity may play a key role in the pathogenesis of chronic kidney disease (CKD). This study hypothesized that plasma folate and vitamin B(12) would modify the association of CKD with total urinary arsenic and blood lead and cadmium levels. We recruited 220 patients with CKD who had an estimated glomerular filtration rate of <60 mL/min/1.73 m(2) for ≥3 consecutive months and 438 sex- and age-matched controls. We performed inductively coupled plasma mass spectrometry to measure blood cadmium and lead levels. The urinary arsenic level was determined using a high-performance liquid chromatography–hydride generator–atomic absorption spectrometry. Plasma vitamin B(12) and folate levels were measured through the SimulTRAC-SNB radioassay. Compared with patients with plasma vitamin B(12) ≤ 6.27 pg/mL, the odds ratio (OR) and 95% confidence interval of CKD for patients with plasma vitamin B(12) > 9.54 pg/mL was 2.02 (1.15–3.55). However, no association was observed between plasma folate concentration and CKD. A high level of plasma vitamin B(12) combined with high levels of blood lead and cadmium level and total urinary arsenic tended to increase the OR of CKD in a dose-response manner, but the interactions were nonsignificant. This is the first study to demonstrate that patients with high plasma vitamin B(12) level exhibit increased OR of CKD related to high levels of blood cadmium and lead and total urinary arsenic.
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spelling pubmed-86250542021-11-27 Plasma Vitamin B(12) and Folate Alter the Association of Blood Lead and Cadmium and Total Urinary Arsenic Levels with Chronic Kidney Disease in a Taiwanese Population Hsueh, Yu-Mei Huang, Ya-Li Lin, Yuh-Feng Shiue, Horng-Sheng Lin, Ying-Chin Chen, Hsi-Hsien Nutrients Article Heavy metals causing chronic nephrotoxicity may play a key role in the pathogenesis of chronic kidney disease (CKD). This study hypothesized that plasma folate and vitamin B(12) would modify the association of CKD with total urinary arsenic and blood lead and cadmium levels. We recruited 220 patients with CKD who had an estimated glomerular filtration rate of <60 mL/min/1.73 m(2) for ≥3 consecutive months and 438 sex- and age-matched controls. We performed inductively coupled plasma mass spectrometry to measure blood cadmium and lead levels. The urinary arsenic level was determined using a high-performance liquid chromatography–hydride generator–atomic absorption spectrometry. Plasma vitamin B(12) and folate levels were measured through the SimulTRAC-SNB radioassay. Compared with patients with plasma vitamin B(12) ≤ 6.27 pg/mL, the odds ratio (OR) and 95% confidence interval of CKD for patients with plasma vitamin B(12) > 9.54 pg/mL was 2.02 (1.15–3.55). However, no association was observed between plasma folate concentration and CKD. A high level of plasma vitamin B(12) combined with high levels of blood lead and cadmium level and total urinary arsenic tended to increase the OR of CKD in a dose-response manner, but the interactions were nonsignificant. This is the first study to demonstrate that patients with high plasma vitamin B(12) level exhibit increased OR of CKD related to high levels of blood cadmium and lead and total urinary arsenic. MDPI 2021-10-28 /pmc/articles/PMC8625054/ /pubmed/34836097 http://dx.doi.org/10.3390/nu13113841 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hsueh, Yu-Mei
Huang, Ya-Li
Lin, Yuh-Feng
Shiue, Horng-Sheng
Lin, Ying-Chin
Chen, Hsi-Hsien
Plasma Vitamin B(12) and Folate Alter the Association of Blood Lead and Cadmium and Total Urinary Arsenic Levels with Chronic Kidney Disease in a Taiwanese Population
title Plasma Vitamin B(12) and Folate Alter the Association of Blood Lead and Cadmium and Total Urinary Arsenic Levels with Chronic Kidney Disease in a Taiwanese Population
title_full Plasma Vitamin B(12) and Folate Alter the Association of Blood Lead and Cadmium and Total Urinary Arsenic Levels with Chronic Kidney Disease in a Taiwanese Population
title_fullStr Plasma Vitamin B(12) and Folate Alter the Association of Blood Lead and Cadmium and Total Urinary Arsenic Levels with Chronic Kidney Disease in a Taiwanese Population
title_full_unstemmed Plasma Vitamin B(12) and Folate Alter the Association of Blood Lead and Cadmium and Total Urinary Arsenic Levels with Chronic Kidney Disease in a Taiwanese Population
title_short Plasma Vitamin B(12) and Folate Alter the Association of Blood Lead and Cadmium and Total Urinary Arsenic Levels with Chronic Kidney Disease in a Taiwanese Population
title_sort plasma vitamin b(12) and folate alter the association of blood lead and cadmium and total urinary arsenic levels with chronic kidney disease in a taiwanese population
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8625054/
https://www.ncbi.nlm.nih.gov/pubmed/34836097
http://dx.doi.org/10.3390/nu13113841
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