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Changes in plasma sclerostin level associated with use of a medium cut-off dialyzer in end-stage renal disease

BACKGROUND: Larger middle molecules are important substances associated with cardiovascular complications in end- stage renal disease. Unfortunately, larger middle molecules are not reliably removed by a high -flux dialyzer. A medium cut-off (MCO) membrane could effectively remove larger middle mole...

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Autores principales: Ahn, Seon-Ho, Ko, Mi Mi, Song, Ju Hung, Jung, Jong Hwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Nephrology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8041631/
https://www.ncbi.nlm.nih.gov/pubmed/33745263
http://dx.doi.org/10.23876/j.krcp.20.173
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author Ahn, Seon-Ho
Ko, Mi Mi
Song, Ju Hung
Jung, Jong Hwan
author_facet Ahn, Seon-Ho
Ko, Mi Mi
Song, Ju Hung
Jung, Jong Hwan
author_sort Ahn, Seon-Ho
collection PubMed
description BACKGROUND: Larger middle molecules are important substances associated with cardiovascular complications in end- stage renal disease. Unfortunately, larger middle molecules are not reliably removed by a high -flux dialyzer. A medium cut-off (MCO) membrane could effectively remove larger middle molecules. This study aimed to identify the long-term effect of the MCO membrane for changes of larger middle molecules. METHODS: Thirty-four patients were prospectively analyzed for 12 months. The enrolled patients were divided into control and MCO groups. We measured the plasma levels of growth differentiation factor 15, sclerostin, and fibroblast growth factor 23 in larger middle molecules and those of biomarkers including small solutes. Single-pool Kt/V (spKt/V) and reduction ratios also were evaluated. RESULTS: Plasma sclerostin did not increase significantly in patients using the MCO dialyzer (135.294 [–637.726 to 908.314], p = 0.715). And there was a significant difference in change of plasma sclerostin level between the two groups (–1,646.916 [–3,015.150 to –278.682], p = 0.033). Furthermore, a negative association between calcium and sclerostin was not observed in the MCO group (r = –0.142, p = 0.587). Solute clearance of larger middle molecules in the MCO group was significantly higher. Moreover, spKt/V values for patients in the MCO group were significantly increased without albumin loss. Values are presented as mean (95% confidence interval [CI]) or adjusted mean (95% CI). CONCLUSION: The MCO dialyzer can increase dialytic adequacy and suppress the increase in plasma sclerostin level without significant albumin loss in patients with end-stage renal disease.
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spelling pubmed-80416312021-04-15 Changes in plasma sclerostin level associated with use of a medium cut-off dialyzer in end-stage renal disease Ahn, Seon-Ho Ko, Mi Mi Song, Ju Hung Jung, Jong Hwan Kidney Res Clin Pract Original Article BACKGROUND: Larger middle molecules are important substances associated with cardiovascular complications in end- stage renal disease. Unfortunately, larger middle molecules are not reliably removed by a high -flux dialyzer. A medium cut-off (MCO) membrane could effectively remove larger middle molecules. This study aimed to identify the long-term effect of the MCO membrane for changes of larger middle molecules. METHODS: Thirty-four patients were prospectively analyzed for 12 months. The enrolled patients were divided into control and MCO groups. We measured the plasma levels of growth differentiation factor 15, sclerostin, and fibroblast growth factor 23 in larger middle molecules and those of biomarkers including small solutes. Single-pool Kt/V (spKt/V) and reduction ratios also were evaluated. RESULTS: Plasma sclerostin did not increase significantly in patients using the MCO dialyzer (135.294 [–637.726 to 908.314], p = 0.715). And there was a significant difference in change of plasma sclerostin level between the two groups (–1,646.916 [–3,015.150 to –278.682], p = 0.033). Furthermore, a negative association between calcium and sclerostin was not observed in the MCO group (r = –0.142, p = 0.587). Solute clearance of larger middle molecules in the MCO group was significantly higher. Moreover, spKt/V values for patients in the MCO group were significantly increased without albumin loss. Values are presented as mean (95% confidence interval [CI]) or adjusted mean (95% CI). CONCLUSION: The MCO dialyzer can increase dialytic adequacy and suppress the increase in plasma sclerostin level without significant albumin loss in patients with end-stage renal disease. The Korean Society of Nephrology 2021-03 2021-03-22 /pmc/articles/PMC8041631/ /pubmed/33745263 http://dx.doi.org/10.23876/j.krcp.20.173 Text en Copyright © 2021 The Korean Society of Nephrology https://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/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ahn, Seon-Ho
Ko, Mi Mi
Song, Ju Hung
Jung, Jong Hwan
Changes in plasma sclerostin level associated with use of a medium cut-off dialyzer in end-stage renal disease
title Changes in plasma sclerostin level associated with use of a medium cut-off dialyzer in end-stage renal disease
title_full Changes in plasma sclerostin level associated with use of a medium cut-off dialyzer in end-stage renal disease
title_fullStr Changes in plasma sclerostin level associated with use of a medium cut-off dialyzer in end-stage renal disease
title_full_unstemmed Changes in plasma sclerostin level associated with use of a medium cut-off dialyzer in end-stage renal disease
title_short Changes in plasma sclerostin level associated with use of a medium cut-off dialyzer in end-stage renal disease
title_sort changes in plasma sclerostin level associated with use of a medium cut-off dialyzer in end-stage renal disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8041631/
https://www.ncbi.nlm.nih.gov/pubmed/33745263
http://dx.doi.org/10.23876/j.krcp.20.173
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