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Dermal tissue remodeling and non-osmotic sodium storage in kidney patients
BACKGROUND: Excess dietary sodium is not only excreted by the kidneys, but can also be stored by non-osmotic binding with glycosaminoglycans in dermal connective tissue. Such storage has been associated with dermal inflammation and lymphangiogenesis. We aim to investigate if skin storage of sodium i...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421653/ https://www.ncbi.nlm.nih.gov/pubmed/30885222 http://dx.doi.org/10.1186/s12967-019-1815-5 |
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author | Hijmans, Ryanne S. van Londen, Marco Sarpong, Kwaku A. Bakker, Stephan J. L. Navis, Gerjan J. Storteboom, Twan T. R. de Jong, Wilhelmina H. A. Pol, Robert A. van den Born, Jacob |
author_facet | Hijmans, Ryanne S. van Londen, Marco Sarpong, Kwaku A. Bakker, Stephan J. L. Navis, Gerjan J. Storteboom, Twan T. R. de Jong, Wilhelmina H. A. Pol, Robert A. van den Born, Jacob |
author_sort | Hijmans, Ryanne S. |
collection | PubMed |
description | BACKGROUND: Excess dietary sodium is not only excreted by the kidneys, but can also be stored by non-osmotic binding with glycosaminoglycans in dermal connective tissue. Such storage has been associated with dermal inflammation and lymphangiogenesis. We aim to investigate if skin storage of sodium is increased in kidney patients and if this storage is associated with clinical parameters of sodium homeostasis and dermal tissue remodeling. METHODS: Abdominal skin tissue of 12 kidney patients (5 on hemodialysis) and 12 healthy kidney donors was obtained during surgery. Skin biopsies were processed for dermal sodium measurement by atomic absorption spectroscopy, and evaluated for CD(68+) macrophages, CD(3+) T-cells, collagen I, podoplanin + lymph vessels, and glycosaminoglycans by qRT-PCR and immunohistochemistry. RESULTS: Dermal sodium content of kidney patients did not differ from healthy individuals, but was inversely associated with plasma sodium values (p < 0.05). Compared to controls, kidney patients showed dermal tissue remodeling by increased CD(68+) macrophages, CD(3+) T-cells and Collagen I expression (all p < 0.05). Also, both N- and O-sulfation of heparan sulfate glycosaminoglycans were increased (all p < 0.05), most outspoken in hemodialysis patients. Plasma and urinary sodium associates with dermal lymph vessel number (both p < 0.05), whereas loss of eGFR, proteinuria and high systolic blood pressure associated with dermal macrophage density (all p < 0.05). CONCLUSION: Kidney patients did not show increased skin sodium storage compared to healthy individuals. Results do indicate that kidney failure associates with dermal inflammation, whereas increased sodium excretion and plasma sodium associate with dermal lymph vessel formation and loss of dermal sodium storage capacity. Trial registration The cohort is registered at clinicaltrials.gov as NCT (September 6, 2017). NCT, NCT03272841. Registered 6 September 2017—Retrospectively registered, https://clinicaltrials.gov |
format | Online Article Text |
id | pubmed-6421653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64216532019-03-28 Dermal tissue remodeling and non-osmotic sodium storage in kidney patients Hijmans, Ryanne S. van Londen, Marco Sarpong, Kwaku A. Bakker, Stephan J. L. Navis, Gerjan J. Storteboom, Twan T. R. de Jong, Wilhelmina H. A. Pol, Robert A. van den Born, Jacob J Transl Med Research BACKGROUND: Excess dietary sodium is not only excreted by the kidneys, but can also be stored by non-osmotic binding with glycosaminoglycans in dermal connective tissue. Such storage has been associated with dermal inflammation and lymphangiogenesis. We aim to investigate if skin storage of sodium is increased in kidney patients and if this storage is associated with clinical parameters of sodium homeostasis and dermal tissue remodeling. METHODS: Abdominal skin tissue of 12 kidney patients (5 on hemodialysis) and 12 healthy kidney donors was obtained during surgery. Skin biopsies were processed for dermal sodium measurement by atomic absorption spectroscopy, and evaluated for CD(68+) macrophages, CD(3+) T-cells, collagen I, podoplanin + lymph vessels, and glycosaminoglycans by qRT-PCR and immunohistochemistry. RESULTS: Dermal sodium content of kidney patients did not differ from healthy individuals, but was inversely associated with plasma sodium values (p < 0.05). Compared to controls, kidney patients showed dermal tissue remodeling by increased CD(68+) macrophages, CD(3+) T-cells and Collagen I expression (all p < 0.05). Also, both N- and O-sulfation of heparan sulfate glycosaminoglycans were increased (all p < 0.05), most outspoken in hemodialysis patients. Plasma and urinary sodium associates with dermal lymph vessel number (both p < 0.05), whereas loss of eGFR, proteinuria and high systolic blood pressure associated with dermal macrophage density (all p < 0.05). CONCLUSION: Kidney patients did not show increased skin sodium storage compared to healthy individuals. Results do indicate that kidney failure associates with dermal inflammation, whereas increased sodium excretion and plasma sodium associate with dermal lymph vessel formation and loss of dermal sodium storage capacity. Trial registration The cohort is registered at clinicaltrials.gov as NCT (September 6, 2017). NCT, NCT03272841. Registered 6 September 2017—Retrospectively registered, https://clinicaltrials.gov BioMed Central 2019-03-18 /pmc/articles/PMC6421653/ /pubmed/30885222 http://dx.doi.org/10.1186/s12967-019-1815-5 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Hijmans, Ryanne S. van Londen, Marco Sarpong, Kwaku A. Bakker, Stephan J. L. Navis, Gerjan J. Storteboom, Twan T. R. de Jong, Wilhelmina H. A. Pol, Robert A. van den Born, Jacob Dermal tissue remodeling and non-osmotic sodium storage in kidney patients |
title | Dermal tissue remodeling and non-osmotic sodium storage in kidney patients |
title_full | Dermal tissue remodeling and non-osmotic sodium storage in kidney patients |
title_fullStr | Dermal tissue remodeling and non-osmotic sodium storage in kidney patients |
title_full_unstemmed | Dermal tissue remodeling and non-osmotic sodium storage in kidney patients |
title_short | Dermal tissue remodeling and non-osmotic sodium storage in kidney patients |
title_sort | dermal tissue remodeling and non-osmotic sodium storage in kidney patients |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421653/ https://www.ncbi.nlm.nih.gov/pubmed/30885222 http://dx.doi.org/10.1186/s12967-019-1815-5 |
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