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Variations in Circulating Active MMP-9 Levels during Renal Replacement Therapy
Renal replacement therapy (RRT) is complicated by a chronic state of inflammation and a high mortality risk. However, different RRT modalities can have a selective impact on markers of inflammation and oxidative stress. We evaluated the levels of active matrix metalloproteinase (MMP)-9 in patients u...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226477/ https://www.ncbi.nlm.nih.gov/pubmed/32225016 http://dx.doi.org/10.3390/biom10040505 |
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author | Rodríguez-Sánchez, Elena Navarro-García, José Alberto Aceves-Ripoll, Jennifer Abarca-Zabalía, Judith Susmozas-Sánchez, Andrea Bada-Bosch, Teresa Hernández, Eduardo Mérida-Herrero, Evangelina Andrés, Amado Praga, Manuel Fernández-Ruiz, Mario Aguado, José María Segura, Julián Ruilope, Luis Miguel Ruiz-Hurtado, Gema |
author_facet | Rodríguez-Sánchez, Elena Navarro-García, José Alberto Aceves-Ripoll, Jennifer Abarca-Zabalía, Judith Susmozas-Sánchez, Andrea Bada-Bosch, Teresa Hernández, Eduardo Mérida-Herrero, Evangelina Andrés, Amado Praga, Manuel Fernández-Ruiz, Mario Aguado, José María Segura, Julián Ruilope, Luis Miguel Ruiz-Hurtado, Gema |
author_sort | Rodríguez-Sánchez, Elena |
collection | PubMed |
description | Renal replacement therapy (RRT) is complicated by a chronic state of inflammation and a high mortality risk. However, different RRT modalities can have a selective impact on markers of inflammation and oxidative stress. We evaluated the levels of active matrix metalloproteinase (MMP)-9 in patients undergoing two types of dialysis (high-flux dialysis (HFD) and on-line hemodiafiltration (OL-HDF)) and in kidney transplantation (KT) recipients. Active MMP-9 was measured by zymography and ELISA before (pre-) and after (post-) one dialysis session, and at baseline and follow-up (7 and 14 days, and 1, 3, 6, and 12 months) after KT. Active MMP-9 decreased post-dialysis only in HFD patients, while the levels in OL-HDF patients were already lower before dialysis. Active MMP-9 increased at 7 and 14 days post-KT and was restored to baseline levels three months post-KT, coinciding with an improvement in renal function and plasma creatinine. Active MMP-9 correlated with pulse pressure as an indicator of arterial stiffness both in dialysis patients and KT recipients. In conclusion, active MMP-9 is better controlled in OL-HDF than in HFD and is restored to baseline levels along with stabilization of renal parameters after KT. Active MMP-9 might act as a biomarker of arterial stiffness in RRT. |
format | Online Article Text |
id | pubmed-7226477 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72264772020-05-18 Variations in Circulating Active MMP-9 Levels during Renal Replacement Therapy Rodríguez-Sánchez, Elena Navarro-García, José Alberto Aceves-Ripoll, Jennifer Abarca-Zabalía, Judith Susmozas-Sánchez, Andrea Bada-Bosch, Teresa Hernández, Eduardo Mérida-Herrero, Evangelina Andrés, Amado Praga, Manuel Fernández-Ruiz, Mario Aguado, José María Segura, Julián Ruilope, Luis Miguel Ruiz-Hurtado, Gema Biomolecules Article Renal replacement therapy (RRT) is complicated by a chronic state of inflammation and a high mortality risk. However, different RRT modalities can have a selective impact on markers of inflammation and oxidative stress. We evaluated the levels of active matrix metalloproteinase (MMP)-9 in patients undergoing two types of dialysis (high-flux dialysis (HFD) and on-line hemodiafiltration (OL-HDF)) and in kidney transplantation (KT) recipients. Active MMP-9 was measured by zymography and ELISA before (pre-) and after (post-) one dialysis session, and at baseline and follow-up (7 and 14 days, and 1, 3, 6, and 12 months) after KT. Active MMP-9 decreased post-dialysis only in HFD patients, while the levels in OL-HDF patients were already lower before dialysis. Active MMP-9 increased at 7 and 14 days post-KT and was restored to baseline levels three months post-KT, coinciding with an improvement in renal function and plasma creatinine. Active MMP-9 correlated with pulse pressure as an indicator of arterial stiffness both in dialysis patients and KT recipients. In conclusion, active MMP-9 is better controlled in OL-HDF than in HFD and is restored to baseline levels along with stabilization of renal parameters after KT. Active MMP-9 might act as a biomarker of arterial stiffness in RRT. MDPI 2020-03-26 /pmc/articles/PMC7226477/ /pubmed/32225016 http://dx.doi.org/10.3390/biom10040505 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Rodríguez-Sánchez, Elena Navarro-García, José Alberto Aceves-Ripoll, Jennifer Abarca-Zabalía, Judith Susmozas-Sánchez, Andrea Bada-Bosch, Teresa Hernández, Eduardo Mérida-Herrero, Evangelina Andrés, Amado Praga, Manuel Fernández-Ruiz, Mario Aguado, José María Segura, Julián Ruilope, Luis Miguel Ruiz-Hurtado, Gema Variations in Circulating Active MMP-9 Levels during Renal Replacement Therapy |
title | Variations in Circulating Active MMP-9 Levels during Renal Replacement Therapy |
title_full | Variations in Circulating Active MMP-9 Levels during Renal Replacement Therapy |
title_fullStr | Variations in Circulating Active MMP-9 Levels during Renal Replacement Therapy |
title_full_unstemmed | Variations in Circulating Active MMP-9 Levels during Renal Replacement Therapy |
title_short | Variations in Circulating Active MMP-9 Levels during Renal Replacement Therapy |
title_sort | variations in circulating active mmp-9 levels during renal replacement therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226477/ https://www.ncbi.nlm.nih.gov/pubmed/32225016 http://dx.doi.org/10.3390/biom10040505 |
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