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Lessons from effect of etelcalcetide on left ventricular hypertrophy in patients with end-stage kidney disease
Patients with end-stage kidney disease (ESKD) frequently develop left ventricular hypertrophy (LVH), which is associated with an exceptionally high risk of cardiovascular events and mortality. This review focuses on interventional studies that modify levels of fibroblast growth factor 23 (FGF23) and...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9394497/ https://www.ncbi.nlm.nih.gov/pubmed/35703173 http://dx.doi.org/10.1097/MNH.0000000000000799 |
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author | Dörr, Katharina Kainz, Alexander Oberbauer, Rainer |
author_facet | Dörr, Katharina Kainz, Alexander Oberbauer, Rainer |
author_sort | Dörr, Katharina |
collection | PubMed |
description | Patients with end-stage kidney disease (ESKD) frequently develop left ventricular hypertrophy (LVH), which is associated with an exceptionally high risk of cardiovascular events and mortality. This review focuses on interventional studies that modify levels of fibroblast growth factor 23 (FGF23) and examine effects on myocardial hypertrophy, cardiovascular events and mortality. RECENT FINDINGS: Quantitative evaluations of trials of calcimimetics found no effects on cardiovascular events and cardiovascular and all-cause mortality when compared with placebo. However, a recent randomized, controlled trial of etelcalcetide versus alfacalcidol showed that etelcalcetide effectively inhibited the progression of LVH in comparison to vitamin D in patients on haemodialysis after 1 year of treatment. Prior to that, oral calcimimetic treatment has already been shown to reduce left ventricular mass in patients on haemodialysis, whereas treatment with active vitamin D or mineralocorticoids was ineffective in patients with ESKD. SUMMARY: Data from a recent trial of etelcalcetide on LVH suggest that FGF23 may be a possible therapeutic target for cardiac risk reduction in patients on haemodialysis. If these findings are confirmed by further research, it might be speculated that a treatment shift from active vitamin D towards FGF23-lowering therapy may occur in patients on haemodialysis. |
format | Online Article Text |
id | pubmed-9394497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-93944972022-08-26 Lessons from effect of etelcalcetide on left ventricular hypertrophy in patients with end-stage kidney disease Dörr, Katharina Kainz, Alexander Oberbauer, Rainer Curr Opin Nephrol Hypertens MINERAL METABOLISM: Edited by Aline Martin and Tamara Isakova Patients with end-stage kidney disease (ESKD) frequently develop left ventricular hypertrophy (LVH), which is associated with an exceptionally high risk of cardiovascular events and mortality. This review focuses on interventional studies that modify levels of fibroblast growth factor 23 (FGF23) and examine effects on myocardial hypertrophy, cardiovascular events and mortality. RECENT FINDINGS: Quantitative evaluations of trials of calcimimetics found no effects on cardiovascular events and cardiovascular and all-cause mortality when compared with placebo. However, a recent randomized, controlled trial of etelcalcetide versus alfacalcidol showed that etelcalcetide effectively inhibited the progression of LVH in comparison to vitamin D in patients on haemodialysis after 1 year of treatment. Prior to that, oral calcimimetic treatment has already been shown to reduce left ventricular mass in patients on haemodialysis, whereas treatment with active vitamin D or mineralocorticoids was ineffective in patients with ESKD. SUMMARY: Data from a recent trial of etelcalcetide on LVH suggest that FGF23 may be a possible therapeutic target for cardiac risk reduction in patients on haemodialysis. If these findings are confirmed by further research, it might be speculated that a treatment shift from active vitamin D towards FGF23-lowering therapy may occur in patients on haemodialysis. Lippincott Williams & Wilkins 2022-07 2022-06-10 /pmc/articles/PMC9394497/ /pubmed/35703173 http://dx.doi.org/10.1097/MNH.0000000000000799 Text en Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | MINERAL METABOLISM: Edited by Aline Martin and Tamara Isakova Dörr, Katharina Kainz, Alexander Oberbauer, Rainer Lessons from effect of etelcalcetide on left ventricular hypertrophy in patients with end-stage kidney disease |
title | Lessons from effect of etelcalcetide on left ventricular hypertrophy in patients with end-stage kidney disease |
title_full | Lessons from effect of etelcalcetide on left ventricular hypertrophy in patients with end-stage kidney disease |
title_fullStr | Lessons from effect of etelcalcetide on left ventricular hypertrophy in patients with end-stage kidney disease |
title_full_unstemmed | Lessons from effect of etelcalcetide on left ventricular hypertrophy in patients with end-stage kidney disease |
title_short | Lessons from effect of etelcalcetide on left ventricular hypertrophy in patients with end-stage kidney disease |
title_sort | lessons from effect of etelcalcetide on left ventricular hypertrophy in patients with end-stage kidney disease |
topic | MINERAL METABOLISM: Edited by Aline Martin and Tamara Isakova |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9394497/ https://www.ncbi.nlm.nih.gov/pubmed/35703173 http://dx.doi.org/10.1097/MNH.0000000000000799 |
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