Protective effects of spironolactone on vascular calcification in chronic kidney disease
Please always quote using this URN: urn:nbn:de:bvb:20-opus-352457
- Background Vascular calcification is common in chronic kidney disease (CKD) and associated with increased cardiovascular mortality. Aldosterone has been implicated as an augmenting factor in the progression of vascular calcification. The present study further explored putative beneficial effects of aldosterone inhibition by the mineralocorticoid receptor antagonist spironolactone on vascular calcification in CKD. Methods Serum calcification propensity was determined in serum samples from the MiREnDa trial, a prospective, randomizedBackground Vascular calcification is common in chronic kidney disease (CKD) and associated with increased cardiovascular mortality. Aldosterone has been implicated as an augmenting factor in the progression of vascular calcification. The present study further explored putative beneficial effects of aldosterone inhibition by the mineralocorticoid receptor antagonist spironolactone on vascular calcification in CKD. Methods Serum calcification propensity was determined in serum samples from the MiREnDa trial, a prospective, randomized controlled clinical trial to investigate efficacy and safety of spironolactone in maintenance hemodialysis patients. Experiments were conducted in mice with subtotal nephrectomy and cholecalciferol treatment, and in calcifying primary human aortic smooth muscle cells (HAoSMCs). Results Serum calcification propensity was improved by spironolactone treatment in patients on hemodialysis from the MiREnDa trial. In mouse models and HAoSMCs, spironolactone treatment ameliorated vascular calcification and expression of osteogenic markers. Conclusions These observations support a putative benefit of spironolactone treatment in CKD-associated vascular calcification. Further research is required to investigate possible improvements in cardiovascular outcomes by spironolactone and whether the benefits outweigh the risks in patients with CKD.…
Author: | Fabian Hammer, Salvatore S. Buehling, Jaber Masyout, Uwe Malzahn, Tobias Hauser, Tilman Auer, Sören Grebe, Martina Feger, Rashad Tuffaha, Gerald Degenhart, Florian Lang, Andreas Pasch, Ioana Alesutan, Christoph Wanner, Vera Krane, Jakob Voelkl |
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URN: | urn:nbn:de:bvb:20-opus-352457 |
Document Type: | Journal article |
Faculties: | Medizinische Fakultät / Medizinische Klinik und Poliklinik I |
Medizinische Fakultät / Deutsches Zentrum für Herzinsuffizienz (DZHI) | |
Language: | English |
Parent Title (English): | Biochemical and Biophysical Research Communications |
Year of Completion: | 2021 |
Volume: | 582 |
Pagenumber: | 28-34 |
Source: | Biochemical and Biophysical Research Communications (2021) 582:28-34. https://doi.org/10.1016/j.bbrc.2021.10.023 |
DOI: | https://doi.org/10.1016/j.bbrc.2021.10.023 |
Dewey Decimal Classification: | 6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit |
Tag: | aldosterone; serum calcification propensity; spironolactone; vascular calcification; vascular smooth muscle cells |
Release Date: | 2024/11/27 |
EU-Project number / Contract (GA) number: | 603288 |
OpenAIRE: | OpenAIRE |
Licence (German): | CC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International |