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Dissociation between progression of coronary artery calcification and endothelial function in hemodialysis patients: a prospective pilot study

Chronic kidney disease profoundly disturbs calcium-phosphate metabolism and predisposes to premature atherosclerosis. Both coronary artery calcification (CAC) and endothelial dysfunction are common in hemodialysis (HD) patients. We hypothesized that a calcium-free phosphate binder would improve endo...

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Autores principales: Kalil, Roberto S., Flanigan, Michael, Stanford, William, Haynes, William G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dustri-Verlag Dr. Karl Feistle 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4407338/
https://www.ncbi.nlm.nih.gov/pubmed/22732331
http://dx.doi.org/10.5414/CN106830
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author Kalil, Roberto S.
Flanigan, Michael
Stanford, William
Haynes, William G.
author_facet Kalil, Roberto S.
Flanigan, Michael
Stanford, William
Haynes, William G.
author_sort Kalil, Roberto S.
collection PubMed
description Chronic kidney disease profoundly disturbs calcium-phosphate metabolism and predisposes to premature atherosclerosis. Both coronary artery calcification (CAC) and endothelial dysfunction are common in hemodialysis (HD) patients. We hypothesized that a calcium-free phosphate binder would improve endothelial function and delay progression of vascular calcification in HD patients. Methods: This was a randomized parallel-group trial in HD patients comparing lanthanum carbonate (LC) with a non-LC phosphorus binders control group (non-LC) at a 1 : 1 randomization. CAC was obtained at baseline, 6, and 12 months, and endothelial function (brachial artery flow-mediated dilation – FMD) at baseline and 6 months. Results: 13 patients were randomized (LC n = 7 and non-LC n = 6). CAC scores (Log ± SE) at baseline were 7.21 ± 0.62 (LC) and 6.07 ± 0.73 (control). CAC increased in the non-LC group (33 ± 17% and 77 ± 22% at 6 and 12 months), but tended to decrease in the LC group (–10 ± 11% and –2 ± 11% at 6 and 12 months). There was statistically less progression in CAC in the LC group compared to control at 6 (p = 0.002) and 12 months (p = 0.003). There was no difference between groups in FMD (p = 0.7). Markers of inflammation did not change significantly. Conclusion: A slower rate of progression of CAC occurred in the LC group, independent of changes in FMD. This is the first study showing dissociation between progression of CAC and FMD in HD patients. Larger studies are warranted to elucidate the impact of different phosphate sequestration therapies on atherosclerosis in HD patients.
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spelling pubmed-44073382015-05-05 Dissociation between progression of coronary artery calcification and endothelial function in hemodialysis patients: a prospective pilot study Kalil, Roberto S. Flanigan, Michael Stanford, William Haynes, William G. Clin Nephrol Research Article Chronic kidney disease profoundly disturbs calcium-phosphate metabolism and predisposes to premature atherosclerosis. Both coronary artery calcification (CAC) and endothelial dysfunction are common in hemodialysis (HD) patients. We hypothesized that a calcium-free phosphate binder would improve endothelial function and delay progression of vascular calcification in HD patients. Methods: This was a randomized parallel-group trial in HD patients comparing lanthanum carbonate (LC) with a non-LC phosphorus binders control group (non-LC) at a 1 : 1 randomization. CAC was obtained at baseline, 6, and 12 months, and endothelial function (brachial artery flow-mediated dilation – FMD) at baseline and 6 months. Results: 13 patients were randomized (LC n = 7 and non-LC n = 6). CAC scores (Log ± SE) at baseline were 7.21 ± 0.62 (LC) and 6.07 ± 0.73 (control). CAC increased in the non-LC group (33 ± 17% and 77 ± 22% at 6 and 12 months), but tended to decrease in the LC group (–10 ± 11% and –2 ± 11% at 6 and 12 months). There was statistically less progression in CAC in the LC group compared to control at 6 (p = 0.002) and 12 months (p = 0.003). There was no difference between groups in FMD (p = 0.7). Markers of inflammation did not change significantly. Conclusion: A slower rate of progression of CAC occurred in the LC group, independent of changes in FMD. This is the first study showing dissociation between progression of CAC and FMD in HD patients. Larger studies are warranted to elucidate the impact of different phosphate sequestration therapies on atherosclerosis in HD patients. Dustri-Verlag Dr. Karl Feistle 2012-07 2011-08-11 /pmc/articles/PMC4407338/ /pubmed/22732331 http://dx.doi.org/10.5414/CN106830 Text en © Dustri-Verlag Dr. K. Feistle http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kalil, Roberto S.
Flanigan, Michael
Stanford, William
Haynes, William G.
Dissociation between progression of coronary artery calcification and endothelial function in hemodialysis patients: a prospective pilot study
title Dissociation between progression of coronary artery calcification and endothelial function in hemodialysis patients: a prospective pilot study
title_full Dissociation between progression of coronary artery calcification and endothelial function in hemodialysis patients: a prospective pilot study
title_fullStr Dissociation between progression of coronary artery calcification and endothelial function in hemodialysis patients: a prospective pilot study
title_full_unstemmed Dissociation between progression of coronary artery calcification and endothelial function in hemodialysis patients: a prospective pilot study
title_short Dissociation between progression of coronary artery calcification and endothelial function in hemodialysis patients: a prospective pilot study
title_sort dissociation between progression of coronary artery calcification and endothelial function in hemodialysis patients: a prospective pilot study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4407338/
https://www.ncbi.nlm.nih.gov/pubmed/22732331
http://dx.doi.org/10.5414/CN106830
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