Cargando…

Fibroblast growth factor 23 and parathyroid hormone predict extent of aortic valve calcifications in patients with mild to moderate chronic kidney disease

BACKGROUND: Cardiac valve calcifications are present in dialysis patients and regarded as dependent on a deranged mineral metabolism. Few data are available for patients with chronic kidney disease (CKD) not on dialysis. This study evaluates the potential association between the extent of cardiac va...

Descripción completa

Detalles Bibliográficos
Autores principales: Di Lullo, Luca, Gorini, Antonio, Bellasi, Antonio, Morrone, Luigi F., Rivera, Rodolfo, Russo, Luigi, Santoboni, Alberto, Russo, Domenico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655786/
https://www.ncbi.nlm.nih.gov/pubmed/26613033
http://dx.doi.org/10.1093/ckj/sfv073
_version_ 1782402218870177792
author Di Lullo, Luca
Gorini, Antonio
Bellasi, Antonio
Morrone, Luigi F.
Rivera, Rodolfo
Russo, Luigi
Santoboni, Alberto
Russo, Domenico
author_facet Di Lullo, Luca
Gorini, Antonio
Bellasi, Antonio
Morrone, Luigi F.
Rivera, Rodolfo
Russo, Luigi
Santoboni, Alberto
Russo, Domenico
author_sort Di Lullo, Luca
collection PubMed
description BACKGROUND: Cardiac valve calcifications are present in dialysis patients and regarded as dependent on a deranged mineral metabolism. Few data are available for patients with chronic kidney disease (CKD) not on dialysis. This study evaluates the potential association between the extent of cardiac valve calcification and levels of intact parathyroid hormone (i-PTH), phosphorus, calcium, 25-OH vitamin D, fibroblast growth factor 23 (FGF-23), Klotho and C-reactive protein (CRP) simultaneously measured in patients with mild to moderate CKD. METHODS: Consecutive non-hospitalized patients referring to five nephrology units were evaluated. Inclusion criteria were age >18 years, CKD Stages 3–4, and the presence of aortic and/or mitral valve calcification assessed by echocardiography as routinely clinical evaluation. Patients underwent clinical examination and routine biochemistry. Baseline i-PTH, phosphorus, calcium, 25-OH vitamin D, FGF-23, Klotho and CRP were simultaneously ascertained. RESULTS: Extent of aortic valve calcification (n = 100 patients) was moderate in 68 patients and mild in the remaining patients. Mitral valve calcification (n = 96 patients) score was 1, 2 and 3 in 61, 34 and 1 patients, respectively. In univariate analysis, no association was found between extent of mitral valve calcification and markers of mineral metabolism and CRP; aortic valve extent of calcification was positively associated with i-PTH (r(2) = 0.212; P = 0.03) and FGF-23 (r(2) = 0.272; P = 0.01), and negatively with Klotho (r(2) = −0.208; P = 0.04). In multivariable analysis, extent of aortic valve calcification was associated with FGF-23 (P = 0.01) and PTH (P = 0.01) levels. CONCLUSIONS: Extent of aortic valve calcification is associated to FGF-23 and PTH in naïve CKD patients with mild to moderate CKD. Further studies should examine whether FGF-23 assay should be included in routine clinical evaluation of CKD as part of cardiovascular risk stratification.
format Online
Article
Text
id pubmed-4655786
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-46557862015-11-26 Fibroblast growth factor 23 and parathyroid hormone predict extent of aortic valve calcifications in patients with mild to moderate chronic kidney disease Di Lullo, Luca Gorini, Antonio Bellasi, Antonio Morrone, Luigi F. Rivera, Rodolfo Russo, Luigi Santoboni, Alberto Russo, Domenico Clin Kidney J Contents BACKGROUND: Cardiac valve calcifications are present in dialysis patients and regarded as dependent on a deranged mineral metabolism. Few data are available for patients with chronic kidney disease (CKD) not on dialysis. This study evaluates the potential association between the extent of cardiac valve calcification and levels of intact parathyroid hormone (i-PTH), phosphorus, calcium, 25-OH vitamin D, fibroblast growth factor 23 (FGF-23), Klotho and C-reactive protein (CRP) simultaneously measured in patients with mild to moderate CKD. METHODS: Consecutive non-hospitalized patients referring to five nephrology units were evaluated. Inclusion criteria were age >18 years, CKD Stages 3–4, and the presence of aortic and/or mitral valve calcification assessed by echocardiography as routinely clinical evaluation. Patients underwent clinical examination and routine biochemistry. Baseline i-PTH, phosphorus, calcium, 25-OH vitamin D, FGF-23, Klotho and CRP were simultaneously ascertained. RESULTS: Extent of aortic valve calcification (n = 100 patients) was moderate in 68 patients and mild in the remaining patients. Mitral valve calcification (n = 96 patients) score was 1, 2 and 3 in 61, 34 and 1 patients, respectively. In univariate analysis, no association was found between extent of mitral valve calcification and markers of mineral metabolism and CRP; aortic valve extent of calcification was positively associated with i-PTH (r(2) = 0.212; P = 0.03) and FGF-23 (r(2) = 0.272; P = 0.01), and negatively with Klotho (r(2) = −0.208; P = 0.04). In multivariable analysis, extent of aortic valve calcification was associated with FGF-23 (P = 0.01) and PTH (P = 0.01) levels. CONCLUSIONS: Extent of aortic valve calcification is associated to FGF-23 and PTH in naïve CKD patients with mild to moderate CKD. Further studies should examine whether FGF-23 assay should be included in routine clinical evaluation of CKD as part of cardiovascular risk stratification. Oxford University Press 2015-12 2015-09-03 /pmc/articles/PMC4655786/ /pubmed/26613033 http://dx.doi.org/10.1093/ckj/sfv073 Text en © The Author 2015. Published by Oxford University Press on behalf of ERA-EDTA. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Contents
Di Lullo, Luca
Gorini, Antonio
Bellasi, Antonio
Morrone, Luigi F.
Rivera, Rodolfo
Russo, Luigi
Santoboni, Alberto
Russo, Domenico
Fibroblast growth factor 23 and parathyroid hormone predict extent of aortic valve calcifications in patients with mild to moderate chronic kidney disease
title Fibroblast growth factor 23 and parathyroid hormone predict extent of aortic valve calcifications in patients with mild to moderate chronic kidney disease
title_full Fibroblast growth factor 23 and parathyroid hormone predict extent of aortic valve calcifications in patients with mild to moderate chronic kidney disease
title_fullStr Fibroblast growth factor 23 and parathyroid hormone predict extent of aortic valve calcifications in patients with mild to moderate chronic kidney disease
title_full_unstemmed Fibroblast growth factor 23 and parathyroid hormone predict extent of aortic valve calcifications in patients with mild to moderate chronic kidney disease
title_short Fibroblast growth factor 23 and parathyroid hormone predict extent of aortic valve calcifications in patients with mild to moderate chronic kidney disease
title_sort fibroblast growth factor 23 and parathyroid hormone predict extent of aortic valve calcifications in patients with mild to moderate chronic kidney disease
topic Contents
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655786/
https://www.ncbi.nlm.nih.gov/pubmed/26613033
http://dx.doi.org/10.1093/ckj/sfv073
work_keys_str_mv AT dilulloluca fibroblastgrowthfactor23andparathyroidhormonepredictextentofaorticvalvecalcificationsinpatientswithmildtomoderatechronickidneydisease
AT goriniantonio fibroblastgrowthfactor23andparathyroidhormonepredictextentofaorticvalvecalcificationsinpatientswithmildtomoderatechronickidneydisease
AT bellasiantonio fibroblastgrowthfactor23andparathyroidhormonepredictextentofaorticvalvecalcificationsinpatientswithmildtomoderatechronickidneydisease
AT morroneluigif fibroblastgrowthfactor23andparathyroidhormonepredictextentofaorticvalvecalcificationsinpatientswithmildtomoderatechronickidneydisease
AT riverarodolfo fibroblastgrowthfactor23andparathyroidhormonepredictextentofaorticvalvecalcificationsinpatientswithmildtomoderatechronickidneydisease
AT russoluigi fibroblastgrowthfactor23andparathyroidhormonepredictextentofaorticvalvecalcificationsinpatientswithmildtomoderatechronickidneydisease
AT santobonialberto fibroblastgrowthfactor23andparathyroidhormonepredictextentofaorticvalvecalcificationsinpatientswithmildtomoderatechronickidneydisease
AT russodomenico fibroblastgrowthfactor23andparathyroidhormonepredictextentofaorticvalvecalcificationsinpatientswithmildtomoderatechronickidneydisease