Phosphorylated fetuin-A-containing calciprotein particles are associated with aortic stiffness and a procalcific milieu in patients with pre-dialysis CKD

Vascular stiffening occurs in normal ageing and is accelerated in chronic kidney disease (CKD). Vascular calcification contributes to this stiffening and to the high incidence of vascular morbidity and mortality in this population. A network of inhibitors work in concert to reduce mineralization ris...

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Published inNephrology, dialysis, transplantation Vol. 27; no. 5; pp. 1957 - 1966
Main Authors Smith, Edward R., Ford, Martin L., Tomlinson, Laurie A., Rajkumar, Chakravarthi, McMahon, Lawrence P., Holt, Stephen G.
Format Journal Article
LanguageEnglish
Published Oxford Oxford University Press 01.05.2012
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ISSN0931-0509
1460-2385
1460-2385
DOI10.1093/ndt/gfr609

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Abstract Vascular stiffening occurs in normal ageing and is accelerated in chronic kidney disease (CKD). Vascular calcification contributes to this stiffening and to the high incidence of vascular morbidity and mortality in this population. A network of inhibitors work in concert to reduce mineralization risk in extra-osseous tissue. Fetuin-A is an important systemic inhibitor of ectopic calcification. A fraction of the total circulating fetuin-A interacts with mineral ions to form stable colloidal complexes, calciprotein particles (CPP), preventing deposition. We sought to assess whether CPP fetuin-A levels were associated with procalcific factors and aortic stiffness in a cohort of patients with Stages 3 and 4 CKD. We measured fetuin-A CPP levels, serum inflammatory markers [C-reactive protein (CRP), interleukin-6, tumour necrosis factor-α], oxidized low-density lipoprotein (oxLDL), bone morphogenetic protein-2 (BMP-2) and -7 (BMP-7) and aortic pulse wave velocity (APWV) in a cohort of 200 CKD patients. Serum measurements were also made in 78 healthy controls. CPP fetuin-A phosphorylation was characterized by phosphate-affinity gel chromatography. Fetuin-A-containing CPPs were only detectable in the serum of CKD patients. Inflammatory markers, oxLDL and BMP-2 levels were all significantly higher in the CKD than control subjects. CPP fetuin-A levels were independently associated with serum phosphate, high-sensitivity C-reactive protein, oxLDL, BMP-2/7 ratio and inversely with estimated glomerular filtration rate (model R(2) = 0.51). After adjusting for confounders, CPP fetuin-A levels were independently associated with APWV. Only phosphorylated fetuin-A was present in serum CPP. Increased CPP fetuin-A levels reflect an increasingly procalcific milieu and are associated with increased aortic stiffness in patients with pre-dialysis CKD.
AbstractList Vascular stiffening occurs in normal ageing and is accelerated in chronic kidney disease (CKD). Vascular calcification contributes to this stiffening and to the high incidence of vascular morbidity and mortality in this population. A network of inhibitors work in concert to reduce mineralization risk in extra-osseous tissue. Fetuin-A is an important systemic inhibitor of ectopic calcification. A fraction of the total circulating fetuin-A interacts with mineral ions to form stable colloidal complexes, calciprotein particles (CPP), preventing deposition. We sought to assess whether CPP fetuin-A levels were associated with procalcific factors and aortic stiffness in a cohort of patients with Stages 3 and 4 CKD.BACKGROUNDVascular stiffening occurs in normal ageing and is accelerated in chronic kidney disease (CKD). Vascular calcification contributes to this stiffening and to the high incidence of vascular morbidity and mortality in this population. A network of inhibitors work in concert to reduce mineralization risk in extra-osseous tissue. Fetuin-A is an important systemic inhibitor of ectopic calcification. A fraction of the total circulating fetuin-A interacts with mineral ions to form stable colloidal complexes, calciprotein particles (CPP), preventing deposition. We sought to assess whether CPP fetuin-A levels were associated with procalcific factors and aortic stiffness in a cohort of patients with Stages 3 and 4 CKD.We measured fetuin-A CPP levels, serum inflammatory markers [C-reactive protein (CRP), interleukin-6, tumour necrosis factor-α], oxidized low-density lipoprotein (oxLDL), bone morphogenetic protein-2 (BMP-2) and -7 (BMP-7) and aortic pulse wave velocity (APWV) in a cohort of 200 CKD patients. Serum measurements were also made in 78 healthy controls. CPP fetuin-A phosphorylation was characterized by phosphate-affinity gel chromatography.METHODSWe measured fetuin-A CPP levels, serum inflammatory markers [C-reactive protein (CRP), interleukin-6, tumour necrosis factor-α], oxidized low-density lipoprotein (oxLDL), bone morphogenetic protein-2 (BMP-2) and -7 (BMP-7) and aortic pulse wave velocity (APWV) in a cohort of 200 CKD patients. Serum measurements were also made in 78 healthy controls. CPP fetuin-A phosphorylation was characterized by phosphate-affinity gel chromatography.Fetuin-A-containing CPPs were only detectable in the serum of CKD patients. Inflammatory markers, oxLDL and BMP-2 levels were all significantly higher in the CKD than control subjects. CPP fetuin-A levels were independently associated with serum phosphate, high-sensitivity C-reactive protein, oxLDL, BMP-2/7 ratio and inversely with estimated glomerular filtration rate (model R(2) = 0.51). After adjusting for confounders, CPP fetuin-A levels were independently associated with APWV. Only phosphorylated fetuin-A was present in serum CPP.RESULTSFetuin-A-containing CPPs were only detectable in the serum of CKD patients. Inflammatory markers, oxLDL and BMP-2 levels were all significantly higher in the CKD than control subjects. CPP fetuin-A levels were independently associated with serum phosphate, high-sensitivity C-reactive protein, oxLDL, BMP-2/7 ratio and inversely with estimated glomerular filtration rate (model R(2) = 0.51). After adjusting for confounders, CPP fetuin-A levels were independently associated with APWV. Only phosphorylated fetuin-A was present in serum CPP.Increased CPP fetuin-A levels reflect an increasingly procalcific milieu and are associated with increased aortic stiffness in patients with pre-dialysis CKD.CONCLUSIONIncreased CPP fetuin-A levels reflect an increasingly procalcific milieu and are associated with increased aortic stiffness in patients with pre-dialysis CKD.
Vascular stiffening occurs in normal ageing and is accelerated in chronic kidney disease (CKD). Vascular calcification contributes to this stiffening and to the high incidence of vascular morbidity and mortality in this population. A network of inhibitors work in concert to reduce mineralization risk in extra-osseous tissue. Fetuin-A is an important systemic inhibitor of ectopic calcification. A fraction of the total circulating fetuin-A interacts with mineral ions to form stable colloidal complexes, calciprotein particles (CPP), preventing deposition. We sought to assess whether CPP fetuin-A levels were associated with procalcific factors and aortic stiffness in a cohort of patients with Stages 3 and 4 CKD. We measured fetuin-A CPP levels, serum inflammatory markers [C-reactive protein (CRP), interleukin-6, tumour necrosis factor-α], oxidized low-density lipoprotein (oxLDL), bone morphogenetic protein-2 (BMP-2) and -7 (BMP-7) and aortic pulse wave velocity (APWV) in a cohort of 200 CKD patients. Serum measurements were also made in 78 healthy controls. CPP fetuin-A phosphorylation was characterized by phosphate-affinity gel chromatography. Fetuin-A-containing CPPs were only detectable in the serum of CKD patients. Inflammatory markers, oxLDL and BMP-2 levels were all significantly higher in the CKD than control subjects. CPP fetuin-A levels were independently associated with serum phosphate, high-sensitivity C-reactive protein, oxLDL, BMP-2/7 ratio and inversely with estimated glomerular filtration rate (model R(2) = 0.51). After adjusting for confounders, CPP fetuin-A levels were independently associated with APWV. Only phosphorylated fetuin-A was present in serum CPP. Increased CPP fetuin-A levels reflect an increasingly procalcific milieu and are associated with increased aortic stiffness in patients with pre-dialysis CKD.
Author Holt, Stephen G.
Tomlinson, Laurie A.
Ford, Martin L.
Smith, Edward R.
Rajkumar, Chakravarthi
McMahon, Lawrence P.
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  fullname: Tomlinson, Laurie A.
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https://www.ncbi.nlm.nih.gov/pubmed/22105144$$D View this record in MEDLINE/PubMed
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IQODW
MBLQV
NTWIH
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CGR
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7X8
ID FETCH-LOGICAL-c317t-d04b5b72dd69fbd6ea16224801182eef48225f69b40c0e240fb864061eaf1c413
ISSN 0931-0509
1460-2385
IngestDate Thu Jul 10 20:00:52 EDT 2025
Thu Apr 03 07:14:06 EDT 2025
Mon Jul 21 09:15:49 EDT 2025
Thu Apr 24 23:03:14 EDT 2025
Tue Jul 01 02:30:18 EDT 2025
IsPeerReviewed true
IsScholarly true
Issue 5
Keywords Kidney disease
Human
Urinary system disease
Hemodialysis
vascular calcification
Inflammation
Particle
Extrarenal dialysis
aortic stiffness
Renal failure
Calcification
fetuin-A
Aorta
Dialysis
Stiffness
bone morphogenetic proteins
Language English
License CC BY 4.0
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c317t-d04b5b72dd69fbd6ea16224801182eef48225f69b40c0e240fb864061eaf1c413
Notes ObjectType-Article-1
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content type line 23
PMID 22105144
PQID 1010638801
PQPubID 23479
PageCount 10
ParticipantIDs proquest_miscellaneous_1010638801
pubmed_primary_22105144
pascalfrancis_primary_25856174
crossref_citationtrail_10_1093_ndt_gfr609
crossref_primary_10_1093_ndt_gfr609
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PublicationCentury 2000
PublicationDate 2012-05-01
PublicationDateYYYYMMDD 2012-05-01
PublicationDate_xml – month: 05
  year: 2012
  text: 2012-05-01
  day: 01
PublicationDecade 2010
PublicationPlace Oxford
PublicationPlace_xml – name: Oxford
– name: England
PublicationTitle Nephrology, dialysis, transplantation
PublicationTitleAlternate Nephrol Dial Transplant
PublicationYear 2012
Publisher Oxford University Press
Publisher_xml – name: Oxford University Press
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Snippet Vascular stiffening occurs in normal ageing and is accelerated in chronic kidney disease (CKD). Vascular calcification contributes to this stiffening and to...
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StartPage 1957
SubjectTerms Aged
Aged, 80 and over
alpha-2-HS-Glycoprotein - metabolism
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Aorta - metabolism
Aorta - physiopathology
Biological and medical sciences
Biomarkers - blood
Bone Morphogenetic Protein 2 - blood
Bone Morphogenetic Protein 7 - blood
C-Reactive Protein - metabolism
Calcinosis - blood
Case-Control Studies
Chronic Disease
Emergency and intensive care: renal failure. Dialysis management
Female
Glomerular Filtration Rate - physiology
Glomerulonephritis
Humans
Intensive care medicine
Interleukin-6 - blood
Kidney Diseases - blood
Kidney Diseases - physiopathology
Lipoproteins, LDL - blood
Male
Medical sciences
Middle Aged
Nephrology. Urinary tract diseases
Nephropathies. Renovascular diseases. Renal failure
Phosphorylation
Tumor Necrosis Factor-alpha - blood
Vascular Stiffness - physiology
Title Phosphorylated fetuin-A-containing calciprotein particles are associated with aortic stiffness and a procalcific milieu in patients with pre-dialysis CKD
URI https://www.ncbi.nlm.nih.gov/pubmed/22105144
https://www.proquest.com/docview/1010638801
Volume 27
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