Aortic Calcification and Arterial Stiffness Burden in a Chronic Kidney Disease Cohort with High Cardiovascular Risk: Baseline Characteristics of the Impact of Phosphate Reduction On Vascular End-Points in Chronic Kidney Disease Trial.
Age Factors
Aged
Aorta
/ diagnostic imaging
Disease Progression
Female
Fibroblast Growth Factor-23
Glomerular Filtration Rate
Heart Disease Risk Factors
Humans
Kidney Failure, Chronic
/ blood
Lanthanum
/ administration & dosage
Male
Middle Aged
Phosphates
/ blood
Pulse Wave Analysis
Sex Factors
Treatment Outcome
Vascular Calcification
/ blood
Vascular Stiffness
/ drug effects
Arterial compliance
Cardiovascular disease
Chronic kidney disease
Chronic kidney disease mineral and bone disorder
Phosphate
Vascular calcification
Journal
American journal of nephrology
ISSN: 1421-9670
Titre abrégé: Am J Nephrol
Pays: Switzerland
ID NLM: 8109361
Informations de publication
Date de publication:
2020
2020
Historique:
received:
09
10
2019
accepted:
31
12
2019
pubmed:
6
2
2020
medline:
25
5
2021
entrez:
6
2
2020
Statut:
ppublish
Résumé
Chronic kidney disease (CKD) is associated with excess cardiovascular morbidity and mortality compared to the general population. Hyperphosphataemia, associated with vascular calcification and arterial stiffness, may play a key role in the pathogenesis of cardiovascular disease (CVD) associated with CKD, although phosphate reduction strategies have not consistently proven to beneficially affect clinically relevant outcomes. The IMpact of Phosphate Reduction On Vascular End-points in CKD (IMPROVE-CKD) study is an international, multi-centre, randomized, placebo-controlled trial investigating the effect of the phosphate binder lanthanum carbonate on intermediate cardiovascular markers in patients with stage 3b-4 CKD. The primary end-point is change in carotid-femoral pulse wave velocity (PWV, SphygmoCor) after 96 weeks. Secondary outcomes include change in abdominal aortic calcification (AAC, computed tomography), serum phosphate and fibroblast growth factor 23 (FGF-23). In total, 278 participants were recruited and randomized, mean age 63 ± 13 years, 69% male, 45% diabetes, 32% CVD, 33% stage 3b CKD and 67% stage 4 CKD. Mean estimated glomerular filtration rate and serum phosphate were 26.6 ± 8.3 mL/min/1.72 m2 and 1.25 ± 0.20 mmol/L, respectively. Median (interquartile range) intact and c-terminal FGF-23 levels were 133.0 (89.1-202) pg/mL and 221.1 (154.3-334.1) RU/mL, respectively. Mean PWV was 10.8 ± 3.6 m/s and 81% had AAC (median Agatston score 1,535 [63-5,744] Hounsfield units). PWV ≥10 m/s was associated with older age, diabetes, CVD, presence of AAC, higher systolic blood pressure (BP), larger waist circumference and higher alkaline phosphatase. AAC was associated with older age, male sex, diabetes, CVD, higher diastolic BP, dyslipidaemia (and use of statins), smoking, larger waist circumference and increased PWV. In conclusion, IMPROVE-CKD participants had high baseline risk for cardiovascular events, as suggested by high baseline PWV and AAC values.
Identifiants
pubmed: 32023606
pii: 000505717
doi: 10.1159/000505717
doi:
Substances chimiques
FGF23 protein, human
0
Phosphates
0
lanthanum carbonate
490D9F069T
Lanthanum
6I3K30563S
Fibroblast Growth Factor-23
7Q7P4S7RRE
Types de publication
Journal Article
Multicenter Study
Randomized Controlled Trial
Langues
eng
Sous-ensembles de citation
IM
Pagination
201-215Informations de copyright
© 2020 S. Karger AG, Basel.