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Serum phosphate is associated with left ventricular mass in patients with chronic kidney disease: a cardiac magnetic resonance study.

Authors :
Chue CD
Edwards NC
Moody WE
Steeds RP
Townend JN
Ferro CJ
Source :
Heart (British Cardiac Society) [Heart] 2012 Feb; Vol. 98 (3), pp. 219-24. Date of Electronic Publication: 2011 Oct 22.
Publication Year :
2012

Abstract

Objective: To explore the relationship between serum phosphate, arterial stiffness and left ventricular mass (LVM) in patients with early-stage chronic kidney disease (CKD).<br />Design: A cross-sectional observational study.<br />Setting: Single centre.<br />Patients: 208 patients with stage 2 to stage 4 non-diabetic CKD.<br />Interventions: Arterial stiffness was determined through measurement of aortic pulse wave velocity (PWV). Cardiac magnetic resonance was used to determine LVM.<br />Main Outcome Measure: Relationship between serum phosphate, aortic PWV and LVM.<br />Results: Mean age was 54 ± 13 years, mean glomerular filtration rate was 50 ± 15 ml/min/1.73 m(2), mean serum phosphate was 1.11 ± 0.21 mmol/l and mean PWV was 8.6 ± 2.1 m/s. When the cohort was divided into quartiles according to serum phosphate, LVM increased across quartiles (p=0.04), with no significant differences in age, kidney function, blood pressure or PWV. Serum phosphate correlated with LVM (r=0.173; p=0.01), but PWV did not (p=0.2). In a regression model containing gender, serum phosphate, office systolic blood pressure, albumin/creatinine ratio and haemoglobin, 30% of the variation in LVM was explained (p<0.0005), with serum phosphate accounting for 5% of the variance.<br />Conclusion: Serum phosphate is independently associated with LVM in patients with CKD. Interventional studies are required to determine whether this association is causative and whether reducing phosphate exposure reduces LVM in this population.

Details

Language :
English
ISSN :
1468-201X
Volume :
98
Issue :
3
Database :
MEDLINE
Journal :
Heart (British Cardiac Society)
Publication Type :
Academic Journal
Accession number :
22021416
Full Text :
https://doi.org/10.1136/heartjnl-2011-300570