Linkage of elevated CaxPO4 product with inflammation in maintenance hemodialysis patients.

Nasri, H. (2006) Linkage of elevated CaxPO4 product with inflammation in maintenance hemodialysis patients. Minerva urologica e nefrologica = The Italian journal of urology and nephrology, 58 (4). pp. 339-45. ISSN 0393-2249

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Abstract

AIM The aim of the paper was to elucidate whether and how, in end-stage renal disease (ESRD) patients on regular hemodialysis, the levels of C-reactive protein (CRP) correlate with CaxPO4 product; thus, a cross-sectional study was conducted on stable hemodialysis patients. METHODS According to the severity of secondary hyperparathyroidism, each patient being treated for secondary hyperparathyroidism was given oral active vitamin D3, calcium carbonate capsule, and Rena-Gel tablet at various doses. Fasting serum 25-hydroxy, vitamin D and intact serum PTH and also serum blood urea nitrogen, serum CRP, albumin, serum calcium, phosphorus and alkaline phosphatase and also serum ferritin were measured using standard METHODS RESULTS There was a total of 41 patients, consisting of 29 nondiabetic hemodialysis patients and 12 diabetic hemodialysis patients. The mean patient age was 46+/-17.6 years. The value of serum CRP of patients was 8.6+/-6.6 mg/L (median 6 mg/L). The value of CaxPO4 product was 50.5+/-15.5 mg(2)/dL(2) (median: 50 mg(2)dL(2)). The present study showed a significant inverse correlation between CaxPO4 product and the age of the patients and a significant positive correlation between logarithm of serum CRP with age and also significant inverse correlations of dialysis adequacy as determined by urea reduction rate (URR) with logarithm of serum CRP and with CaxPO4 product. Furthermore, significant positive correlation of logarithm of serum CRP with CaxPO4 product was found too. CONCLUSIONS Our findings showed the need to pay further attention to hyperphosphatemia and uncontrolled secondary hyperparathyroidism in maintenance hemodialysis patients.

Item Type: Article
Subjects: WJ Urogenital System
WK Endocrine System
QU Biochemistry
Divisions: Faculty of Medicine > Department of Clinical Sciences > Department of Internal Medicine
Depositing User: zahra bagheri .
Date Deposited: 20 Aug 2017 05:23
Last Modified: 20 Aug 2017 05:23
URI: http://eprints.skums.ac.ir/id/eprint/3236

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