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A high calcium-phosphate product is associated with high C-reactive protein concentrations in hemodialysis patients
Insights
In hemodialysis patients, a high calcium-phosphate (Ca x PO4) product is linked to elevated C-reactive protein (CRP) levels, a marker of inflammation. Lowering the Ca x PO4 product effectively reduces CRP, suggesting a therapeutic target for cardiovascular risk reduction.
Area of Science:
- Nephrology
- Cardiovascular Medicine
- Biochemistry
Background:
- Elevated calcium-phosphate (Ca x PO4) product and C-reactive protein (CRP) are linked to cardiovascular mortality in hemodialysis (HD) patients.
- The relationship between Ca x PO4 and CRP in HD patients requires further elucidation.
Purpose of the Study:
- To investigate the correlation between Ca x PO4 product and CRP levels in chronic HD patients.
- To assess the impact of correcting a high Ca x PO4 product on CRP levels.
Main Methods:
- Cross-sectional and interventional study of 47 chronic HD patients without active inflammation.
- Measured CRP, Ca, PO4, and other biochemical markers; analyzed the correlation between Ca x PO4 and CRP.
- Intervention involved intensive lowering of Ca x PO4 in patients with elevated levels.
Main Results:
- A significant hyperbolic correlation was found between Ca x PO4 and CRP, with a breakpoint at 55 mg2/dl2.
- Patients with Ca x PO4 > 55 mg2/dl2 exhibited significantly higher CRP levels.
- Intensive lowering of Ca x PO4 product in a subgroup of patients led to a significant reduction in both Ca x PO4 and CRP levels.
Conclusions:
- In stable chronic HD patients, a high Ca x PO4 product is associated with elevated CRP concentrations.
- Therapeutic reduction of the Ca x PO4 product can effectively lower CRP levels in HD patients.
Background:
An elevated CaxPO4 product and C-reactive protein (CRP) have been associated with coronary artery calcification and increased cardiovascular mortality in hemodialysis (HD) patients. However, it has not been defined, so far, whether and how both parameters are related to each other. For this reason we have evaluated in a cross-sectional and in an interventional study the possible correlation between CaxPO4 and CRP and the effect of the correction of a high CaxPO4 on CRP levels.
Methods:
47 uremic patients (age 65 +/- 16 years) on regular chronic HD were selected from a total population of 125 prevalent patients treated at our Institution. Patients had no clinical evidence of either acute infectious or inflammatory diseases for at least 4 weeks before the study. They were on regular bicarbonate HD for 6-329 months (median 42). CRP, hemoglobin (Hb), serum albumin (sAlb), protein catabolic rate (PCRn), serum calcium (Ca), serum phosphorus (PO4), CaxPO4, intact PTH, Kt/V, presence of ischemic heart disease (IHD) and/or peripheral vascular disease (PVD) were recorded. CRP was Ln-transformed in all statistical analyses because of positive skewness.
Results:
The main findings were: LnCRP 2.17 +/- 0.77 mg/l, Ca 10.1 +/- 0.4 mg/dl, PO4 5.8 +/- 0.6 mg/dl, CaxPO4 59 +/- 6 mg2/dl2, andPTHint 218 +/- 195 ng/ml. 18/47 had IHD, 18/47 PVD. A significant hyperbolic correlation between CaxPO4 and CRP was observed. A piecewise linear regression model analysis identified a break-point for CaxPO4 at 55 mg2/dl2. Comparison of CRP levels after the division of the patients into two groups according to CaxPO4 break-point (group A, CaxPO4 < or = 55 mg2/dl2, n = 16 patients; group B, CaxPO4 >55 mg2/dl2, n = 31 patients) showed that CRP levels were significantly lower in patients in group A (LnCRP 1.43 +/- 0.22 mg/l) than in group B (LnCRP 2.55 +/- 0.67 mg/l, p < 0.0001). Multiple regression analysis bearing LnCRP as dependent variable confirmed CaxPO4 as the most significant variable among the other variables examined. In 22 patients with CaxPO4 > or = 60 mg2/dl2, we performed intensive lowering of the CaxPO4 product in order to reach and maintain a CaxPO4 , or =55 mg2/dl2 for 3 months. At the end of observation, a significant reduction in CaxPO4 and LnCRP was observed (CaxPO4 pre 62.8 +/- 1.9 vs. post 46.3 +/- 6.2 mg2/dl2: p < 0.0001; LnCRP pre 2.32 +/-0.36 vs. post 1.83 +/- 0.14 mg/l: p < 0.0001). No significant variation in the other biochemical parameters was observed.
Conclusions:
Our data show that in chronic HD patients in steady clinical conditions with no clinical evidence of either infectious or inflammatory diseases, a high CaxPO4 is associated with high CRP concentrations. Intensive lowering of CaxPO4 reduces CRP
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