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Calcium and phosphorus metabolic changes in children with hepatic bilharziasis
Insights
Children with hepatic bilharziasis show altered calcium and phosphorus metabolism, with increased urinary excretion and impaired renal handling of these minerals. Ascitic cases exhibited more pronounced metabolic disturbances.
Area of Science:
- Pediatric Nephrology
- Hepatology
- Mineral Metabolism
Background:
- Hepatic bilharziasis (schistosomiasis) is a significant parasitic disease affecting the liver.
- Mineral metabolism, particularly calcium and phosphorus, can be disrupted in chronic liver diseases.
- Understanding these metabolic changes is crucial for managing pediatric patients with hepatic bilharziasis.
Purpose of the Study:
- To investigate the specific alterations in calcium and phosphorus metabolism in children with hepatic bilharziasis.
- To compare metabolic profiles between non-ascitic and ascitic pediatric patients with hepatic bilharziasis and healthy controls.
Main Methods:
- Cross-sectional study involving 35 children with hepatic bilharziasis (12 with ascites) and 13 healthy controls.
- Serum and urinary calcium and inorganic phosphate levels were measured.
- Creatinine clearance, phosphate excretion index (PEI), and tubular reabsorption of phosphate (% TRP) were assessed.
- Response to phosphate loading and intravenous calcium loading tests were evaluated.
Main Results:
- Children with hepatic bilharziasis had normal serum calcium and inorganic phosphate but increased urinary levels.
- Ascitic fluid calcium and phosphate were 70% and 90.2% of serum levels, respectively.
- Significantly diminished creatinine clearance, increased PEI, and decreased % TRP were observed, more so in ascitic cases.
- Bilharzial patients showed a more rapid decrease in serum inorganic phosphate after phosphate load and significant calcium retention after calcium load.
Conclusions:
- Hepatic bilharziasis in children is associated with significant disturbances in calcium and phosphorus metabolism, including renal wasting.
- Ascites exacerbates these metabolic abnormalities.
- Altered mineral handling suggests potential renal involvement and impaired bone health in these patients.
Abstract:
Investigations were done to study the calcium and phosphorus metabolic changes in 35 children with hepatic bilharziasis, of whom 12 were ascitic. Thirteen normal children served as controls. Despite a normal serum level of both calcium and inorganic phosphate in the Bilharzial group, yet both were increased in urine. The mean values obtained from the ascitic fluid were 70% and 90.2% of their serum levels, respectively. The corrected creatinine clearance was significantly diminished, while PEI was significantly increased, and the % TRP significantly decreased, with still a more marked decrease in the ascitic cases. Following a phosphate lead the serum inorganic phosphate level showed a significantly more rapid lowering in both bilharzial groups, as compared to the control group. On the other hand bilharzial cases responded to the intravenous calcium load by a significant retention of calcium in the serum.
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