Chronic kidney disease (CKD) affects approximately 26 million Americans with many more at risk for disease development. Elevated serum phosphorus (P) and related abnormalities in P homeostasis due to progressive loss of kidney function are primary driving forces behind cardiovascular dysfunction and mortality in CKD patients. Intestinal P absorption is an critical aspect in P homeostasis but has been understudied, particularly in the early stages of CKD progression. This study aims to determine P absorption in patients with moderate CKD compared to healthy adults.
Study Type
OBSERVATIONAL
Enrollment
20
Subjects will undergo a radiophosphorus (P-33) absorption test over two days, that will include an oral administration of P-33 on the 1st day of the test, and an IV administration of P-33 on the 2nd day of the test. P-33 activity from serial serum and urine collections will be determined by scintillation counting, and fractional phosphorus absorption calculated by kinetic modeling.
Purdue University Nutrition Science Department
West Lafayette, Indiana, United States
Fractional Phosphorus Absorption
Radiophosphorus (P-33) activity determined by liquid scintillation counting in serum and urine after oral and IV administration will be used to determine fractional phosphate absorption.
Time frame: Measured from serial blood draws over a 4-hour time frame
Serum FGF23
serum intact and c-terminal FGF23
Time frame: Measured from baseline measures and serial blood draws over a 4-hour time frame
Serum 1,25(OH)2D
serum 1,25-dihydroxyvitamin D
Time frame: Measured from baseline measures and serial blood draws over a 4-hour time frame
Serum parathyroid hormone (PTH)
serum intact parathyroid hormone
Time frame: Measured from baseline measures and serial blood draws over a 4-hour time frame
Serum phosphate
serum phosphate
Time frame: Measured from baseline measures and serial blood draws over a 4-hour time frame
24h Urine phosphate
24h urine phosphate
Time frame: measured from two, 24-hour urine collections
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