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Original Research Communication |
1 From the Research Department of Human Nutrition, The Royal Veterinary and Agricultural University, Frederiksberg, Denmark (ABB, SB, CM, MH, and BS); the Department of Earth Sciences, Dartmouth College, Hanover, NH (SS); and the Department of Clinical Physiology and Nuclear Medicine, The Copenhagen University Hospital, Copenhagen (MJ and OWK).
Background: Dietary calcium absorption can be determined only with the use of isotope techniques. Currently used isotope techniques require exclusive equipment or are not true tracer approaches.
Objective: The objective was to compare a dual-isotope method combining radioisotopes and stable isotopes with a whole-body radioisotope retention method for measuring calcium absorption.
Design: Seven healthy adults aged 2127 y consumed a test meal containing 63 ± 14 (
± SD) mg Ca together with a water solution of 47Ca (0.11 MBq). One hour after ingestion, 18 mg 44Ca was administered intravenously. All feces and urine were collected for 5 and 6 d, respectively. Calcium absorption was estimated from whole-body retention of the radioisotope 12 times over 3 wk after ingestion and from the excretion of 47Ca and 44Ca in a 24-h urine sample collected on day 2. 44Ca in urine was determined by inductively coupled plasma mass spectrometry.
Results: Mean (± SD) calcium absorption was 75 ± 9% with the dual-isotope method and was 74 ± 8% with the whole-body radioisotope retention method. There was a high degree of agreement between the methods.
Conclusion: The dual-isotope method is a valid approach for measuring calcium absorption from a single meal.
Key Words: Calcium absorption radioisotopes 47Ca stable isotopes 44Ca whole-body counting inductively coupled plasma mass spectrometry ICPMS
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