Demonstration of a difference in urinary calcium, not calcium absorption, in black and white adolescents

Bone mineral density (BMD) of the forearm, lumbar spine, and femoral neck is greater in black than in white children. Studies were performed to determine whether differences in intestinal absorption of calcium or urinary calcium or both account for an assumed more positive calcium balance and greater bone mass in black children. Normal black and white boys and girls were admitted to a metabolic ward and given a constant daily diet containing 1000 mg calcium, 60% as calcium carbonate, for 2½ days (study I) or 3½ days (study II). Fasting blood and 24 h urine collections were obtained, and in study II, unidirectional fractional absorption of calcium (α) was determined with stable isotopes of calcium. It was found that (1) serum 25‐hydroxyvitamin D (25‐OHD) and urinary calcium were lower and serum 1,25‐dihydroxyvitamin D [1,25‐(OH)2D] was higher in black than in white children, and (2) α was higher in boys than in girls with no racial difference, and (3) there were significant positive correlations between α and urinary calcium in the blacks and in the black and white children together. It is concluded that (1) α is higher in boys than in girls and (2) a lower urinary calcium, not increased intestinal absorption of calcium, is the means for a more positive calcium balance in blacks that accounts for the racial difference in BMD.

[1]  N. Bell,et al.  Increased calcium intake does not suppress circulating 1,25-dihydroxyvitamin D in normocalcemic patients with sarcoidosis. , 1993, The Journal of clinical investigation.

[2]  N. Bell,et al.  Demonstration that bone mass is greater in black than in white children , 1991, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[3]  B. Specker,et al.  Bone mineral content in black and white children 1 to 6 years of age. Early appearance of race and sex differences. , 1989, American journal of diseases of children.

[4]  R. Eastell,et al.  One‐day test using stable isotopes to measure true fractional calcium absorption , 1989, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[5]  S. Epstein,et al.  Evidence of a probable role for 25‐hydroxyvitamin D in the regulation of human calcium metabolism , 1988, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[6]  D. Covell,et al.  Direct measurement of dietary fractional absorption using calcium isotopic tracers. , 1987, Biomedical & environmental mass spectrometry.

[7]  S. Epstein,et al.  Evidence for alteration of the vitamin D-endocrine system in blacks. , 1985, The Journal of clinical investigation.

[8]  S. Epstein,et al.  Evidence for alteration of the vitamin D-endocrine system in obese subjects. , 1985, The Journal of clinical investigation.

[9]  J. Adams,et al.  INCREASED SKIN PIGMENT REDUCES THE CAPACITY OF SKIN TO SYNTHESISE VITAMIN D3 , 1982, The Lancet.

[10]  H. DeLuca,et al.  Intestinal calcium absorption and serum vitamin D metabolites in normal subjects and osteoporotic patients: effect of age and dietary calcium. , 1979, The Journal of clinical investigation.

[11]  J. Lemann,et al.  The effects of oral CaCO3 loading and dietary calcium deprivation on plasma 1,25-dihydroxyvitamin D concentrations in healthy adults. , 1979, The Journal of clinical endocrinology and metabolism.

[12]  H. DeLuca,et al.  A rapid assay for 25-OH-vitamin D3 without preparative chromatography. , 1974, The Journal of clinical endocrinology and metabolism.

[13]  H. Bartels,et al.  [Micro-determination of creatinine]. , 1971, Clinica chimica acta; international journal of clinical chemistry.

[14]  M. Modlin Urinary calcium in normal adults and in patients with renal stone: An interracial study , 1967 .

[15]  C. H. Fiske,et al.  THE COLORIMETRIC DETERMINATION OF PHOSPHORUS , 1925 .

[16]  R. Horst,et al.  A microassay for 1,25-dihydroxyvitamin D not requiring high performance liquid chromatography: application to clinical studies. , 1984, The Journal of clinical endocrinology and metabolism.