Clinical Chemistry
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Clinical Chemistry 0: clinchem.2005.059568v1, 2005; 10.1373/clinchem.2005.059568
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
clinchem.2005.059568v1
52/2/248    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Al-oanzi, Z. H.
Right arrow Articles by Datta, H. K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Al-oanzi, Z. H.
Right arrow Articles by Datta, H. K.

Received on August 23, 2005
Accepted on November 17, 2005

Endocrinology and Metabolism

Assessment of Vitamin D Status in Male Osteoporosis

Ziad H. Al-oanzi 1, Stephen P. Tuck 1, Nicholas Raj 2, John S. Harrop 2, Gregory D. Summers 2, David B. Cook 1, Roger M. Francis 1, Harish K. Datta 1*

1 School of Clinical & Laboratory Sciences and School of Clinical Medical Sciences, The Medical School, University of Newcastle, Newcastle upon Tyne, United Kingdom
2 Departments of Rheumatology and Biochemistry, Derbyshire Royal Infirmary, Derby, United Kingdom

* To whom correspondence should be addressed. E-mail: h.k.datta{at}ncl.ac.uk.

Background: Clinical assessment of vitamin D status often relies on measuring total circulating 25-hydroxyvitamin D3 (25OHD3), but much of each vitamin D metabolite is bound to plasma vitamin D-binding protein (DBP), such that the percentage of free vitamin is very low. We hypothesized that measurement of free rather than total 1,25-dihydroxyvitamin D3 [1,25(OH)2D3] and 25OHD3 may provide better assessment of vitamin D status. We therefore aimed to assess vitamin D status in men with idiopathic osteoporosis, in whom possible secondary causes of osteoporosis had been excluded, and to determine the extent of change in biologically active "free" vitamin D caused by variation in plasma DBP concentrations.

Methods: We measured 1,25(OH)2D3 and 25OHD3 in plasma samples from 56 men with idiopathic osteoporosis [mean (SD) age, 59.6 (13.6); range, 21-86 years] and 114 male controls [62.4 (10.4) years; range, 44-82 years].

Results: Mean total plasma 25OHD3 in the 56 men with osteoporosis and the 114 controls was 44.7 (21) and 43.3 (17) nmol/L, respectively; total plasma 1,25(OH)2D3 measured in randomly selected men with osteoporosis (n = 50) and controls (n = 50) was 90 (37) and 103 (39) pmol/L, respectively. Mean plasma DBP was significantly higher (P <0.001) in men with osteoporosis [224 (62) mg/L; n = 56] than in the controls [143 (34) mg/L; n = 114], but calculated free plasma 25OHD3 and 1,25(OH)2D3 were significantly lower in the osteoporotic men than in controls [6.1 (3.1) vs 9.1 (4.4) pmol/L (P <0.00001) and 77 (37) vs 142 (58) fmol/L (P <0.00001), respectively].

Conclusions: Measurement of total vitamin D metabolites alone, although providing a crude assessment of vitamin D status, may not give an accurate indication of the free (biologically active) form of the vitamin. The ratio of total 25OHD3 and 1,25(OH)2D3 to plasma DBP, rather than total circulating vitamin D metabolites, may provide a more useful index of biological activity. Further studies are required to substantiate this hypothesis.




The following articles in journals at HighWire Press have cited this article:


Home page
J. Clin. Endocrinol. Metab.Home page
K. E. Ensrud, B. C. Taylor, M. L. Paudel, J. A. Cauley, P. M. Cawthon, S. R. Cummings, H. A. Fink, E. Barrett-Connor, J. M. Zmuda, J. M. Shikany, et al.
Serum 25-Hydroxyvitamin D Levels and Rate of Hip Bone Loss in Older Men
J. Clin. Endocrinol. Metab., August 1, 2009; 94(8): 2773 - 2780.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
S. M Smith, K. K Gardner, J. Locke, and S. R Zwart
Vitamin D supplementation during Antarctic winter
Am. J. Clinical Nutrition, April 1, 2009; 89(4): 1092 - 1098.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
A. Prentice, G. R Goldberg, and I. Schoenmakers
Vitamin D across the lifecycle: physiology and biomarkers
Am. J. Clinical Nutrition, August 1, 2008; 88(2): 500S - 506S.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
J. E Zerwekh
Blood biomarkers of vitamin D status
Am. J. Clinical Nutrition, April 1, 2008; 87(4): 1087S - 1091S.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Copyright © 2005 by the American Association for Clinical Chemistry.