| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Submitted on October 16, 2006
Accepted on March 26, 2007
University of Wisconsin Osteoporosis Clinical Research Program, Madison, WI; Human Nutrition, Food and Animal Sciences, University of Hawaii at Manoa, Honolulu, HI; Laboratory Medicine, University of Wisconsin, Madison, WI; Medical University of South Carolina, Charleston, SC
* To whom correspondence should be addressed. E-mail: nbinkley{at}wisc.edu.
Context: Lack of sun exposure is widely accepted as the primary cause of epidemic low vitamin D status worldwide. However, some individuals with seemingly adequate UV exposure have been reported to have low serum 25-hydroxyvitamin D (25(OH)D) concentration; results which might have been confounded by imprecision of the assays employed.
Objective: The objective of this study was to document the 25(OH)D status of healthy individuals with habitually high sun exposure.
Setting: This study was conducted in a convenience sample of adults in Honolulu, HI, (latitude 21°).
Participants: The study population consisted of 93 adults 30 women and 63 men, mean (SEM) age and BMI of 24.0 (0.7) years and 23.6 (0.4) kg/m2 respectively. Their self-reported sun exposure was 28.9 (1.5) hours/week yielding a calculated sun exposure index of 11.1 (0.7).
Main Outcome Measures: Serum 25(OH)D concentration was measured using a precise HPLC assay. Low vitamin D status was defined as a circulating 25(OH)D concentration < 30 ng/ml.
Results: Mean serum 25(OH)D concentration was 31.6 ng/ml. Using a cutpoint of 30 ng/ml, 51% of this population had low vitamin D status. The highest 25(OH)D concentration was 62 ng/ml.
Conclusion: These data suggest that variable responsivity to UVB radiation is evident among individuals, causing some to have low vitamin D status despite abundant sun exposure. Additionally, as the maximal 25(OH)D concentration produced by natural UV exposure appears to be
60 ng/ml, it seems prudent to utilize this value as an upper limit when prescribing vitamin D supplementation.
This article has been cited by other articles:
![]() |
R. P Heaney, L. A. Armas, J. R Shary, N. H Bell, N. Binkley, and B. W Hollis 25-Hydroxylation of vitamin D3: relation to circulating vitamin D3 under various input conditions Am. J. Clinical Nutrition, June 1, 2008; 87(6): 1738 - 1742. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. F Aloia, M. Patel, R. DiMaano, M. Li-Ng, S. A Talwar, M. Mikhail, S. Pollack, and J. K Yeh Vitamin D intake to attain a desired serum 25-hydroxyvitamin D concentration Am. J. Clinical Nutrition, June 1, 2008; 87(6): 1952 - 1958. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. C. Fleet, C. Gliniak, Z. Zhang, Y. Xue, K. B. Smith, R. McCreedy, and S. A. Adedokun Serum Metabolite Profiles and Target Tissue Gene Expression Define the Effect of Cholecalciferol Intake on Calcium Metabolism in Rats and Mice J. Nutr., June 1, 2008; 138(6): 1114 - 1120. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Binkley, D. Krueger, D. Gemar, and M. K. Drezner Correlation among 25-Hydroxy-Vitamin D Assays J. Clin. Endocrinol. Metab., May 1, 2008; 93(5): 1804 - 1808. [Abstract] [Full Text] [PDF] |
||||
![]() |
S T Weiss and A A Litonjua Author's reply Thorax, March 1, 2008; 63(3): 293 - 293. [Full Text] [PDF] |
||||
Read all eLetters
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |
| Endocrinology | Endocrine Reviews | J. Clin. End. & Metab. |
| Molecular Endocrinology | Recent Prog. Horm. Res. | All Endocrine Journals |