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Letters to the Editor |
Unit of Hormonal Biology, Hôpital Saint-Louis, Assistance Publique, Hôpitaux de Paris, Paris, France
aAddress correspondence to this author at: Unit of Hormonal Biology, Saint-Louis University Hospital (AP-HP) and INSERM U 671, 1 avenue Claude Vellefaux, 75475 Paris cedex 10, France. Fax 33-1-42-49-42-80; e-mail philippe.boudou@sls.aphp.fr.
| The first 20% of the full text of this article appears below. |
To the Editor:
The major problem in measuring 25-hydroxyvitamin D (25-OHD) is attributable to the molecule itself (1). Thus, an analytical method must be selected that will accurately estimate total circulating 25-OHD independent of the circulating concentrations of 25OHD2 and 25OHD3. Although HPLC remains the method of choice, many convergent data indicate that the 25-OHD RIA (DiaSorin Inc) should be incorporated as a secondary reference method (2)(3). With the RIA method actually used in our laboratory, we evaluated the 25-OHD LIAISON® chemiluminescent immunoassay (CLIA) proposed by the same manufacturer as an alternative assay. We also investigated whether a 25-OHD value <50 nmol/L, a well-known arbitrary RIA cutoff value to define vitamin D insufficiency, is applicable to CLIA.
We studied 199 people [79 men/120 women; mean (SD) age 48.1 (19.8) years] who were residents of Paris and its suburbs and who suffered primary hyperparathyroidism (HPT), secondary HPT with hemodialysis or obesity, mild asthenia, depression, and/or osteopenia/osteoporosis. This study was approved by the ethics
The following articles in journals at HighWire Press have cited this article:
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E. Hypponen, S. Turner, P. Cumberland, C. Power, and I. Gibb Serum 25-Hydroxyvitamin D Measurement in a Large Population Survey with Statistical Harmonization of Assay Variation to an International Standard J. Clin. Endocrinol. Metab., December 1, 2007; 92(12): 4615 - 4622. [Abstract] [Full Text] [PDF] |
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