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Multiple Sclerosis InternationalVolume 2012 2012, Article ID 650462, 2 pages

Letter to the Editor

Department of Chemistry and Chemical Engineering, Royal Military College of Canada and Department of Nutritional Sciences, University of Toronto, Toronto, ON, Canada M5S 3E2

Neurosciences and Mental Health, Hospital for Sick Children, University of Toronto, Toronto, ON, Canada M5G 1X8

Received 21 June 2012; Accepted 2 October 2012

Copyright © 2012 Samantha M. Kimball and Heather E. Hanwell. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Regarding the recent article by Shaygannejad et al. 1, we are writing to express serious concerns about the portrayal of the intervention and the authors’ interpretation and discussion of the findings. Of predominate concern is that the authors utilized a calcitriol intervention in their study but referred to it as “vitamin D”. The erroneous use of the term “vitamin D” is of concern for several reasons.

Firstly, vitamin D is the biologically inactive form that can be synthesized in the skin when exposed to ultraviolet B radiation and is found in foods. In order to produce the active metabolite, calcitriol or 1,25-dihydroxyvitamin D; 1,25OH2D, vitamin D must be hydroxylated in two subsequent reactions by two separate hydroxylases. The second hydroxylation step—conversion of 25-hydroxyvitamin D 25OHD to 1,25OH2D via 1α-hydroxylase—is under tight regulatory control. By providing adequate substrate i.e., vitamin D, circulating 25OHD concentrations increase and cells are able to locally produce and use 1,25OH2D in a self-regulated manner without affecting circulating levels of calcitriol. In contrast, supplying calcitriol directly produces a systemic increase in calcitriol, thus bypassing the key regulatory steps and increases risk of hypercalcemia. On the other hand, supplementation with vitamin D is quite safe at levels up to 10,000 IU-d 2, 3. Wingerchuk et al. 4 have previously demonstrated the risk of hypercalcemia with calcitriol treatment in patients with MS. With this sole exception 4, none of the published vitamin D-related trials in patients with MS have administered calcitriol; the authors failed to note this or compare the findings of their calcitriol intervention to the only other published calcitriol intervention in MS. The differences in the safety profile and activity of vitamin D versus calcitriol alone are significant and necessitate accurate nomenclature.

Next, the authors indicate “no unusual or unexpected safety risks found with vitamin D therapy in our study population with RRMS”; however, not only did they administer calcitriol rather than vitamin D, but also no characterization of the dosage nor description of the rationale for the selected dosage was present. Furthermore, since there is neither mention of serum calcium, urine calcium nor 1,25OH2D levels in response to therapy dose, we cannot assess the effect of oral calcitriol 1,25OH2D supplementation on biochemical outcomes in these patients.

Overall, the authors’ naivety regarding metabolism of vitamin D is evidenced in that they i neglected to monitor calcium or calcitriol levels when treating with calcitriol, ii monitored 25OHD levels—which are the biomarker of vitamin D status in the normal situation but are not relevant during calcitriol therapy, and iii directly compare studies of supplementation with vitamin D, calcitriol, and alphacalcidiol a synthetic analogue of calcitriol without distinguishing the various forms and their inherently different activity.

In conclusion, the work presented here “a calcitriol intervention in adults with MS” cannot be directly compared with the majority of the previous vitamin D-related MS interventions in the literature. Barring instances of genetic mutations causing dysfunction of the 1-alpha hydroxylase, at present, there is no rationale to support the use of calcitriol over vitamin D.

Authors’ Contribution

The authors contributed equally.


V. Shaygannejad, M. Janghorbani, F. Ashtari, and H. Dehghan -Effects of adjunct low-dose vitamin d on relapsing-remitting multiple sclerosis progression: preliminary findings of a randomized placebo-controlled trial,- Neurological Research, vol. 2012, Article ID 452541, 7 pages, 2012. View at Publisher · View at Google Scholar · View at ScopusR. Vieth -Vitamin D supplementation, 25-hydroxyvitamin D concentrations, and safety,- American Journal of Clinical Nutrition, vol. 69, no. 5, pp. 842–856, 1999. View at Google Scholar · View at ScopusJ. N. Hathcock, A. Shao, R. Vieth, and R. Heaney -Risk assessment for vitamin D,- American Journal of Clinical Nutrition, vol. 85, no. 1, pp. 6–18, 2007. View at Google Scholar · View at ScopusD. M. Wingerchuk, J. Lesaux, G. P. A. Rice, M. Kremenchutzky, and G. C. Ebers -A pilot study of oral calcitriol 1,25-dihydroxyvitamin D3 for relapsing-remitting multiple sclerosis,- Journal of Neurology, Neurosurgery and Psychiatry, vol. 76, no. 9, pp. 1294–1296, 2005. View at Publisher · View at Google Scholar · View at Scopus

Autor: Samantha M. Kimball and Heather E. Hanwell

Fuente: https://www.hindawi.com/


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