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Investigation of biomarker responses to depletion/repletion with vitamin B12

Published online by Cambridge University Press:  09 September 2010

C. F. Hughes
Affiliation:
Northern Ireland Centre for Food and Health, University of Ulster, Coleraine BT52 1SA, UK
M. Ward
Affiliation:
Northern Ireland Centre for Food and Health, University of Ulster, Coleraine BT52 1SA, UK
L. Hoey
Affiliation:
Northern Ireland Centre for Food and Health, University of Ulster, Coleraine BT52 1SA, UK
A. Molloy
Affiliation:
Trinity College, School of Biochemistry and Immunology, Dublin, Ireland
K. Pentieva
Affiliation:
Northern Ireland Centre for Food and Health, University of Ulster, Coleraine BT52 1SA, UK
J. M. Scott
Affiliation:
Trinity College, School of Biochemistry and Immunology, Dublin, Ireland
F. Tracey
Affiliation:
Causeway Hospital, Coleraine BT52 IHS, UK
H. McNulty
Affiliation:
Northern Ireland Centre for Food and Health, University of Ulster, Coleraine BT52 1SA, UK
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Abstract

Type
Abstract
Copyright
Copyright © The Authors 2010

Despite dietary intakes well above current recommendations, low biomarker status of vitamin B12 is a common problem in older adults, largely as a result of malabsorption of food-bound vitamin B12. This arises mainly from atrophic gastritis which leads to reduced gastric acid production (hypochlorhydria). Hydrochloric acid is essential for the absorption of food-bound vitamin B12, and thus vitamin B12 absorption is reduced in states of hypochlorhydria, although in theory free vitamin B12 (from supplements or fortified) should still be absorbed. Gastric acid suppressant medications, such as proton pump inhibitors (PPI) drugs induce hypochlorhydria and therefore a state similar to atrophic gastritis. The aim of the present study is to investigate the effect of hypochlorhydria on absorption of food-bound vitamin B12 and to determine whether low-dose supplemental vitamin B12 would overcome any vitamin B12 malabsorption. Forty-one healthy males, aged 18–45, participated in a vitamin B12 depletion/repletion trial. During the depletion phase (week 0–6) all subjects were administered with a PPI (omeprazole, 20 mg/d); after which they were randomised (by vitamin B12 status as measured by serum holotranscobalamin; holoTC; the metabolically active fraction of total circulating vitamin B12) into one of the two treatment groups to receive; omeprazole (20 mg/d) plus supplemental vitamin B12 (10 μg/d) or omeprazole (20 mg/d) plus placebo for the repletion phase of the study (week 7–12).

Fig. 1. Serum total B12 and holoTC responses to vitamin B12 depletion/repletion were compared by repeated measures ANOVA on log transformed data.

Contrary to expectations, no significant change in vitamin B12 status (as assessed by either total vitamin B12 or holoTC) was observed during the depletion phase of the study. During the repletion phase of the study, an increase in vitamin B12 status was observed in the treatment group, but this was significant (P=0.006) only using the biomarker holoTC, with the response for total vitamin B12 failing to reach significance. In conclusion, these results supports the emerging view that holoTC (compared with the traditional biomarker of status, serum total vitamin B12) is a more sensitive biomarker in detecting small changes in vitamin B12 intake. Although the acute administration of PPI drugs did not significantly suppress vitamin B12, repletion with 10 μg/d of supplemental vitamin B12 was sufficient to significantly increase biomarker status within just 4 weeks. The consequence of long-term PPI therapy on vitamin B12 status is still to be determined.

Figure 0

Fig. 1. Serum total B12 and holoTC responses to vitamin B12 depletion/repletion were compared by repeated measures ANOVA on log transformed data.