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Uptake of cobalamin and markers of cobalamin status: a longitudinal study of healthy pregnant women

  • Eva Greibe , Birgitte Horst Andreasen , Dorte L. Lildballe , Anne L. Morkbak , Anne-Mette Hvas and Ebba Nexo
Published/Copyright: August 30, 2011

Abstract

Background: Currently, it is unknown whether the decline in plasma cobalamin observed during pregnancy is caused by malabsorption of the vitamin. This study examined cobalamin absorption and markers of cobalamin status during normal pregnancy.

Methods: Twenty-seven pregnant Danish women were examined at gestation weeks 13, 24 and 36. The absorption test CobaSorb was performed in all women implying measurement of holotranscobalamin or cyanocobalamin bound to transcobalamin before and after 2 days intake of 3×9 μg cobalamin. Serum cobalamin and the two cobalamin binding proteins transcobalamin and haptocorrin, including haptocorrin saturated with cobalamin or analogues, were measured, and so was plasma methylmalonic acid and homocysteine.

Results: No change in the uptake of cobalamin was observed throughout pregnancy. Serum cobalamin displayed a gradual decline during pregnancy (p<0.0001), while holotranscobalamin remained unchanged, despite an increase in total transcobalamin (p<0.0001). In accord with these results, total haptocorrin showed a decline from the 1st to 3rd trimester (p=0.007) and cobalamin bound to haptocorrin declined (p<0.0001). Interestingly, the amount of cobalamin analogues attached to haptocorrin remained unchanged. Methylmalonic acid (p=0.002) and homocysteine (p<0.0001) increased during pregnancy.

Conclusions: Cobalamin absorption remains unchanged during normal pregnancy, as judged by the CobaSorb test. No change was observed in the biological active holotranscobalamin during pregnancy. Thus, the pregnancy-related decline in cobalamin is caused by alternations in haptocorrin-bound cobalamin. Surprisingly, no pregnancy-related change was observed in the amount of analogues attached to haptocorrin.


Corresponding author: Eva Greibe, Department of Clinical Biochemistry, Aarhus University Hospital, Norrebrogade 44, building 9, 8000 Aarhus C, Denmark Phone: +45 8949 3018, Fax: +45 8949 3060,

Received: 2011-2-28
Accepted: 2011-7-27
Published Online: 2011-08-30
Published in Print: 2011-11-01

©2011 by Walter de Gruyter Berlin Boston

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