Disorders of cobalamin (Vitamin B12) metabolism: Emerging concepts in pathophysiology, diagnosis and treatment
Summary
Although cobalamin (vitamin B12) was isolated almost 60 years ago, its biochemical, physiologic and neurologic effects remain incompletely defined. New observations suggest renal regulation of cobalamin metabolism; actions of cobalamin on nucleic acid and protein function; and a role for cobalamin in cytokine and growth factor regulation. Clinically, no gold standard has emerged for the diagnosis of cobalamin deficiency. Moreover, cobalamin resistance may occur in diabetes, renal insufficiency and advanced age, leading to functional cobalamin deficiency despite adequate cobalamin nutriture. Finally, high-dose cobalamin therapy may have salutary pharmacologic effects on neurologic function in a variety of disorders. Many studies lacked appropriate control groups. However, at this time, therapeutic trials with pharmacologic doses of cobalamin are suggested when findings consistent with cobalamin deficiency are present regardless of the results of diagnostic tests. While oral cobalamin immediate-release is adequate for many patients, its effectiveness in reversing neurologic abnormalities has yet to be established.
Abbreviations: Cbl, Cobalamin, MMA, Methylmalonic acid, HCys, Homocysteine, THF, Tetrahydrofolate, RDI, Recommended dietary intake, HIV, Human immunodeficiency virus-1, TNF, Tumor necrosis factor α, EGF, Epidermal growth factor, IL-6, Interleukin 6, OCS, Oral contraceptives, DM, Diabetes mellitus, TCA, Tricarboxylic acid
Keywords: Cobalamin, Methylmalonic acid, Homocysteine, Vitamin B12, Diabetes mellitus
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PII: S0268-960X(06)00039-7
doi:10.1016/j.blre.2006.05.001
© 2006 Elsevier Ltd. All rights reserved.
