Measuring and Interpreting Holo-Transcobalamin (Holo-Transcobalamin II)

钴胺素 无症状的 甲基丙二酸 亚临床感染 内科学 同型半胱氨酸 维生素B12 化学 内分泌学 医学 胃肠病学
作者
Ralph Carmel
出处
期刊:Clinical Chemistry [Oxford University Press]
卷期号:48 (3): 407-409 被引量:69
标识
DOI:10.1093/clinchem/48.3.407
摘要

At one time, diagnosing cobalamin deficiency was fairly simple, usually involving a patient with clinical problems, and was usually settled by determining whether the serum cobalamin concentration was low or not. As reviewed elsewhere (1), things began to change after sensitive metabolic tests were introduced and as attention extended to the cobalamin status of asymptomatic persons. Metabolic studies confirmed that most low cobalamin concentrations in asymptomatic patients and seemingly healthy persons represented subclinical cobalamin insufficiency, but ∼30–40% of these cobalamin concentrations did not represent insufficiency and thus could be considered “falsely low”. The diagnostic reliability of serum cobalamin was further challenged by metabolic demonstrations of “falsely normal” cobalamin concentrations; these too occurred most often, but not exclusively, in asymptomatic persons. The search continues for the optimal test to diagnose deficiency because the metabolic tests also have disadvantages. Increased plasma total homocysteine is too nonspecific; methylmalonic acid determination, although posing fewer problems of specificity, is complex and expensive; and the deoxyuridine suppression test is too unwieldy for practical use. Interest has been drawn to the possible benefit of measuring only the cobalamin attached to transcobalamin (TC; also called TC II; the TC-cobalamin complex is called holo-TC or holo-TC II) rather than the total cobalamin content of plasma. The concept, suggested by Lindemans et al. in 1983 (2), is simple and attractive: holo-TC contains the biologically available cobalamin because only TC promotes specific uptake of its cobalamin by all cells. The much larger fraction of serum cobalamin carried by haptocorrin (HC; also called TC I, R binder, or sometimes cobalophilin) is considered metabolically inert because no cellular receptors exist for holo-HC (also called holo-TC I). However, the physiologic cycle of holo-TC is quite complex: ( a ) ileal holo-TC enters the portal circulation, carrying cobalamin absorbed from the gut (3); ( b ) some of the …
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