Zuckier L S, Chervu L R
J Nucl Med. 1984 Sep;25(9):1032-9.
The Schilling examination remains a popular means of evaluating in vivo absorption of vitamin B12. When absorption is abnormally low, the test may be repeated with addition of exogenous intrinsic factor (IF) in order to correct the IF deficiency that characterizes pernicious anemia. A dual-isotope variation provides a means of performing both stages of the test simultaneously, thereby speeding up the test and reducing dependence on complete urine collection. The dual-tracer test depends on no exchange of B12 moieties on the IF molecule. In vitro studies suggest that this exchange does take place, in a manner dependent on time, temperature, and pH. Furthermore, in vivo studies indicate that, when administered simultaneously, the absorption of unbound B12 is elevated, and IF-bound B12 is reduced, in pernicious-anemia patients, relative to the classic two-stage examination. A number of clinical studies indicate significant difficulty in resolving clinical diagnoses with the dual-tracer test. The potential weaknesses of the test discussed herein can be overcome by temporally separating the administration of the two B12 doses and by treating secondary malabsorption where it exists. An algorithm is offered for selecting the most suitable variation of the Schilling test to improve the accuracy of test results and the ease of performance.
希林试验仍然是评估维生素B12体内吸收情况的常用方法。当吸收异常低下时,可添加外源性内因子(IF)重复该试验,以纠正恶性贫血所特有的内因子缺乏。双同位素变体提供了一种同时进行试验两个阶段的方法,从而加快试验速度并减少对完整尿液收集的依赖。双示踪剂试验不依赖于IF分子上B12部分的交换。体外研究表明这种交换确实会发生,且方式取决于时间、温度和pH值。此外,体内研究表明,在恶性贫血患者中,同时给药时,相对于经典的两阶段检查,未结合B12的吸收增加,而结合IF的B12吸收减少。多项临床研究表明,双示踪剂试验在解决临床诊断方面存在显著困难。本文讨论的试验潜在弱点可通过在时间上分开给予两种B12剂量以及治疗存在的继发性吸收不良来克服。提供了一种算法,用于选择希林试验最合适的变体,以提高试验结果的准确性和操作的简便性。