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同时给予游离及内因子结合放射性氰钴胺素用于诊断老年人恶性贫血的评估

An evaluation of simultaneously administered free and intrinsic factor bound radioactive cyanocobalamin in the diagnosis of pernicious anaemia in the elderly.

作者信息

Pathy M S, Kirkman S, Molloy M J

出版信息

J Clin Pathol. 1979 Mar;32(3):244-50. doi: 10.1136/jcp.32.3.244.

Abstract

The definitive diagnosis of pernicious anaemia (PA) in the elderly is by no means always straightforward, particularly when inappropriate medication has been introduced before the institution of specific investigatory procedures. A detailed haematological study was carried out on 301 patients aged 60-95 with a serum B(12) concentration at the laboratory's lower level of normal of 150 ng per litre (Euglena gracilis assay). The diagnosis of PA was based on strict predetermined haematological criteria. All patients were subsequently studied by the simultaneous oral administration of the dual isotopes (57)Co-labelled B(12) bound to intrinsic factor and free (58)Co-labelled B(12) (Dicopac test), and urine was collected over 24 hours after an intramuscular dose of 1 mg nonradioactive B(12) for estimation of the (57)Co/(58)Co B(12) ratio; 255 patients satisfied all criteria for final analysis. The Radiochemical Centre, Amersham suggests an upper limit of the normal range for the (57)Co/(58)Co ratio of 1.3 with a lower limit for PA of 2.0. We were unable to show a sharp borderline in the (57)Co/(58)Co B(12) ratio between those patients shown by other criteria to have PA and those who do not have PA; 34% of the 71 established patients had a ratio below 2.0. From our series a ratio borderline drawn at 1.4 gave only one false negative (1.4% of the PA group). Of the 175 non-PA cases, nine (5%) gave false positive results; four of these had (58)Co excretion levels high enough to make misdiagnosis unlikely. In a proportion of patients the (57)Co/(58)Co B(12) ratio was estimated at regular intervals for 36-hour periods. Maximum accuracy of isotope measurement on a single specimen was obtained 8-20 hours after isotope dosing. The Dicopac investigation is a useful simple screening test in the differential diagnosis of patients with a megaloblastic bone marrow and combined low serum B(12) and folate concentrations. When carried out by the standard technique, the degree of discrimination between normal and abnormal ratios is of limited diagnostic significance in one-third of patients.

摘要

老年恶性贫血(PA)的明确诊断绝非总是直截了当,尤其是在进行特定检查程序之前就已使用不恰当药物的情况下。对301例年龄在60 - 95岁、血清维生素B₁₂浓度处于实验室正常下限150 ng/升(纤细裸藻试验)的患者进行了详细的血液学研究。PA的诊断基于严格预先确定的血液学标准。随后所有患者同时口服与内因子结合的⁵⁷Co标记的维生素B₁₂和游离的⁵⁸Co标记的维生素B₁₂(双同位素试验),并在肌内注射1 mg非放射性维生素B₁₂后收集24小时尿液,以估算⁵⁷Co/⁵⁸Co维生素B₁₂比值;255例患者满足所有标准用于最终分析。阿默舍姆放射化学中心表明,⁵⁷Co/⁵⁸Co比值正常范围的上限为1.3,PA的下限为2.0。我们无法在通过其他标准诊断为PA的患者和未患PA的患者之间的⁵⁷Co/⁵⁸Co维生素B₁₂比值上显示出明显的界限;在71例确诊患者中,34%的患者比值低于2.0。在我们的系列研究中,以1.4为界限得出的比值仅产生1例假阴性(PA组的1.4%)。在175例非PA病例中,9例(5%)给出了假阳性结果;其中4例的⁵⁸Co排泄水平高到足以使误诊不太可能。在一部分患者中,每隔36小时定期估算⁵⁷Co/⁵⁸Co维生素B₁₂比值。同位素给药后8 - 20小时,单个标本的同位素测量获得最大准确度。双同位素试验在鉴别诊断具有巨幼细胞性骨髓且血清维生素B₁₂和叶酸浓度均低的患者中是一种有用的简单筛查试验。当采用标准技术进行时,正常与异常比值之间的区分程度在三分之一的患者中具有有限的诊断意义。

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