低血清促红细胞生成素-原发性红细胞增多症的一个强有力的诊断标准,即使在正常血红蛋白水平。

M. Messinezy, N. Westwood, S. Woodcock, R. Strong, Thomas C. Pearson
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引用次数: 61

摘要

采用酶免疫测定(EIA)试剂盒对42例原发性红细胞增多症患者和41例继发性红细胞增多症患者及47例特发性红细胞增多症患者进行血清促红细胞生成素水平测定。大多数原发性多红细胞血症患者正在接受静脉切除治疗,因此在促红细胞生成素估计时Hb水平在正常范围内。在原发性红细胞增多症中,从每个患者身上采集的第一批样本中有64%低于正常人血清促红细胞生成素的参考范围。当从每位患者中抽取两个样本时,其中一个或两个样本中72%的值较低。在对照组中,对采集了两个样本的患者进行分析,结果显示只有一个人患有继发性红细胞增多症,而没有一个人患有特发性红细胞增多症,其血清促红细胞生成素水平低于参考范围。原发性多红细胞血症患者血清促红细胞生成素水平低,即使由于静脉切除Hb水平正常,也具有很高的诊断特异性(很少有假阳性结果)和有用的诊断敏感性(28%假阴性结果)。建议将来原发性红细胞增多症的诊断标准应包括在不同场合采集的两份血清样本中至少有一份血清促红细胞生成素水平低于正常下限。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low serum erythropoietin--a strong diagnostic criterion of primary polycythaemia even at normal haemoglobin levels.
Estimations of serum erythropoietin level by enzyme immunoassay (EIA) kit were made in 42 patients with primary polycythaemia, and in a comparison group consisting of 41 patients with secondary polycythaemia and 47 patients with idiopathic erythrocytosis. The majority of patients with primary polycythaemia were undergoing treatment by venesection and therefore had Hb levels in the normal range at the time of erythropoietin estimation. In primary polycythaemia, 64% of the first samples taken from each patient were below the reference range for serum erythropoietin in normal individuals. When two samples were taken from each patient 72% had low values in one or both samples. In the comparison group, analysis of those patients who had two samples taken showed only one individual with secondary polycythaemia and none with idiopathic erythrocytosis who had a serum erythropoietin level below the reference range. The finding of low serum erythropoietin in patients with primary polycythaemia, even when Hb levels are normal due to venesection, is of high diagnostic specificity (few false positive results) and useful diagnostic sensitivity (28% false negative results). It is proposed that future diagnostic criteria of primary polycythaemia should include the finding of a serum erythropoietin level below the lower limit of normal in at least one of two serum samples taken on different occasions.
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