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通过内源性红系集落测定而非血清促红细胞生成素水平预测特发性红细胞增多症患者的临床病程。

Prediction of clinical course in patients with idiopathic erythrocytosis by endogenous erythroid colony assay but not by serum erythropoietin levels.

作者信息

Shih L Y, Lee C T, Ou Y C

机构信息

Department of Internal Medicine, Chang Gung College of Medicine and Technology, Chang Gung Memorial Hospital, Taipei, Taiwan.

出版信息

Exp Hematol. 1997 Apr;25(4):288-92.

PMID:9131002
Abstract

We studied the in vitro culture growth of bone marrow and blood erythroid progenitors and serum erythropoietin (EPO) levels by radioimmunoassay in 24 patients with idiopathic erythrocytosis (IE). All patients had an increased red blood cell (RBC) mass and lacked a cause of secondary polycythemia, but did not fulfill the diagnostic criteria of polycythemia vera (PV). Marrow and blood cultures were obtained simultaneously; the results of endogenous (EPO-independent) erythroid colony (EEC) growth were parallel in both cultures. EECs were present in five patients, all of them developed PV 3 to 48 months later. The EEC number did not correlate with the time to the progression of PV. In contrast, none of the 19 EEC-negative patients had PV evolution during a median follow-up period of 38 months. Three of the five IE patients in whom EECs formed displayed vascular complications during their clinical course compared with three of 19 patients who did not have EEC. The serum EPO levels were variable: low in five, normal in 14, and high in five patients. Serial measurements of serum EPO levels in three of five patients who had high initial levels showed persistently elevated values; the underlying cause of the increased EPO production could not be defined during a follow-up period of more than 36 months. Of the five patients who subsequently developed PV, two had low serum EPO levels and three had normal values at initial evaluation. Serum EPO levels did not correlate with the occurrence of thrombotic complications. Our results show that serum EPO levels have limited value in determining the underlying cause of IE and cannot predict the clinical course of patients with IE, whereas the assessment of EEC in bone marrow or blood can identify IE patients who will have PV evolution.

摘要

我们通过放射免疫分析法研究了24例特发性红细胞增多症(IE)患者的骨髓和血液红系祖细胞的体外培养生长情况以及血清促红细胞生成素(EPO)水平。所有患者红细胞(RBC)量均增加,且无继发性红细胞增多症的病因,但不符合真性红细胞增多症(PV)的诊断标准。同时获取骨髓和血液培养物;内源性(不依赖EPO)红系集落(EEC)生长结果在两种培养物中平行。5例患者存在EEC,所有这些患者在3至48个月后均发展为PV。EEC数量与PV进展时间无关。相比之下,19例EEC阴性患者在中位随访期38个月内均未发生PV演变。形成EEC的5例IE患者中有3例在临床病程中出现血管并发症,而19例未出现EEC的患者中有3例出现血管并发症。血清EPO水平各不相同:5例患者较低,14例患者正常,5例患者较高。5例初始水平较高的患者中有3例的血清EPO水平连续测量显示持续升高;在超过36个月的随访期内无法确定EPO产生增加的根本原因。在随后发展为PV的5例患者中,2例初始评估时血清EPO水平较低,3例正常。血清EPO水平与血栓形成并发症的发生无关。我们的结果表明,血清EPO水平在确定IE的根本原因方面价值有限,无法预测IE患者的临床病程,而评估骨髓或血液中的EEC可以识别出将发生PV演变的IE患者。

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