Parisotto R, Gore C J, Emslie K R, Ashenden M J, Brugnara C, Howe C, Martin D T, Trout G J, Hahn A G
Department of Physiology, Australian Institute of Sport, P.O. Box 176, Belconnen ACT 2616, Australia.
Haematologica. 2000 Jun;85(6):564-72.
The use of recombinant human erythropoietin (r-HuEPO) to enhance athletic performance is prohibited. Existing tests cannot readily differentiate between exogenous and endogenous EPO. Therefore the aim of our study was to investigate possible indirect detection of r-HuEPO use via blood markers of altered erythropoiesis.
Twenty-seven recreational athletes were assigned to three groups prior to a 25 day drug administration phase, with the following protocols: EPO+IM group (n = 10), 50 Ukg(-1) r-HuEPO at a frequency of 3wk(-1), 100 mg intramuscular (IM) iron 1wk(-1) and a sham iron tablet daily; EPO+OR group (n = 8), 50 U.kg(-1) r-HuEPO 3wk(-1), sham iron injection 1wk(-1) and 105 mg of oral elemental iron daily; placebo group (n = 9), sham r-HuEPO injections 3wk(-1), sham iron injections 1wk(-1) and sham iron tablets daily. Each group was monitored during and for 4 weeks after drug administration.
Models incorporating combinations of the variables reticulocyte hematocrit (RetHct), serum EPO, soluble transferrin receptor, hematocrit (Hct) and % macrocytes were analyzed by logistic regression. One model (ON-model) repeatedly identified 94-100% of r-HuEPO group members during the final 2 wk of the r-HuEPO administration phase. One false positive was recorded from a possible 189. Another model (OFF-model) incorporating RetHct, EPO and Hct was applied during the wash-out phase and, during the period of 12-21 days after the last r-HuEPO injection, it repeatedly identified 67-72% of recent users with no false positives.
Multiple indirect hematologic and biochemical markers used simultaneously are potentially effective for identifying current or recent users of r-HuEPO.
使用重组人促红细胞生成素(r-HuEPO)来提高运动成绩是被禁止的。现有的检测方法难以轻易区分外源性和内源性促红细胞生成素。因此,我们研究的目的是通过红细胞生成改变的血液标志物来调查r-HuEPO使用的可能间接检测方法。
27名业余运动员在25天的药物给药阶段之前被分为三组,采用以下方案:EPO+IM组(n = 10),50 Ukg(-1) r-HuEPO,给药频率为3wk(-1),100 mg肌肉注射(IM)铁剂,1wk(-1),每天服用一片安慰剂铁剂;EPO+OR组(n = 8),50 U.kg(-1) r-HuEPO,3wk(-1),1wk(-1)进行安慰剂铁剂注射,每天口服105 mg元素铁;安慰剂组(n = 9),3wk(-1)进行安慰剂r-HuEPO注射,1wk(-1)进行安慰剂铁剂注射,每天服用安慰剂铁剂。在给药期间及给药后4周对每组进行监测。
通过逻辑回归分析包含网织红细胞压积(RetHct)、血清促红细胞生成素、可溶性转铁蛋白受体、血细胞比容(Hct)和大红细胞百分比等变量组合的模型。一个模型(ON模型)在r-HuEPO给药阶段的最后2周反复识别出94%-100%的r-HuEPO组成员。在可能的189次检测中记录到1例假阳性。另一个包含RetHct、促红细胞生成素和Hct的模型(OFF模型)在洗脱阶段应用,在最后一次r-HuEPO注射后的12-21天期间,它反复识别出67%-72%的近期使用者,无假阳性。
同时使用多种间接血液学和生化标志物可能有效地识别当前或近期使用r-HuEPO的人。