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外周血基因表达谱检测生长激素滥用。

Detection of growth hormone doping by gene expression profiling of peripheral blood.

机构信息

Pituitary Research Unit, Garvan Institute of Medical Research, 384 Victoria Street, Darlinghurst New South Wales 2010, Sydney, Australia.

出版信息

J Clin Endocrinol Metab. 2009 Dec;94(12):4703-9. doi: 10.1210/jc.2009-1038. Epub 2009 Oct 29.

Abstract

CONTEXT

GH abuse is a significant problem in many sports, and there is currently no robust test that allows detection of doping beyond a short window after administration.

OBJECTIVE

Our objective was to evaluate gene expression profiling in peripheral blood leukocytes in-vivo as a test for GH doping in humans.

DESIGN

Seven men and thirteen women were administered GH, 2 mg/d sc for 8 wk. Blood was collected at baseline and at 8 wk. RNA was extracted from the white cell fraction. Microarray analysis was undertaken using Agilent 44K G4112F arrays using a two-color design. Quantitative RT-PCR using TaqMan gene expression assays was performed for validation of selected differentially expressed genes.

RESULTS

GH induced an approximately 2-fold increase in circulating IGF-I that was maintained throughout the 8 wk of the study. GH induced significant changes in gene expression with 353 in women and 41 in men detected with a false discovery rate of less than 5%. None of the differentially expressed genes were common between men and women. The maximal changes were a doubling for up-regulated or halving for down-regulated genes, similar in magnitude to the variation between individuals. Quantitative RT-PCR for seven target genes showed good concordance between microarray and quantitative PCR data in women but not in men.

CONCLUSION

Gene expression analysis of peripheral blood leukocytes is unlikely to be a viable approach for the detection of GH doping.

摘要

背景

生长激素滥用在许多运动项目中是一个严重的问题,目前还没有一种强大的测试方法可以在给药后很短的时间窗口之外检测到兴奋剂。

目的

我们的目的是评估体内外周血白细胞基因表达谱作为人类生长激素滥用的检测方法。

设计

7 名男性和 13 名女性接受了 GH,每天 2 毫克/天 sc 给药 8 周。在基线和 8 周时采集血液。从白细胞部分提取 RNA。使用 Agilent 44K G4112F 阵列进行微阵列分析,采用双色设计。使用 TaqMan 基因表达测定进行定量 RT-PCR 验证了选定的差异表达基因。

结果

GH 诱导循环 IGF-I 约增加 2 倍,在整个 8 周的研究中维持不变。GH 诱导基因表达发生显著变化,女性有 353 个,男性有 41 个,假发现率低于 5%。在男性和女性之间没有共同的差异表达基因。最大的变化是上调基因的两倍或下调基因的减半,与个体之间的差异幅度相似。对七个靶基因的定量 RT-PCR 显示,女性的微阵列和定量 PCR 数据之间具有良好的一致性,但男性则不然。

结论

外周血白细胞的基因表达分析不太可能成为检测生长激素滥用的可行方法。

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