Detection of Growth Hormone Doping by Gene Expression Profiling of Peripheral Blood

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