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

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.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Doping in Sports / methods*
  • Double-Blind Method
  • Female
  • Gene Expression / drug effects*
  • Gene Expression Profiling
  • Human Growth Hormone / pharmacology*
  • Humans
  • Insulin-Like Growth Factor I / metabolism
  • Male
  • Oligonucleotide Array Sequence Analysis
  • RNA / biosynthesis
  • RNA / isolation & purification
  • Recombinant Proteins / pharmacology*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sex Characteristics
  • Young Adult

Substances

  • Recombinant Proteins
  • Human Growth Hormone
  • RNA
  • Insulin-Like Growth Factor I