The I-IEF pattern from the urine sample obtained immediately following the run detected multiple glycosylated proteins that looked nearly identical to that generated by small quantities of Epoetin-β (Roche), strongly suggesting the presence of this drug in the runner’s blood. This “positive” result was not seen in urine donated as little as one hour after the run. The fact that Epo has a plasma half-life of more than eight hours suggested that the first result was a false positive, perhaps related to the transient post-exercise proteinuria. The authors then retested the “positive” urine samples by a different technique — immunoblotting after protein denaturation and separation and size fractionation by electrophoresis — and found that the protein detected by the “Epo-specific” monoclonal antibody used in both assays was substantially larger than Epoetin-β, and so must be different. Their interpretation, based on the fact that this larger protein was only detected in the sample generated during a period of transient proteinuria, was that this larger protein was a normal serum protein component to which the anti-Epo monoclonal antibody was cross-reacting.
In Brief
This result, which confirmed similar suggestions raised as possibilities in the clinical chemistry literature, clearly demonstrated many lessons that physicians and scientists know only too well. Every result is only as reliable as the measurement techniques it uses; no “specific” reagent, whether it is monoclonal antibody or an RNAi, is really specific until it is proven to be so; and, most of all, our laboratory preconceptions need to be carefully validated and reconsidered when we translate these into the clinic, let alone the hurly-burly of the non-medical world. Maintaining this strong, continuously self-correcting relationship with the public and its understanding of science is among our highest responsibilities as scientists, physicians, and citizens.
Competing Interests
Dr. Emerson indicated no relevant conflicts of interest.