Evidence map›Paper›PMID 25679398›Full record

Trial reportPloS one2015

Serum proteomic changes after randomized prolonged erythropoietin treatment and/or endurance training: detection of novel biomarkers.

Britt Christensen, Maja Ludvigsen, Birgitte Nellemann, John J Kopchick, Bent Honoré, Jens Otto L Jørgensen

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01320449 (Identification of New Serum Markers for Detection of Abuse With Erythropoietin), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.8field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01320449 nacompletednot on this map

Identification of New Serum Markers for Detection of Abuse With Erythropoietin

TypeinterventionalSponsorUniversity of AarhusRan2011 to 2012Enrolled35ConditionsSubstance Abuse ProblemArmsrecombinant human erythropoietin, Training, Placebo
3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 7 citations in OpenAlex.

  1. Trial
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Britt ChristensenDepartment of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark; Medical Research Laboratories, Aarhus University, Aarhus, Denmark; Research Laboratory for Biochemical Pathology, Institute for Clinical Medicine, Aarhus University Hospital, Aarhus, Denmark.
Maja LudvigsenDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Birgitte NellemannDepartment of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark; Medical Research Laboratories, Aarhus University, Aarhus, Denmark.
John J KopchickEdison Biotechnology Institute Ohio University, Athens, Ohio, United States of America; Department of Biomedical Sciences, Heritage College of Osteopathic Medicine, Ohio University, Athens, Ohio, United States of America.
Bent HonoréDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Jens Otto L JørgensenDepartment of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark.
Aarhus University · DKAarhus University Hospital · DKBiotechnology Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDespite implementation of the biological passport to detect erythropoietin abuse, a need for additional biomarkers remains. We used a proteomic approach to identify novel serum biomarkers of prolonged erythropoiesis-stimulating agent (ESA) exposure (Darbepoietin-α) and/or aerobic training. TRIAL

designThirty-six healthy young males were randomly assigned to the following groups: Sedentary-placebo (n = 9), Sedentary-ESA (n = 9), Training-placebo (n = 10), or Training-ESA (n = 8). They were treated with placebo/Darbepoietin-α subcutaneously once/week for 10 weeks followed by a 3-week washout period. Training consisted of supervised biking 3/week for 13 weeks at the highest possible intensity. Serum was collected at baseline, week 3 (high dose Darbepoietin-α), week 10 (reduced dose Darbepoietin-α), and after a 3-week washout period.

methodsSerum proteins were separated according to charge and molecular mass (2D-gel electrophoresis). The identity of proteins from spots exhibiting altered intensity was determined by mass spectrometry.

resultsSix protein spots changed in response to Darbepoietin-α treatment. Comparing all 4 experimental groups, two protein spots (serotransferrin and haptoglobin/haptoglobin related protein) showed a significant response to Darbepoietin-α treatment. The haptoglobin/haptoglobin related protein spot showed a significantly lower intensity in all subjects in the training-ESA group during the treatment period and increased during the washout period.

conclusionAn isoform of haptoglobin/haptoglobin related protein could be a new anti-doping marker and merits further research.

trial registrationClinicalTrials.gov NCT01320449.

Indexed as

Blood ProteinsPhysical EnduranceProteomeProteomicsAdolescentAdultBiomarkersChromatography, LiquidDarbepoetin alfaElectrophoresis, Gel, Two-DimensionalErythrocyte IndicesErythropoietinHaptoglobinsHumansMaleOxygen ConsumptionBiomarkersBlood ProteinsDarbepoetin alfaErythropoietinHaptoglobinsProteome

Identifiers

PMID25679398
PMCPMC4332672
OpenAlexW2024384142

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.