Evidence map›Paper›PMID 36450940›Full record

Trial reportMetabolomics : Official journal of the Metabolomic Society2022

Metabolomics of testosterone enanthate administration during severe-energy deficit.

Jesse A Stein, J Philip Karl, Claire E Berryman, Melissa N Harris, Jennifer C Rood, Stefan M Pasiakos, Harris R Lieberman

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Metabolomics : Official journal of the Metabolomic Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 42% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Testosterone administration partially modulates gut microbiota responses to severe energy deficit.American journal of physiology. Endocrinology and metabolism · 2026
    Trial
  2. Trial
  3. Article
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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

7 authors at 3 institutions in 1 country.

Jesse A SteinMilitary Nutrition Division, US Army Research Institute of Environmental Medicine (USARIEM), Natick, MA, USA.
J Philip KarlMilitary Nutrition Division, US Army Research Institute of Environmental Medicine (USARIEM), Natick, MA, USA.
Claire E BerrymanMilitary Nutrition Division, US Army Research Institute of Environmental Medicine (USARIEM), Natick, MA, USA.
Melissa N HarrisLouisiana State University's Pennington Biomedical Research Center, Baton Rouge, LA, USA.
Jennifer C RoodLouisiana State University's Pennington Biomedical Research Center, Baton Rouge, LA, USA.
Stefan M PasiakosMilitary Nutrition Division, US Army Research Institute of Environmental Medicine (USARIEM), Natick, MA, USA.
Harris R LiebermanMilitary Nutrition Division, US Army Research Institute of Environmental Medicine (USARIEM), Natick, MA, USA. harris.r.lieberman.civ@mail.mil.ORCID 0000-0002-1519-0156
U.S. Army Research Institute of Environmental Medicine · USPennington Biomedical Research Center · USFlorida State University · US

Funding

Research BaseP30DK072476 · NIDDK · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI ROBERT A KESTERSON · 2005 to 2026
$26.5M
NIDDK NIH HHS P30 DK072476
6 · The paper itself

Abstract

introductionTestosterone administration attenuates reductions in total body mass and lean mass during severe energy deficit (SED).

objectivesThis study examined the effects of testosterone administration on the serum metabolome during SED.

methodsIn a double-blind, placebo-controlled clinical trial, non-obese men were randomized to receive 200-mg testosterone enanthate/wk (TEST) (n = 24) or placebo (PLA) (n = 26) during a 28-d inpatient, severe exercise- and diet-induced energy deficit. This study consisted of three consecutive phases. Participants were free-living and provided a eucaloric diet for 14-d during Phase 1. During Phase 2, participants were admitted to an inpatient unit, randomized to receive testosterone or placebo, and underwent SED for 28-d. During Phase 3, participants returned to their pre-study diet and physical activity habits. Untargeted metabolite profiling was conducted on serum samples collected during each phase. Body composition was measured using dual-energy X-ray absorptiometry after 11-d of Phase 1 and after 25-d of Phase 2 to determine changes in fat and lean mass.

resultsTEST had higher (Benjamini-Hochberg adjusted, q < 0.05) androgenic steroid and acylcarnitine, and lower (q < 0.05) amino acid metabolites after SED compared to PLA. Metabolomic differences were reversed by Phase 3. Changes in lean mass were associated (Bonferroni-adjusted, p < 0.05) with changes in androgenic steroid metabolites (r = 0.42-0.70), acylcarnitines (r = 0.37-0.44), and amino acid metabolites (r = - 0.36-- 0.37). Changes in fat mass were associated (p < 0.05) with changes in acylcarnitines (r = - 0.46-- 0.49) and changes in urea cycle metabolites (r = 0.60-0.62).

conclusionTestosterone administration altered androgenic steroid, acylcarnitine, and amino acid metabolites, which were associated with changes in body composition during SED.

Indexed as

MetabolomicsTestosteroneAmino AcidsCarnitineHumansMalePolyestersacylcarnitineAmino AcidsCarnitinePolyestersTestosteronetestosterone enanthateAnabolicMilitary stressSemi-starvationSport metabolomics

Identifiers

PMID36450940
PMCPMC9712311
OpenAlexW4310644690

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.