Evidence map›Paper›PMID 20660052›Full record

Trial reportThe Journal of clinical endocrinology and metabolism2010

Testosterone suppresses hepcidin in men: a potential mechanism for testosterone-induced erythrocytosis.

Eric Bachman, Rui Feng, Thomas Travison, Michelle Li, Gordana Olbina, Vaughn Ostland, Jagadish Ulloor, Anqi Zhang, Shehzad Basaria, Tomas Ganz and 2 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of clinical endocrinology and metabolism, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 99 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed, 4 pooled it
–field-weighted citation impact
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

99 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

39 more citing papers are in PubMed but not listed here.

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

12 authors.

Eric BachmanDepartment of Medicine, Boston University School of Medicine, 670 Albany Street, Boston, Massachusetts 02118, USA. eric.bachman@bmc.org
Rui Feng
Thomas Travison
Michelle Li
Gordana Olbina
Vaughn Ostland
Jagadish Ulloor
Anqi Zhang
Shehzad Basaria
Tomas Ganz
Mark Westerman
Shalender Bhasin

Funding

TUFTS--FIELDINGP30AG031679 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI LEWIS LIPSITZ · 2008 to 2026
$23.9M
TESTOSTERONE SUPPLEMENTATION FOR MEN WITH SARCOPENIAU01AG014369 · NIA · BOSTON MEDICAL CENTER · PI BHASIN, SHALENDER · 2005 to 2011
$4.6M
NIA NIH HHS P30 AG031679NIA NIH HHS U01 AG014369NIA NIH HHS U01AG14369
6 · The paper itself

Abstract

contextThe mechanisms by which testosterone increases hemoglobin and hematocrit are unknown.

objectiveThe aim was to test the hypothesis that testosterone-induced increase in hematocrit is associated with suppression of the iron regulatory peptide hepcidin.

participantsHealthy younger men (ages 19-35 yr; n = 53) and older men (ages 59-75 yr; n = 56) were studied.

methodsWeekly doses of testosterone enanthate (25, 50, 125, 300, and 600 mg) were administered over 20 wk, whereas endogenous testosterone was suppressed by monthly GnRH agonist administration. Blood and serum parameters from each individual were measured at wk 0, 1, 2, 4, 8, and 20. Longitudinal analyses were performed to examine the relationship between hepcidin, hemoglobin, hematocrit, and testosterone while controlling for potential confounders.

resultsHigh levels of testosterone markedly suppressed serum hepcidin within 1 wk. Hepcidin suppression in response to testosterone administration was dose-dependent in older men and more pronounced than in young men, and this corresponded to a greater rise in hemoglobin in older men. Serum hepcidin levels at 4 and 8 wk were predictive of change in hematocrit from baseline to peak levels.

conclusionTestosterone administration is associated with suppression of serum hepcidin. Greater increases in hematocrit in older men during testosterone therapy are related to greater suppression of hepcidin.

Indexed as

AdultAgedAgingAntimicrobial Cationic PeptidesDose-Response Relationship, DrugDouble-Blind MethodDown-RegulationDrug Administration ScheduleHepcidinsHumansInjectionsLeuprolideMaleMiddle AgedPolycythemiaTestosteroneAntimicrobial Cationic PeptidesHAMP protein, humanHepcidinsLeuprolideTestosterone

Identifiers

PMID20660052
PMCPMC3050108

What OpenQuestion holds

Textmetadata
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.