Evidence map›Paper›PMID 24646101›Full record

Trial reportThe Journal of clinical endocrinology and metabolism2014

FSH suppression does not affect bone turnover in eugonadal men.

Alexander V Uihlein, Joel S Finkelstein, Hang Lee, Benjamin Z Leder

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of clinical endocrinology and metabolism, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.6field-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.

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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Extra-Gonadal and Non-Canonical Effects of FSH in Males.Pharmaceuticals (Basel, Switzerland) · 2023
    Review
  2. Review
  3. Observational
  4. Review
  5. FSH Level and Changes in Bone Mass and Body Composition in Older Women and Men.The Journal of clinical endocrinology and metabolism · 2021
    Article
  6. First-in-class humanized FSH blocking antibody targets bone and fat.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  7. Review
  8. FSH Beyond Fertility.Frontiers in endocrinology · 2019
    Review
  9. Modulation of Gonadotropins Activity by Antibodies.Frontiers in endocrinology · 2019
    Review
  10. Review
  11. Review
  12. Estrogens, the be-all and end-all of male hypogonadal bone loss?Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2015
    Article
  13. Sex steroid actions in male bone.Endocrine reviews · 2014
    Review
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

4 authors at 1 institution in 1 country.

Alexander V UihleinEndocrine Unit (A.V.U., J.S.F., B.Z.L.) and Biostatistics Center (H.L.), Massachusetts General Hospital, Boston, Massachusetts 02114.
Joel S Finkelstein
Hang Lee
Benjamin Z Leder
Massachusetts General Hospital · US

Funding

ZD6416 Analgesic--Painful Distal Symmetrical PolyneuropaM01RR001066 · NCRR · MASSACHUSETTS GENERAL HOSPITAL · PI HOGE, ELIZABETH A · 1985 to 2008
$37.4M
Physiologic effects of androgen and estrogen deficiency in young and old menR01AG030545 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI FINKELSTEIN, JOEL S · 2007 to 2011
$3.1M
EFFECTS OF ANDROGENS, ESTROGENS, AND PTH ON BONEK24DK002759 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI FINKELSTEIN, JOEL S · 1999 to 2008
$1.2M
NCRR NIH HHS M01 RR001066NCRR NIH HHS RR-1066NIA NIH HHS R01 AG030545NIDDK NIH HHS K24 DK002759PHS HHS K24 KD02759
6 · The paper itself

Abstract

contextIn vitro and animal studies have reported conflicting results regarding an independent role for FSH in the regulation of bone turnover.

objectiveOur objective was to test the hypothesis that suppressing serum FSH while holding serum gonadal steroid levels stable in the eugonadal range will affect biochemical markers of bone metabolism in healthy men. PARTICIPANTS, DESIGN, AND

settingEugonadal men aged 20 to 50 years participated in this randomized controlled trial at a tertiary care academic teaching hospital.

interventionsParticipants received monthly GnRH analog injections to suppress FSH secretion plus daily topical testosterone gel in prespecified doses (intervention group). Controls received matching placebos (control group). Subjects in the intervention group were individually matched with subjects in the control group to ensure that the mean testosterone and estradiol levels (measured every 4 weeks during the 16-week study period) in the 2 groups were similar.

main outcome measuresBiochemical markers of bone resorption (serum N-terminal telopeptide and C-terminal telopeptide), bone formation (serum osteocalcin), and FSH were measured at baseline and after 16 weeks of treatment.

resultsSerum FSH declined by 2% in the control group and by 60% in the intervention group (P < .0001 for the between-group difference). Despite the substantial suppression of serum FSH in the intervention group, serum N-terminal telopeptide, C-terminal telopeptide, and osteocalcin did not change in the intervention group, nor were any between-group differences observed.

conclusionWhen gonadal steroid levels are held constant, short-to midterm suppression of FSH does not affect bone turnover in men. FSH does not appear to be a significant regulator of bone metabolism in eugonadal men.

Indexed as

AdultBone RemodelingCollagen Type IEstradiolFollicle Stimulating HormoneGonadal Steroid HormonesGonadsGoserelinHumansMaleMiddle AgedPeptidesTestosteroneYoung AdultCollagen Type Icollagen type I trimeric cross-linked peptideEstradiolFollicle Stimulating HormoneGonadal Steroid HormonesGoserelinPeptidesTestosterone

Identifiers

PMID24646101
PMCPMC4079307
OpenAlexW2085202924

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.