Evidence map›Paper›PMID 24823464›Full record

Trial reportThe Journal of clinical endocrinology and metabolism2014

5α-reductase type 1 modulates insulin sensitivity in men.

Rita Upreti, Katherine A Hughes, Dawn E W Livingstone, Calum D Gray, Fiona C Minns, David P Macfarlane, Ian Marshall, Laurence H Stewart, Brian R Walker, Ruth Andrew

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 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

40 citing papers in PubMed, 85 citations in OpenAlex.

  1. Trial
  2. Aromatase Inhibition Reduces Insulin Sensitivity in Healthy Men.The Journal of clinical endocrinology and metabolism · 2016
    Trial
  3. Dual-5α-Reductase Inhibition Promotes Hepatic Lipid Accumulation in Man.The Journal of clinical endocrinology and metabolism · 2016
    Trial
  4. Trial
  5. Article
  6. Review
  7. Article
  8. Article
  9. Metabolic Messengers: testosterone.Nature metabolism · 2026
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. The association of new-onset diabetes mellitus and medical therapy for benign prostatic hyperplasia: A population-based study.Canadian Urological Association journal = Journal de l'Association des urologues du Canada · 2021
    Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Rita UpretiUniversity/British Heart Foundation Centre for Cardiovascular Science (R.U., K.A.H., D.E.W.L., D.P.M., I.M., B.R.W., R.A.) and Clinical Research Imaging Centre (C.D.G.), University of Edinburgh, Queen's Medical Research Institute, Edinburgh EH16 4TJ, United Kingdom; and Radiology (F.C.M.) and Urology (L.H.S.) Departments, National Health Service Lothian University Hospitals Division, Western General Hospital, Edinburgh EH4 2XU, United Kingdom.
Katherine A Hughes
Dawn E W Livingstone
Calum D Gray
Fiona C Minns
David P Macfarlane
Ian Marshall
Laurence H Stewart
Brian R Walker
Ruth Andrew
British Heart Foundation Centre for Cardiovascular Science · GBBritish Heart Foundation · GBThe Queen's Medical Research Institute · GBWestern General Hospital · GB

Funding

British Heart Foundation RG/11/4/28734Chief Scientist Office CZB/4/642
6 · The paper itself

Abstract

context5α-Reductase (5αR) types 1 and 2 catalyze the A-ring reduction of steroids, including androgens and glucocorticoids. 5α-R inhibitors lower dihydrotestosterone in benign prostatic hyperplasia; finasteride inhibits 5αR2, and dutasteride inhibits both 5αR2 and 5αR1. In rodents, loss of 5αR1 promotes fatty liver.

objectiveOur objective was to test the hypothesis that inhibition of 5αR1 causes metabolic dysfunction in humans. DESIGN, SETTING, AND

participantsThis double-blind randomized controlled parallel group study at a clinical research facility included 46 men (20-85 years) studied before and after intervention.

interventionOral dutasteride (0.5 mg daily; n = 16), finasteride (5 mg daily; n = 16), or control (tamsulosin; 0.4 mg daily; n = 14) was administered for 3 months.

main outcome measureGlucose disposal was measured during a stepwise hyperinsulinemic-euglycemic clamp. Data are mean (SEM).

resultsDutasteride and finasteride had similar effects on steroid profiles, with reduced urinary androgen and glucocorticoid metabolites and reduced circulating DHT but no change in plasma or salivary cortisol. Dutasteride, but not finasteride, reduced stimulation of glucose disposal by high-dose insulin (dutasteride by -5.7 [3.2] μmol/kg fat-free mass/min, versus finasteride +7.2 [3.0], and tamsulosin +7.0 [2.0]). Dutasteride also reduced suppression of nonesterified fatty acids by insulin and increased body fat (by 1.6% [0.6%]). Glucose production and glycerol turnover were unchanged. Consistent with metabolic effects of dutasteride being mediated in peripheral tissues, mRNA for 5αR1 but not 5αR2 was detected in human adipose tissue.

conclusionDual inhibition of 5αRs, but not inhibition of 5αR2 alone, modulates insulin sensitivity in human peripheral tissues rather than liver. This may have important implications for patients prescribed dutasteride for prostatic disease.

Indexed as

Insulin Resistance3-Oxo-5-alpha-Steroid 4-Dehydrogenase5-alpha Reductase InhibitorsAdipose TissueAdultAgedAged, 80 and overAzasteroidsBlood GlucoseBody CompositionDouble-Blind MethodDutasterideFinasterideHumansMaleMiddle Aged3-Oxo-5-alpha-Steroid 4-Dehydrogenase5-alpha Reductase InhibitorsAzasteroidsBlood GlucoseDutasterideFinasteride

Identifiers

PMID24823464
PMCPMC4207930
OpenAlexW2136383818

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.