Evidence map›Paper›PMID 23678038›Full record

Trial reportThe Journal of clinical endocrinology and metabolism2013

Metabolic effects of oral versus transdermal 17β-estradiol (E₂): a randomized clinical trial in girls with Turner syndrome.

L Torres-Santiago, V Mericq, M Taboada, N Unanue, K O Klein, R Singh, J Hossain, R J Santen, J L Ross, N Mauras

3 registry-linked trialsOpen access · bronzeAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in The Journal of clinical endocrinology and metabolism, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 31 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 3 pooled it
5.6field-weighted citation impact, top 4% 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.

NCT00837616 phase4completednot on this map

Estrogen Dosing in Turner Syndrome:Pharmacology & Metabolism

TypeinterventionalSponsorNemours Children's ClinicRan2009 to 2012Enrolled41ConditionsTurner Syndrome, Hypogonadism, Premature Ovarian FailureArms17 B estradiol orally, 17 B estradiol
NCT06544473 phase4recruitingnot on this mapstarted 2021, after this paper: background citation

Determining Dose Equivalence Between Oral and Transdermal Estrogen Treatment in Women With Turner Syndrome - A Randomized Study

TypeinterventionalSponsorAarhus University HospitalRan2021 to 2026Enrolled50ConditionsTurner Syndrome, Hypogonadism, Ovarian, Hormone Replacement TherapyArms17-beta estradiol
NCT06570460 phase4recruitingnot on this mapstarted 2021, after this paper: background citation

Long Term Effects of Oral Versus Transdermal Estrogen Replacement Therapy in Turner Syndrome - A Randomized Trial

TypeinterventionalSponsorAarhus University HospitalRan2021 to 2026Enrolled50ConditionsTurner Syndrome, Hypogonadism, Ovarian, Hormone Replacement TherapyArms17-beta estradiol
3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 3 syntheses or guidelines pooled it, 98 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Review
  6. Article
  7. Article
  8. Article
  9. Lifelong medical challenges and immunogenetics of Turner syndrome.Clinical and experimental pediatrics · 2024
    Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Perspectives on growth promoting treatment for patients with Turner syndrome in Japan.Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology · 2020
    Review
  19. Article
  20. Glucose Metabolism in Turner Syndrome.Frontiers in endocrinology · 2019
    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

10 authors at 9 institutions in 2 countries.

L Torres-SantiagoNemours Children’s Clinic, Jacksonville, Florida 32207, USA.
V Mericq
M Taboada
N Unanue
K O Klein
R Singh
J Hossain
R J Santen
J L Ross
N Mauras
Nemours Children's Clinic · USCommunity Health Systems - Dupont Hospital · USDuPont (United States) · USJefferson College · USMayo Clinic · USNemours Children's Clinic · USUniversity of California San Diego · USUniversity of Chile · CLUniversity of Virginia Medical Center · US

Funding

MAYO CLINIC CENTER FOR TRANSLATIONAL SCIENCE ACTIVITIESUL1RR024150 · NCRR · MAYO CLINIC ROCHESTER · PI RIZZA, ROBERT A. · 2006 to 2011
$66.4M
Center for Pediatric ResearchP20GM103464 · NIGMS · NEMOURS CHILDREN'S HOSPITAL, DELAWARE · PI SHAFFER, THOMAS H · 2012 to 2014
$5.6M
NCRR NIH HHS UL1 RR024150NCRR NIH HHS UL1 RR024150-05-NIH/NCRRNIGMS NIH HHS P20 GM103464
6 · The paper itself

Abstract

contextThe long-term effects of pure 17β-estradiol (E₂) depending on route of administration have not been well characterized.

objectiveOur objective was to assess metabolic effects of oral vs transdermal (TD) 17β-E₂ replacement using estrogen concentration-based dosing in girls with Turner syndrome (TS). PATIENTS: Forty girls with TS, mean age 16.7 ± 1.7 years, were recruited.

designSubjects were randomized to 17β-E₂ orally or TD. Doses were titrated using mean E₂ concentrations of normally menstruating girls as therapeutic target. E₂, estrone (E₁), and E₁ sulfate (E₁S) were measured by liquid chromatography tandem mass spectrometry and a recombinant cell bioassay; metabolites were measured, and dual-energy x-ray absorptiometry scan and indirect calorimetry were performed. MAIN OUTCOME: Changes in body composition and lipid oxidation were evaluated.

resultsE₂ concentrations were titrated to normal range in both groups; mean oral dose was 2 mg, and TD dose was 0.1 mg. After 6 and 12 months, fat-free mass and percent fat mass, bone mineral density accrual, lipid oxidation, and resting energy expenditure rates were similar between groups. IGF-1 concentrations were lower on oral 17β-E₂, but suppression of gonadotropins was comparable with no significant changes in lipids, glucose, osteocalcin, or highly sensitive C-reactive protein between groups. However, E₁, E₁S, SHBG, and bioestrogen concentrations were significantly higher in the oral group.

conclusionsWhen E₂ concentrations are titrated to the normal range, the route of delivery of 17β-E₂ does not affect differentially body composition, lipid oxidation, and lipid concentrations in hypogonadal girls with TS. However, total estrogen exposure (E₁, E₁S, and total bioestrogen) is significantly higher after oral 17β-E₂. TD 17β-E₂ results in a more physiological estrogen milieu than oral 17β-E₂ administration in girls with TS.

Indexed as

Estrogen Replacement TherapyAdministration, OralAdolescentAdultBasal MetabolismBiotransformationBody CompositionBone DensityDrug MonitoringEnergy MetabolismEstradiolEstroneFeasibility StudiesFemaleHumansLipid MetabolismEstradiolEstroneestrone sulfate

Identifiers

PMID23678038
PMCPMC5393461
OpenAlexW2110808214

What Socratic holds

Textmetadata
Read underepoch 390

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 Socratic graph.