Evidence map›Paper›PMID 29144249›Full record

Trial reportThe Journal of pediatrics2017

Effect of Antiandrogen, Aromatase Inhibitor, and Gonadotropin-releasing Hormone Analog on Adult Height in Familial Male Precocious Puberty.

Ellen Werber Leschek, Armando C Flor, Joy C Bryant, Janet V Jones, Kevin M Barnes, Gordon B Cutler

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in The Journal of pediatrics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 33 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Short Adult Height After Rapid-tempo Puberty: When is it too Late to Treat?Journal of clinical research in pediatric endocrinology · 2024
    Article
  5. Article
  6. Article
  7. Familial Male-limited Precocious Puberty (FMPP) and Testicular Germ Cell Tumors.The Journal of clinical endocrinology and metabolism · 2022
    Review
  8. Article
  9. Article
  10. Review
  11. A Case of Familial Male-limited Precocious Puberty with a Novel MutationJournal of clinical research in pediatric endocrinology · 2021
    Article
  12. Review
  13. Review
  14. [Reconsideration of the third-generation non-steroidal aromatase inhibitors in pediatrics].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2020
    Article
  15. Article
  16. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Ellen Werber LeschekNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD. Electronic address: LeschekE@extra.niddk.nih.gov.
Armando C FlorMedImmune, Gaithersburg, MD.
Joy C BryantNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD.
Janet V JonesBastrop, TX.
Kevin M BarnesThe Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD.
Gordon B CutlerDeltaville, VA.
National Institutes of Health · USDelta Air Lines (United States) · USEunice Kennedy Shriver National Institute of Child Health and Human Development · US

Funding

Intramural NIH HHS Z99 DK999999
6 · The paper itself

Abstract

objectiveAntiandrogen, aromatase inhibitor, and gonadotropin-releasing hormone analog (GnRHa) treatment normalizes growth rate and bone maturation and increases predicted adult height (AH) in boys with familial male-limited precocious puberty (FMPP). To evaluate the effect of long-term antiandrogen, aromatase inhibitor, and GnRHa on AH, boys with FMPP who were treated were followed to AH. STUDY

designTwenty-eight boys with FMPP, referred to the National Institutes of Health, were started on antiandrogen and aromatase inhibitor at 4.9 ± 1.5 years of age; GnRHa was added at 6.9 ± 1.5 years of age. Treatment was discontinued at 12.2 ± 0.5 years of age (bone age, 14.4 ± 1.3). AH was assessed at 16.4 ± 1.3 years of age (bone age, 18.5 ± 0.6).

resultsAH (mean ± SD) for all treated subjects was 173.6 ± 6.8 cm (-0.4 ± 1.0 SD relative to adult US males). For 25 subjects with pretreatment predicted AH, AH significantly exceeded predicted AH at treatment onset (173.8 ± 6.9 vs 164.9 ± 10.7 cm; P < .001), but fell short of predicted AH at treatment discontinuation (177.3 ± 9.0 cm; P < .001). For 11 subjects with maternal or sporadic inheritance, the mean AH was 3.1 cm (0.4 SD score) below sex-adjusted midparental height (175.4 ± 5.8 vs 178.5 ± 3.1 cm [midparental height]; P = .10). For 16 subjects with affected and untreated fathers, AH was significantly greater than fathers' AH (172.8 ± 7.4 vs 168.8 ± 7.2 cm; P < .05).

conclusionsLong-term treatment with antiandrogen, aromatase inhibitor, and GnRHa in boys with FMPP results in AH modestly below sex-adjusted midparental height and within the range for adult males in the general population.

Indexed as

AdultAnastrozoleAndrogen AntagonistsAromatase InhibitorsBody HeightChildChild, PreschoolDrug Administration ScheduleDrug Therapy, CombinationFollow-Up StudiesGonadotropin-Releasing HormoneHumansLeuprolideMaleNitrilesPuberty, PrecociousAnastrozoleAndrogen AntagonistsAromatase InhibitorsdeslorelinGonadotropin-Releasing HormoneLeuprolideNitrilesSpironolactoneTestolactoneTriazolesTriptorelin Pamoatefamilial male-limited precocious pubertygonadotropin-independent precocious pubertytestotoxicosis

Identifiers

PMID29144249
PMCPMC5726420
OpenAlexW2765172961

What OpenQuestion holds

Textmetadata
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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.