Evidence map›Paper›PMID 38040920›Full record

ArticleJournal of endocrinological investigation2024

Aromatase inhibitors: a useful additional therapeutic option for slowing down advanced bone age in boys with growth hormone deficiency.

G Akın Kağızmanlı, D Özalp Kızılay, Ö Besci, K Yüksek Acinikli, S Özen, K Demir, R D Gökşen Şimşek, E Böber, Ş Darcan, A Abacı

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Journal of endocrinological investigation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. Article
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.

G Akın KağızmanlıDepartment of Pediatric Endocrinology, Dokuz Eylül University Faculty of Medicine, İzmir, Turkey.ORCID http://orcid.org/0000-0002-6158-9002
D Özalp KızılayDepartment of Pediatric Endocrinology, Ege University Faculty of Medicine, İzmir, Turkey.ORCID http://orcid.org/0000-0003-4529-4404
Ö BesciDepartment of Pediatric Endocrinology, Dokuz Eylül University Faculty of Medicine, İzmir, Turkey.ORCID http://orcid.org/0000-0003-3135-9617
K Yüksek AcinikliDepartment of Pediatric Endocrinology, Dokuz Eylül University Faculty of Medicine, İzmir, Turkey.ORCID http://orcid.org/0000-0001-9492-4834
S ÖzenDepartment of Pediatric Endocrinology, Ege University Faculty of Medicine, İzmir, Turkey.ORCID http://orcid.org/0000-0001-7037-2713
K DemirDepartment of Pediatric Endocrinology, Dokuz Eylül University Faculty of Medicine, İzmir, Turkey.ORCID http://orcid.org/0000-0002-8334-2422
R D Gökşen ŞimşekDepartment of Pediatric Endocrinology, Ege University Faculty of Medicine, İzmir, Turkey.ORCID http://orcid.org/0000-0001-6108-0591
E BöberDepartment of Pediatric Endocrinology, Dokuz Eylül University Faculty of Medicine, İzmir, Turkey.ORCID http://orcid.org/0000-0001-8828-0892
Ş DarcanDepartment of Pediatric Endocrinology, Ege University Faculty of Medicine, İzmir, Turkey.ORCID http://orcid.org/0000-0002-1330-6397
A AbacıDepartment of Pediatric Endocrinology, Dokuz Eylül University Faculty of Medicine, İzmir, Turkey. ayhan.abaci@deu.edu.tr.ORCID http://orcid.org/0000-0002-1812-0321

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAromatase inhibitors (AIs) have been used to slow down estrogen-dependent skeletal maturation in pubertal boys with short stature. In the literature, few data evaluate the effectiveness and safety of AIs in boys with growth hormone deficiency (GHD). This study aimed to evaluate the auxologic effects and short-term laboratory profiles of combined AI and rhGH therapy for 1 year in adolescent males with GHD. SUBJECTS AND

methodsMale subjects between the ages of 10 and 16 with GHD from two different centers were included in the study. Patients were divided into two groups: (i) those who only used recombinant human growth hormone (rhGH) therapy (Group I; G-I) and (ii) those who also used AI therapy (anastrozole or letrozole) along with rhGH (Group II; G-II).

resultsForty-one patients (G-I, 46%; G-II, 54%) were included in the study. All the subjects had isolated GHD. At the beginning of the treatment, the chronological ages (CAs) of the patients in the G-I and G-II groups were 11.8 (10.9-13.7) and 12.8 (12.0-14.3) years, respectively. The ratios of bone age (BA)/CA for the two groups were 0.8 (0.8-0.9) and 1.0 (0.9-1.1), respectively (p < 0.001). After the treatment, the height standard deviation (SD) scores and predicted adult height (PAH) significantly increased from baseline in all subjects in the G-I and G-II groups (p < 0.001; p < 0.001, respectively). There was no significant change in the ratio of BA/CA post-therapy in the G-I group (p = 0.1), while there was a significant decrease in the G-II group (p < 0.001). The growth velocities of the patients in the G-I and G-II groups were 9.1 (7.4-10.1) cm/year [1.5 (0.8-5.0) SD score] and 8.7 (7.5-9.9) cm/year [1.1 (0.3-3.1) SD score], respectively (p = 0.6). While post-therapy serum testosterone concentrations were seen to increase in the G-II group, none of the patients exhibited hematocrit above 50 percent, and the fasting glucose concentrations were normal.

conclusionsWhen used in addition to rhGH therapy in boys with GHD and advanced BA, AIs were observed to slow down the tempo of BA maturation after 1 year, compared to those who received rhGH treatment alone. AI therapy was found to be safe during the 1-year observation period and thus could be considered for preserving growth potential in these patients.

Indexed as

Age Determination by SkeletonAromatase InhibitorsHuman Growth HormoneAdolescentBody HeightBone DevelopmentChildDwarfism, PituitaryFollow-Up StudiesGrowth DisordersHumansMaleAromatase InhibitorsHuman Growth HormoneAromatase inhibitorGrowth hormone deficiencyHeight incrementShort stature

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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.