Evidence map›Paper›PMID 38152128›Full record

ArticleFrontiers in endocrinology2023

Pubertal attainment and Leydig cell function following pediatric hematopoietic stem cell transplantation: a three-decade longitudinal assessment.

Alessandro Cattoni, Maria Laura Nicolosi, Giulia Capitoli, Alberto Gadda, Silvia Molinari, Sotiris Louka, Andrea Buonsante, Simona Orlandi, Gianluca Salierno, Iacopo Bellani and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 9% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. 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

16 authors at 4 institutions in 1 country.

Alessandro CattoniDepartment of Pediatrics, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
Maria Laura NicolosiDepartment of Pediatrics, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
Giulia CapitoliBicocca Bioinformatics, Biostatistics and Bioimaging B4 Centre, University of Milano-Bicocca, Monza, Italy.
Alberto GaddaBicocca Bioinformatics, Biostatistics and Bioimaging B4 Centre, University of Milano-Bicocca, Monza, Italy.
Silvia MolinariDepartment of Pediatrics, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
Sotiris LoukaDepartment of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.
Andrea BuonsanteDepartment of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.
Simona OrlandiDepartment of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.
Gianluca SaliernoDepartment of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.
Iacopo BellaniDepartment of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy.
Francesca VendeminiDepartment of Pediatrics, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
Giorgio OttavianoDepartment of Pediatrics, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
Alberto GaieroDepartment of Pediatrics and Neonatology, IRCCS Gaslini Savona e Pietra Ligure, Savona, Italy.
Graziella FicheraDepartment of Endocrinology, Ospedale San Paolo, Savona, Italy.
Andrea BiondiDepartment of Pediatrics, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
Adriana BalduzziDepartment of Pediatrics, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
University of Milano-Bicocca · ITAzienda Ospedaliera San Gerardo · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITOspedale San Paolo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Impaired testosterone secretion is a frequent Methods: Monocentric, retrospective analysis. Male patients transplanted <18 years between 1992 and 2021, surviving ≥2 years after HSCT and showing, upon enrollment, clinical and biochemical signs consistent with pubertal onset and progression were included. Clinical and biochemical data collected every 6-12 months were recorded. Results: Of 130 patients enrolled, 56% were prepubertal, while 44% were peri-/postpubertal upon HSCT. Overall, 44% showed spontaneous progression into puberty and normal gonadal profile, while the remaining experienced pubertal arrest (1%), isolated increase of FSH (19%), compensated (23%) or overt (13%) hypergonadotropic hypogonadism. Post-pubertal testicular volume (TV) was statistically smaller among patients still pre-pubertal upon HSCT ( Conclusions: a) patients pre-pubertal upon HSCT showed a reduced risk of testicular endocrine dysfunction, despite smaller adult TV; b) patients showed downwards trend in testosterone levels after full pubertal attainment, despite a compensatory increase in LH; c) treosulfan was associated to a statistically lower occurrence of hypogonadism than busulfan, with a trend towards larger TV, higher testosterone levels and lower gonadotropins.

Indexed as

Hematopoietic Stem Cell TransplantationHypogonadismAdultBusulfanChildHumansLeydig CellsMaleRetrospective StudiesTestosteroneBusulfanTestosteronetreosulfanbusulfangonadal disordershematopoietic stem cell transplantationhypogonadismtestosteronetotal body irradiationtreosulfan

Identifiers

PMID38152128
PMCPMC10751351
OpenAlexW4389679071

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.