Evidence map›Paper›PMID 38436980›Full record

ReviewEndocrine reviews2024

Mini-Puberty, Physiological and Disordered: Consequences, and Potential for Therapeutic Replacement.

Julia Rohayem, Emma C Alexander, Sabine Heger, Anna Nordenström, Sasha R Howard

Open access · hybridAbstract readReview
In one paragraph

Review in Endocrine reviews, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 3 pooled it
44.0field-weighted citation impact, top 1% 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

61 citing papers in PubMed, 3 syntheses or guidelines pooled it, 82 citations in OpenAlex.

  1. Guideline
  2. Reversal of Congenital Hypogonadotropic Hypogonadism.The Journal of clinical endocrinology and metabolism · 2026
    Pooled it
  3. Pooled it
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  6. Review
  7. Review
  8. Article
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  11. Review
  12. Article
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  16. Article
  17. The ontogeny of sex differences in exercise performance.Journal of the Endocrine Society · 2026
    Article
  18. Article
  19. Article
  20. Review

1 more citing papers are in PubMed but not listed here.

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

5 authors at 4 institutions in 3 countries.

Julia RohayemDepartment of Pediatric Endocrinology and Diabetology, Children's Hospital of Eastern Switzerland, 9006 St. Gallen, Switzerland.
Emma C AlexanderCentre for Endocrinology, William Harvey Research Institute, Queen Mary University of London, London EC1M 6BQ, UK.ORCID 0000-0001-7063-6846
Sabine HegerDepartment of Pediatric Endocrinology, Children's Hospital Auf der Bult, 30173 Hannover, Germany.
Anna NordenströmPediatric Endocrinology, Karolinska Institutet, Astrid Lindgren Children's Hospital, Karolinska University Hospital, 17176 Stockholm, Sweden.ORCID 0000-0003-0405-3401
Sasha R HowardCentre for Endocrinology, William Harvey Research Institute, Queen Mary University of London, London EC1M 6BQ, UK.ORCID 0000-0002-6698-903X
Queen Mary University of London · GBKarolinska University Hospital · SEKinderkrankenhaus auf der Bult · DEUniversity of Münster · DE

Funding

ESPE Research UnitKarolinska InstitutetNIHR Academic Clinical FellowshipStockholm City CouncilWellcome Trust
6 · The paper itself

Abstract

There are 3 physiological waves of central hypothalamic-pituitary-gonadal (HPG) axis activity over the lifetime. The first occurs during fetal life, the second-termed "mini-puberty"-in the first months after birth, and the third at puberty. After adolescence, the axis remains active all through adulthood. Congenital hypogonadotropic hypogonadism (CHH) is a rare genetic disorder characterized by a deficiency in hypothalamic gonadotropin-releasing hormone (GnRH) secretion or action. In cases of severe CHH, all 3 waves of GnRH pulsatility are absent. The absence of fetal HPG axis activation manifests in around 50% of male newborns with micropenis and/or undescended testes (cryptorchidism). In these boys, the lack of the mini-puberty phase accentuates testicular immaturity. This is characterized by a low number of Sertoli cells, which are important for future reproductive capacity. Thus, absent mini-puberty will have detrimental effects on later fertility in these males. The diagnosis of CHH is often missed in infants, and even if recognized, there is no consensus on optimal therapeutic management. Here we review physiological mini-puberty and consequences of central HPG axis disorders; provide a diagnostic approach to allow for early identification of these conditions; and review current treatment options for replacement of mini-puberty in male infants with CHH. There is evidence from small case series that replacement with gonadotropins to mimic "mini-puberty" in males could have beneficial outcomes not only regarding testis descent, but also normalization of testis and penile sizes. Moreover, such therapeutic replacement regimens in disordered mini-puberty could address both reproductive and nonreproductive implications.

Indexed as

HypogonadismGonadotropin-Releasing HormoneHormone Replacement TherapyHumansHypothalamo-Hypophyseal SystemMalePubertyGonadotropin-Releasing Hormonecongenital hypogonadotropic hypogonadismcryptorchidismgonadotropinshypogonadisminfancyKallmann syndromemicropenismini-pubertypuberty

Identifiers

PMID38436980
PMCPMC11244267
OpenAlexW4392756877

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.