Evidence map›Paper›PMID 41689273›Full record

ArticleThe Journal of clinical endocrinology and metabolism2026

Glucocorticoid trajectories in preterm infants-born too soon, wired differently.

Tanja Kuiri-Hänninen, Christa Flück, Sanna Silvennoinen, Michael Groessl, Ulla Sankilampi

Abstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

  1. Glucocorticoid trajectories in preterm infants-born too soon, wired differently.The Journal of clinical endocrinology and metabolism · 2026
    Article
  2. 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

5 authors.

Tanja Kuiri-HänninenDepartment of Pediatrics, Kuopio University Hospital, 70210 Kuopio, Finland.ORCID 0000-0002-5081-1392
Christa FlückPediatric Endocrinology, Diabetology and Metabolism, Department of Pediatrics, Inselspital Bern University Hospital, University of Bern, 3010 Bern, Switzerland.
Sanna SilvennoinenDepartment of Pediatrics, Kuopio University Hospital, 70210 Kuopio, Finland.
Michael GroesslDepartment of Biomedical Research, University Hospital Inselspital, University of Bern, 3010 Bern, Switzerland.
Ulla SankilampiDepartment of Pediatrics, Kuopio University Hospital, 70210 Kuopio, Finland.

Funding

Kuopion Yliopistollinen SairaalaPäivikki ja Sakari Sohlbergin SäätiöThe Foundation for Pediatric Research
6 · The paper itself

Abstract

contextLevels of glucocorticoid (GC) precursors are elevated in preterm infants, whereas clinical signs of GC deficiency are frequently observed in neonatal intensive care units.

objectiveTo describe the maturation of the GC metabolic pathway in preterm infants during the first year of life. DESIGN AND

settingSpot urinary samples (n = 154) were collected in the neonatal intensive care unit and at follow-up visits.

participantsSixteen preterm infants (8 boys) born <30 weeks of gestational age. Data of full-term infants were available from the same laboratory.

main outcome measuresUrinary levels of GC precursor metabolites and 13 GC metabolites were quantitated by gas chromatography-mass spectrometry. Enzyme activities were calculated by product/substrate ratios. Mixed models were used for statistical analyses.

resultsThe levels of GC precursors remained high in preterm infants until term-equivalent age (TEA), after which they decreased (P < .001). However, GC production, estimated by the sum of 13 GC metabolites did not change significantly over time in preterm infants and was higher in preterm than in full-term infants after 1 week of age (P = .044 -<.001). The sum of 13 GC metabolites/tetrahydro-11-deoxycortisol ratio (representing CYP11B1 activity) increased in preterm infants after TEA (P < .001), whereas the 16α-OH-DHEA/5-PT ratio (representing 17,20-lyase activity) decreased (P < .001). The ratio of cortisone metabolites to cortisol metabolites was higher in preterm infants before TEA than thereafter (P < .001).

conclusionDespite a high production rate of GC precursors in preterm infants, the total GC production remained relatively constant and was regulated at the level of CYP11B1. Persisting differences between preterm and full-term infants in GC precursor levels as well as in GC production were observed, indicating possible programming effects of preterm birth.

Indexed as

GlucocorticoidsInfant, PrematureFemaleFollow-Up StudiesGas Chromatography-Mass SpectrometryGestational AgeHumansInfantInfant, NewbornIntensive Care Units, NeonatalMaleGlucocorticoidsfetal adrenal cortexfetal-neonatal transitionGC-MSglucocorticoidprematurity

Identifiers

PMID41689273
PMCPMC13271798

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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.