Evidence map›Paper›PMID 40795401›Full record

ArticleEuropean journal of endocrinology2025

Leptin and adiponectin in children and young persons with congenital adrenal hyperplasia.

Irina A Bacila, Neil R Lawrence, Sabah Alvi, Timothy D Cheetham, Elizabeth Crowne, Urmi Das, Mehul T Dattani, Justin H Davies, Evelien Gevers, Brian Keevil and 7 more

Abstract readMulticenter Study
In one paragraph

Article in European journal of endocrinology, 2025. 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. 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

17 authors.

Irina A BacilaDivision of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Western Bank, Sheffield S10 2TH, United Kingdom.ORCID 0000-0001-7726-4299
Neil R LawrenceDivision of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Western Bank, Sheffield S10 2TH, United Kingdom.
Sabah AlviDepartment of Paediatric Endocrinology, Leeds General Infirmary, Leeds LS1 3EX, United Kingdom.
Timothy D CheethamGreat North Children's Hospital, University of Newcastle, Newcastle NE1 7RU, United Kingdom.
Elizabeth CrowneBristol Royal Hospital for Children, University Hospitals Bristol Foundation Trust, Bristol BS2 8BJ, United Kingdom.
Urmi DasDepartment of Paediatric Endocrinology, Alder Hey Children's Hospital, Liverpool L14 5AB, United Kingdom.
Mehul T DattaniDepartment of Paediatric Endocrinology, Great Ormond Street Hospital, London WC1N 3BH, United Kingdom.
Justin H DaviesDepartment of Paediatric Endocrinology, University Hospital Southampton, Southampton SO16 6YD, United Kingdom.
Evelien GeversCentre for Endocrinology, William Harvey Research Institute, Queen Mary University London, London and Barts Health NHS Trust-the Royal London Hospital, London EC1M 6BQ, United Kingdom.ORCID 0000-0002-4397-4126
Brian KeevilDepartment of Biochemistry, Manchester University NHS Foundation Trust, Manchester M13 9WL, United Kingdom.
Ruth E KroneDepartment of Paediatric Endocrinology, Birmingham Women's & Children's Hospital, Birmingham B4 6NH, United Kingdom.
Allan LawrieNational Heart and Lung Institute, Faculty of Medicine, Imperial College London, London  SW3 6LY, United Kingdom.ORCID 0000-0003-4192-9505
Leena PatelDepartment of Paediatric Endocrinology, Royal Manchester Children's Hospital, Manchester University NHS Foundation Trust and Division of Medical Education, the University of Manchester, Manchester M13 9WL, United Kingdom.
Tabitha RandellDepartment of Paediatric Endocrinology, Nottingham Children's Hospital, Nottingham NG7 2UH, United Kingdom.
Fiona J RyanOxford Children's Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford OX3 9DU, United Kingdom.
S Faisal AhmedDevelopmental Endocrinology Research Group, University of Glasgow, Glasgow G12 8QQ, United Kingdom.ORCID 0000-0003-0689-5549
Nils P KroneDivision of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Western Bank, Sheffield S10 2TH, United Kingdom.ORCID 0000-0002-3402-4727

Funding

British Heart Foundation FS/18/52/33808National Institute of Health Research NIHR RD TRC
6 · The paper itself

Abstract

objectivesPatients with congenital adrenal hyperplasia (CAH) have increased prevalence of metabolic problems. We studied adiponectin, leptin and resistin in children with CAH, in relation to BMI, treatment, hormonal and metabolic biomarkers. DESIGN AND

methodsWe analysed 101 patients with 21-hydroxylase deficiency (54 females, 13.0 ± 2.92 years) from 13 centres in the United Kingdom, and 83 sex- and age-matched controls. Blood parameters (leptin, adiponectin, resistin, metabolic and hormonal markers) were measured in fasted state, between 09:00 and 11:00, after the first glucocorticoid (GC) dose.

resultsA difference in adipokines between patients and controls was only found for leptin in males (patients > control, P = .033). In patients and controls, leptin had a positive relationship with BMI-SDS (P < .001). However, adiponectin decreased with the BMI only in patients (P  <  .001). Contrary to published evidence on the effect of synthetic steroids on leptin, in our cohort, leptin decreased with the increasing first daily hydrocortisone (HC) dose (Log10Leptin  =  4.1- 0.08xfirstGCdose (mg/m2), P  =  .009) but not with the total daily dose. When correcting for BMI, a positive relationship between leptin and insulin was only found in controls (P  <  .001). Adiponectin decreased with steroid precursor and androgen concentrations (17-hydroxyprogesterone, androstenedione, testosterone, 11-hydroxyandrostenedione, 11-ketotestosterone) in patients.

conclusionOur findings indicate a decrease in leptin with the HC dose, consistent with a detrimental effect of glucocorticoid on satiety and hunger pathways in CAH. Adiponectin was decreased in patients with increased androgens concentrations, suggesting it may be used as an indicator of metabolic risk associated with poor hormonal CAH control.

Indexed as

AdiponectinAdrenal Hyperplasia, CongenitalLeptinAdolescentBiomarkersBody Mass IndexCase-Control StudiesChildFemaleGlucocorticoidsHumansHydrocortisoneMaleAdiponectinADIPOQ protein, humanBiomarkersGlucocorticoidsHydrocortisoneLeptinadiponectinandrogenscongenital adrenal hyperplasiaglucocorticoid treatmentleptin

Identifiers

PMID40795401
PMCPMC12396446

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Registered trials

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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.