Evidence map›Paper›PMID 41339369›Full record

Observational studyScientific reports2025

In vitro dexamethasone suppression of cytokine production assay and plasma total and free cortisol responses to ACTH in healthy volunteers.

Gladness Dakalo Nethathe, Jeremy Cohen, Jeffrey Lipman, Ronald Anderson, Karen Elizabeth Hay, Carel J Pretorius, Charles Feldman

Abstract readObservational Study
In one paragraph

Observational study in Scientific reports, 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. 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

7 authors.

Gladness Dakalo NethatheSchool of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, Johannesburg, South Africa. gladness.nethathe@wits.ac.za.
Jeremy CohenFaculty of Medicine, The University of Queensland, Brisbane, QLD, Australia.
Jeffrey LipmanFaculty of Medicine, The University of Queensland, Brisbane, QLD, Australia.
Ronald AndersonThe Clinical and Translational Research Unit of the Medical Oncology Centre of Rosebank Oncology Centre, Johannesburg, South Africa.
Karen Elizabeth HayQIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Carel J PretoriusDepartment of Chemical Pathology, Pathology Queensland, Royal Brisbane and Women's Hospital, Herston, Brisbane, QLD, Australia.
Charles FeldmanSchool of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, Johannesburg, South Africa.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glucocorticoid sensitivity varies between individuals, influencing stress and inflammatory responses, however its relationship with the synthetic ACTH [1-24] stimulation test, is not well evaluated. To evaluate glucocorticoid sensitivity and plasma total cortisol (TC) and plasma free cortisol (PFC) responses to stimulation with 250 μg of synthetic ACTH [1-24]) in healthy adults. Prospective, single-centre observational study. Forty-eight healthy adults (24 females, 24 males) underwent basal and stimulated TC and PFC level measurements using liquid chromatography-tandem mass spectrometry. Peak cortisol values were defined as the highest TC or PFC at either 30- or 60-min. Glucocorticoid sensitivity was measured using the dexamethasone suppression of cytokine production (DSCP) assay, based on interleukin-6 (IL-6) and tumour necrosis factor-α (TNF-α) production from lipopolysaccharide-stimulated (LPS) monocytes. A whole blood sample was incubated with buffer, LPS, or LPS with dexamethasone (Dex). TNF-α and IL-6 concentrations were measured in the supernatants (ng/L). The ratio of cytokine levels between LPS + Dex and LPS indicated glucocorticoid sensitivity. Data from 45 participants were analysed. Peak TC levels ranged from 391 to 1570 nmol/L (median: 618 nmol/L, IQR: 555-729), while PFC levels ranged from 27 to 133 nmol/L (median: 62 nmol/L, IQR: 53-73). No significant associations were found between baseline or peak TC and PFC levels and glucocorticoid sensitivity ratios. Synthetic ACTH (1-24) test results did not predict glucocorticoid sensitivity. Males exhibited higher BMI (median: 26 vs. 22; p = 0.031), however no significant differences were observed in age, baseline PFC and TC levels between sexes. In this exploratory study, ACTH [1-24]-stimulated cortisol responses did not correlate with glucocorticoid sensitivity measured by the DSCP assay. Findings should be interpreted as preliminary and hypothesis-generating given current assay limitations.

Indexed as

Adrenocorticotropic HormoneCytokinesDexamethasoneHydrocortisoneAdultFemaleGlucocorticoidsHealthy VolunteersHumansInterleukin-6LipopolysaccharidesMaleMiddle AgedProspective StudiesTumor Necrosis Factor-alphaYoung AdultAdrenocorticotropic HormoneCytokinesDexamethasoneGlucocorticoidsHydrocortisoneInterleukin-6LipopolysaccharidesTumor Necrosis Factor-alphaAdrenal insufficiencyFree cortisolGlucocorticoid sensitivityStress responseSynthetic ACTH (1-24) stimulationTotal cortisol

Identifiers

PMID41339369
PMCPMC12678605

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.